The DOI matches its Crossref record; 230 of the 241 references it cites were found in a registry or an index; 133 of the 232 sources its claims cite were checked for support.
Main Pathogenic Mechanisms and Recent Advances in COPD Peripheral Skeletal Muscle Wasting
Open accessAbstract
Chronic obstructive pulmonary disease (COPD) is a worldwide prevalent respiratory disease mainly caused by tobacco smoke exposure. COPD is now considered as a systemic disease with several comorbidities. Among them, skeletal muscle dysfunction affects around 20% of COPD patients and is associated with higher morbidity and mortality. Although the histological alterations are well characterized, including myofiber atrophy, a decreased proportion of slow-twitch myofibers, and a decreased capillarization and oxidative phosphorylation capacity, the molecular basis for muscle atrophy is complex and remains partly unknown. Major difficulties lie in patient heterogeneity, accessing patients’ samples, and complex multifactorial process including extrinsic mechanisms, such as tobacco smoke or disuse, and intrinsic mechanisms, such as oxidative stress, hypoxia, or systemic inflammation. Muscle wasting is also a highly dynamic process whose investigation is hampered by the differential protein regulation according to the stage of atrophy. In this review, we report and discuss recent data regarding the molecular alterations in COPD leading to impaired muscle mass, including inflammation, hypoxia and hypercapnia, mitochondrial dysfunction, diverse metabolic changes such as oxidative and nitrosative stress and genetic and epigenetic modifications, all leading to an impaired anabolic/catabolic balance in the myocyte. We recapitulate data concerning skeletal muscle dysfunction obtained in the different rodent models of COPD. Finally, we propose several pathways that should be investigated in COPD skeletal muscle dysfunction in the future.
Overview
AI snapshot
Written from the paper’s full text.
TL;DR
This review summarizes molecular mechanisms of peripheral skeletal muscle wasting in COPD, including inflammation, hypoxia/hypercapnia, mitochondrial dysfunction, oxidative/nitrosative stress, metabolic changes, and genetic/epigenetic alterations. It emphasizes that these pathways converge on an impaired anabolic/catabolic balance and discusses patient heterogeneity, limited sample access, and inconsistent rodent models as barriers to mechanistic understanding.
Key findings
- Skeletal muscle dysfunction affects around 20% of COPD patients in the abstract and up to 35% depending on the considered population in the introduction; histologically it includes myofiber atrophy, decreased cross-sectional area, a shift from oxidative type I/IIa to glycolytic type IIx/IIb fibers, decreased capillarization, and adipose infiltration.
- Multiple intrinsic and extrinsic mechanisms are implicated: inflammation (TNF-α, IL-6, IL-8, IL-18, IL-15, IFN-γ, IL-10), hypoxia and hypercapnia, mitochondrial dysfunction (reduced density/activity, increased mitophagy, apoptosis), oxidative and nitrosative stress, altered amino acid/creatine/calcium metabolism, and genetic/epigenetic modifications including miRNAs.
- These processes converge on impaired muscle mass regulation, with increased catabolism via the ubiquitin–proteasome system (Atrogin-1/MAFbx, MuRF-1), autophagy, and myostatin, alongside decreased IGF/Akt/mTOR protein synthesis signaling; however, data are often contradictory. For example, a transcriptomic study in 79 COPD patients found coordinated mitochondrial gene changes, and a 91-patient quadriceps study found decreased Akt phosphorylation but increased S6- or 4EBP1-phosphorylations.
- Rodent COPD models allow access to all muscles and time-course studies, but reported skeletal muscle alterations are inconsistent across models; the review proposes future investigation of pathways, patient profiles, disease time course, and multiomic approaches.
Methods
- Design: narrative review of current knowledge on molecular alterations leading to decreased muscle mass and function in COPD, with a focus on peripheral skeletal muscle and preclinical models.
- Data/sample: cited human studies using peripheral muscle biopsies (mainly quadriceps/vastus lateralis), cultured myoblasts/myotubes from COPD patients, and rodent COPD models (cigarette smoke exposure, elastase or lipopolysaccharide instillations, transgenic models, etc.).
- Main analysis: qualitative synthesis of histopathological, molecular, and preclinical evidence; no primary data collection, systematic search, or meta-analysis is reported.
Limitations
- Stated in the paper: limited access to patients’ samples because muscle biopsy is not routine; coexisting conditions such as lung cancer introduce bias; the origin of muscle wasting is multifactorial and difficult to assess in heterogeneous sarcopenic patients; peripheral muscles are heterogeneous; muscle wasting is dynamic with molecules up- or downregulated according to stage; no validated clinical criteria exist for the stage of muscle function impairment.
- Stated in the paper: rodent models are inconsistent and not perfectly adapted to human skeletal muscle dysfunction, partly because rodents have four myofiber types (I, IIa, IIx, IIb) whereas humans have three (lacking type IIb); many mechanisms lack direct evidence in COPD muscle (e.g., HIF-1α, calpain, caspase, IL-10, IL-15 human data).
- Evident from the text: as a narrative review, it does not describe a systematic search strategy or formal quality appraisal, and it repeatedly notes conflicting findings across studies due to differences in patient selection, measurement methods, normalization approaches, and timing of assessment.
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Claims the paper makes
133 of 232 cited sources checked · 70 supported · 3 flagged · accuracy not yet measured
At least one cited source doesn’t support this claim or points to a different paper, and none confirmed it — see the verdicts below.
In the paper
“Finally, another study reported an increase in the phosphoULK1/ULK1 ratio—ULK1 is a kinase protein essential for autophagy initiation and progression [183].”
§ Main Pathogenic Mechanisms and Recent Advances in COPD Peripheral Skeletal Muscle Wasting > 9. Consequences on Muscle Mass Regulation > 9.1. Protein Degradation
What the sources say
- Disputedcites [183] Kneppers, 2017, Increased Myogenic and Protein Turnover Signaling in Skeletal Muscle of Chronic Obstructive Pulmonary Disease Patients With Sarcopenia, J. Am. Med. Dir. Assoc. sourceExperimental — accuracy not yet measured
In “Progressively Increased Autophagy Signaling in COPD and Sarcopenic COPD” (Figure 4I, K), the paper reports that relative ULK1 phosphorylation—the phospho-ULK1/ULK1 ratio—was lower at Ser757 in COPD muscle and unaltered at Ser555. It reports only a trend toward higher absolute Ser555 phosphorylation in sarcopenic COPD muscle (Figure 4L), not an increased ratio. Page numbers are unavailable in our copy. (LLM, conf=0.88)
Checked by a reasoning model — may be wrong.
Strength:plain· not yet calibratedCausal:direct· not yet calibratedTests✓ Asserted: passes✓ Checkable: passes? Load-bearing: unclear✓ Based: passes- Disputed
At least one cited source doesn’t support this claim or points to a different paper, and none confirmed it — see the verdicts below.
In the paper
“A significant number of studies reported an increased LC3BII/LC3BI ratio and/or LC3B lipidation (another marker of activation) in COPD quadriceps [123,182,183].”
§ Main Pathogenic Mechanisms and Recent Advances in COPD Peripheral Skeletal Muscle Wasting > 9. Consequences on Muscle Mass Regulation > 9.1. Protein Degradation
What the sources say
- Not checked — no full text of the sourcecites [123] Rodriguez, 2015, Oxidative Stress, Redox Signaling Pathways, and Autophagy in Cachectic Muscles of Male Patients with Advanced COPD and Lung Cancer, Free Radic. Biol. Med. source
- Could not verifycites [182] Guo, 2013, Autophagy in Locomotor Muscles of Patients with Chronic Obstructive Pulmonary Disease, Am. J. Respir. Crit. Care Med. sourceExperimental — accuracy not yet measured
Searches for the LC3BII/LC3BI ratio, LC3B lipidation, and quadriceps findings returned no relevant full-text passage. The only matching statement was labeled Abstract, which is not admissible evidence under the stated rubric. (LLM, conf=0.65)
- Disputedcites [183] Kneppers, 2017, Increased Myogenic and Protein Turnover Signaling in Skeletal Muscle of Chronic Obstructive Pulmonary Disease Patients With Sarcopenia, J. Am. Med. Dir. Assoc. sourceExperimental — accuracy not yet measured
The Results section reports a lower LC3BII/I ratio in sarcopenic COPD patients than in controls, with LC3BII levels unaltered. The Discussion repeats the lower-ratio finding; it does not report increased LC3B lipidation in this cohort. The paper therefore does not support the claimed increase for this cited study. (LLM, conf=0.86)
Checked by a reasoning model — may be wrong.
Tests✓ Asserted: passes✓ Checkable: passes✓ Load-bearing: passes✓ Based: passesThe cited sources support only part of this claim — read each source’s verdict below.
In the paper
“a recent study has found that the downregulation of histone deacetylase 2 (HDAC2) by RNA interference in cultured primary myotubes increased TNF-α production and cell apoptosis [37].”
§ Main Pathogenic Mechanisms and Recent Advances in COPD Peripheral Skeletal Muscle Wasting > 3. Inflammation > 3.1. Tumor Necrosis Factor α (TNF-α)
What the sources say
- Partly supportedcites [37] To, 2017, Reduced HDAC2 in Skeletal Muscle of COPD Patients, Respir. Res. sourceExperimental — accuracy not yet measured
The Results report that HDAC2 siRNA increased TNF-α production and apoptosis in cultured primary skeletal muscle cells. The Methods describe these cells and their transfection but do not identify them as myotubes, so that more specific cell description is unsupported. (LLM, conf=0.86)
Tests✓ Asserted: passes✓ Checkable: passes✓ Load-bearing: passes✓ Based: passes- Partly supported
The cited sources support only part of this claim — read each source’s verdict below.
In the paper
“A specific metabolic alteration in COPD muscle (as opposed to aging muscle for example) is the shift in fiber type, from fatigue-resistant oxidative (type I and type IIa) to force-predominant glycolytic muscle fibers (type IIx and, specifically for rodents, type IIb) [12]”
§ Main Pathogenic Mechanisms and Recent Advances in COPD Peripheral Skeletal Muscle Wasting > 2. Histopathological Alterations of COPD Skeletal Muscle Tissue
What the sources say
- Partly supportedcites [12] Gosker, 2002, Muscle Fiber Type IIX Atrophy Is Involved in the Loss of Fat-Free Mass in Chronic Obstructive Pulmonary Disease, Am. J. Clin. Nutr. sourceExperimental — accuracy not yet measured
The Results and Discussion report selective atrophy of type IIA/IIX and IIX fibers in COPD, along with disturbed enzyme activity in many type IIX fibers. They do not establish a shift in fiber-type composition from types I and IIA toward IIX, or address rodent type IIb fibers. The study compared patients with age-matched controls but did not establish the claimed contrast with aging muscle. (LLM, conf=0.84)
Strength:plain· not yet calibratedCausal:direct· not yet calibratedTests✓ Asserted: passes✓ Checkable: passes? Load-bearing: unclear✓ Based: passes- Partly supported
Every source the paper cites for this claim was checked and supports it.
In the paper
“However, this correlation seems to be consistent only in cachectic patients [26].”
§ Main Pathogenic Mechanisms and Recent Advances in COPD Peripheral Skeletal Muscle Wasting > 3. Inflammation > 3.1. Tumor Necrosis Factor α (TNF-α)
What the sources say
- Supportedcites [26] Eagan, 2012, TNF-α Is Associated with Loss of Lean Body Mass Only in Already Cachectic COPD Patients, Respir. Res. source
The Discussion reports that sustained high circulating TNF-α was associated with faster loss of fat-free mass over three years, with an interaction analysis suggesting this occurred only in patients already cachectic at study entry. The Measurement considerations section likewise says the association with change in fat-free mass index was found only in already cachectic COPD patients. (LLM, conf=0.92)
Strength:hedged· not yet calibratedCausal:correlational· not yet calibratedTests✓ Asserted: passes✓ Checkable: passes? Load-bearing: unclear✓ Based: passes- Supported
The cited sources support only part of this claim — read each source’s verdict below.
In the paper
“In muscle from COPD patients, IL-6 has been reported as unchanged at the transcriptional level (at both stable and exacerbation states) compared to that of healthy controls [27,28].”
§ Main Pathogenic Mechanisms and Recent Advances in COPD Peripheral Skeletal Muscle Wasting > 3. Inflammation > 3.2. Interleukin-6 (IL-6)
What the sources say
- Partly supportedcites [27] Barreiro, 2008, Cytokine Profile in Quadriceps Muscles of Patients with Severe COPD, Thorax sourceExperimental — accuracy not yet measured
The 'Expression of IL6, Interferon c and TGFb' section reports no difference in quadriceps IL-6 between COPD patients and controls, but it measured protein by ELISA, not transcription. 'METHODS Subjects' identifies the patients as having stable COPD; this paper does not report an exacerbation-state comparison. Page numbers were not available in our copy. (LLM, conf=0.90)
- Not checked — no full text of the sourcecites [28] Crul, 2007, Markers of Inflammation and Disuse in Vastus Lateralis of Chronic Obstructive Pulmonary Disease Patients, Eur. J. Clin. Investig. source
Strength:plain· not yet calibratedTests✓ Asserted: passes✓ Checkable: passes? Load-bearing: unclear✓ Based: passes- Partly supported
Every source the paper cites for this claim was checked and supports it.
In the paper
“The decreased fibers’ CSA has been reported to be predominant on type IIx fibers [12].”
§ Main Pathogenic Mechanisms and Recent Advances in COPD Peripheral Skeletal Muscle Wasting > 2. Histopathological Alterations of COPD Skeletal Muscle Tissue
What the sources say
- Supportedcites [12] Gosker, 2002, Muscle Fiber Type IIX Atrophy Is Involved in the Loss of Fat-Free Mass in Chronic Obstructive Pulmonary Disease, Am. J. Clin. Nutr. source
The Discussion reports that fiber atrophy in patients with COPD was mainly confined to type IIA/IIX and IIX fibers and also describes it as predominantly affecting type IIX fibers. The cited claim accurately paraphrases that finding, although the paper also identifies the hybrid IIA/IIX type. (LLM, conf=0.92)
Strength:plain· not yet calibratedCausal:correlational· not yet calibratedTests✓ Asserted: passes✓ Checkable: passes? Load-bearing: unclear✓ Based: passes- Supported
The cited sources support only part of this claim — read each source’s verdict below.
In the paper
“Capillarization has notably been found impaired specifically in type I muscle fibers, which has a deep impact on the muscle’s oxidative capacity [14,15]”
§ Main Pathogenic Mechanisms and Recent Advances in COPD Peripheral Skeletal Muscle Wasting > 2. Histopathological Alterations of COPD Skeletal Muscle Tissue
What the sources say
- Partly supportedcites [14] Eliason, 2010, Alterations in the Muscle-to-Capillary Interface in Patients with Different Degrees of Chronic Obstructive Pulmonary Disease, Respir. Res. sourceExperimental — accuracy not yet measured
The Discussion reports that the muscle-to-capillary interface measure was significantly reduced in type I, but not type IIa, fibres in patients with moderate or severe COPD. The Introduction links capillary supply to oxidative metabolism, but the paper does not establish that this finding had a deep impact on muscle oxidative capacity. (LLM, conf=0.85)
- Not checked — no full text of the sourcecites [15] Whittom, 1998, Histochemical and Morphological Characteristics of the Vastus Lateralis Muscle in Patients with Chronic Obstructive Pulmonary Disease, Med. Sci. Sport. Exerc. source
Strength:plain· not yet calibratedCausal:direct· not yet calibratedTests✓ Asserted: passes✓ Checkable: passes? Load-bearing: unclear✓ Based: passes- Partly supported
The cited sources support only part of this claim — read each source’s verdict below.
In the paper
“Like TNF-α, IL-6 is considered as a “double-edged sword” with proinflammatory (catabolic) and anti-inflammatory (anabolic) effects (see the review in [46]) according to local immune cells and the cytokines’ microenvironment.”
§ Main Pathogenic Mechanisms and Recent Advances in COPD Peripheral Skeletal Muscle Wasting > 3. Inflammation > 3.2. Interleukin-6 (IL-6)
What the sources say
- Partly supportedcites [46] Borges, 2016, Skeletal Muscle Wasting and Renewal: A Pivotal Role of Myokine IL-6, SpringerPlus sourceExperimental — accuracy not yet measured
The Background and Final remarks describe IL-6 as promoting muscle repair in some conditions and muscle wasting in others; the Satellite cells and skeletal muscle renewal section also identifies regenerative and anti-inflammatory roles. The review discusses local immune cells and cytokines, but does not establish that those cells and the cytokine microenvironment determine which of IL-6’s opposing effects occurs. It instead emphasizes IL-6 levels, duration of release, and signaling pathways. (LLM, conf=0.82)
Strength:plain· not yet calibratedCausal:direct· not yet calibratedTests✓ Asserted: passes✓ Checkable: passes? Load-bearing: unclear✓ Based: passes- Partly supported
The cited sources support only part of this claim — read each source’s verdict below.
In the paper
“Two studies outside the COPD context also point towards a prominent role of the Toll-like receptor (TLR)-4 pathway in muscle wasting, via the activation of the p38-MAPK atrophy pathway [63,64].”
§ Main Pathogenic Mechanisms and Recent Advances in COPD Peripheral Skeletal Muscle Wasting > 3. Inflammation > 3.8. Other Myokines
What the sources say
- Supportedcites [63] Doyle, 2011, Toll-like Receptor 4 Mediates Lipopolysaccharide-Induced Muscle Catabolism via Coordinate Activation of Ubiquitin-Proteasome and Autophagy-Lysosome Pathways, FASEB J. source
The Discussion (page not provided) states that TLR4 regulates muscle proteolysis and that p38 MAPK mediates its catabolic signaling. The Results also report that p38 MAPK inhibition abolished LPS-induced muscle proteolysis in mice. This supports the claim for this study outside the COPD context. (LLM, conf=0.94)
- Partly supportedcites [64] Tang, 2010, TLR4 Activation Is Required for IL-17–Induced Multiple Tissue Inflammation and Wasting in Mice, J. Immunol. sourceExperimental — accuracy not yet measured
The section on TLR4-deficient mice reports that they were protected from IL-17-induced gastrocnemius muscle atrophy, supporting a role for TLR4 in muscle wasting outside COPD. The paper attributes the atrophy to the ubiquitin-proteasome pathway, but the passages do not establish activation of a p38-MAPK atrophy pathway (searched: p38-MAPK, p38). Page numbers were unavailable in our copy. (LLM, conf=0.88)
Strength:plain· not yet calibratedCausal:direct· not yet calibratedTests✓ Asserted: passes✓ Checkable: passes? Load-bearing: unclear✓ Based: passes- Supported
- It may state two separate claims as one. 97
- Probably not a substantial claim. 23
At least one cited source doesn’t support this claim or points to a different paper, and none confirmed it — see the verdicts below.
In the paper
“While some authors have found an increased COX activity in COPD patients with resting hypoxemia [96] and with exercise hypoxemia [97], others have not found any significant increase [98].”
§ Main Pathogenic Mechanisms and Recent Advances in COPD Peripheral Skeletal Muscle Wasting > 5. Mitochondrial Dysfunction > 5.2. Reduced Mitochondrial Activity
What the sources say
- Not checked — no full text of the sourcecites [96] Sauleda, 1998, Cytochrome Oxidase Activity and Mitochondrial Gene Expression in Skeletal Muscle of Patients with Chronic Obstructive Pulmonary Disease, Am. J. Respir. Crit. Care Med. source
- Disputedcites [97] Godoy, 2009, Abnormal Mitochondrial Function in Locomotor and Respiratory Muscles of COPD Patients, Eur. Respir. J. sourceExperimental — accuracy not yet measured
The citation [98] supports the clause saying that others found no significant increase in COX activity. In the Mitochondrial function section, this paper instead reports significantly higher COX activity in COPD patients than in controls in both muscles studied; the Previous studies section says its results agree with an earlier report of increased COX activity. The supplied passages do not give page numbers. (LLM, conf=0.93)
Checked by a reasoning model — may be wrong.
- Not checked — no full text of the sourcecites [98] Picard, 2008, The Mitochondrial Phenotype of Peripheral Muscle in Chronic Obstructive Pulmonary Disease: Disuse or Dysfunction?, Am. J. Respir. Crit. Care Med. source
Strength:plain· not yet calibratedCausal:correlational· not yet calibratedTests✓ Asserted: passes✓ Checkable: passes? Load-bearing: unclear✓ Based: passesIt may state two separate claims as one.
The cited sources support only part of this claim — read each source’s verdict below.
In the paper
“COPD should not be limited to its respiratory features and is now considered as a systemic inflammatory disease implicating a wild range of cytokines and chemokines [5] and including several comorbidities.”
§ Main Pathogenic Mechanisms and Recent Advances in COPD Peripheral Skeletal Muscle Wasting > 1. Introduction
What the sources say
- Partly supportedcites [5] Henrot, P., Prevel, R., Berger, P., and Dupin, I. (2019). Chemokines in COPD: From Implication to Therapeutic Use. Int. J. Mol. Sci., 20. sourceExperimental — accuracy not yet measured
The Introduction identifies chemokines as cytokines with a pivotal role in COPD, and §3 describes chemokines produced in both the lung and systemic circulation. But §3.3.2 describes a systemic inflammatory response specifically during virus-associated exacerbations; it does not establish the broader characterization of COPD as a systemic inflammatory disease. The comorbidities phrase follows the citation and is not assessed as attributed to this source. (LLM, conf=0.82)
Strength:plain· not yet calibratedTests✓ Asserted: passes✓ Checkable: passes✗ Load-bearing: fails✓ Based: passesProbably not a substantial claim. The paper’s conclusions may not depend on it. It may state two separate claims as one.
- Partly supported
The sources with a verdict support this claim; the rest weren’t checked yet, have no full text we could read, or their verdicts aren’t rated yet.
In the paper
“Structural alterations of peripheral skeletal muscle are well characterized and include a global muscle atrophy (with both loss in number and size of muscle fibers), macroscopically reflected by a decrease in thigh diameter [11] and microscopically reflected by a decreased fibers’ cross-sectional area (CSA) [12]”
§ Main Pathogenic Mechanisms and Recent Advances in COPD Peripheral Skeletal Muscle Wasting > 2. Histopathological Alterations of COPD Skeletal Muscle Tissue
What the sources say
- Not checked — no full text of the sourcecites [11] Bernard, 1998, Peripheral Muscle Weakness in Patients with Chronic Obstructive Pulmonary Disease, Am. J. Respir. Crit. Care Med. source
- Supportedcites [12] Gosker, 2002, Muscle Fiber Type IIX Atrophy Is Involved in the Loss of Fat-Free Mass in Chronic Obstructive Pulmonary Disease, Am. J. Clin. Nutr. source
Citation [12] is attached to the microscopic finding of decreased muscle-fiber cross-sectional area, not the separate thigh-diameter claim cited to [11]. The Results report lower overall mean fiber CSA in patients with COPD than in controls, with the reduction concentrated in IIA/IIX and IIX fibers. Page numbers were not available in our copy. (LLM, conf=0.93)
Tests✓ Asserted: passes✓ Checkable: passes✓ Load-bearing: passes✓ Based: passesIt may state two separate claims as one.
The sources with a verdict support this claim; the rest weren’t checked yet, have no full text we could read, or their verdicts aren’t rated yet.
In the paper
“with regards to muscular TNF-α, significantly elevated, decreased, and unaltered levels have been reported in the quadriceps of COPD patients [27,28,29], or even undetected at the protein level [30,31]”
§ Main Pathogenic Mechanisms and Recent Advances in COPD Peripheral Skeletal Muscle Wasting > 3. Inflammation > 3.1. Tumor Necrosis Factor α (TNF-α)
What the sources say
- Supportedcites [27] Barreiro, 2008, Cytokine Profile in Quadriceps Muscles of Patients with Severe COPD, Thorax source
The Discussion and ELISA results report significantly reduced quadriceps TNF-α protein levels in patients with severe COPD compared with controls. This supports the 'decreased' finding in the sentence’s list of reports; the other findings are attributed to other citations. (LLM, conf=0.94)
- Not checked — no full text of the sourcecites [28] Crul, 2007, Markers of Inflammation and Disuse in Vastus Lateralis of Chronic Obstructive Pulmonary Disease Patients, Eur. J. Clin. Investig. source
- Supportedcites [29] Torres, 2005, Skeletal Muscle Inflammation and Nitric Oxide in Patients with COPD, Eur. Respir. J. source
The Muscle biopsy section identifies the sampled muscle as the vastus lateralis of the quadriceps. The Results report markedly higher skeletal-muscle TNF-α in COPD patients than in healthy controls, supporting the elevated-level finding for which this source is cited. The other findings in the citing sentence are accompanied by other citations. (LLM, conf=0.92)
- Supportedcites [30] Koechlin, 2005, Hypoxaemia Enhances Peripheral Muscle Oxidative Stress in Chronic Obstructive Pulmonary Disease, Thorax source
The citation to this paper supports the clause about TNF-α being undetected, not the differing levels attributed to [27–29]. The Inflammatory markers section reports that muscle TNF-α was not detected by immunostaining in quadriceps biopsy specimens, either at rest or after exercise, in either COPD group. (LLM, conf=0.94)
- Could not verifycites [31] Remels, 2010, TNF-α Impairs Regulation of Muscle Oxidative Phenotype: Implications for Cachexia?, FASEB J. sourceExperimental — accuracy not yet measured
The retrieved copy contains the paper’s title and bibliographic material (section labeled Abstract, no page), but no passage about quadriceps TNF-α levels in COPD patients. Searches for elevated, decreased, unaltered, and undetected muscle TNF-α did not find evidence to assess the claim. (LLM, conf=0.70)
Strength:plain· not yet calibratedTests✓ Asserted: passes✓ Checkable: passes? Load-bearing: unclear✓ Based: passesIt may state two separate claims as one.
- Supported
The cited sources support only part of this claim — read each source’s verdict below.
In the paper
“Circulating IL-6 is also classically elevated in COPD patients compared to healthy subjects, both during and outside exacerbations [44] and associated with reduced quadriceps strength [45].”
§ Main Pathogenic Mechanisms and Recent Advances in COPD Peripheral Skeletal Muscle Wasting > 3. Inflammation > 3.2. Interleukin-6 (IL-6)
What the sources say
- Partly supportedcites [44] Sin, 2008, Interleukin-6: A Red Herring or a Real Catch in COPD?, Chest sourceExperimental — accuracy not yet measured
The Interleukin-6 section links circulating IL-6 to COPD exacerbations, and the References list a study reporting elevated serum IL-6 during acute exacerbations. But its comparison with healthy controls during clinical stability concerns CRP, fibrinogen, leukocytes, and platelets—not IL-6—so it does not establish that part of the claim. Reduced quadriceps strength has a separate citation [45] in the citing sentence and is not judged against this source. (LLM, conf=0.83)
- Supportedcites [45] Yende, 2006, Inflammatory Markers Are Associated with Ventilatory Limitation and Muscle Dysfunction in Obstructive Lung Disease in Well Functioning Elderly Subjects, Thorax source
Citation [45] is attached to the association with reduced quadriceps strength, not the preceding claim about IL-6 during and outside exacerbations. The Discussion reports that IL-6 levels were inversely associated with quadriceps strength in participants with stable obstructive lung disease; the study population was well-functioning older adults. (LLM, conf=0.92)
Strength:plain· not yet calibratedCausal:correlational· not yet calibratedTests✓ Asserted: passes✓ Checkable: passes? Load-bearing: unclear✓ Based: passesIt may state two separate claims as one.
- Partly supported
Every source the paper cites for this claim was checked and supports it.
In the paper
“Chronic, low-grade inflammation induces muscle catabolism via pleiotropic mechanisms mediated by the inflammatory secretome [20], whereas acute inflammation (exercise-mediated or in acute muscle injury models) activates anabolic pathways leading to muscle regeneration.”
§ Main Pathogenic Mechanisms and Recent Advances in COPD Peripheral Skeletal Muscle Wasting > 3. Inflammation
What the sources say
- Supportedcites [20] Nelke, 2019, Skeletal Muscle as Potential Central Link between Sarcopenia and Immune Senescence, EBioMedicine source
The cited paper’s section “Sarcopenia and immune senescence: a bidirectional link” states the clause immediately preceding citation [20] nearly verbatim. The acute-inflammation clause follows the citation and is not attributed to this source by that citation. (LLM, conf=0.95)
Tests✓ Asserted: passes✓ Checkable: passes✓ Load-bearing: passes✓ Based: passesIt may state two separate claims as one.
- Supported
Every source the paper cites for this claim was checked and supports it.
In the paper
“The authors also evidenced a decrease of HDAC2 level in the quadriceps of COPD patients, associated with an increase in the NF-кB pathway.”
§ Main Pathogenic Mechanisms and Recent Advances in COPD Peripheral Skeletal Muscle Wasting > 3. Inflammation > 3.1. Tumor Necrosis Factor α (TNF-α)
What the sources say
- Supportedcites [37] To, 2017, Reduced HDAC2 in Skeletal Muscle of COPD Patients, Respir. Res. source
The Abstract’s Methods and results report significantly lower HDAC2 protein in quadriceps biopsies from COPD patients and significantly higher NF-κB DNA-binding activity, which correlated with the HDAC2 decrease. The Discussion likewise describes increased NF-κB activity in skeletal muscle from COPD patients. (LLM, conf=0.94)
Tests✓ Asserted: passes✓ Checkable: passes✓ Load-bearing: passes✓ Based: passesIt may state two separate claims as one.
- Supported
The cited sources support only part of this claim — read each source’s verdict below.
In the paper
“In myocytes, the binding of TNF-α to its receptor TNF-R activates the p38-mitogen-activated protein kinase (MAPK) pathway, leading to a silencing of target genes such as Pax7 and Notch1 (via an epigenetic control), promoting satellite cell differentiation into myotubes [39]”
§ Main Pathogenic Mechanisms and Recent Advances in COPD Peripheral Skeletal Muscle Wasting > 3. Inflammation > 3.1. Tumor Necrosis Factor α (TNF-α)
What the sources say
- Partly supportedcites [39] Tidball, 2017, Regulation of Muscle Growth and Regeneration by the Immune System, Nat. Rev. Immunol. sourceExperimental — accuracy not yet measured
In “Muscle–myeloid cell interactions during the early, proliferative stage of muscle regeneration” (page unavailable), the review describes TNF signalling through p38α repressing PAX7 via EZH2 and promoting differentiation of myogenic precursor cells. The same section describes TNF-induced epigenetic silencing of NOTCH1, but does not establish that p38α mediates that silencing; it also does not specify TNF-receptor binding as the initiating step or directly link this pathway to myotube formation. (LLM, conf=0.85)
Strength:plain· not yet calibratedCausal:direct· not yet calibratedTests✓ Asserted: passes✓ Checkable: passes? Load-bearing: unclear✓ Based: passesIt may state two separate claims as one.
- Partly supported
Every source the paper cites for this claim was checked and supports it.
In the paper
“However, inflammation is not the sole driver as exercise can affect factors regulating muscle hypertrophy and regeneration without affecting the levels of systemic or local muscle inflammation [19].”
§ Main Pathogenic Mechanisms and Recent Advances in COPD Peripheral Skeletal Muscle Wasting > 3. Inflammation
What the sources say
- Supportedcites [19] Vogiatzis, 2007, Effects of Rehabilitative Exercise on Peripheral Muscle TNFalpha, IL-6, IGF-I and MyoD Expression in Patients with COPD, Thorax source
The Discussion reports that exercise training increased factors regulating muscle hypertrophy and regeneration in patients with COPD while neither systemic inflammatory mediator levels nor local muscle TNFα and IL-6 expression decreased. This supports the claim that muscle adaptation can occur without a reduction in the measured inflammation markers. No page number is provided in our copy. (LLM, conf=0.93)
Tests✓ Asserted: passes✓ Checkable: passes✓ Load-bearing: passes✓ Based: passesIt may state two separate claims as one.
- Supported
Every source the paper cites for this claim was checked and supports it.
In the paper
“HIF1α and its downstream target vascular endothelial growth factor (VEGF) were found elevated in quadriceps biopsies of COPD patients and correlated to the level of muscular TNF-α.”
§ Main Pathogenic Mechanisms and Recent Advances in COPD Peripheral Skeletal Muscle Wasting > 3. Inflammation > 3.1. Tumor Necrosis Factor α (TNF-α)
What the sources say
- Supportedcites [36] Remels, 2015, TNF-α-Induced NF-ΚB Activation Stimulates Skeletal Muscle Glycolytic Metabolism through Activation of HIF-1α, Endocrinology source
The Subjects section identifies the samples as quadriceps muscle biopsies from COPD patients. The results section reports elevated HIF-1α and VEGF mRNA compared with controls, with the increases most pronounced in patients with high muscle TNF-α; the Discussion describes this as an association. The source supports the claimed relationship, though it reports expression and association rather than a formal correlation of each marker with TNF-α. (LLM, conf=0.90)
Strength:plain· not yet calibratedCausal:correlational· not yet calibratedTests✓ Asserted: passes✓ Checkable: passes? Load-bearing: unclear✓ Based: passesIt may state two separate claims as one.
- Supported
The cited sources support only part of this claim — read each source’s verdict below.
In the paper
“therapies against TNF-α have not proven to be effective for various outcomes such as dyspnea or a number of exacerbations [43], suggesting that this cytokine is not the primary or at least the sole driver of COPD inflammation.”
§ Main Pathogenic Mechanisms and Recent Advances in COPD Peripheral Skeletal Muscle Wasting > 3. Inflammation > 3.1. Tumor Necrosis Factor α (TNF-α)
What the sources say
- Partly supportedcites [43] Aaron, 2013, TNFα Antagonists for Acute Exacerbations of COPD: A Randomised Double-Blind Controlled Trial, Thorax sourceExperimental — accuracy not yet measured
The Secondary outcomes section (page unavailable) reports that dyspnoea improved in both groups, with no significant difference between etanercept and prednisone. The Discussion (page unavailable) also reports no benefit of etanercept over prednisone for treating acute exacerbations and cites a separate trial finding no dyspnoea benefit from infliximab in stable COPD. This paper does not establish that TNF-α therapies reduce the number of exacerbations; its own trial studied treatment of an exacerbation, not prevention of future ones. (LLM, conf=0.86)
Strength:hedged· not yet calibratedTests✓ Asserted: passes✓ Checkable: passes? Load-bearing: unclear✓ Based: passesIt may state two separate claims as one.
- Partly supported
The sources with a verdict support this claim; the rest weren’t checked yet, have no full text we could read, or their verdicts aren’t rated yet.
In the paper
“the pilot study of Tsujinaka and colleagues showed that transgenic mice chronically overexpressing IL-6 exhibit a marked muscle atrophy [47]; however, the knockout of IL-6 was not sufficient to prevent sarcopenia in a sepsis mouse model [48].”
§ Main Pathogenic Mechanisms and Recent Advances in COPD Peripheral Skeletal Muscle Wasting > 3. Inflammation > 3.2. Interleukin-6 (IL-6)
What the sources say
- Supportedcites [47] Tsujinaka, 1996, Interleukin 6 Receptor Antibody Inhibits Muscle Atrophy and Modulates Proteolytic Systems in Interleukin 6 Transgenic Mice, J. Clin. Investig. source
The Discussion states that chronic IL-6 overproduction in transgenic mice causes muscle weight loss, and the Abstract reports muscle atrophy in those mice. The sepsis-model knockout finding has a separate citation [48] and is not attributed to this paper. (LLM, conf=0.93)
- Not checked — no full text of the sourcecites [48] Williams, 1998, Sepsis in Mice Stimulates Muscle Proteolysis in the Absence of IL-6, Am. J. Physiol. source
Strength:plain· not yet calibratedCausal:direct· not yet calibratedTests✓ Asserted: passes✓ Checkable: passes? Load-bearing: unclear✓ Based: passesIt may state two separate claims as one.
- Supported
The cited sources support only part of this claim — read each source’s verdict below.
In the paper
“Adipose tissue infiltration has also been reported in COPD muscle, in a similar way to senescent muscle in the aging population, particularly in the obese sarcopenic phenotype where adipose inflammation leads to the redistribution of fat to the intra-abdominal area and skeletal muscle tissue [16,17]”
§ Main Pathogenic Mechanisms and Recent Advances in COPD Peripheral Skeletal Muscle Wasting > 2. Histopathological Alterations of COPD Skeletal Muscle Tissue
What the sources say
- Partly supportedcites [16] Persson, 2022, Skeletal Myosteatosis Is Associated with Systemic Inflammation and a Loss of Muscle Bioenergetics in Stable COPD, J. Inflamm. Res. sourceExperimental — accuracy not yet measured
The Introduction defines muscle fat infiltration in COPD, and the Discussion reports excess thigh-muscle fat infiltration and visceral adipose tissue in the COPD cohort. The paper does not establish that infiltration occurs particularly in an obese sarcopenic phenotype or that adipose inflammation causes fat to redistribute into the abdomen and muscle. Instead, it describes those fat deposits as possible sources of systemic inflammation. (LLM, conf=0.88)
- Partly supportedcites [17] Li, 2022, Pathogenesis of Sarcopenia and the Relationship with Fat Mass: Descriptive Review, J. Cachexia Sarcopenia Muscle sourceExperimental — accuracy not yet measured
The Abstract and Figure 2 caption describe ageing-related adipose inflammation redistributing fat to visceral depots and skeletal muscle, with a possible contribution to sarcopenic obesity (page numbers unavailable). The section on chronic disease mentions muscle fat infiltration in COPD, but specifically discusses lean patients; it does not establish that this process occurs particularly in an obese sarcopenic COPD phenotype. (LLM, conf=0.88)
Strength:plain· not yet calibratedCausal:direct· not yet calibratedTests✓ Asserted: passes✓ Checkable: passes? Load-bearing: unclear✓ Based: passesIt may state two separate claims as one.
- Partly supported
Every source the paper cites for this claim was checked and supports it.
In the paper
“a mouse model exposed to CS and exhibiting increased circulating TNF-α levels, which were correlated to detrimental outcomes such as muscle mass, decreased capillarization, and increased catabolism [41].”
§ Main Pathogenic Mechanisms and Recent Advances in COPD Peripheral Skeletal Muscle Wasting > 3. Inflammation > 3.1. Tumor Necrosis Factor α (TNF-α)
What the sources say
- Supportedcites [41] Tang, 2010, TNF-Alpha-Mediated Reduction in PGC-1alpha May Impair Skeletal Muscle Function after Cigarette Smoke Exposure, J. Cell. Physiol. source
The Discussion (Early COPD-like locomotor skeletal muscle phenotype; page unavailable) reports higher circulating TNF-α in smoke-exposed mice alongside reduced capillarity and atrophy-related gene expression. The Discussion summary also reports muscle atrophy, while the Results (Gene expression of muscle ubiquitin ligases; page unavailable) document increases in atrogin-1 and MuRF-1, supporting the claim’s reference to catabolic changes. (LLM, conf=0.87)
Strength:plain· not yet calibratedCausal:correlational· not yet calibratedTests✓ Asserted: passes✓ Checkable: passes? Load-bearing: unclear✓ Based: passesIt may state two separate claims as one.
- Supported
The cited sources support only part of this claim — read each source’s verdict below.
In the paper
“IFN-γ has been reported as unchanged at the protein level in COPD quadriceps compared to controls [27]. However, a recent transcriptional analysis shows a globally downregulated interferon response in COPD quadriceps [56].”
§ Main Pathogenic Mechanisms and Recent Advances in COPD Peripheral Skeletal Muscle Wasting > 3. Inflammation > 3.6. Interferon-γ (IFN-γ)
What the sources say
- Supportedcites [27] Barreiro, 2008, Cytokine Profile in Quadriceps Muscles of Patients with Severe COPD, Thorax source
The “Expression of IL6, Interferon c and TGFb” section reports no significant difference in quadriceps interferon-γ protein levels between patients with COPD and controls, measured by ELISA. The separate transcriptional-analysis statement cites [56], not this source. (LLM, conf=0.94)
- Partly supportedcites [56] Cano, 2018, Network Modules Uncover Mechanisms of Skeletal Muscle Dysfunction in COPD Patients, J. Transl. Med. sourceExperimental — accuracy not yet measured
The Results section on skeletal muscle alterations at rest reports systematic down-regulation of IFIT genes in an interferon-response module. The Methods identify the sampled muscle as the vastus lateralis, part of the quadriceps. The paper does not establish that the interferon response as a whole was globally downregulated; the separate protein-level claim is cited to [27], not this source. (LLM, conf=0.82)
Load-bearingStrength:plain· not yet calibratedTests✓ Asserted: passes✓ Checkable: passes✓ Load-bearing: passes✓ Based: passesIt may state two separate claims as one.
- Supported
The cited sources support only part of this claim — read each source’s verdict below.
In the paper
“a recent study pointed out a possible role of intermittent hypoxia (such as the nocturnal hypoxemia seen in obstructive sleep apnea disorder, frequent among COPD patients [83]) in skeletal muscle wasting, driven by mitochondrial dysfunction and a lower activity [84].”
§ Main Pathogenic Mechanisms and Recent Advances in COPD Peripheral Skeletal Muscle Wasting > 4. Hypoxia and Hypercapnia
What the sources say
- Partly supportedcites [84] Attaway, 2022, Adaptive Exhaustion during Prolonged Intermittent Hypoxia Causes Dysregulated Skeletal Muscle Protein Homeostasis, J. Physiol. sourceExperimental — accuracy not yet measured
The Results report smaller myotube diameter during prolonged intermittent hypoxia and reduced mitochondrial oxidative function and respiratory-chain complex activity. The paper does not establish lower physical activity as a driver of muscle wasting; its reported lower activity is mitochondrial complex activity. It also distinguishes its prolonged nocturnal-hypoxia model from the brief episodes typical of obstructive sleep apnea. (LLM, conf=0.82)
Tests✓ Asserted: passes✓ Checkable: passes✓ Load-bearing: passes✓ Based: passesIt may state two separate claims as one.
- Partly supported
The cited sources support only part of this claim — read each source’s verdict below.
In the paper
“The same authors confirmed their observations in 2017 on a different cohort of COPD patients matched to healthy controls based on the same physical activity, in order to avoid disuse bias. They observed a diminished state 3 CI-driven respiration, and a trend to a lower state 3:CI+CII driven respiration.”
§ Main Pathogenic Mechanisms and Recent Advances in COPD Peripheral Skeletal Muscle Wasting > 5. Mitochondrial Dysfunction > 5.2. Reduced Mitochondrial Activity
What the sources say
- Partly supportedcites [101] Gifford, 2015, Quadriceps Exercise Intolerance in Patients with Chronic Obstructive Pulmonary Disease: The Potential Role of Altered Skeletal Muscle Mitochondrial Respiration, J. Appl. Physiol. sourceExperimental — accuracy not yet measured
Split into 2 atoms — 0 confirmed, 2 partially supported, 0 disputed, 0 misattributed, 0 unverifiable. Expand the claim to see per-atom verdicts.
Load-bearingStrength:plain· not yet calibratedTests✓ Asserted: passes✓ Checkable: passes✓ Load-bearing: passes✓ Based: passesIt may state two separate claims as one.
- Partly supported
Every source the paper cites for this claim was checked and supports it.
In the paper
“they concluded that this reduction was largely driven by diminished CI-driven respiration rather than CII-driven respiration.”
§ Main Pathogenic Mechanisms and Recent Advances in COPD Peripheral Skeletal Muscle Wasting > 5. Mitochondrial Dysfunction > 5.2. Reduced Mitochondrial Activity
What the sources say
- Supportedcites [101] Gifford, 2015, Quadriceps Exercise Intolerance in Patients with Chronic Obstructive Pulmonary Disease: The Potential Role of Altered Skeletal Muscle Mitochondrial Respiration, J. Appl. Physiol. source
The section “CI vs. CII-driven respiration in COPD” explicitly states that the reduction in State 3:CI+CII in patients with COPD was largely driven by diminished CI-driven, rather than CII-driven, respiration. It also reports that State 3:CI was significantly reduced compared with controls while State 3:CII was not. (LLM, conf=0.95)
Tests✓ Asserted: passes✓ Checkable: passes✓ Load-bearing: passes✓ Based: passesProbably not a substantial claim.
- Supported
Every source the paper cites for this claim was checked and supports it.
In the paper
“Importantly, transfecting the defective CII subunit C to mice muscles significantly increased both mitochondrial function (respiration) and oxidative myofibers’ proportion, indicating that mitochondrial function could regulate the muscle fiber phenotype in vivo.”
§ Main Pathogenic Mechanisms and Recent Advances in COPD Peripheral Skeletal Muscle Wasting > 5. Mitochondrial Dysfunction > 5.2. Reduced Mitochondrial Activity
What the sources say
- Supportedcites [102] Balnis, 2021, Succinate Dehydrogenase (SDH)-Subunit C Regulates Muscle Oxygen Consumption and Fatigability in an Animal Model of Pulmonary Emphysema, Am. J. Respir. Cell Mol. Biol. source
In the in vivo overexpression section (page unavailable), the paper reports significantly increased oxygen consumption after SDHC electroporation in IL13 transgenic mouse muscle. The fiber-type section (page unavailable) reports more oxidative type 2A and 2X fibers and fewer type 2B fibers, while cautiously suggesting that fiber identity could change downstream of increased oxidative capacity. The intervention restored expression of downregulated SDHC; the paper does not describe transfecting a defective SDHC construct. (LLM, conf=0.88)
Tests✓ Asserted: passes✓ Checkable: passes✓ Load-bearing: passes✓ Based: passesIt may state two separate claims as one.
- Supported
Every source the paper cites for this claim was checked and supports it.
In the paper
“only one study investigated HIF-1α expression and found an increased mRNA level in the quadriceps of COPD patients, related to increased TNF-α signaling [36].”
§ Main Pathogenic Mechanisms and Recent Advances in COPD Peripheral Skeletal Muscle Wasting > 4. Hypoxia and Hypercapnia
What the sources say
- Supportedcites [36] Remels, 2015, TNF-α-Induced NF-ΚB Activation Stimulates Skeletal Muscle Glycolytic Metabolism through Activation of HIF-1α, Endocrinology source
The Subjects section identifies quadriceps biopsies from COPD patients and healthy controls. The HIF-1α and VEGF results section reports higher muscle HIF-1α mRNA in COPD patients, most pronounced in those with high muscle TNF-α; the Discussion describes this as an association with TNF-α expression. (LLM, conf=0.90)
Strength:hedged· not yet calibratedCausal:correlational· not yet calibratedTests✓ Asserted: passes✓ Checkable: passes? Load-bearing: unclear✓ Based: passesIt may state two separate claims as one.
- Supported
The cited sources support only part of this claim — read each source’s verdict below.
In the paper
“Hypoxia seems to play a prominent role in the skeletal muscle wasting of COPD patients, as suggested by a network-analysis transcriptomic studies evidencing upregulation of four histone deacetylase in the muscle of COPD patients (HDAC 9 and 4, SIRT 2 and 3) compared to that of healthy subjects and correlated with oxygen availability [66].”
§ Main Pathogenic Mechanisms and Recent Advances in COPD Peripheral Skeletal Muscle Wasting > 4. Hypoxia and Hypercapnia
What the sources say
- Partly supportedcites [66] Turan, N., Kalko, S., Stincone, A., Clarke, K., Sabah, A., Howlett, K., Curnow, S.J., Rodriguez, D.A., Cascante, M., and O’Neill, L. (2011). A Systems Biology Approach Identifies Molecular Networks Defining Skeletal Muscle Abnormalities in Chronic Obstructive Pulmonary Disease. PLoS Comput. Biol., 7. sourceExperimental — accuracy not yet measured
Split into 2 atoms — 0 confirmed, 2 partially supported, 0 disputed, 0 misattributed, 0 unverifiable. Expand the claim to see per-atom verdicts.
Tests✓ Asserted: passes✓ Checkable: passes✓ Load-bearing: passes✓ Based: passesIt may state two separate claims as one.
- Partly supported
The cited sources support only part of this claim — read each source’s verdict below.
In the paper
“The expressions of electron transport chain (ETC) complex proteins I, II, III, and V have, for example, been reported as unchanged in patients with mild COPD (GOLD II) but decreased in patients with severe or very severe COPD (GOLD III-IV) [89].”
§ Main Pathogenic Mechanisms and Recent Advances in COPD Peripheral Skeletal Muscle Wasting > 5. Mitochondrial Dysfunction > 5.1. Reduced Mitochondrial Density/Dynamics
What the sources say
- Partly supportedcites [89] Haji, 2020, COPDMAP consortium Mitochondrial Dysfunction in Airways and Quadriceps Muscle of Patients with Chronic Obstructive Pulmonary Disease, Respir. Res. sourceExperimental — accuracy not yet measured
The Results section on quadriceps muscle reports unchanged levels of ETC complex proteins I, II, III and V in GOLD Grade 2 patients and significantly reduced levels in GOLD Grade 3/4 patients. The claim omits that this pattern is specific to quadriceps muscle: the airway Results report reduced complex I and II expression in GOLD Grade 2 patients. (LLM, conf=0.86)
Strength:hedged· not yet calibratedCausal:correlational· not yet calibratedTests✓ Asserted: passes✓ Checkable: passes? Load-bearing: unclear✓ Based: passesIt may state two separate claims as one.
- Partly supported
The cited sources support only part of this claim — read each source’s verdict below.
In the paper
“A study showed that exercise training improved functional capacity in both normoxemic and hypoxemic COPD patients, however the structural improvements (increased mitochondrial density, capillary-to-fiber ratio, and fibers’ CSA) occurred only in the normoxemic ones [80].”
§ Main Pathogenic Mechanisms and Recent Advances in COPD Peripheral Skeletal Muscle Wasting > 4. Hypoxia and Hypercapnia
What the sources say
- Partly supportedcites [80] Costes, 2015, Impaired Exercise Training-Induced Muscle Fiber Hypertrophy and Akt/MTOR Pathway Activation in Hypoxemic Patients with COPD, J. Appl. Physiol. sourceExperimental — accuracy not yet measured
Split into 2 atoms — 1 confirmed, 1 partially supported, 0 disputed, 0 misattributed, 0 unverifiable. Expand the claim to see per-atom verdicts.
Tests✓ Asserted: passes✓ Checkable: passes✓ Load-bearing: passes✓ Based: passesIt may state two separate claims as one.
- Partly supported
Every source the paper cites for this claim was checked and supports it.
In the paper
“Only one study investigated dynamin-1-like protein DNML1 (also known as DRP1, a GTPase regulating mitochondrial fission) expression in COPD quadriceps and found a decreased protein level [88].”
§ Main Pathogenic Mechanisms and Recent Advances in COPD Peripheral Skeletal Muscle Wasting > 5. Mitochondrial Dysfunction > 5.1. Reduced Mitochondrial Density/Dynamics
What the sources say
- Supportedcites [88] Leermakers, 2018, Molecular Signalling towards Mitochondrial Breakdown Is Enhanced in Skeletal Muscle of Patients with Chronic Obstructive Pulmonary Disease (COPD), Sci. Rep. source
The Results section reports that DNM1L protein levels were lower in the vastus lateralis (a quadriceps muscle) of patients with COPD than in controls. The Introduction identifies DNM1L as DRP1. The phrase “only one study” describes the citing authors’ survey of the literature, rather than a finding this study needs to establish. (LLM, conf=0.92)
Strength:plain· not yet calibratedTests✓ Asserted: passes✓ Checkable: passes? Load-bearing: unclear✓ Based: passesIt may state two separate claims as one.
- Supported
The cited sources support only part of this claim — read each source’s verdict below.
In the paper
“Remels and colleagues observed low levels of peroxisome proliferator-activated receptor-gamma coactivator 1 alpha (PGC1-α, the master regulator of mitochondrial biogenesis) and its downstream effector, mitochondrial transcription factor A (TFAM), in COPD quadriceps; these differences were further enhanced in cachectic COPD patients [90].”
§ Main Pathogenic Mechanisms and Recent Advances in COPD Peripheral Skeletal Muscle Wasting > 5. Mitochondrial Dysfunction > 5.1. Reduced Mitochondrial Density/Dynamics
What the sources say
- Partly supportedcites [90] Remels, 2007, Peroxisome Proliferator-Activated Receptor Expression Is Reduced in Skeletal Muscle in COPD, Eur. Respir. J. sourceExperimental — accuracy not yet measured
The Methods section identifies the biopsied muscle as quadriceps. The PGC-1a and TFAM results sections report lower PGC-1a mRNA and TFAM protein in COPD, with a further TFAM reduction in cachectic patients. But PGC-1a mRNA did not differ between cachectic and noncachectic patients, and PGC-1a protein was not measured; the claim overstates the cachexia finding for PGC-1a. (LLM, conf=0.93)
Strength:plain· not yet calibratedCausal:correlational· not yet calibratedTests✓ Asserted: passes✓ Checkable: passes? Load-bearing: unclear✓ Based: passesIt may state two separate claims as one.
- Partly supported
The cited sources support only part of this claim — read each source’s verdict below.
In the paper
“During exacerbations, mitochondrial respiration seems to be further decreased, as confirmed by a study investigating the transcriptomic profile of quadriceps biopsies between exacerbating COPD patients and stable COPD controls, and evidencing a decreased aspartate catabolism as well as COX6C activity [104].”
§ Main Pathogenic Mechanisms and Recent Advances in COPD Peripheral Skeletal Muscle Wasting > 5. Mitochondrial Dysfunction > 5.2. Reduced Mitochondrial Activity
What the sources say
- Partly supportedcites [104] Crul, 2010, Gene Expression Profiling in Vastus Lateralis Muscle During an Acute Exacerbation of COPD, Cell. Physiol. Biochem. sourceExperimental — accuracy not yet measured
The Discussion reports downregulated aspartate catabolism and mitochondrial respiratory-chain pathways in vastus lateralis muscle during exacerbation. The Real-time PCR data section reports lower COX6C mRNA in exacerbating patients than in stable COPD patients, but it does not establish decreased COX6C activity; that part of the claim overstates the measurement. (LLM, conf=0.88)
Tests✓ Asserted: passes✓ Checkable: passes✓ Load-bearing: passes✓ Based: passesIt may state two separate claims as one.
- Partly supported
Every source the paper cites for this claim was checked and supports it.
In the paper
“The evidence for DNA damage is scarce but includes higher (8-OHdG) levels in COPD quadriceps compared to controls [87].”
§ Main Pathogenic Mechanisms and Recent Advances in COPD Peripheral Skeletal Muscle Wasting > 6. Oxidative and Nitrosative Stress
What the sources say
- Supportedcites [87] Konokhova, 2016, Failed Upregulation of TFAM Protein and Mitochondrial DNA in Oxidatively Deficient Fibers of Chronic Obstructive Pulmonary Disease Locomotor Muscle, Skelet. Muscle source
The Results section reports 50% higher 8-OHdG in COPD vastus lateralis muscle than in controls; the vastus lateralis is part of the quadriceps. The Discussion says oxidative damage to lipids and proteins had been measured most commonly and describes this as the first finding of higher 8-OHdG in COPD muscle, consistent with the claim that DNA-damage evidence was scarce. Page numbers are not provided in our copy. (LLM, conf=0.93)
Strength:plain· not yet calibratedCausal:correlational· not yet calibratedTests✓ Asserted: passes✓ Checkable: passes? Load-bearing: unclear✓ Based: passesIt may state two separate claims as one.
- Supported
The cited sources support only part of this claim — read each source’s verdict below.
In the paper
“For example, several studies have found an increased lipofuscin accumulation in COPD quadriceps [126] and higher levels of hydroxy-2-nonenal (4-HNE) in quadriceps tissue [87,127], as well as in cultured myotubes from COPD patients [128].”
§ Main Pathogenic Mechanisms and Recent Advances in COPD Peripheral Skeletal Muscle Wasting > 6. Oxidative and Nitrosative Stress
What the sources say
- Not checked — no full text of the sourcecites [126] Allaire, 2002, Lipofuscin Accumulation in the Vastus Lateralis Muscle in Patients with Chronic Obstructive Pulmonary Disease, Muscle Nerve source
- Supportedcites [87] Konokhova, 2016, Failed Upregulation of TFAM Protein and Mitochondrial DNA in Oxidatively Deficient Fibers of Chronic Obstructive Pulmonary Disease Locomotor Muscle, Skelet. Muscle source
The citation to this paper is attached to the higher 4-HNE levels in quadriceps tissue, not to lipofuscin or cultured myotubes. The Results section (‘Higher prevalence of oxidative damage and mtDNA deletions in COPD muscle’) reports that 4-hydroxynonenal adducts were twice as high in COPD vastus lateralis muscle as in age-matched controls. (LLM, conf=0.94)
- Supportedcites [127] Barreiro, 2009, Chronic Endurance Exercise Induces Quadriceps Nitrosative Stress in Patients with Severe COPD, Thorax source
This source is cited for the quadriceps-tissue 4-HNE finding, not the separately cited lipofuscin or cultured-myotube findings. The Muscle redox balance section reports significantly higher baseline HNE-protein adducts in COPD quadriceps than in controls. (LLM, conf=0.94)
- Partly supportedcites [128] Rodriguez, 2015, Reduced Myotube Diameter, Atrophic Signalling and Elevated Oxidative Stress in Cultured Satellite Cells from COPD Patients, J. Cell. Mol. Med. sourceExperimental — accuracy not yet measured
The Results section reports higher measured 4-HNE levels in cultured myotubes from COPD patients than in controls, which supports the portion attributed to this paper. It describes the difference as a tendency (P = 0.065), however, so the unqualified claim of higher levels overstates the evidence. The lipofuscin and quadriceps-tissue claims have other citations. (LLM, conf=0.87)
Strength:plain· not yet calibratedCausal:correlational· not yet calibratedTests✓ Asserted: passes✓ Checkable: passes? Load-bearing: unclear✓ Based: passesIt may state two separate claims as one.
Every source the paper cites for this claim was checked and supports it.
In the paper
“Finally, the antioxidant protein carnosine, mainly present in type II myofibers, has been reported to be unchanged in the muscle of COPD patients compared to healthy controls; however, in COPD patients, carnosine was decreased in the quadriceps of GOLD III–IV patients compared to GOLD I–II, despite their increased proportion of type II myofibers [125].”
§ Main Pathogenic Mechanisms and Recent Advances in COPD Peripheral Skeletal Muscle Wasting > 6. Oxidative and Nitrosative Stress
What the sources say
- Supportedcites [125] Burtin, 2021, Carnosine, Oxidative and Carbonyl Stress, Antioxidants, and Muscle Fiber Characteristics of Quadriceps Muscle of Patients with COPD, J. Appl. Physiol. source
The paper’s conclusion and New & Noteworthy passage state that quadriceps carnosine was similar in patients with COPD and healthy controls. They also report 31% lower carnosine in severe/very severe than mild/moderate COPD, despite a high proportion of fast-twitch fibers. No page number is available in our copy. (LLM, conf=0.93)
Strength:hedged· not yet calibratedTests✓ Asserted: passes✓ Checkable: passes? Load-bearing: unclear✓ Based: passesIt may state two separate claims as one.
- Supported
Every source the paper cites for this claim was checked and supports it.
In the paper
“It is also likely that oxidative stress enhances proteolysis via the calpain and caspase pathways [133], whereas this has not been directly demonstrated in COPD muscle.”
§ Main Pathogenic Mechanisms and Recent Advances in COPD Peripheral Skeletal Muscle Wasting > 6. Oxidative and Nitrosative Stress
What the sources say
- Supportedcites [133] Powers, 2010, Reactive Oxygen Species Are Signalling Molecules for Skeletal Muscle Adaptation, Exp. Physiol. source
The section on redox signalling during prolonged disuse says oxidative stress could contribute to muscle atrophy by activating proteolytic pathways, including calpain and caspase-3. The citation is attached to that proposed mechanism; the subsequent COPD-specific caveat is the citing authors’ qualification. (LLM, conf=0.91)
Strength:hedged· not yet calibratedCausal:conditional· not yet calibratedTests✓ Asserted: passes✓ Checkable: passes? Load-bearing: unclear✓ Based: passesIt may state two separate claims as one.
- Supported
The cited sources support only part of this claim — read each source’s verdict below.
In the paper
“In the muscle, ROS mainly originate from mitochondrial respiration and membrane (NAPDH oxidase). In the lung, by contrast, ROS are produced by alveolar macrophages and activated neutrophils [117].”
§ Main Pathogenic Mechanisms and Recent Advances in COPD Peripheral Skeletal Muscle Wasting > 6. Oxidative and Nitrosative Stress
What the sources say
- Partly supportedcites [117] Barreiro, E. (2016). Role of Protein Carbonylation in Skeletal Muscle Mass Loss Associated with Chronic Conditions. Proteomes, 4. sourceExperimental — accuracy not yet measured
Section 3 says skeletal-muscle ROS are mainly produced by the mitochondrial respiratory chain and also identifies NADPH oxidase as a source. Section 8.2 identifies mitochondria and membrane NADPH oxidase as the main sources specifically in respiratory and limb muscles of patients with severe COPD. Our copy does not support the separate claim that lung ROS are produced by alveolar macrophages and activated neutrophils (searched for alveolar macrophages). (LLM, conf=0.86)
Strength:plain· not yet calibratedCausal:direct· not yet calibratedTests✓ Asserted: passes✓ Checkable: passes? Load-bearing: unclear✓ Based: passesIt may state two separate claims as one.
- Partly supported
The cited sources support only part of this claim — read each source’s verdict below.
In the paper
“Oxidative stress is increased both at the systemic and muscular levels in COPD [10,89,116].”
§ Main Pathogenic Mechanisms and Recent Advances in COPD Peripheral Skeletal Muscle Wasting > 6. Oxidative and Nitrosative Stress
What the sources say
- Not checked — no full text of the sourcecites [10] Barreiro, 2016, Molecular and Biological Pathways of Skeletal Muscle Dysfunction in Chronic Obstructive Pulmonary Disease, Chronic Respir. Dis. source
- Partly supportedcites [89] Haji, 2020, COPDMAP consortium Mitochondrial Dysfunction in Airways and Quadriceps Muscle of Patients with Chronic Obstructive Pulmonary Disease, Respir. Res. sourceExperimental — accuracy not yet measured
The Abstract Results report increased ROS in quadriceps muscle from patients with COPD, supporting the muscular part of the claim. The Background describes increased oxidative-stress markers in COPD, but does not locate them at the systemic level; the reported measurements are from airway and muscle tissue, not systemic samples. (LLM, conf=0.85)
- Not checked — no full text of the sourcecites [116] Mano, 2022, Oxidative Stress Causes Muscle Structural Alterations via P38 MAPK Signaling in COPD Mouse Model, J. Bone Miner. Metab. source
Load-bearingStrength:plain· not yet calibratedTests✓ Asserted: passes✓ Checkable: passes✓ Load-bearing: passes✓ Based: passesIt may state two separate claims as one.
The cited sources support only part of this claim — read each source’s verdict below.
In the paper
“Increased lipid peroxidation has also been observed, possibly favored by reduced UCP3 levels [112].”
§ Main Pathogenic Mechanisms and Recent Advances in COPD Peripheral Skeletal Muscle Wasting > 6. Oxidative and Nitrosative Stress
What the sources say
- Partly supportedcites [112] Gosker, 2003, Uncoupling Protein-3 Content Is Decreased in Peripheral Skeletal Muscle of Patients with COPD, Eur. Respir. J. sourceExperimental — accuracy not yet measured
The Discussion (page unavailable) reports reduced UCP3 in COPD muscle and cites observations of an imbalance between oxygen species and antioxidant status. It does not report increased lipid peroxidation, and says whether reduced UCP3 is involved in defence against reactive oxygen species needs further examination. (LLM, conf=0.85)
Strength:hedged· not yet calibratedCausal:conditional· not yet calibratedTests✓ Asserted: passes✓ Checkable: passes? Load-bearing: unclear✓ Based: passesIt may state two separate claims as one.
- Partly supported
Every source the paper cites for this claim was checked and supports it.
In the paper
“Ferroptosis, a newly discovered type of cell death resulting from iron-dependent lipid peroxide accumulation, has been reported to be increased both in vitro in CS-exposed C2C12 myotubes and in vivo in a mouse model of COPD [129].”
§ Main Pathogenic Mechanisms and Recent Advances in COPD Peripheral Skeletal Muscle Wasting > 6. Oxidative and Nitrosative Stress
What the sources say
- Supportedcites [129] Zhang, 2022, Myostatin/HIF2α-Mediated Ferroptosis Is Involved in Skeletal Muscle Dysfunction in Chronic Obstructive Pulmonary Disease, Int. J. Chronic Obstr. Pulm. Dis. source
The Discussion states that chronic cigarette-smoke exposure induced ferroptosis in skeletal muscles of COPD mice and that the finding was recapitulated in C2C12 myotubes exposed to cigarette-smoke extract (CSE). The Abstract Results also reports ferroptosis-related changes in both models. In vitro, the myotubes received CSE rather than cigarette smoke directly. (LLM, conf=0.94)
Strength:plain· not yet calibratedTests✓ Asserted: passes✓ Checkable: passes? Load-bearing: unclear✓ Based: passesIt may state two separate claims as one.
- Supported
The cited sources support only part of this claim — read each source’s verdict below.
In the paper
“For example, increased Mn-superoxide dismutase (SOD) and Cu-Zn-SOD protein levels have been demonstrated in the quadriceps [118,127], whereas unchanged SOD content and decreased SOD activity have been reported in another study [122], and unchanged MnSOD, Cu/ZnSOD, and catalase expressions in cultured COPD myoblasts and myotubes have been found [128].”
§ Main Pathogenic Mechanisms and Recent Advances in COPD Peripheral Skeletal Muscle Wasting > 6. Oxidative and Nitrosative Stress
What the sources say
- Partly supportedcites [118] Fermoselle, 2012, Does Oxidative Stress Modulate Limb Muscle Atrophy in Severe COPD Patients?, Eur. Respir. J. sourceExperimental — accuracy not yet measured
Split into 3 atoms — 0 confirmed, 1 partially supported, 0 disputed, 0 misattributed, 0 unverifiable, 2 not checked. Expand the claim to see per-atom verdicts.
- Partly supportedcites [127] Barreiro, 2009, Chronic Endurance Exercise Induces Quadriceps Nitrosative Stress in Patients with Severe COPD, Thorax sourceExperimental — accuracy not yet measured
The Muscle redox balance section (page unavailable) reports higher baseline quadriceps SOD activity in patients with COPD than in controls. It does not report increased protein levels of Mn-SOD or Cu-Zn-SOD, which is the specific finding attributed to this paper. The other findings in the citing sentence have separate citations and are not assessed here. (LLM, conf=0.82)
- Not checked — no full text of the sourcecites [122] Rodriguez, 2012, Muscle and Blood Redox Status after Exercise Training in Severe COPD Patients, Free Radic. Biol. Med. source
- Partly supportedcites [128] Rodriguez, 2015, Reduced Myotube Diameter, Atrophic Signalling and Elevated Oxidative Stress in Cultured Satellite Cells from COPD Patients, J. Cell. Mol. Med. sourceExperimental — accuracy not yet measured
Split into 3 atoms — 2 confirmed, 1 partially supported, 0 disputed, 0 misattributed, 0 unverifiable. Expand the claim to see per-atom verdicts.
Strength:boosted· not yet calibratedTests✓ Asserted: passes✓ Checkable: passes? Load-bearing: unclear✓ Based: passesIt may state two separate claims as one.
- Partly supported
Every source the paper cites for this claim was checked and supports it.
In the paper
“Mitochondrial permeability transition pore (mPTP) is a key regulator of mitochondria during cell death [115].”
§ Main Pathogenic Mechanisms and Recent Advances in COPD Peripheral Skeletal Muscle Wasting > 5. Mitochondrial Dysfunction > 5.4. Apoptosis
What the sources say
- Supportedcites [115] Bonora, 2014, The Mitochondrial Permeability Transition Pore and Cancer: Molecular Mechanisms Involved in Cell Death, Front. Oncol. source
The Background on mPTP Structure identifies the mPTP as the pore responsible for mitochondrial permeability transition (MPT). The Introduction describes MPT as a strategic regulator of cell death and explains its effects on mitochondria, supporting the citing sentence’s broad paraphrase. (LLM, conf=0.91)
Strength:plain· not yet calibratedCausal:direct· not yet calibratedTests✓ Asserted: passes✓ Checkable: passes✗ Load-bearing: fails✓ Based: passesProbably not a substantial claim. The paper’s conclusions may not depend on it.
- Supported
The cited sources support only part of this claim — read each source’s verdict below.
In the paper
“Skeletal muscle tissue usually compensates the excessive oxidative stress (induced for example by exercise training) by increasing the levels of antioxidants [122,127], but in COPD, this protective mechanism seems to be defective, although contradictory data have been reported.”
§ Main Pathogenic Mechanisms and Recent Advances in COPD Peripheral Skeletal Muscle Wasting > 6. Oxidative and Nitrosative Stress
What the sources say
- Not checked — no full text of the sourcecites [122] Rodriguez, 2012, Muscle and Blood Redox Status after Exercise Training in Severe COPD Patients, Free Radic. Biol. Med. source
- Partly supportedcites [127] Barreiro, 2009, Chronic Endurance Exercise Induces Quadriceps Nitrosative Stress in Patients with Severe COPD, Thorax sourceExperimental — accuracy not yet measured
The Muscle oxidative stress section reports that exercise increased antioxidant SOD activity in healthy controls but not in patients with severe COPD, supporting a defective exercise-induced response. The Muscle redox balance section also reports higher baseline SOD activity in patients, but the paper does not identify this or other findings as contradictory reports. Its direct evidence is limited to the exercise response studied. (LLM, conf=0.84)
Load-bearingStrength:hedged· not yet calibratedTests✓ Asserted: passes✓ Checkable: passes✓ Load-bearing: passes✓ Based: passesIt may state two separate claims as one.
The cited sources that could be checked couldn’t confirm or dispute this claim.
In the paper
“Since the early reports of Agusti and colleagues and Gosker and colleagues, who observed, respectively, an increased and unchanged myonuclear fragmentation in muscle cells [111,112]”
§ Main Pathogenic Mechanisms and Recent Advances in COPD Peripheral Skeletal Muscle Wasting > 5. Mitochondrial Dysfunction > 5.4. Apoptosis
What the sources say
- Not checked — no full text of the sourcecites [111] Sauleda, 2002, Skeletal Muscle Apoptosis and Weight Loss in Chronic Obstructive Pulmonary Disease, Am. J. Respir. Crit. Care Med. source
- Could not verifycites [112] Gosker, 2003, Uncoupling Protein-3 Content Is Decreased in Peripheral Skeletal Muscle of Patients with COPD, Eur. Respir. J. sourceExperimental — accuracy not yet measured
The Methods describe muscle-fibre staining and protein measurements, while the Results report fibre types and UCP3 content; neither section reports myonuclear fragmentation. Searches for myonuclear fragmentation and apoptosis-related nuclear measures found no passage addressing whether fragmentation was unchanged in COPD patients. Page numbers were unavailable in our copy. (LLM, conf=0.76)
Strength:plain· not yet calibratedTests✓ Asserted: passes✓ Checkable: passes? Load-bearing: unclear✓ Based: passesIt may state two separate claims as one.
The cited sources support only part of this claim — read each source’s verdict below.
In the paper
“Surprisingly, few data are available to date in COPD despite the fact that caspase-induced apoptosis is a known contributor of muscle wasting [114].”
§ Main Pathogenic Mechanisms and Recent Advances in COPD Peripheral Skeletal Muscle Wasting > 5. Mitochondrial Dysfunction > 5.4. Apoptosis
What the sources say
- Partly supportedcites [114] Moresi, V., Garcia-Alvarez, G., Pristerà, A., Rizzuto, E., Albertini, M.C., Rocchi, M., Marazzi, G., Sassoon, D., Adamo, S., and Coletti, D. (2009). Modulation of Caspase Activity Regulates Skeletal Muscle Regeneration and Function in Response to Vasopressin and Tumor Necrosis Factor. PLoS ONE, 4. sourceExperimental — accuracy not yet measured
The Introduction (page unavailable) links muscle wasting and impaired regeneration to TNF and caspase activity. But it describes the relevant caspase activation as non-apoptotic, so it does not establish the cited assertion that caspase-induced apoptosis contributes to muscle wasting. The paper also does not assess how much evidence is available in COPD. (LLM, conf=0.84)
Strength:plain· not yet calibratedCausal:direct· not yet calibratedTests✓ Asserted: passes✓ Checkable: passes? Load-bearing: unclear✓ Based: passesIt may state two separate claims as one.
- Partly supported
Every source the paper cites for this claim was checked and supports it.
In the paper
“Later, miR-1, miR-206, and miR-133 were found significantly elevated in the plasma of patients with COPD, as well as miR-499, encoded within the slow myosin heavy chain (MHC) gene and thus promoting type I fibers [156].”
§ Main Pathogenic Mechanisms and Recent Advances in COPD Peripheral Skeletal Muscle Wasting > 8. Genetic Predisposition and Epigenetic Modifications
What the sources say
- Supportedcites [156] Donaldson, 2013, Increased Skeletal Muscle-Specific MicroRNA in the Blood of Patients with COPD, Thorax source
The Results section reports significantly elevated plasma miR-1, miR-206, miR-133 and miR-499 in patients with COPD versus controls. The Introduction says miR-499 is encoded within a slow MHC gene and modulates fibre type; the Discussion describes its role in type I fibre maintenance. Page numbers are not available in the supplied copy. (LLM, conf=0.92)
Strength:plain· not yet calibratedCausal:direct· not yet calibratedTests✓ Asserted: passes✓ Checkable: passes? Load-bearing: unclear✓ Based: passesIt may state two separate claims as one.
- Supported
Every source the paper cites for this claim was checked and supports it.
In the paper
“Hyperammonemic stress is also known to be associated with COPD, and a recent study evidenced new pathways associated with hyperammonemia in skeletal muscle (in addition to the already-known mitochondrial dysfunction, oxidative stress, and senescence), such as antiapoptotic B-cell leukemia/lymphoma 2 family protein expression, increased calcium flux, and increased protein glycosylation [144].”
§ Main Pathogenic Mechanisms and Recent Advances in COPD Peripheral Skeletal Muscle Wasting > 7. Other Metabolic Processes
What the sources say
- Supportedcites [144] Welch, 2021, Integrated Multiomics Analysis Identifies Molecular Landscape Perturbations during Hyperammonemia in Skeletal Muscle and Myotubes, J. Biol. Chem. source
Split into 2 atoms — 2 confirmed, 0 partially supported, 0 disputed, 0 misattributed, 0 unverifiable. Expand the claim to see per-atom verdicts.
Strength:boosted· not yet calibratedCausal:correlational· not yet calibratedTests✓ Asserted: passes✓ Checkable: passes? Load-bearing: unclear✓ Based: passesIt may state two separate claims as one.
- Supported
The cited sources support only part of this claim — read each source’s verdict below.
In the paper
“Finally, a recent study evidenced elevated circulating kynurenine levels in COPD patients, as well as reduced muscle levels of kynurenine aminotransferases; this dysregulated kynurenine clearance was attributed to impaired PGC1α signaling [145].”
§ Main Pathogenic Mechanisms and Recent Advances in COPD Peripheral Skeletal Muscle Wasting > 7. Other Metabolic Processes
What the sources say
- Partly supportedcites [145] Gosker, H.R., Clarke, G., de Theije, C.C., Cryan, J.F., and Schols, A.M.W.J. (2019). Impaired Skeletal Muscle Kynurenine Metabolism in Patients with Chronic Obstructive Pulmonary Disease. J. Clin. Med., 8. sourceExperimental — accuracy not yet measured
The Results report higher plasma kynurenine and lower muscle KAT4 expression in COPD, but KAT1 and KAT3 were unchanged and KAT2 protein was higher—not a general reduction in kynurenine aminotransferases. The Conclusions suggest impaired muscle PGC1α signaling might be involved; the Discussion says its role in regulating KAT4 remains to be established, so the proposed mechanism is not demonstrated. (LLM, conf=0.90)
Strength:plain· not yet calibratedCausal:direct· not yet calibratedTests✓ Asserted: passes✓ Checkable: passes? Load-bearing: unclear✓ Based: passesIt may state two separate claims as one.
- Partly supported
The sources with a verdict support this claim; the rest weren’t checked yet, have no full text we could read, or their verdicts aren’t rated yet.
In the paper
“The ubiquitin–proteasome system plays a major role in protein content turnover by degrading misfolded or defective proteins [163,164].”
§ Main Pathogenic Mechanisms and Recent Advances in COPD Peripheral Skeletal Muscle Wasting > 9. Consequences on Muscle Mass Regulation > 9.1. Protein Degradation
What the sources say
- Supportedcites [163] Kitajima, 2020, The Ubiquitin–Proteasome System in Regulation of the Skeletal Muscle Homeostasis and Atrophy: From Basic Science to Disorders, J. Physiol. Sci. source
The Introduction states that the ubiquitin–proteasome system degrades the majority of misfolded or defective cellular proteins and describes its substrate-specific protein degradation mechanism. This supports the claim that it plays a major role in protein turnover through that degradation. (LLM, conf=0.94)
- Not checked — no full text of the sourcecites [164] Gavriilidis, 2018, The MTM1–UBQLN2–HSP Complex Mediates Degradation of Misfolded Intermediate Filaments in Skeletal Muscle, Nat. Cell Biol. source
Strength:plain· not yet calibratedCausal:direct· not yet calibratedTests✓ Asserted: passes✓ Checkable: passes✗ Load-bearing: fails✓ Based: passesProbably not a substantial claim. The paper’s conclusions may not depend on it.
- Supported
Every source the paper cites for this claim was checked and supports it.
In the paper
“An increase in the maternally imprinted miR-675 was found in the quadriceps of COPD patients with a low fat-free mass index (FFMI), and this was associated with an inhibition of myoblast proliferation in vitro [159].”
§ Main Pathogenic Mechanisms and Recent Advances in COPD Peripheral Skeletal Muscle Wasting > 8. Genetic Predisposition and Epigenetic Modifications
What the sources say
- Supportedcites [159] Lewis, 2016, Increased Expression of H19/MiR-675 Is Associated with a Low Fat-Free Mass Index in Patients with COPD, J. Cachexia Sarcopenia Muscle source
The Introduction identifies miR-675 as arising from maternally expressed H19. The Results (Muscle array validation) report higher quadriceps miR-675 in COPD patients with low FFMI and an inverse correlation with FFMI; the Results (Altered regeneration in low FFMI patients) state that miR-675 inhibited C2C12 cell proliferation in vitro. The paper does not establish that elevated miR-675 caused reduced proliferation in the patients themselves. (LLM, conf=0.91)
Tests✓ Asserted: passes✓ Checkable: passes✓ Load-bearing: passes✓ Based: passesIt may state two separate claims as one.
- Supported
The cited sources support only part of this claim — read each source’s verdict below.
In the paper
“Of note, the study of Adami and colleagues identified an SNP in the same gene, that was close to be significantly associated with muscle aerobic capacity response [140].”
§ Main Pathogenic Mechanisms and Recent Advances in COPD Peripheral Skeletal Muscle Wasting > 7. Other Metabolic Processes
What the sources say
- Partly supportedcites [140] Adami, 2018, Genetic Variants Predicting Aerobic Capacity Response to Training Are Also Associated with Skeletal Muscle Oxidative Capacity in Moderate-to-Severe COPD, Physiol. Genom. sourceExperimental — accuracy not yet measured
The Results report that rs24575771 within SLC22A3 approached nominal significance (P = 0.058) for association with muscle oxidative capacity, measured by the recovery rate constant k. The study did not test response to training; the Abstract says the candidate SNPs had previously been associated with changes in aerobic capacity following training. (LLM, conf=0.87)
Strength:plain· not yet calibratedCausal:correlational· not yet calibratedTests✓ Asserted: passes✓ Checkable: passes✗ Load-bearing: fails✓ Based: passesProbably not a substantial claim. The paper’s conclusions may not depend on it.
- Partly supported
Every source the paper cites for this claim was checked and supports it.
In the paper
“Furthermore, levels of miR-499 were associated with nuclear NF-κB p50 in mild/moderate COPD, whereas in severe and very severe disease, miR-206 and miR-133 were associated with circulating cytokines, emphasizing the link with inflammation.”
§ Main Pathogenic Mechanisms and Recent Advances in COPD Peripheral Skeletal Muscle Wasting > 8. Genetic Predisposition and Epigenetic Modifications
What the sources say
- Supportedcites [156] Donaldson, 2013, Increased Skeletal Muscle-Specific MicroRNA in the Blood of Patients with COPD, Thorax source
The Results section, “Plasma miR-499 with markers of inflammation” (page not provided), reports a correlation between miR-499 and nuclear NFκB p50 in GOLD I/II COPD and associations between plasma miR-206 and miR-133 and circulating cytokines, particularly in GOLD III/IV disease. The Discussion, “Disease process and mechanism” (page not provided), links these findings to a possible role for inflammation while retaining uncertainty about the mechanism. (LLM, conf=0.93)
Strength:plain· not yet calibratedCausal:correlational· not yet calibratedTests✓ Asserted: passes✓ Checkable: passes? Load-bearing: unclear✓ Based: passesIt may state two separate claims as one.
- Supported
The cited sources support only part of this claim — read each source’s verdict below.
In the paper
“Among them, one SNPs was located in the DEPTOR gene, of particular interest as it is associated with the regulation of the contractile properties of glycolytic muscles [151].”
§ Main Pathogenic Mechanisms and Recent Advances in COPD Peripheral Skeletal Muscle Wasting > 8. Genetic Predisposition and Epigenetic Modifications
What the sources say
- Partly supportedcites [151] Meng, 2013, BAF60c Drives Glycolytic Muscle Formation and Improves Glucose Homeostasis through Deptor-Mediated AKT Activation, Nat. Med. sourceExperimental — accuracy not yet measured
The paper reports that Deptor is enriched in glycolytic muscles and mediates BAF60c-driven AKT activation and glycolytic metabolism (Abstract; page unavailable). It attributes the observed contractile changes to BAF60c, but does not establish that Deptor itself regulates contractile properties. The COPD SNP finding is the citing authors’ own result, not a finding attributed to this source. (LLM, conf=0.84)
Strength:plain· not yet calibratedCausal:correlational· not yet calibratedTests✓ Asserted: passes✓ Checkable: passes? Load-bearing: unclear✓ Based: passesIt may state two separate claims as one.
- Partly supported
The cited sources support only part of this claim — read each source’s verdict below.
In the paper
“miR-1 is also associated with insulin-like growth factor-1 (IGF-1) regulation, providing a possible explanation for reduced protein synthesis (cf. infra).”
§ Main Pathogenic Mechanisms and Recent Advances in COPD Peripheral Skeletal Muscle Wasting > 8. Genetic Predisposition and Epigenetic Modifications
What the sources say
- Partly supportedcites [155] Lewis, 2012, Downregulation of the Serum Response Factor/MiR-1 Axis in the Quadriceps of Patients with COPD, Thorax sourceExperimental — accuracy not yet measured
The Results (Reduced expression of targets of miR-1 in patients with COPD; page unavailable) report increased IGF-1 mRNA and an inverse association between miR-1 and Akt phosphorylation, supporting a link to IGF-1 regulation. The Discussion (miR-1 in muscle biology; page unavailable) raises synthetic resistance as a possible explanation for increased hypertrophy signalling despite muscle wasting, but does not establish that miR-1 regulation explains reduced protein synthesis. (LLM, conf=0.84)
Strength:hedged· not yet calibratedCausal:correlational· not yet calibratedTests✓ Asserted: passes✓ Checkable: passes? Load-bearing: unclear✓ Based: passesIt may state two separate claims as one.
- Partly supported
The cited sources support only part of this claim — read each source’s verdict below.
In the paper
“Later, Adami and colleagues investigated the association between the same SNPs and the muscle oxygen consumption recovery rate constant (k), assessed with near infrared spectroscopy, which reflects skeletal muscle oxidative capacity. Although no significant association was evidenced in COPD patients, three SNPs were associated with k specifically in moderate-to-severe COPD patients [140].”
§ Main Pathogenic Mechanisms and Recent Advances in COPD Peripheral Skeletal Muscle Wasting > 8. Genetic Predisposition and Epigenetic Modifications
What the sources say
- Partly supportedcites [140] Adami, 2018, Genetic Variants Predicting Aerobic Capacity Response to Training Are Also Associated with Skeletal Muscle Oxidative Capacity in Moderate-to-Severe COPD, Physiol. Genom. sourceExperimental — accuracy not yet measured
Split into 2 atoms — 1 confirmed, 1 partially supported, 0 disputed, 0 misattributed, 0 unverifiable. Expand the claim to see per-atom verdicts.
Strength:plain· not yet calibratedCausal:correlational· not yet calibratedTests✓ Asserted: passes✓ Checkable: passes? Load-bearing: unclear✓ Based: passesIt may state two separate claims as one.
- Partly supported
Every source the paper cites for this claim was checked and supports it.
In the paper
“The pioneer study in the matter was conducted by Lewis and colleagues and showed a decreased expression of miR-1 in COPD quadriceps, as well as an increase in its target, histone deacetylase 4 (HDCA4) at the protein level [155].”
§ Main Pathogenic Mechanisms and Recent Advances in COPD Peripheral Skeletal Muscle Wasting > 8. Genetic Predisposition and Epigenetic Modifications
What the sources say
- Supportedcites [155] Lewis, 2012, Downregulation of the Serum Response Factor/MiR-1 Axis in the Quadriceps of Patients with COPD, Thorax source
The Results section on miRNA expression in quadriceps reports lower miR-1 expression in patients with COPD than in controls. The Results section on miR-1 targets reports higher HDAC4 protein in patients, while identifying HDAC4 as a miR-1 target. Page numbers were not provided in the supplied passages. (LLM, conf=0.94)
Tests✓ Asserted: passes✓ Checkable: passes✓ Load-bearing: passes✓ Based: passesIt may state two separate claims as one.
- Supported
Every source the paper cites for this claim was checked and supports it.
In the paper
“Among them, miRNAs represent a growing body of interest in COPD, and they have been associated with several features of the disease in the lung [154].”
§ Main Pathogenic Mechanisms and Recent Advances in COPD Peripheral Skeletal Muscle Wasting > 8. Genetic Predisposition and Epigenetic Modifications
What the sources say
- Supportedcites [154] Osei, 2015, Unravelling the Complexity of COPD by MicroRNAs: It’s a Small World after All, Eur. Respir. J. source
The Introduction says the review covers miRNAs in several aspects of COPD pathogenesis, including inflammation, emphysema, tissue repair and lung function. The Differential miRNA expression in COPD section reports altered miRNA expression in lung tissue from patients with COPD and associations with disease stage and impaired lung function. (LLM, conf=0.93)
Strength:plain· not yet calibratedCausal:correlational· not yet calibratedTests✓ Asserted: passes✓ Checkable: passes✗ Load-bearing: fails✓ Based: passesProbably not a substantial claim. The paper’s conclusions may not depend on it.
- Supported
The cited sources support only part of this claim — read each source’s verdict below.
In the paper
“Of note, some studies have failed to report a significant difference between COPD patients and healthy subjects [166], possibly due to the timing of the assessment.”
§ Main Pathogenic Mechanisms and Recent Advances in COPD Peripheral Skeletal Muscle Wasting > 9. Consequences on Muscle Mass Regulation > 9.1. Protein Degradation
What the sources say
- Partly supportedcites [166] Natanek, 2013, MuRF-1 and Atrogin-1 Protein Expression and Quadriceps Fiber Size and Muscle Mass in Stable Patients with COPD, COPD sourceExperimental — accuracy not yet measured
The Results report no significant difference in MuRF-1 protein between COPD patients and controls, but atrogin-1 protein was significantly lower in the COPD group. The Discussion considers measurement timing as a possible reason ubiquitin-ligase levels may not be elevated in stable patients; it does not establish timing as the cause of the MuRF-1 result. Thus the claim is supported for MuRF-1, not for both atrogenes. (LLM, conf=0.89)
Strength:hedged· not yet calibratedTests✓ Asserted: passes✓ Checkable: passes? Load-bearing: unclear✓ Based: passesIt may state two separate claims as one.
- Partly supported
Every source the paper cites for this claim was checked and supports it.
In the paper
“To our knowledge, only one study has investigated the calpain expression in COPD quadriceps and reported an unchanged expression compared to that of the control group [187].”
§ Main Pathogenic Mechanisms and Recent Advances in COPD Peripheral Skeletal Muscle Wasting > 9. Consequences on Muscle Mass Regulation > 9.1. Protein Degradation
What the sources say
- Supportedcites [187] Constantin, 2013, Skeletal Muscle Molecular Responses to Resistance Training and Dietary Supplementation in COPD, Thorax source
The Muscle biopsy analysis section says the study measured calpain-3 in quadriceps samples. Table 2 (indexed under Discussion; page not supplied) reports similar baseline calpain-3 protein expression in healthy controls (0.50) and patients with COPD (0.52), with no significant difference marked. The claim that this was the only study is framed as the citing authors’ knowledge, not a finding attributed to this paper. (LLM, conf=0.91)
Strength:hedged· not yet calibratedTests✓ Asserted: passes✓ Checkable: passes? Load-bearing: unclear✓ Based: passesIt may state two separate claims as one.
- Supported
The cited sources support only part of this claim — read each source’s verdict below.
In the paper
“However, a recent clinical trial using a monoclonal antibody blocking its receptor has not shown potent results in treating skeletal muscle wasting for COPD patients [177], despite promising results previously obtained in cancer models [178].”
§ Main Pathogenic Mechanisms and Recent Advances in COPD Peripheral Skeletal Muscle Wasting > 9. Consequences on Muscle Mass Regulation > 9.1. Protein Degradation
What the sources say
- Partly supportedcites [177] Polkey, 2019, Activin Type II Receptor Blockade for Treatment of Muscle Depletion in Chronic Obstructive Pulmonary Disease. A Randomized Trial, Am. J. Respir. Crit. Care Med. sourceExperimental — accuracy not yet measured
The Abstract identifies bimagrumab as a monoclonal antibody blocking activin type II receptors, and the Results report no significant improvement in walking distance or most measures of muscle strength and mobility. But the Abstract and Discussion report substantial gains in thigh muscle volume and lean body mass, so the trial did show a benefit for muscle wasting, though not for functional performance. The cancer-model claim carries a separate citation and is not assessed here. (LLM, conf=0.88)
- Not checked — no full text of the sourcecites [178] Murphy, 2011, Antibody-Directed Myostatin Inhibition Enhances Muscle Mass and Function in Tumor-Bearing Mice, Am. J. Physiol. Regul. Integr. Comp. Physiol. source
Strength:plain· not yet calibratedTests✓ Asserted: passes✓ Checkable: passes? Load-bearing: unclear✓ Based: passesIt may state two separate claims as one.
- Partly supported
The cited sources support only part of this claim — read each source’s verdict below.
In the paper
“Its expression is increased in the quadriceps of COPD patients [176], possibly related to hypoxia [72].”
§ Main Pathogenic Mechanisms and Recent Advances in COPD Peripheral Skeletal Muscle Wasting > 9. Consequences on Muscle Mass Regulation > 9.1. Protein Degradation
What the sources say
- Partly supportedcites [176] Man, 2010, Quadriceps Myostatin Expression in COPD, Eur. Respir. J. sourceExperimental — accuracy not yet measured
In “Quadriceps myostatin expression in COPD” (page unavailable), the paper reports increased quadriceps myostatin expression in some COPD patients with low strength, exercise capacity, or physical activity—not in COPD patients generally. The hypoxia explanation is attached to a different citation [72] and is not judged here. (LLM, conf=0.88)
- Not checked — no full text of the sourcecites [72] Hayot, 2011, Myostatin Up-Regulation Is Associated with the Skeletal Muscle Response to Hypoxic Stimuli, Mol. Cell. Endocrinol. source
Strength:hedged· not yet calibratedCausal:conditional· not yet calibratedTests✓ Asserted: passes✓ Checkable: passes? Load-bearing: unclear✓ Based: passesIt may state two separate claims as one.
- Partly supported
Every source the paper cites for this claim was checked and supports it.
In the paper
“It is already established that autophagy is increased in the lungs of COPD patients [180].”
§ Main Pathogenic Mechanisms and Recent Advances in COPD Peripheral Skeletal Muscle Wasting > 9. Consequences on Muscle Mass Regulation > 9.1. Protein Degradation
What the sources say
- Supportedcites [180] Chen, Z.-H., Kim, H.P., Sciurba, F.C., Lee, S.-J., Feghali-Bostwick, C., Stolz, D.B., Dhir, R., Landreneau, R.J., Schuchert, M.J., and Yousem, S.A. (2008). Egr-1 Regulates Autophagy in Cigarette Smoke-Induced Chronic Obstructive Pulmonary Disease. PLoS ONE, 3. source
The Results section, “Increased autophagy in human COPD lung tissues,” reports significantly increased autophagy-related proteins and markedly more autophagic vacuoles in COPD lung tissue than in controls. This directly supports the citing sentence. (LLM, conf=0.94)
Strength:boosted· not yet calibratedCausal:direct· not yet calibratedTests✓ Asserted: passes✓ Checkable: passes✗ Load-bearing: fails✓ Based: passesProbably not a substantial claim. The paper’s conclusions may not depend on it.
- Supported
The cited sources support only part of this claim — read each source’s verdict below.
In the paper
“Nedd4, another muscle-specific E3-ubiquitin ligase acting through Notch1 signaling [167], has recently drawn attention because of its implication in denervation-induced muscle atrophy [168], here unrelated to Notch1 activation.”
§ Main Pathogenic Mechanisms and Recent Advances in COPD Peripheral Skeletal Muscle Wasting > 9. Consequences on Muscle Mass Regulation > 9.1. Protein Degradation
What the sources say
- Not checked — no full text of the sourcecites [167] Koncarevic, 2006, The Ubiquitin-Protein Ligase Nedd4 Targets Notch1 in Skeletal Muscle and Distinguishes the Subset of Atrophies Caused by Reduced Muscle Tension, FASEB J. source
- Partly supportedcites [168] Nagpal, P., Plant, P.J., Correa, J., Bain, A., Takeda, M., Kawabe, H., Rotin, D., Bain, J.R., and Batt, J.A.E. (2012). The Ubiquitin Ligase Nedd4-1 Participates in Denervation-Induced Skeletal Muscle Atrophy in Mice. PLoS ONE, 7. sourceExperimental — accuracy not yet measured
The Discussion reports that deleting Nedd4-1 from skeletal muscle protected mice from early denervation-induced atrophy. It also says the authors found no evidence that Nedd4-1 engages Notch-1 to mediate that atrophy. Calling the mechanism definitively unrelated to Notch-1 activation is stronger than the paper’s qualified conclusion. (LLM, conf=0.86)
Strength:plain· not yet calibratedCausal:direct· not yet calibratedTests✓ Asserted: passes✓ Checkable: passes? Load-bearing: unclear✓ Based: passesIt may state two separate claims as one.
The cited sources support only part of this claim — read each source’s verdict below.
In the paper
“In COPD, increased proteolysis is mainly mediated by an overactivation of the ubiquitin (26S)–proteasome system, activated via the muscle-specific E3-ubiquitin ligases Atrogin-1/MAFbx and TRIM63/MuRF-1, also named atrogenes, which are increased in COPD quadriceps [118,165].”
§ Main Pathogenic Mechanisms and Recent Advances in COPD Peripheral Skeletal Muscle Wasting > 9. Consequences on Muscle Mass Regulation > 9.1. Protein Degradation
What the sources say
- Partly supportedcites [118] Fermoselle, 2012, Does Oxidative Stress Modulate Limb Muscle Atrophy in Severe COPD Patients?, Eur. Respir. J. sourceExperimental — accuracy not yet measured
The Ubiquitin-proteasome system section reports greater protein ubiquitination and atrogin-1 in the vastus lateralis of muscle-wasted COPD patients, supporting part of the claim. It explicitly reports that MuRF-1 did not differ between study groups; the discussion describes the system's role in severe COPD muscle atrophy as likely rather than establishing that increased proteolysis is mainly mediated by its overactivation. (LLM, conf=0.90)
- Not checked — no full text of the sourcecites [165] Doucet, 2007, Muscle Atrophy and Hypertrophy Signaling in Patients with Chronic Obstructive Pulmonary Disease, Am. J. Respir. Crit. Care Med. source
Tests✓ Asserted: passes✓ Checkable: passes✓ Load-bearing: passes✓ Based: passesIt may state two separate claims as one.
- Partly supported
The cited sources that could be checked couldn’t confirm or dispute this claim.
In the paper
“Myostatin is a ligand of the TGF-β pathway in skeletal muscle and a well-known negative regulator of muscle mass, as it inhibits satellite cells’ proliferation and differentiation [174].”
§ Main Pathogenic Mechanisms and Recent Advances in COPD Peripheral Skeletal Muscle Wasting > 9. Consequences on Muscle Mass Regulation > 9.1. Protein Degradation
What the sources say
- Could not verifycites [174] Liu, 2001, TGF-Beta Inhibits Muscle Differentiation through Functional Repression of Myogenic Transcription Factors by Smad3, Genes Dev. sourceExperimental — accuracy not yet measured
The opening passage reports that TGF-β inhibits differentiation in cultured myoblasts without affecting their proliferation; the Discussion likewise concerns TGF-β, not myostatin. Searches for myostatin, satellite cells, and muscle mass found no passage addressing the claim about myostatin. The proliferation finding for TGF-β does not establish what myostatin does. (LLM, conf=0.76)
Tests✓ Asserted: passes✓ Checkable: passes✓ Load-bearing: passes✓ Based: passesIt may state two separate claims as one.
- Could not verify
Every source the paper cites for this claim was checked and supports it.
In the paper
“However, experimental models do not reflect the complexity of human disease, as currently illustrated in the field of cancer research [190], and are quite heterogeneous in their ability to reproduce every characteristic of COPD sarcopenia.”
§ Main Pathogenic Mechanisms and Recent Advances in COPD Peripheral Skeletal Muscle Wasting > 9. Consequences on Muscle Mass Regulation > 9.2. Protein Synthesis
What the sources say
- Supportedcites [190] Mueller, T.C., Bachmann, J., Prokopchuk, O., Friess, H., and Martignoni, M.E. (2016). Molecular Pathways Leading to Loss of Skeletal Muscle Mass in Cancer Cachexia—Can Findings from Animal Models Be Translated to Humans?. BMC Cancer, 16. source
The Discussion section, under “General issues in cancer cachexia research and clinical trials,” says no animal model can reflect all contributing factors in human cancer cachexia or simulate its complex biology. This supports the cited cancer-research illustration; the subsequent COPD-sarcopenia clause is the citing authors’ application, not a finding attributed to this source. (LLM, conf=0.92)
Strength:plain· not yet calibratedTests✓ Asserted: passes✓ Checkable: passes? Load-bearing: unclear✓ Based: passesIt may state two separate claims as one.
- Supported
A claim is checked only against the cited paper’s full text, never its abstract, and none is available for its sources.
In the paper
“Classically, circulating TNF-α is reported to be higher in COPD patients than controls and negatively correlated to lean mass [23,24]”
§ Main Pathogenic Mechanisms and Recent Advances in COPD Peripheral Skeletal Muscle Wasting > 3. Inflammation > 3.1. Tumor Necrosis Factor α (TNF-α)
What the sources say
- Not checked — no full text of the sourcecites [23] Kochetkova, 2016, The Role of Tumor Necrosis Factor Alpha and TNF Superfamily Members in Bone Damage in Patients with End-Stage Chronic Obstructive Lung Disease Prior to Lung Transplantation, Calcif. Tissue Int. source
- Not checked — no full text of the sourcecites [24] Wouters, 2002, Systemic Effects in COPD, Chest source
Strength:hedged· not yet calibratedCausal:correlational· not yet calibratedTests✓ Asserted: passes✓ Checkable: passes? Load-bearing: unclear✓ Based: passesIt may state two separate claims as one.
In the paper
“IL-15 was increased and correlated with TNF-α in a rat model of COPD (induced by CS exposure as well as LPS instillations), in the serum and in both peripheral and respiratory skeletal muscles [54].”
§ Main Pathogenic Mechanisms and Recent Advances in COPD Peripheral Skeletal Muscle Wasting > 3. Inflammation > 3.5. Interleukin-15 (IL-15)
What the sources say
- Not checked — no full text of the sourcecites [54] Liu, 2015, The Role of Interleukin 15 in Protein Degradation in Skeletal Muscles in Rats of Chronic Obstructive Pulmonary Disease, Int. J. Clin. Exp. Med.
Strength:plain· not yet calibratedCausal:correlational· not yet calibratedTests✓ Asserted: passes✓ Checkable: passes? Load-bearing: unclear✓ Based: passesIt may state two separate claims as one.
In the paper
“an overexpression of TNF-α in the lung leads to an increased muscle fatigue, decreased muscle mass and mitochondrial content, and increased catabolism (mostly in male mice) [42].”
§ Main Pathogenic Mechanisms and Recent Advances in COPD Peripheral Skeletal Muscle Wasting > 3. Inflammation > 3.1. Tumor Necrosis Factor α (TNF-α)
What the sources say
- Not checked — no full text of the sourcecites [42] Tang, 2013, Impaired Exercise Capacity and Skeletal Muscle Function in a Mouse Model of Pulmonary Inflammation, J. Appl. Physiol. source
Strength:plain· not yet calibratedCausal:direct· not yet calibratedTests✓ Asserted: passes✓ Checkable: passes? Load-bearing: unclear✓ Based: passesIt may state two separate claims as one.
In the paper
“Other known histological alterations include a decreased capillarity, with both a decrease in capillaries density as well as in the capillary-to-fiber ratio [13]”
§ Main Pathogenic Mechanisms and Recent Advances in COPD Peripheral Skeletal Muscle Wasting > 2. Histopathological Alterations of COPD Skeletal Muscle Tissue
What the sources say
- Not checked — no full text of the sourcecites [13] Jobin, 1998, Chronic Obstructive Pulmonary Disease: Capillarity and Fiber-Type Characteristics of Skeletal Muscle, J. Cardiopulm. Rehabil. Prev. source
Strength:boosted· not yet calibratedTests✓ Asserted: passes✓ Checkable: passes? Load-bearing: unclear✓ Based: passesIt may state two separate claims as one.
A claim is checked only against the cited paper’s full text, never its abstract, and none is available for its sources.
In the paper
“In vitro, IL-6 bears anabolic effects by regulating satellite cells’ function and enhancing glucose metabolism; furthermore, a loss of IL-6 signaling in myoblasts results in a reduced proliferation and migration [49,50].”
§ Main Pathogenic Mechanisms and Recent Advances in COPD Peripheral Skeletal Muscle Wasting > 3. Inflammation > 3.2. Interleukin-6 (IL-6)
What the sources say
- Not checked — no full text of the sourcecites [49] 2004, P38 MAPK-Induced Nuclear Factor-KappaB Activity Is Required for Skeletal Muscle Differentiation: Role of Interleukin-6, Mol. Biol. Cell source
- Not checked — no full text of the sourcecites [50] Serrano, 2008, Interleukin-6 Is an Essential Regulator of Satellite Cell-Mediated Skeletal Muscle Hypertrophy, Cell Metab. source
Strength:plain· not yet calibratedCausal:direct· not yet calibratedTests✓ Asserted: passes✓ Checkable: passes? Load-bearing: unclear✓ Based: passesIt may state two separate claims as one.
In the paper
“CD34+ muscle stem cells are specifically affected by hypoxia: Pagé and colleagues found a worse outcome for CD34−/− mice exposed to hypoxia compared to wild-type littermates, with a lower number of fibro-adipogenic progenitors in CD34−/− mice and a greater muscle atrophy as well as a worse functional impairment of the extensor digitorum longus muscle [68].”
§ Main Pathogenic Mechanisms and Recent Advances in COPD Peripheral Skeletal Muscle Wasting > 4. Hypoxia and Hypercapnia
What the sources say
- Not checked — no full text of the sourcecites [68] Maheux, 2019, CD34 Regulates the Skeletal Muscle Response to Hypoxia, J. Muscle Res. Cell Motil. source
Tests✓ Asserted: passes✓ Checkable: passes✓ Load-bearing: passes✓ Based: passesIt may state two separate claims as one.
In the paper
“Chronic hypoxia in healthy subjects (implicated in altitude expeditions) induces a loss of muscle mass and decreased fibers’ CSA and mitochondrial density, without affecting the capillary network [65].”
§ Main Pathogenic Mechanisms and Recent Advances in COPD Peripheral Skeletal Muscle Wasting > 4. Hypoxia and Hypercapnia
What the sources say
- Not checked — no full text of the sourcecites [65] Hoppeler, 1990, Morphological Adaptations of Human Skeletal Muscle to Chronic Hypoxia, Int. J. Sport. Med. source
Strength:plain· not yet calibratedCausal:direct· not yet calibratedTests✓ Asserted: passes✓ Checkable: passes? Load-bearing: unclear✓ Based: passesIt may state two separate claims as one.
In the paper
“First, Picard and colleagues observed a decreased state 2 and state 3 respiration in COPD fibers compared to healthy controls. However, a normalization with respect to the citrate synthase activity abolished these differences [98].”
§ Main Pathogenic Mechanisms and Recent Advances in COPD Peripheral Skeletal Muscle Wasting > 5. Mitochondrial Dysfunction > 5.2. Reduced Mitochondrial Activity
What the sources say
- Not checked — no full text of the sourcecites [98] Picard, 2008, The Mitochondrial Phenotype of Peripheral Muscle in Chronic Obstructive Pulmonary Disease: Disuse or Dysfunction?, Am. J. Respir. Crit. Care Med. source
Load-bearingStrength:plain· not yet calibratedTests✓ Asserted: passes✓ Checkable: passes✓ Load-bearing: passes✓ Based: passesIt may state two separate claims as one.
In the paper
“The current knowledge considers that state 3 respiration (ADP-stimulated) is impaired in COPD patients; however, contradictory data are reported regarding complex I- (CI) or complex II-, succinate dehydrogenase (CII-SDH), driven respiration states [100].”
§ Main Pathogenic Mechanisms and Recent Advances in COPD Peripheral Skeletal Muscle Wasting > 5. Mitochondrial Dysfunction > 5.2. Reduced Mitochondrial Activity
What the sources say
- Not checked — no full text of the sourcecites [100] Meyer, 2013, Skeletal Muscle Mitochondrial Dysfunction during Chronic Obstructive Pulmonary Disease: Central Actor and Therapeutic Target, Exp. Physiol. source
Strength:plain· not yet calibratedTests✓ Asserted: passes✓ Checkable: passes? Load-bearing: unclear✓ Based: passesIt may state two separate claims as one.
In the paper
“no specific and efficient pharmaceutic therapy is available to date, and pulmonary rehabilitation remains the only validated treatment [9].”
§ Main Pathogenic Mechanisms and Recent Advances in COPD Peripheral Skeletal Muscle Wasting > 1. Introduction
What the sources say
- Not checked — no full text of the sourcecites [9] Spruit, 2013, An Official American Thoracic Society/European Respiratory Society Statement: Key Concepts and Advances in Pulmonary Rehabilitation, Am. J. Respir. Crit. Care Med. source
Load-bearingStrength:plain· not yet calibratedTests✓ Asserted: passes✓ Checkable: passes✓ Load-bearing: passes✓ Based: passesIt may state two separate claims as one.
In the paper
“Finally, the same team performed a similar study in COPD patients according to their inflammatory status and found an increase in BNIP3 at the protein level in COPD patients with high circulating C-reactive protein (CRP) compared to other COPD patients, pointing out that mitophagy was associated with systemic inflammation [110].”
§ Main Pathogenic Mechanisms and Recent Advances in COPD Peripheral Skeletal Muscle Wasting > 5. Mitochondrial Dysfunction > 5.3. Increased Mitophagy
What the sources say
- Not checked — no full text of the sourcecites [110] Gosker, 2018, Systemic Inflammation Is Associated with Mitophagy Signalling in Skeletal Muscle of COPD Patients, Eur. Respir. J. source
Tests✓ Asserted: passes✓ Checkable: passes✓ Load-bearing: passes✓ Based: passesIt may state two separate claims as one.
In the paper
“Of note, mitochondrial respiration can be affected by external factors, such as glucocorticoid use [105]”
§ Main Pathogenic Mechanisms and Recent Advances in COPD Peripheral Skeletal Muscle Wasting > 5. Mitochondrial Dysfunction > 5.2. Reduced Mitochondrial Activity
What the sources say
- Not checked — no full text of the sourcecites [105] Liu, 2016, Mitochondrial Dysfunction Launches Dexamethasone-Induced Skeletal Muscle Atrophy via AMPK/FOXO3 Signaling, Mol. Pharm. source
Strength:plain· not yet calibratedCausal:conditional· not yet calibratedTests✓ Asserted: passes✓ Checkable: passes✗ Load-bearing: fails✓ Based: passesProbably not a substantial claim. The paper’s conclusions may not depend on it.
In the paper
“The same authors simultaneously investigated COPD patients’ quadriceps biopsies and found decreased FUNDC1 and PINK1 at the protein level, whereas Parkin was increased. Moreover, no change was observed at the mRNA level [109].”
§ Main Pathogenic Mechanisms and Recent Advances in COPD Peripheral Skeletal Muscle Wasting > 5. Mitochondrial Dysfunction > 5.3. Increased Mitophagy
What the sources say
- Not checked — no full text of the sourcecites [109] Leermakers, 2016, Peripheral Muscle Mitophagy Is Enhanced in Patients with COPD, Eur. Respir. J. source
Load-bearingStrength:plain· not yet calibratedTests✓ Asserted: passes✓ Checkable: passes✓ Load-bearing: passes✓ Based: passesIt may state two separate claims as one.
In the paper
“The first study was performed in a murine model of lung injury (induced by LPS instillation) and showed an enhanced transcription of mitophagy-related genes such as BNIP3L and PARKIN and a decrease of FUNDC1 [108].”
§ Main Pathogenic Mechanisms and Recent Advances in COPD Peripheral Skeletal Muscle Wasting > 5. Mitochondrial Dysfunction > 5.3. Increased Mitophagy
What the sources say
- Not checked — no full text of the sourcecites [108] Leermakers, 2016, Activation of Skeletal Muscle Mitophagy in a Murine Model of Pulmonary and Systemic Inflammation, Eur. Respir. J. source
Strength:plain· not yet calibratedCausal:direct· not yet calibratedTests✓ Asserted: passes✓ Checkable: passes? Load-bearing: unclear✓ Based: passesIt may state two separate claims as one.
In the paper
“However, other observations tend to show that metabolic and contractile properties are controlled by distinct signaling pathways [103].”
§ Main Pathogenic Mechanisms and Recent Advances in COPD Peripheral Skeletal Muscle Wasting > 5. Mitochondrial Dysfunction > 5.2. Reduced Mitochondrial Activity
What the sources say
- Not checked — no full text of the sourcecites [103] Schiaffino, 2011, Fiber Types in Mammalian Skeletal Muscles, Physiol. Rev. source
Strength:hedged· not yet calibratedCausal:conditional· not yet calibratedTests✓ Asserted: passes✓ Checkable: passes✗ Load-bearing: fails✓ Based: passesProbably not a substantial claim. The paper’s conclusions may not depend on it.
A conclusion the paper draws from its own results — it cites no other source for it, so there is none to check. The quote shows it is in the paper.
In the paper
“Overall, hypoxia is an important contributor of muscle wasting, although direct mechanistic evidence in COPD muscle is lacking.”
§ Main Pathogenic Mechanisms and Recent Advances in COPD Peripheral Skeletal Muscle Wasting > 4. Hypoxia and Hypercapnia
Tests✓ Asserted: passes✓ Checkable: passes✓ Load-bearing: passes✓ Based: passesIt may state two separate claims as one.
In the paper
“The authors concluded that CIII was the main site of ROS production in COPD skeletal muscle and attributed this to the absence of matrix antioxidant in close vicinity (contrary to complex I).”
§ Main Pathogenic Mechanisms and Recent Advances in COPD Peripheral Skeletal Muscle Wasting > 6. Oxidative and Nitrosative Stress
What the sources say
- Not checked — no full text of the sourcecites [85] Tejedor, 2012, Site of Mitochondrial Reactive Oxygen Species Production in Skeletal Muscle of Chronic Obstructive Pulmonary Disease and Its Relationship with Exercise Oxidative Stress, Am. J. Respir. Cell Mol. Biol. source
Tests✓ Asserted: passes✓ Checkable: passes✓ Load-bearing: passes✓ Based: passesIt may state two separate claims as one.
In the paper
“Of note, some studies report no difference in oxidative stress markers between COPD patients and healthy smokers [130], implying that oxidative stress could mainly be attributed to CS extracts and not the specificity of systemic involvement of COPD.”
§ Main Pathogenic Mechanisms and Recent Advances in COPD Peripheral Skeletal Muscle Wasting > 6. Oxidative and Nitrosative Stress
What the sources say
- Not checked — no full text of the sourcecites [130] Barreiro, 2010, ENIGMA in COPD Project Cigarette Smoke-Induced Oxidative Stress: A Role in Chronic Obstructive Pulmonary Disease Skeletal Muscle Dysfunction, Am. J. Respir. Crit. Care Med. source
Strength:hedged· not yet calibratedCausal:conditional· not yet calibratedTests✓ Asserted: passes✓ Checkable: passes? Load-bearing: unclear✓ Based: passesIt may state two separate claims as one.
In the paper
“Picard and colleagues reported that there was more resistance to Ca2+-induced mPTP opening in permeabilized muscle fibers from COPD patients than in those from healthy control subjects, attributed to the increased proportion of type II fibers, which are intrinsically more resistant to Ca2+-induced mPTP opening [98].”
§ Main Pathogenic Mechanisms and Recent Advances in COPD Peripheral Skeletal Muscle Wasting > 5. Mitochondrial Dysfunction > 5.4. Apoptosis
What the sources say
- Not checked — no full text of the sourcecites [98] Picard, 2008, The Mitochondrial Phenotype of Peripheral Muscle in Chronic Obstructive Pulmonary Disease: Disuse or Dysfunction?, Am. J. Respir. Crit. Care Med. source
Strength:plain· not yet calibratedCausal:direct· not yet calibratedTests✓ Asserted: passes✓ Checkable: passes? Load-bearing: unclear✓ Based: passesIt may state two separate claims as one.
In the paper
“only one study reported increased terminal deoxynucleotidyl transferase mediated dUTP nick-end labeling (TUNEL)-positive cells in quadriceps and diaphragm muscles [113]. However, no ultrastructural difference in apoptotic nuclei was noticed.”
§ Main Pathogenic Mechanisms and Recent Advances in COPD Peripheral Skeletal Muscle Wasting > 5. Mitochondrial Dysfunction > 5.4. Apoptosis
What the sources say
- Not checked — no full text of the sourcecites [113] Barreiro, 2011, Inflammatory Cells and Apoptosis in Respiratory and Limb Muscles of Patients with COPD, J. Appl. Physiol. source
Strength:plain· not yet calibratedTests✓ Asserted: passes✓ Checkable: passes? Load-bearing: unclear✓ Based: passesIt may state two separate claims as one.
A conclusion the paper draws from its own results — it cites no other source for it, so there is none to check. The quote shows it is in the paper.
In the paper
“Discrepancies might also come from the fact that Agusti and colleagues reported an increased apoptosis specifically in COPD patients with low BMI, whereas Gosker and colleagues investigated moderate-to-severe COPD patients without weight indication, and Barreiro and colleagues reported COPD patients with normal body composition.”
§ Main Pathogenic Mechanisms and Recent Advances in COPD Peripheral Skeletal Muscle Wasting > 5. Mitochondrial Dysfunction > 5.4. Apoptosis
Strength:hedged· not yet calibratedCausal:conditional· not yet calibratedTests✓ Asserted: passes✓ Checkable: passes✗ Load-bearing: fails✓ Based: passesProbably not a substantial claim. The paper’s conclusions may not depend on it. It may state two separate claims as one.
In the paper
“Recently, miR542-3p/5p has been found elevated in COPD quadriceps. In vitro data showed its implication in mitochondrial stress and transforming growth factor beta (TGF-β) canonical signaling, and an in vivo experimental study confirmed its role in muscle wasting through a decrease of mitochondrial function [160].”
§ Main Pathogenic Mechanisms and Recent Advances in COPD Peripheral Skeletal Muscle Wasting > 8. Genetic Predisposition and Epigenetic Modifications
What the sources say
- Not checked — no full text of the sourcecites [160] Garros, 2017, MicroRNA-542 Promotes Mitochondrial Dysfunction and SMAD Activity and Is Elevated in Intensive Care Unit-Acquired Weakness, Am. J. Respir. Crit. Care Med. source
Strength:plain· not yet calibratedCausal:direct· not yet calibratedTests✓ Asserted: passes✓ Checkable: passes? Load-bearing: unclear✓ Based: passesIt may state two separate claims as one.
In the paper
“Epigenetic modifications, whether methylation, acetylation, or muscle-specific micro-RNAs (myomiRNAs) play essential roles in muscle physiology, including embryogenesis and adaptation to environmental factors (for a comprehensive review, see [152]).”
§ Main Pathogenic Mechanisms and Recent Advances in COPD Peripheral Skeletal Muscle Wasting > 8. Genetic Predisposition and Epigenetic Modifications
What the sources say
- Not checked — no full text of the sourcecites [152] Barreiro, 2013, Epigenetic Regulation of Muscle Phenotype and Adaptation: A Potential Role in COPD Muscle Dysfunction, J. Appl. Physiol. source
Strength:plain· not yet calibratedCausal:direct· not yet calibratedTests✓ Asserted: passes✓ Checkable: passes✗ Load-bearing: fails✓ Based: passesProbably not a substantial claim. The paper’s conclusions may not depend on it.
A conclusion the paper draws from its own results — it cites no other source for it, so there is none to check. The quote shows it is in the paper.
In the paper
“These discrepancies are possibly explained by the absence of matching for smoking and physical activity in the first study. Differences in timing of miRNA secretion can also be invoked.”
§ Main Pathogenic Mechanisms and Recent Advances in COPD Peripheral Skeletal Muscle Wasting > 8. Genetic Predisposition and Epigenetic Modifications
Strength:hedged· not yet calibratedCausal:conditional· not yet calibratedTests✓ Asserted: passes✓ Checkable: passes✗ Load-bearing: fails✓ Based: passesProbably not a substantial claim. The paper’s conclusions may not depend on it. It may state two separate claims as one.
A conclusion the paper draws from its own results — it cites no other source for it, so there is none to check. The quote shows it is in the paper.
In the paper
“All mechanisms detailed above converge to deleterious consequences on muscle mass regulation, destabilizing the atrophy/hypertrophy balance.”
§ Main Pathogenic Mechanisms and Recent Advances in COPD Peripheral Skeletal Muscle Wasting > 9. Consequences on Muscle Mass Regulation
Tests✓ Asserted: passes✓ Checkable: passes✓ Load-bearing: passes✓ Based: passesIt may state two separate claims as one.
- Rests on an assumption: Muscle protein turnover is impaired in COPD through both enhanced degradation and reduced synthesis.
None of the sources cited for this claim have been checked yet.
In the paper
“Willis-Owen and colleagues also reported an increase of FST, encoding follistatin, a propeptide inhibiting myostatin signaling and promoting myogenic differentiation. Thus, this upregulation might represent a compensatory mechanism.”
§ Main Pathogenic Mechanisms and Recent Advances in COPD Peripheral Skeletal Muscle Wasting > 7. Other Metabolic Processes
Strength:hedged· not yet calibratedCausal:conditional· not yet calibratedTests✓ Asserted: passes✓ Checkable: passes✗ Load-bearing: fails✓ Based: passesProbably not a substantial claim. The paper’s conclusions may not depend on it. It may state two separate claims as one.
In the paper
“Maternally imprinted genes are usually associated with limiting growth, whereas paternal genes bear the reverse effect [158].”
§ Main Pathogenic Mechanisms and Recent Advances in COPD Peripheral Skeletal Muscle Wasting > 8. Genetic Predisposition and Epigenetic Modifications
What the sources say
- Not checked — no full text of the sourcecites [158] Kemp, 2017, Epigenetics and Susceptibility to Muscle Wasting in COPD, Arch. Bronconeumol. source
Strength:plain· not yet calibratedCausal:correlational· not yet calibratedTests✓ Asserted: passes✓ Checkable: passes✗ Load-bearing: fails✓ Based: passesProbably not a substantial claim. The paper’s conclusions may not depend on it. It may state two separate claims as one.
In the paper
“Among them, two genes were confirmed as in vitro modifiers of muscle mass, as their silencing with RNA interference increased the length of myotubes.”
§ Main Pathogenic Mechanisms and Recent Advances in COPD Peripheral Skeletal Muscle Wasting > 8. Genetic Predisposition and Epigenetic Modifications
What the sources say
- Not checked — no full text of the sourcecites [148] Gonzales, 2019, Genome-Wide Associations Reveal Human-Mouse Genetic Convergence and Modifiers of Myogenesis, CPNE1 and STC2, Am. J. Hum. Genet. source
Strength:plain· not yet calibratedCausal:direct· not yet calibratedTests✓ Asserted: passes✓ Checkable: passes? Load-bearing: unclear✓ Based: passesIt may state two separate claims as one.
What the paper did — it cites no source for this, so there is none to check. The quote shows it is in the paper.
In the paper
“However, patients and controls were not matched for physical activity, unravelling a well-known bias due to deconditioning in COPD patients.”
§ Main Pathogenic Mechanisms and Recent Advances in COPD Peripheral Skeletal Muscle Wasting > 7. Other Metabolic Processes
Strength:boosted· not yet calibratedCausal:direct· not yet calibratedTests✓ Asserted: passes✓ Checkable: passes? Load-bearing: unclear✓ Based: passesIt may state two separate claims as one.
In the paper
“Furthermore, in 2010, a study conducted by Timmons and colleagues identified 11 single-nucleotide polymorphisms (SNPs) associated with the increase in maximal oxygen uptake (VO2max) after exercise training in the general population [150].”
§ Main Pathogenic Mechanisms and Recent Advances in COPD Peripheral Skeletal Muscle Wasting > 8. Genetic Predisposition and Epigenetic Modifications
What the sources say
- Not checked — no full text of the sourcecites [150] Timmons, 2010, Using Molecular Classification to Predict Gains in Maximal Aerobic Capacity Following Endurance Exercise Training in Humans, J. Appl. Physiol. source
Strength:plain· not yet calibratedCausal:correlational· not yet calibratedTests✓ Asserted: passes✓ Checkable: passes✗ Load-bearing: fails✓ Based: passesProbably not a substantial claim. The paper’s conclusions may not depend on it.
In the paper
“Epigenetic modifications are believed to control muscle fiber type, and can be influenced by external factors such as nutrition [153].”
§ Main Pathogenic Mechanisms and Recent Advances in COPD Peripheral Skeletal Muscle Wasting > 8. Genetic Predisposition and Epigenetic Modifications
What the sources say
- Not checked — no full text of the sourcecites [153] Baar, 2010, Epigenetic Control of Skeletal Muscle Fibre Type, Acta Physiol. source
Strength:hedged· not yet calibratedCausal:conditional· not yet calibratedTests✓ Asserted: passes✓ Checkable: passes✗ Load-bearing: fails✓ Based: passesProbably not a substantial claim. The paper’s conclusions may not depend on it. It may state two separate claims as one.
In the paper
“These results point towards an impairment of the muscle energy production and are consistent with other studies showing low baseline creatine kinase and ATP concentrations [121].”
§ Main Pathogenic Mechanisms and Recent Advances in COPD Peripheral Skeletal Muscle Wasting > 7. Other Metabolic Processes
What the sources say
- Not checked — no full text of the sourcecites [121] Barreiro, 2005, Expression and Carbonylation of Creatine Kinase in the Quadriceps Femoris Muscles of Patients with Chronic Obstructive Pulmonary Disease, Am. J. Respir. Cell Mol. Biol. source
Tests✓ Asserted: passes✓ Checkable: passes✓ Load-bearing: passes✓ Based: passesIt may state two separate claims as one.
What the paper did — it cites no source for this, so there is none to check. The quote shows it is in the paper.
In the paper
“However, in that study, although the authors performed muscular biopsies, they did not investigate the level of miRNA in the quadriceps, which would have allowed them to perform correlations with plasma levels.”
§ Main Pathogenic Mechanisms and Recent Advances in COPD Peripheral Skeletal Muscle Wasting > 8. Genetic Predisposition and Epigenetic Modifications
Strength:plain· not yet calibratedTests✓ Asserted: passes✓ Checkable: passes✗ Load-bearing: fails✓ Based: passesProbably not a substantial claim. The paper’s conclusions may not depend on it. It may state two separate claims as one.
In the paper
“More recently, Balnis and colleagues showed in satellite cells a defective autophagic flux associated with important proteins’ upregulation such as Beclin-1. In that work, autophagy seemed to be correlated to satellite cell dysfunction contributing to the pathogenesis of emphysema in a transgenic mouse model [185].”
§ Main Pathogenic Mechanisms and Recent Advances in COPD Peripheral Skeletal Muscle Wasting > 9. Consequences on Muscle Mass Regulation > 9.1. Protein Degradation
What the sources say
- Not checked — no full text of the sourcecites [185] Balnis, 2022, Deaccelerated Myogenesis and Autophagy in Genetically Induced Pulmonary Emphysema, Am. J. Respir. Cell Mol. Biol. source
Strength:hedged· not yet calibratedCausal:correlational· not yet calibratedTests✓ Asserted: passes✓ Checkable: passes? Load-bearing: unclear✓ Based: passesIt may state two separate claims as one.
In the paper
“In the quadriceps of exacerbating COPD patients, IGF-1 was found downregulated at the mRNA level, as well as myoD at the protein level [28].”
§ Main Pathogenic Mechanisms and Recent Advances in COPD Peripheral Skeletal Muscle Wasting > 9. Consequences on Muscle Mass Regulation > 9.2. Protein Synthesis
What the sources say
- Not checked — no full text of the sourcecites [28] Crul, 2007, Markers of Inflammation and Disuse in Vastus Lateralis of Chronic Obstructive Pulmonary Disease Patients, Eur. J. Clin. Investig. source
Strength:plain· not yet calibratedTests✓ Asserted: passes✓ Checkable: passes? Load-bearing: unclear✓ Based: passesIt may state two separate claims as one.
What the paper did — it cites no source for this, so there is none to check. The quote shows it is in the paper.
In the paper
“However, that study lacked the assessment of the LC3BII/LC3BI ratio (reflecting the active form) as well as that of other autophagy markers.”
§ Main Pathogenic Mechanisms and Recent Advances in COPD Peripheral Skeletal Muscle Wasting > 9. Consequences on Muscle Mass Regulation > 9.1. Protein Degradation
Strength:plain· not yet calibratedTests✓ Asserted: passes✓ Checkable: passes? Load-bearing: unclear✓ Based: passesIt may state two separate claims as one.
In the paper
“Yet, its expression has not been thoroughly investigated in COPD, with only one report indicating an increased expression in COPD quadriceps [169].”
§ Main Pathogenic Mechanisms and Recent Advances in COPD Peripheral Skeletal Muscle Wasting > 9. Consequences on Muscle Mass Regulation > 9.1. Protein Degradation
What the sources say
- Not checked — no full text of the sourcecites [169] Plant, 2010, Cellular Markers of Muscle Atrophy in Chronic Obstructive Pulmonary Disease, Am. J. Respir. Cell Mol. Biol. source
Strength:plain· not yet calibratedTests✓ Asserted: passes✓ Checkable: passes✗ Load-bearing: fails✓ Based: passesProbably not a substantial claim. The paper’s conclusions may not depend on it.
What the paper did — it cites no source for this, so there is none to check. The quote shows it is in the paper.
In the paper
“Of note, this study was not conducted on the same patients (exacerbating versus stable COPD patients).”
§ Main Pathogenic Mechanisms and Recent Advances in COPD Peripheral Skeletal Muscle Wasting > 9. Consequences on Muscle Mass Regulation > 9.1. Protein Degradation
Strength:plain· not yet calibratedTests✓ Asserted: passes✓ Checkable: passes✗ Load-bearing: fails✓ Based: passesProbably not a substantial claim. The paper’s conclusions may not depend on it.
A conclusion the paper draws from its own results — it cites no other source for it, so there is none to check. The quote shows it is in the paper.
In the paper
“These discrepancies might come from the diversity in patients’ recruitment and warrant further investigations, although once again, the timing of the investigation is probably the most crucial point.”
§ Main Pathogenic Mechanisms and Recent Advances in COPD Peripheral Skeletal Muscle Wasting > 9. Consequences on Muscle Mass Regulation > 9.1. Protein Degradation
Strength:hedged· not yet calibratedCausal:conditional· not yet calibratedTests✓ Asserted: passes✓ Checkable: passes✗ Load-bearing: fails✓ Based: passesProbably not a substantial claim. The paper’s conclusions may not depend on it. It may state two separate claims as one.
In the paper
“Puig-Vilanova and colleagues reported an increase in p38-MAPK levels in COPD quadriceps but an unchanged ERK1/2 expression [123].”
§ Main Pathogenic Mechanisms and Recent Advances in COPD Peripheral Skeletal Muscle Wasting > 9. Consequences on Muscle Mass Regulation > 9.1. Protein Degradation
What the sources say
- Not checked — no full text of the sourcecites [123] Rodriguez, 2015, Oxidative Stress, Redox Signaling Pathways, and Autophagy in Cachectic Muscles of Male Patients with Advanced COPD and Lung Cancer, Free Radic. Biol. Med. source
Strength:plain· not yet calibratedTests✓ Asserted: passes✓ Checkable: passes? Load-bearing: unclear✓ Based: passesIt may state two separate claims as one.
In the paper
“Upon binding to its receptor, the activin receptor type II A/B, it activates catabolic pathways via the phosphorylation of downstream effectors Smad2/3 and simultaneously inhibits anabolic pathways [175].”
§ Main Pathogenic Mechanisms and Recent Advances in COPD Peripheral Skeletal Muscle Wasting > 9. Consequences on Muscle Mass Regulation > 9.1. Protein Degradation
What the sources say
- Not checked — no full text of the sourcecites [175] Morissette, 2009, Myostatin Inhibits IGF-I-Induced Myotube Hypertrophy through Akt, Am. J. Physiol. Cell Physiol. source
Tests✓ Asserted: passes✓ Checkable: passes✓ Load-bearing: passes✓ Based: passesIt may state two separate claims as one.
A conclusion the paper draws from its own results — it cites no other source for it, so there is none to check. The quote shows it is in the paper.
In the paper
“In skeletal muscle, protein synthesis is mainly mediated by the IGF/Akt/mTOR pathway, which seems globally decreased, although contradictory data between mRNA and protein levels of different components of the cascade have been reported.”
§ Main Pathogenic Mechanisms and Recent Advances in COPD Peripheral Skeletal Muscle Wasting > 9. Consequences on Muscle Mass Regulation > 9.2. Protein Synthesis
Tests✓ Asserted: passes✓ Checkable: passes✓ Load-bearing: passes✓ Based: passesIt may state two separate claims as one.
In the paper
“A major other proteolytic pathway is autophagy-induced lysosomal degradation, an essential process leading to the degradation of cytoplasmic portions of variable sizes in the lysosomes (see the review by [179]).”
§ Main Pathogenic Mechanisms and Recent Advances in COPD Peripheral Skeletal Muscle Wasting > 9. Consequences on Muscle Mass Regulation > 9.1. Protein Degradation
What the sources say
- Not checked — no full text of the sourcecites [179] Hussain, 2013, Role of Autophagy in COPD Skeletal Muscle Dysfunction, J. Appl. Physiol. source
Strength:plain· not yet calibratedCausal:direct· not yet calibratedTests✓ Asserted: passes✓ Checkable: passes✗ Load-bearing: fails✓ Based: passesProbably not a substantial claim. The paper’s conclusions may not depend on it.
In the paper
“It also seems to play an essential role in skeletal muscle wasting, as muscle-autophagy-deficient mice (muscle-specific deletion of Atg7) exhibit sarcopenia features [181].”
§ Main Pathogenic Mechanisms and Recent Advances in COPD Peripheral Skeletal Muscle Wasting > 9. Consequences on Muscle Mass Regulation > 9.1. Protein Degradation
What the sources say
- Not checked — no full text of the sourcecites [181] Masiero, 2009, Autophagy Is Required to Maintain Muscle Mass, Cell Metab. source
Strength:hedged· not yet calibratedCausal:conditional· not yet calibratedTests✓ Asserted: passes✓ Checkable: passes? Load-bearing: unclear✓ Based: passesIt may state two separate claims as one.
A conclusion the paper draws from its own results — it cites no other source for it, so there is none to check. The quote shows it is in the paper.
In the paper
“Although conflicting results have been reported, the global conclusion is that autophagy is enhanced in COPD locomotor muscles.”
§ Main Pathogenic Mechanisms and Recent Advances in COPD Peripheral Skeletal Muscle Wasting > 9. Consequences on Muscle Mass Regulation > 9.1. Protein Degradation
Tests✓ Asserted: passes✓ Checkable: passes✓ Load-bearing: passes✓ Based: passesIt may state two separate claims as one.
In the paper
“For example, a study performed on the quadriceps of 91 COPD patients showed that Akt phosphorylation was decreased in COPD compared to healthy subjects as well as in sarcopenic versus nonsarcopenic patients. However, other markers of protein synthesis signaling such as S6- or 4EBP1-phosphorylations were increased in both cases [188].”
§ Main Pathogenic Mechanisms and Recent Advances in COPD Peripheral Skeletal Muscle Wasting > 9. Consequences on Muscle Mass Regulation > 9.2. Protein Synthesis
What the sources say
- Not checked — no full text of the sourcecites [188] Kneppers, 2016, Impaired Coordination of Skeletal Muscle Protein Turnover Signalling in Sarcopenic COPD Patients, Eur. Respir. J. source
Tests✓ Asserted: passes✓ Checkable: passes? Load-bearing: unclear✓ Based: passesIt may state two separate claims as one.
A conclusion the paper draws from its own results — it cites no other source for it, so there is none to check. The quote shows it is in the paper.
In the paper
“Discrepancies between studies might come from the complex interconnection between pathways, as well as the patients’ selection and the fact that biopsies are taken at different time courses of the disease.”
§ Main Pathogenic Mechanisms and Recent Advances in COPD Peripheral Skeletal Muscle Wasting > 9. Consequences on Muscle Mass Regulation > 9.2. Protein Synthesis
Strength:hedged· not yet calibratedCausal:conditional· not yet calibratedTests✓ Asserted: passes✓ Checkable: passes✗ Load-bearing: fails✓ Based: passesProbably not a substantial claim. The paper’s conclusions may not depend on it. It may state two separate claims as one.
A conclusion the paper draws from its own results — it cites no other source for it, so there is none to check. The quote shows it is in the paper.
In the paper
“In this regard, experimental models can help study every stage of muscle wasting, provided that their functional and histological characteristics fit those of the disease.”
§ Main Pathogenic Mechanisms and Recent Advances in COPD Peripheral Skeletal Muscle Wasting > 10. Conclusions
Strength:plain· not yet calibratedCausal:conditional· not yet calibratedTests✓ Asserted: passes✓ Checkable: passes✗ Load-bearing: fails✗ Based: failsProbably not a substantial claim. The paper’s conclusions may not depend on it. The paper may give no reason why it holds.
A conclusion the paper draws from its own results — it cites no other source for it, so there is none to check. The quote shows it is in the paper.
In the paper
“Skeletal muscle wasting is a crucial issue for COPD patients, both associated with an impaired quality of life and a significant mortality.”
§ Main Pathogenic Mechanisms and Recent Advances in COPD Peripheral Skeletal Muscle Wasting > 10. Conclusions
Tests✓ Asserted: passes✓ Checkable: passes✓ Load-bearing: passes? Based: unclearIt may state two separate claims as one.
A conclusion the paper draws from its own results — it cites no other source for it, so there is none to check. The quote shows it is in the paper.
In the paper
“Indeed, skeletal muscle tissue alterations in rodent models are inconsistent, partly due to the diversity of the experimental procedures used (CS exposure, elastase or lipopolysaccharide instillations, transgenic models, etc.).”
§ Main Pathogenic Mechanisms and Recent Advances in COPD Peripheral Skeletal Muscle Wasting > 9. Consequences on Muscle Mass Regulation > 9.2. Protein Synthesis
Strength:plain· not yet calibratedCausal:conditional· not yet calibratedTests✓ Asserted: passes✓ Checkable: passes? Load-bearing: unclear✓ Based: passesIt may state two separate claims as one.
A conclusion the paper draws from its own results — it cites no other source for it, so there is none to check. The quote shows it is in the paper.
In the paper
“The underlying pathophysiology is vastly multifactorial and implies both extrinsic and intrinsic factors.”
§ Main Pathogenic Mechanisms and Recent Advances in COPD Peripheral Skeletal Muscle Wasting > 10. Conclusions
Tests✓ Asserted: passes✓ Checkable: passes✓ Load-bearing: passes✓ Based: passesIt may state two separate claims as one.
The paper relies on this without support.
Physical inactivity is a major confounding factor, challenging to rule out in comparative studies including healthy subjects and COPD patients.
“physical inactivity is a major confounding factor, challenging to rule out in comparative studies including healthy subjects and COPD patients.”
The paper relies on this without support.
Cancer is a well-known contributor of muscle wasting.
“cancer is a well-known contributor of muscle wasting.”
The paper relies on this without support.
Peripheral muscles are a heterogeneous group comprising locomotor muscles (mainly lower limb muscles) and upper limb muscles, both submitted to different force constraints.
“peripheral muscles are actually a heterogeneous group comprising locomotor muscles (mainly lower limb muscles) and upper limb muscles, both submitted to different force constraints.”
The paper relies on this without support.
Muscle wasting is a dynamic process where the same molecules can be up- or downregulated according to the regenerative stage.
“muscle wasting is a dynamic process where the same molecules can be up- or downregulated according to the regenerative stage.”
The paper relies on this without support.
Experimental animal models of COPD allow access to every muscle as well as time-course studies.
“Several clues can be provided by experimental animal models of COPD, which allow access to every muscle as well as time-course studies.”
The paper relies on this without support.
HIF-1α is a major effector of hypoxic pathways.
“The transcription factor hypoxia-inducible-factor-1α (HIF-1α) is a major effector of hypoxic pathways.”
The paper relies on this without support.
Muscle protein turnover is impaired in COPD through both enhanced degradation and reduced synthesis.
“A consensual statement is that muscle protein turnover is impaired both through enhanced degradation and reduced synthesis.”
The paper relies on this without support.
The mechanisms reviewed (mitochondrial dysfunction, oxidative stress, metabolic alterations, genetic and epigenetic changes) are pathogenic for COPD peripheral skeletal muscle wasting.
“All mechanisms detailed above converge to deleterious consequences on muscle mass regulation, destabilizing the atrophy/hypertrophy balance.”
Self-check
Percentages, sums and reported differences re-computed from the paper’s own numbers.
Each contradiction between two passages listed here was confirmed by an independent check.
Hypoxia findings are said to align with a cited opposite result
MinorThe text says reduced MyoD expression under hypoxia is in line with reference 79, whose listed title reports hypoxia-induced up-regulation of MyoD and a positive effect on myogenic differentiation.
“In an experimental model of hindlimb ischemia, hypoxia induced a reduced protein expression of the skeletal-muscle differentiation markers (myogenic differentiation 1 (MyoD) and myogenin) [78]. These observations were in line with that already shown in vitro [79].”
“79. Kook S.-H. Son Y.-O. Lee K.-Y. Lee H.-J. Chung W.-T. Choi K.-C. Lee J.-C. Hypoxia Affects Positively the Proliferation of Bovine Satellite Cells and Their Myogenic Differentiation through Up-Regulation of MyoD”
Citations
Cites
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“Since mitochondrial oxidative phosphorylation is incomplete, mitochondria are a major source of ROS production [119].”
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Schiaffino, S., & Reggiani, C. (2011) · Physiological Reviews · doi:10.1152/physrev.00031.2010 · Cited by 3,022 · cited 1×
“However, other observations tend to show that metabolic and contractile properties are controlled by distinct signaling pathways [103].”
BackgroundChronic Obstructive Pulmonary Disease
Flavin, K., Morkane, C. M., & Marsh, S. (2018) · Cambridge University Press eBooks · doi:10.1017/9781108233712.025 · Cited by 2,687
Wallace, D. C. (2012) · Nature Reviews Cancer · doi:10.1038/nrc3365 · Cited by 2,404 · cited 1×
“IDH2 is the enzyme responsible for the oxidative decarboxylation of isocitrate to α-ketoglutarate, and its lower activity is largely described in oncology, where it leads to a reduced metabolic activity [95].”
BackgroundSystemic manifestations and comorbidities of COPD
Barnes, P. J., & Celli, B. R. (2009) · European Respiratory Journal · doi:10.1183/09031936.00128008 · Cited by 1,863 · cited 1×
“Indeed, it has been hypothesized that COPD muscle atrophy would be a consequence of the “spill over” of inflammatory molecules from the lungs into the systemic circulation [18].”
BackgroundZhao, J., Brault, J. J., Schild, A., Cao, P., Sandri, M., Schiaffino, S., Lecker, S. H., & Goldberg, A. L. (2007) · Cell Metabolism · doi:10.1016/j.cmet.2007.11.004 · Cited by 1,489 · cited 1×
“Indeed, it has been shown that FOXO3 overexpression in C2C12 myotubes, as well as in isolated mouse muscle fibers, enhanced proteolysis mainly via lysosomal degradation [186].”
BackgroundAutophagy is required to maintain muscle mass.
Masiero, E., Agatea, L., Mammucari, C., Blaauw, B., Loro, E., Komatsu, M., Metzger, D., Reggiani, C., Schiaffino, S., & Sandri, M. (2009) · Cell Metabolism · doi:10.1016/j.cmet.2009.10.008 · Cited by 1,282 · cited 1×
“It also seems to play an essential role in skeletal muscle wasting, as muscle-autophagy-deficient mice (muscle-specific deletion of Atg7) exhibit sarcopenia features [181].”
BackgroundMaltais, F., Decramer, M., Casaburi, R. H., Barreiro, E., Burelle, Y., Debigaré, R., Dekhuijzen, P. N. R., Franssen, F. M. E., Gayan‐Ramirez, G., Gea, J., et al. (2014) · American Journal of Respiratory and Critical Care Medicine · doi:10.1164/rccm.201402-0373st · Cited by 1,165 · cited 1×
“Among them, skeletal muscle wasting is a prevalent and severe condition, affecting up to 35% of the patients depending on the considered population (ambulatory or nursinghome-based), and responsible for substantial morbidity and mortality [6,7].”
BackgroundSelf-citationChronic Obstructive Pulmonary Disease
Barnes, P. J. (2000) · New England Journal of Medicine · doi:10.1056/nejm200007273430407 · Cited by 1,078 · cited 1×
“Lung features of COPD include both airway obstruction, currently used to diagnose the disease and the disruption of alveolar walls called emphysema [4].”
BackgroundChronic obstructive pulmonary disease
Rabe, K. F., & Watz, H. (2017) · The Lancet · doi:10.1016/s0140-6736(17)31222-9 · Cited by 1,030 · cited 1×
“It is a chronic respiratory disease primarily linked to inhaled noxious particles exposure, mainly tobacco smoke, but also biomass fuel in developing countries [2], although recent research increasingly considers the role of different risk factors in very early life (i.”
BackgroundInterleukin-6 Is an Essential Regulator of Satellite Cell-Mediated Skeletal Muscle Hypertrophy
Serrano, A. L., Baeza-Raja, B., Perdiguero, E., Jardí, M., & Muñoz-Cánoves, P. (2008) · Cell Metabolism · doi:10.1016/j.cmet.2007.11.011 · Cited by 873 · cited 1×
“In vitro, IL-6 bears anabolic effects by regulating satellite cells’ function and enhancing glucose metabolism; furthermore, a loss of IL-6 signaling in myoblasts results in a reduced proliferation and migration [49,50].”
BackgroundVanfleteren, L. E. G. W., Spruit, M. A., Groenen, M. T. J., Gaffron, S., van Empel, V. P. M., Bruijnzeel, P. L. B., Rutten, E. P. A., Roodt, J. O. ’., Wouters, E. F. �., & Franssen, F. M. E. (2013) · American Journal of Respiratory and Critical Care Medicine · doi:10.1164/rccm.201209-1665oc · Cited by 829 · cited 1×
“Among them, skeletal muscle wasting is a prevalent and severe condition, affecting up to 35% of the patients depending on the considered population (ambulatory or nursinghome-based), and responsible for substantial morbidity and mortality [6,7].”
BackgroundPeripheral Muscle Weakness in Patients with Chronic Obstructive Pulmonary Disease
BERNARD, S., LeBLANC, P., WHITTOM, F., CARRIER, G., JOBIN, J., BELLEAU, R., & MALTAIS, F. (1998) · American Journal of Respiratory and Critical Care Medicine · doi:10.1164/ajrccm.158.2.9711023 · Cited by 817 · cited 2×
“Structural alterations of peripheral skeletal muscle are well characterized and include a global muscle atrophy (with both loss in number and size of muscle fibers), macroscopically reflected by a decrease in thigh diameter [11] and microscopically reflected by a decreased fibers’ cr ss-sectional area (CSA) [12] (Figu…”
BackgroundRegulation of Muscle Growth and Regeneration by the Immune System
Tidball, J. G. (2017) · Nature Reviews Immunology · doi:10.1038/nri.2016.150 · Cited by 740 · cited 1×
“In myocytes, the binding of TNF-α to its receptor TNF-R activates the p38-mitogen-activated protein kinase (MAPK) pathway, leading to a silencing of target genes such as Pax7 and Notch1 (via an epigenetic control), promoting satellite cell differentiation into myotubes [39], in contrast to that previously reported [40…”
ResultPathogenesis of sarcopenia and the relationship with fat mass: descriptive review
Li, C., Yu, K., Shyh‐Chang, N., Jiang, Z., Liu, T., Ma, S., Luo, L., Guang, L., Liang, K., Ma, W., et al. (2022) · Journal of Cachexia, Sarcopenia and Muscle · doi:10.1002/jcsm.12901 · Cited by 626 · cited 1×
“Adipose tissue infiltration has also been reported in COPD muscle, in a similar way to senescent muscle in the aging population, particularly in the obese sarcopenic phenotype where adipose inflammation leads to the redistribution of fat to the intra-abdominal area and skeletal muscle tissue [16,17] (Figure 1).”
BackgroundMitophagy-dependent necroptosis contributes to the pathogenesis of COPD
Mizumura, K., Cloonan, S. M., Nakahira, K., Bhashyam, A. R., Cervo, M., Kitada, T., Glass, K., Owen, C. A., Mahmood, A., Washko, G. R., et al. (2014) · Journal of Clinical Investigation · doi:10.1172/jci74985 · Cited by 611 · cited 1×
“Evidence of increased mitophagy, mainly attributed to CS exposure, has already been reported in the lung [106].”
BackgroundRisk factors and early origins of chronic obstructive pulmonary disease
Postma, D. S., Bush, A., & van den Berge, M. (2014) · The Lancet · doi:10.1016/s0140-6736(14)60446-3 · Cited by 539 · cited 1×
“, in utero and during early childhood) in the development of COPD [3].”
BackgroundIL-4 Acts as a Myoblast Recruitment Factor during Mammalian Muscle Growth
Horsley, V., Jansen, K. M., Mills, S. T., & Pavlath, G. K. (2003) · Cell · doi:10.1016/s0092-8674(03)00319-2 · Cited by 532 · cited 1×
“Other myokines can also play a role in the control of muscle mass, most of which having not been thoroughly investigated in COPD, such as IL-4 (promoting myoblast fusion in vitro) [61], IL-7, which secretion by skeletal muscle gradually decreases with age [20], or irisin, known to decrease oxidant-induced apoptosis in…”
BackgroundEgr-1 Regulates Autophagy in Cigarette Smoke-Induced Chronic Obstructive Pulmonary Disease
Chen, Z.-H., Kim, H. P., Sciurba, F. C., Lee, S.-J., Feghali-Bostwick, C., Stolz, D. B., Dhir, R., Landreneau, R. J., Schuchert, M. J., Yousem, S. A., et al. (2008) · PLoS ONE · doi:10.1371/journal.pone.0003316 · Cited by 459 · cited 2×
“After that, several reports pointed out an enhanced autophagy in COPD muscle, confirming the data observed in the lung [180].”
BackgroundResultWHITTOM, F., JOBIN, J., SIMARD, P.-M., LEBLANC, P., SIMARD, C., BERNARD, S., BELLEAU, R., & MALTAIS, F. (1998) · Medicine & Science in Sports & Exercise · doi:10.1097/00005768-199810000-00001 · Cited by 447 · cited 1×
“Capillarization has notably been found impaired specifically in type I muscle fibers, which has a deep impact on the muscle’s oxidative capacity [14,15].”
BackgroundReactive Oxygen Species Are Signalling Molecules for Skeletal Muscle Adaptation
Powers, S. K., Duarte, J., Kavazis, A. N., & Talbert, E. E. (2010) · Experimental Physiology · doi:10.1113/expphysiol.2009.050526 · Cited by 440 · cited 1×
“It is also likely that oxidative stress enhances proteolysis via the calpain and caspase pathways [133], whereas this has not been directly demonstrated in COPD muscle.”
BackgroundSkeletal Muscle as Potential Central Link between Sarcopenia and Immune Senescence
Nelke, C., Dziewas, R., Minnerup, J., Meuth, S. G., & Ruck, T. (2019) · eBioMedicine · doi:10.1016/j.ebiom.2019.10.034 · Cited by 437 · cited 3×
“Chronic, low-grade inflammation induces muscle catabolism via pleiotropic mechanisms mediated by the inflammatory secretome [20], whereas acute inflammation (exercise-mediated or in acute muscle injury models) activates anabolic pathways leading to muscle regeneration.”
BackgroundTsujinaka, T., Fujita, J., Ebisui, C., Yano, M., Kominami, E., Suzuki, K., Tanaka, K., Katsume, A., Ohsugi, Y., Shiozaki, H., et al. (1996) · Journal of Clinical Investigation · doi:10.1172/jci118398 · Cited by 421 · cited 1×
“Overall, the pilot study of Tsujinaka and colleagues showed that transgenic mice chronically overexpressing IL-6 exhibit a marked muscle atrophy [47]; however, the knockout of IL-6 was not sufficient to”
BackgroundLiu, D., Black, B. L., & Derynck, R. (2001) · Genes & Development · doi:10.1101/gad.925901 · Cited by 399 · cited 1×
“Myostatin is a ligand of the TGF-β pathway in skeletal muscle and a well-known negative regulator of muscle mass, as it inhibits satellite cells’ proliferation and differentiation [174].”
BackgroundTimmons, J. A., Knudsen, S., Rankinen, T., Koch, L. G., Sarzynski, M., Jensen, T., Keller, P., Scheele, C., Vollaard, N. B. J., Nielsen, S., et al. (2010) · Journal of Applied Physiology · doi:10.1152/japplphysiol.01295.2009 · Cited by 358 · cited 1×
“Furthermore, in 2010, a study conducted by Timmons and colleagues identified 11 single-nucleotide polymorphisms (SNPs) associated with the increase in maximal oxygen uptake (VO2max) after exercise training in the general population [150].”
BackgroundSkeletal Muscle Apoptosis and Weight Loss in Chronic Obstructive Pulmonary Disease
Agustí, A. G. N., Sauleda, J., Miralles, C., Gomez, C., Togores, B., Sala, E., Batle, S., & Busquets, X. (2002) · American Journal of Respiratory and Critical Care Medicine · doi:10.1164/rccm.2108013 · Cited by 343 · cited 1×
“Since the early reports of Agusti and colleagues and Gosker and colleagues, who observed, respectively, an increased and unchanged myonuclear fragmentation in muscle cells [111,112], only one study reported increased terminal deoxynucleotidyl transferase mediated dUTP nick-end labeling (TUNEL)-positive cells in quadri…”
ResultLach-Trifilieff, E., Minetti, G. C., Sheppard, K., Ibebunjo, C., Feige, J. N., Hartmann, S., Brachat, S., Rivet, H., Koelbing, C., Morvan, F., et al. (2014) · Molecular and Cellular Biology · doi:10.1128/mcb.01307-13 · Cited by 306
Wouters, E. F. M., Creutzberg, E. C., & Schols, A. M. W. J. (2002) · Chest · doi:10.1378/chest.121.5_suppl.127s · Cited by 301 · cited 1×
“Classically, circulating TNF-α is reported to be higher in COPD patients than controls and negatively correlated to lean mass [23,24], as well as to muscle strength, including upper muscles [25].”
BackgroundVillalta, S. A., Rinaldi, C., Deng, B., Liu, G., Fedor, B., & Tidball, J. G. (2011) · Human Molecular Genetics · doi:10.1093/hmg/ddq523 · Cited by 299 · cited 1×
“As a cytokine implicated in muscle regeneration in acute injury models (see below), its potential protective role in muscular dystrophy is not surprising [60].”
BackgroundII. Morphological Adaptations of Human Skeletal Muscle to Chronic Hypoxia*
Hoppeler, H., Kleinert, E., Schlegel, C., Claassen, H., Howald, H., Kayar, S., & Cerretelli, P. (1990) · International Journal of Sports Medicine · doi:10.1055/s-2007-1024846 · Cited by 290 · cited 1×
“Chronic hypoxia in healthy subjects (implicated in altitude expeditions) induces a loss of muscle mass and decreased fibers’ CSA and mitochondrial density, without affecting the capillary network [65].”
BackgroundP38 MAPK Links Oxidative Stress to Autophagy-Related Gene Expression in Cachectic Muscle Wasting
McClung, J. M., Judge, A. R., Powers, S. K., & Yan, Z. (2010) · American Journal of Physiology-Cell Physiology · doi:10.1152/ajpcell.00192.2009 · Cited by 277 · cited 8×
“The authors concluded that CIII was the main site of ROS production in COPD skeletal muscle and attributed this to the absence of matrix antioxidant in close vicinity (contrary to complex I).”
BackgroundInfluentialYende, S. (2005) · Thorax · doi:10.1136/thx.2004.034181 · Cited by 276 · cited 1×
“Circulating IL-6 is also classically elevated in COPD patients compared to healthy subjects, both during and outside exacerbations [44] and associated with reduced quadriceps strength [45].”
BackgroundInflammation induced loss of skeletal muscle
Londhe, P., & Guttridge, D. C. (2015) · Bone · doi:10.1016/j.bone.2015.03.015 · Cited by 276 · cited 1×
“This section focuses on myokines and recent data regarding their role in COPD skeletal muscle; for a general review on each cytokine, see [21] or [22].”
BackgroundBarreiro, E., Peinado, V. I., Galdiz, J. B., Ferrer, E., Marin-Corral, J., Sánchez, F., Gea, J., & Barberà, J. A. (2010) · American Journal of Respiratory and Critical Care Medicine · doi:10.1164/rccm.200908-1220oc · Cited by 272 · cited 1×
“Of note, some studies report no difference in oxidative stress markers between COPD patients and healthy smokers [130], implying that oxidative stress could mainly be attributed to CS extracts and not the specificity of systemic involvement of COPD.”
BackgroundDoyle, A., Zhang, G., Fattah, E. A. A., Eissa, N. T., & Li, Y. (2011) · The FASEB Journal · doi:10.1096/fj.10-164152 · Cited by 256 · cited 1×
“Two studies outside the COPD context also point towards a prominent role of the Toll-like receptor (TLR)-4 pathway in muscle wasting, via the activation of the p38-MAPK atrophy pathway [63,64].”
BackgroundTNF-α is a mitogen in skeletal muscle
Li, Y.-P. (2003) · American Journal of Physiology-Cell Physiology · doi:10.1152/ajpcell.00453.2002 · Cited by 249 · cited 1×
“Other data support the anabolic effects of TNF-α, which acts as a mitogen for satellite cells [38].”
ResultBeckett, E., Stevens, R. L., Jarnicki, A., Kim, R., Hanish, I., Hansbro, N. G., Deane, A., Keely, S., Horvat, J. C., Yang, M., et al. (2013) · Journal of Allergy and Clinical Immunology · doi:10.1016/j.jaci.2012.11.053 · Cited by 248
Baeza-Raja, B., & Muñoz-Cánoves, P. (2004) · Molecular Biology of the Cell · doi:10.1091/mbc.e03-08-0585 · Cited by 247 · cited 1×
“In vitro, IL-6 bears anabolic effects by regulating satellite cells’ function and enhancing glucose metabolism; furthermore, a loss of IL-6 signaling in myoblasts results in a reduced proliferation and migration [49,50].”
BackgroundSkeletal Muscle Wasting and Renewal: A Pivotal Role of Myokine IL-6
Belizário, J. E., Fontes-Oliveira, C. C., Borges, J. P., Kashiabara, J. A., & Vannier, E. (2016) · SpringerPlus · doi:10.1186/s40064-016-2197-2 · Cited by 244
Muscle Atrophy and Hypertrophy Signaling in Patients with Chronic Obstructive Pulmonary Disease
Doucet, M., Russell, A. P., Léger, B., Debigaré, R., Joanisse, D. R., Caron, M.-A., LeBlanc, P., & Maltais, F. (2007) · American Journal of Respiratory and Critical Care Medicine · doi:10.1164/rccm.200605-704oc · Cited by 243 · cited 2×
“In COPD, increased proteolysis is mainly mediated by an overactivation of the ubiquitin (26S)–proteasome system, activated via the muscle-specific E3-ubiquitin ligases Atrogin-1/MAFbx and TRIM63/MuRF-1, also named atrogenes, which are increased in COPD quadriceps [118,165].”
BackgroundMyostatin Inhibits IGF-I-Induced Myotube Hypertrophy through Akt
Morissette, M. R., Cook, S. A., Buranasombati, C., Rosenberg, M. A., & Rosenzweig, A. (2009) · American Journal of Physiology-Cell Physiology · doi:10.1152/ajpcell.00043.2009 · Cited by 231 · cited 1×
“Upon binding to its receptor, the activin receptor type II A/B, it activates catabolic pathways via the phosphorylation of downstream effectors Smad2/3 and simultaneously inhibits anabolic pathways [175].”
BackgroundQuinn, L. S., Anderson, B. G., Drivdahl, R. H., Alvarez, B., & Argilés, J. M. (2002) · Experimental Cell Research · doi:10.1006/excr.2002.5624 · Cited by 226 · cited 1×
“In vitro, IL-15 has an anabolic effect by inducing myosin chain synthesis in myotubes [52], notably in response to TNF-α stimulation [53].”
BackgroundChronic Obstructive Pulmonary Disease: Capillarity and Fiber-Type Characteristics of Skeletal Muscle
Jobin, J., Maltais, F., Doyon, J.-F., LeBlanc, P., Simard, P.-M., Simard, A.-A., & Simard, C. (1998) · Journal of Cardiopulmonary Rehabilitation · doi:10.1097/00008483-199811000-00005 · Cited by 224 · cited 1×
“Other known histological alterations include a decreased capillarity, with both a decrease in capillaries density as well as in the capillary-to-fiber ratio [13] (Figure 1).”
BackgroundLoss of Skeletal Muscle HIF-1α Results in Altered Exercise Endurance
Mason, S. D., Howlett, R. A., Kim, M. J., Olfert, I. M., Hogan, M. C., McNulty, W., Hickey, R. P., Wagner, P. D., Kahn, C. R., Giordano, F. J., et al. (2004) · PLoS Biology · doi:10.1371/journal.pbio.0020288 · Cited by 210 · cited 1×
“Some effects of hypoxia are HIF-1α-independent [76], and interestingly, low levels of HIF-1α in skeletal muscle resulted in a more altered phenotype in a mouse model, with an impaired exercise response [77], indicating either that hypoxia-mediated deleterious effects could be independent of HIF-1 α, or that HIF-1α ele…”
BackgroundInterleukin-6 Causes Myocardial Failure and Skeletal Muscle Atrophy in Rats
Janssen, S. P. M., Gayan‐Ramirez, G., den Bergh, A. V., Herijgers, P., Maes, K., Verbeken, E. K., & Decramer, M. (2005) · Circulation · doi:10.1161/01.cir.0000156469.96135.0d · Cited by 208 · cited 9×
“A study showed that exercise training improved functional capacity in both normoxemic and hypoxemic COPD patients, however the structural improvements (increased mitochondrial density, capillary-to-fiber ratio, and fibers’ CSA) occurred only in the normoxemic ones [80].”
BackgroundInfluentialBonora, M., & Pinton, P. (2014) · Frontiers in Oncology · doi:10.3389/fonc.2014.00302 · Cited by 208 · cited 1×
“Mitochondrial permeability transition pore (mPTP) is a key regulator of mitochondria during cell death [115].”
BackgroundBakkar, N., Wang, J., Ladner, K. J., Wang, H., Dahlman, J. M., Carathers, M., Acharyya, S., Rudnicki, M. A., Hollenbach, A. D., & D, D. C. G. (2008) · The Journal of Cell Biology · doi:10.1083/jcb.200707179 · Cited by 208 · cited 1×
“In myocytes, the binding of TNF-α to its receptor TNF-R activates the p38-mitogen-activated protein kinase (MAPK) pathway, leading to a silencing of target genes such as Pax7 and Notch1 (via an epigenetic control), promoting satellite cell differentiation into myotubes [39], in contrast to that previously reported [40…”
ResultGosker, H. R., Engelen, M. P., van Mameren, H., van Dijk, P. J., van der Vusse, G. J., Wouters, E. F., & Schols, A. M. (2002) · The American Journal of Clinical Nutrition · doi:10.1093/ajcn/76.1.113 · Cited by 200 · cited 13×
“A study showed that exercise training improved functional capacity in both normoxemic and hypoxemic COPD patients, however the structural improvements (increased mitochondrial density, capillary-to-fiber ratio, and fibers’ CSA) occurred only in the normoxemic ones [80].”
BackgroundInfluentialCellular Markers of Muscle Atrophy in Chronic Obstructive Pulmonary Disease
Plant, P. J., Brooks, D., Faughnan, M., Bayley, T., Bain, J., Singer, L., Correa, J., Pearce, D., Binnie, M., & Batt, J. (2010) · American Journal of Respiratory Cell and Molecular Biology · doi:10.1165/rcmb.2008-0382oc · Cited by 190 · cited 2×
“Yet, its expression has not been thoroughly investigated in COPD, with only one report indicating an increased expression in COPD quadriceps [169].”
BackgroundCytokine Profile in Quadriceps Muscles of Patients with Severe COPD
Barreiro, E., Schols, A. M. W. J., Polkey, M. I., Galdiz, J. B., Gosker, H. R., Swallow, E. B., Coronell, C., Gea, J., & on behalf of the ENIGMA in COPD project (2007) · Thorax · doi:10.1136/thx.2007.078030 · Cited by 175 · cited 2×
“In muscle from COPD patients, IL-6 has been reported as unchanged at the transcriptional level (at both stable and exacerbation states) compared to that of healthy controls [27,28].”
ResultBakkar, N., Wang, J., Ladner, K. J., Wang, H., Dahlman, J. M., Carathers, M., Acharyya, S., Rudnicki, M. A., Hollenbach, A. D., & D, D. C. G. (2013) · The Journal of Cell Biology · doi:10.1083/jcb.20070717908082013c · Cited by 174
Abnormal Mitochondrial Function in Locomotor and Respiratory Muscles of COPD Patients
Puente-Maestu, L., Pérez-Parra, J., Godoy, R., Moreno, N., Tejedor, A., González-Aragoneses, F., Bravo, J.-L., Villar Álvarez, F., Camaño, S., & Agustí, A. (2009) · European Respiratory Journal · doi:10.1183/09031936.00112408 · Cited by 172 · cited 1×
“While some authors have found an increased COX activity in COPD patients with resting hypoxemia [96] and with exercise hypoxemia [97], others have not found any significant increase [98].”
BackgroundCytokine Signaling in Skeletal Muscle Wasting
Zhou, J., Liu, B., Liang, C., Li, Y., & Song, Y.-H. (2016) · Trends in Endocrinology & Metabolism · doi:10.1016/j.tem.2016.03.002 · Cited by 172 · cited 1×
“This section focuses on myokines and recent data regarding their role in COPD skeletal muscle; for a general review on each cytokine, see [21] or [22].”
BackgroundKitajima, Y., Yoshioka, K., & Suzuki, N. (2020) · The Journal of Physiological Sciences · doi:10.1186/s12576-020-00768-9 · Cited by 171 · cited 1×
“The ubiquitin–proteasome system plays a major role in protein content turnover by degrading misfolded or defective proteins [163,164].”
BackgroundPeroxisome Proliferator-Activated Receptor Expression Is Reduced in Skeletal Muscle in COPD
Remels, A. H., Schrauwen, P., Broekhuizen, R., Willems, J., Kersten, S., Gosker, H. R., & Schols, A. M. (2007) · European Respiratory Journal · doi:10.1183/09031936.00144106 · Cited by 168 · cited 1×
“Remels and colleagues observed low levels of peroxisome proliferator-activated receptor-gamma coactivator 1 alpha (PGC1-α, the master regulator of mitochondrial biogenesis) and its downstream effector, mitochondrial transcription factor A (TFAM), in COPD quadriceps; these differences were further enhanced in cachectic…”
BackgroundPuig-Vilanova, E., Rodriguez, D. A., Lloreta, J., Ausin, P., Pascual-Guardia, S., Broquetas, J., Roca, J., Gea, J., & Barreiro, E. (2015) · Free Radical Biology and Medicine · doi:10.1016/j.freeradbiomed.2014.11.006 · Cited by 167 · cited 4×
“A significant number of studies reported an increased LC3BII/LC3BI ratio and/or LC3B lipidation (another marker of activation) in COPD quadriceps [123,182,183].”
BackgroundInfluentialTriggers and mechanisms of skeletal muscle wasting in chronic obstructive pulmonary disease
LANGEN, R. C. J., Gosker, H. R., Remels, A. H. V., & Schols, A. M. W. J. (2013) · The International Journal of Biochemistry & Cell Biology · doi:10.1016/j.biocel.2013.06.015 · Cited by 167 · cited 1×
“For a comprehensive review of potential triggers leading to impaired muscle mass regulation (including deconditioning and use of glucocorticoids), see [162].”
BackgroundDownregulation of the Serum Response Factor/MiR-1 Axis in the Quadriceps of Patients with COPD
Lewis, A., Riddoch-Contreras, J., Natanek, S. A., Donaldson, A., Man, W. D.-C., Moxham, J., Hopkinson, N. S., Polkey, M. I., & Kemp, P. R. (2012) · Thorax · doi:10.1136/thoraxjnl-2011-200309 · Cited by 156 · cited 2×
“The pioneer study in the matter was conducted by Lewis and colleagues and showed a decreased expression of miR-1 in COPD quadriceps, as well as an increase in its target, histone deacetylase 4 (HDCA4) at the protein level [155].”
BackgroundSAULEDA, J., GARCÍA-PALMER, F., WIESNER, R. J., TARRAGA, S., HARTING, I., TOMÁS, P., GÓMEZ, C., SAUS, C., PALOU, A., & AGUSTÍ, A. G. N. (1998) · American Journal of Respiratory and Critical Care Medicine · doi:10.1164/ajrccm.157.5.9710039 · Cited by 154 · cited 1×
“While some authors have found an increased COX activity in COPD patients with resting hypoxemia [96] and with exercise hypoxemia [97], others have not found any significant increase [98].”
BackgroundDoes Oxidative Stress Modulate Limb Muscle Atrophy in Severe COPD Patients?
Fermoselle, C., Rabinovich, R., Ausín, P., Puig-Vilanova, E., Coronell, C., Sanchez, F., Roca, J., Gea, J., & Barreiro, E. (2012) · European Respiratory Journal · doi:10.1183/09031936.00137211 · Cited by 148 · cited 5×
“For example, increased Mn-superoxide dismutase (SOD) and Cu-Zn-SOD protein levels have been demonstrated in the quadriceps [118,127], whereas unchanged SOD content and decreased SOD activity have been reported in another study [122], and unchanged MnSOD, Cu/ZnSOD, and catalase expressions in cultured COPD myoblasts an…”
BackgroundResultInfluentialHypoxia Inhibits Myogenic Differentiation through Accelerated MyoD Degradation
Carlo, A. D., Mori, R. D., Martelli, F., Pompilio, G., Capogrossi, M. C., & Germani, A. (2004) · Journal of Biological Chemistry · doi:10.1074/jbc.m313931200 · Cited by 147 · cited 2×
“Hypoxia also alters the terminal maturation of myotubes by decreasing myosin heavy chain’s expression [71].”
BackgroundMeng, Z.-X., Li, S., Wang, L., Ko, H. J., Lee, Y., Jung, D. Y., Okutsu, M., Yan, Z., Kim, J. K., & Lin, J. D. (2013) · Nature Medicine · doi:10.1038/nm.3144 · Cited by 146 · cited 1×
“Among them, one SNPs was located in the DEPTOR gene, of particular interest as it is associated with the regulation of the contractile properties of glycolytic muscles [151].”
BackgroundMitochondrial Dysfunction in COPD Patients with Low Body Mass Index
Rabinovich, R. A., Bastos, R., Ardite, E., Llinàs, L., Orozco-Levi, M., Gea, J., Vilaró, J., Barberà, J. A., Rodríguez-Roisin, R., Fernández-Checa, J. C., et al. (2007) · European Respiratory Journal · doi:10.1183/09031936.00086306 · Cited by 144 · cited 2×
“The first study was performed in isolated mitochondria and showed a diminished state 3:CII respiration in low-body-mass-index (BMI) COPD patients compared to both normal BMI and healthy subjects [99].”
BackgroundHypoxaemia Enhances Peripheral Muscle Oxidative Stress in Chronic Obstructive Pulmonary Disease
Koechlin, C. (2005) · Thorax · doi:10.1136/thx.2004.037531 · Cited by 143 · cited 2×
“Moreover, with regards to muscular TNF-α, significantly elevated, decreased, and unaltered levels have been reported in the quadriceps of COPD patients [27–29], or even undetected at the protein level [30,31], although the effects of TNF-α could also be mediated by the elevated circulating levels.”
BackgroundMuscle Wasting and Impaired Muscle Regeneration in a Murine Model of Chronic Pulmonary Inflammation
LANGEN, R. C. J., Schols, A. M. W. J., KELDERS, M. C. J. M., van der Velden, J. L. J., Wouters, E. F. �., & Janssen-Heininger, Y. M. W. (2006) · American Journal of Respiratory Cell and Molecular Biology · doi:10.1165/rcmb.2006-0103oc · Cited by 138 · cited 1×
“Transgenic mouse TNF-α+/+ Decreased muscle mass and exercise capacity, increased ex vivo fatigue, decreased in vivo regenerative capacity Decreased myofibers’ CSA Increased catabolism (mRNA level), decreased citrate synthase activity [42,207]”
BackgroundJaitovich, A., Angulo, M., Lecuona, E., Dada, L. A., Welch, L. C., Cheng, Y., Gusarova, G., Ceco, E., Liu, C., Shigemura, M., et al. (2015) · Journal of Biological Chemistry · doi:10.1074/jbc.m114.625715 · Cited by 137 · cited 1×
“Conversely, hypercapnia led to AMPK/FoxO3a/MuRF1-dependent muscle fiber size reduction in an experimental model [73].”
BackgroundMuscle Wasting and Changes in Muscle Protein Metabolism in Chronic Obstructive Pulmonary Disease
Jagoe, R. T., & Engelen, M. P. K. J. (2003) · European Respiratory Journal · doi:10.1183/09031936.03.00004608 · Cited by 134
Chronic Endurance Exercise Induces Quadriceps Nitrosative Stress in Patients with Severe COPD
Barreiro, E., Rabinovich, R., Marin-Corral, J., Barbera, J. A., Gea, J., & Roca, J. (2008) · Thorax · doi:10.1136/thx.2008.105163 · Cited by 133 · cited 4×
“tissue [87,127], as well as in cultured myotubes from COPD patients [128].”
BackgroundInfluentialLiu, J., Peng, Y., Wang, X., Fan, Y., Qin, C., Shi, L., Tang, Y., Cao, K., Li, H., Long, J., et al. (2016) · Molecular Pharmaceutics · doi:10.1021/acs.molpharmaceut.5b00516 · Cited by 133 · cited 1×
“Of note, mitochondrial respiration can be affected by external factors, such as glucocorticoid use [105], and the specific role of COPD in altered respiration remains to be elucidated.”
BackgroundChemokines in COPD: From Implication to Therapeutic Use
Henrot, P., Prevel, R., Berger, P., & Dupin, I. (2019) · International Journal of Molecular Sciences · doi:10.3390/ijms20112785 · Cited by 131 · cited 1×
“However, COPD should not be limited to its respiratory features and is now considered as a systemic inflammatory disease implicating a wild range of cytokines and chemokines [5] and including several comorbidities.”
BackgroundSelf-citationRinaldi, M., Maes, K., Vleeschauwer, S. D., Thomas, D., Verbeken, E. K., Decramer, M., Janssens, W., & Gayan‐Ramirez, G. (2012) · Disease Models & Mechanisms · doi:10.1242/dmm.008508 · Cited by 129 · cited 1×
“Nose-only (from 8 weeks to 6 months) Decreased muscle mass; decreased strength Fiber-type switch [198,199]”
BackgroundIncreased Skeletal Muscle-Specific MicroRNA in the Blood of Patients with COPD
Donaldson, A., Natanek, S. A., Lewis, A., Man, W. D.-C., Hopkinson, N. S., Polkey, M. I., & Kemp, P. R. (2013) · Thorax · doi:10.1136/thoraxjnl-2012-203129 · Cited by 128 · cited 1×
“Later, miR-1, miR-206, and miR-133 were found significantly elevated in the plasma of patients with COPD, as well as miR-499, encoded within the slow myosin heavy chain (MHC) gene and thus promoting type I fibers [156].”
BackgroundFavier, F. B., Costes, F., Defour, A., Bonnefoy, R., Lefai, E., Baugé, S., Peinnequin, A., Benoit, H., & Freyssenet, D. (2010) · American Journal of Physiology-Regulatory, Integrative and Comparative Physiology · doi:10.1152/ajpregu.00550.2009 · Cited by 127 · cited 2×
“In the study of Favier and colleagues, hypoxia was followed by a downregulation of the anabolic pathway’s mechanistic target of rapamycin (mTOR) [67] (see Section 9.”
BackgroundTang, K., Wagner, P. D., & Breen, E. C. (2010) · Journal of Cellular Physiology · doi:10.1002/jcp.21955 · Cited by 125 · cited 1×
“Other models tend to corroborate in vitro data, such as a mouse model exposed to CS and exhibiting increased circulating TNF-α levels, which were correlated to detrimental outcomes such as muscle mass, decreased capillarization, and increased catabolism [41].”
van den Borst, B., Slot, I. G. M., Hellwig, V. A. C. V., Vosse, B. A. H., KELDERS, M. C. J. M., Barreiro, E., Schols, A. M. W. J., & Gosker, H. R. (2012) · Journal of Applied Physiology · doi:10.1152/japplphysiol.00508.2012 · Cited by 124 · cited 1×
“Intuitive functional implications arise from these observations, as oxidative stress is negatively correlated to contractile performance [124].”
BackgroundSkeletal Muscle Inflammation and Nitric Oxide in Patients with COPD
Montes de Oca, M., Torres, S. H., De Sanctis, J., Mata, A., Hernández, N., & Tálamo, C. (2005) · European Respiratory Journal · doi:10.1183/09031936.05.00107404 · Cited by 123
Vogiatzis, I., Stratakos, G., Simoes, D. C. M., Terzis, G., Georgiadou, O., Roussos, C., & Zakynthinos, S. (2007) · Thorax · doi:10.1136/thx.2006.069310 · Cited by 122 · cited 1×
“However, inflammation is not the sole driver as exercise can affect factors regulating muscle hypertrophy and regeneration without affecting the levels of systemic or local muscle inflammation [19].”
BackgroundTNF-α impairs regulation of muscle oxidative phenotype: implications for cachexia?
Remels, A. H. V., Gosker, H. R., Schrauwen, P., Hommelberg, P. P. H., Sliwinski, P., Polkey, M., Galdiz, J., Wouters, E. F. M., Langen, R. C. J., & Schols, A. M. W. J. (2010) · The FASEB Journal · doi:10.1096/fj.09-150714 · Cited by 122
Crul, T., Spruit, M. A., Gayan‐Ramirez, G., Quarck, R., Gosselink, R., Troosters, T., Pitta, F., & Decramer, M. (2007) · European Journal of Clinical Investigation · doi:10.1111/j.1365-2362.2007.01867.x · Cited by 117 · cited 3×
“In muscle from COPD patients, IL-8 has been reported as unchanged at the transcriptional level (at both stable and exacerbation states) compared to that of healthy controls [28].”
BackgroundResultAutophagy in Locomotor Muscles of Patients with Chronic Obstructive Pulmonary Disease
Guo, Y., Gosker, H. R., Schols, A. M. W. J., Kapchinsky, S., Bourbeau, J., Sandri, M., Jagoe, R. T., Debigaré, R., Maltais, F., Taivassalo, T., et al. (2013) · American Journal of Respiratory and Critical Care Medicine · doi:10.1164/rccm.201304-0732oc · Cited by 117 · cited 3×
“A significant number of studies reported an increased LC3BII/LC3BI ratio and/or LC3B lipidation (another marker of activation) in COPD quadriceps [123,182,183].”
BackgroundEngelen, M. P., Wouters, E. F., Deutz, N. E., Menheere, P. P., & Schols, A. M. (2000) · The American Journal of Clinical Nutrition · doi:10.1093/ajcn/72.6.1480 · Cited by 116 · cited 1×
“These alterations seem to be further enhanced in emphysema patients with a decrease in almost all AA levels [138].”
BackgroundPOUW, E. M., SCHOLS, A. M. W. J., DEUTZ, N. E. P., & WOUTERS, E. F. M. (1998) · American Journal of Respiratory and Critical Care Medicine · doi:10.1164/ajrccm.158.3.9708097 · Cited by 114 · cited 1×
“Alterations in amino acid (AA) profiles have been reviewed by Jagoe and Engelen [136] and include decreased glutamate and glutathione levels in COPD quadriceps [137].”
BackgroundAntibody-Directed Myostatin Inhibition Enhances Muscle Mass and Function in Tumor-Bearing Mice
Murphy, K. T., Chee, A., Gleeson, B. G., Naim, T., Swiderski, K., Koopman, R., & Lynch, G. S. (2011) · American Journal of Physiology-Regulatory, Integrative and Comparative Physiology · doi:10.1152/ajpregu.00121.2011 · Cited by 111 · cited 1×
“However, a recent clinical trial using a monoclonal antibody blocking its receptor has not shown potent results in treating skeletal muscle wasting for COPD patients [177], despite promising results previously obtained in cancer models [178].”
BackgroundPolkey, M. I., Praestgaard, J., Berwick, A., Franssen, F. M. E., Singh, D., Steiner, M. C., Casaburi, R., Tillmann, H.-C., Lach-Trifilieff, E., Roubenoff, R., et al. (2019) · American Journal of Respiratory and Critical Care Medicine · doi:10.1164/rccm.201802-0286oc · Cited by 111 · cited 2×
“However, a recent clinical trial using a monoclonal antibody blocking its receptor has not shown potent results in treating skeletal muscle wasting for COPD patients [177], despite promising results previously obtained in cancer models [178].”
BackgroundProtein Carbonylation in Skeletal Muscles: Impact on Function
Barreiro, E., & Hussain, S. N. A. (2010) · Antioxidants & Redox Signaling · doi:10.1089/ars.2009.2808 · Cited by 108
Ren, H., Accili, D., & Duan, C. (2010) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0909570107 · Cited by 106
TNFα Antagonists for Acute Exacerbations of COPD: A Randomised Double-Blind Controlled Trial
Aaron, S. D., Vandemheen, K. L., Maltais, F., Field, S. K., Sin, D. D., Bourbeau, J., Marciniuk, D. D., FitzGerald, J. M., Nair, P., & Mallick, R. (2013) · Thorax · doi:10.1136/thoraxjnl-2012-202432 · Cited by 103 · cited 1×
“Of note, therapies against TNF-α have not proven to be effective for various outcomes such as dyspnea or a number of exacerbations [43], suggesting that this cytokine is not the primary or at least the sole driver of COPD inflammation.”
BackgroundMuscle and Blood Redox Status after Exercise Training in Severe COPD Patients
Rodriguez, D. A., Kalko, S., Puig-Vilanova, E., Perez-Olabarría, M., Falciani, F., Gea, J., Cascante, M., Barreiro, E., & Roca, J. (2012) · Free Radical Biology and Medicine · doi:10.1016/j.freeradbiomed.2011.09.022 · Cited by 102
Metformin: Experimental and Clinical Evidence for a Potential Role in Emphysema Treatment
Polverino, F., Wu, T. D., Rojas-Quintero, J., Wang, X., Mayo, J., Tomchaney, M., Tram, J., Packard, S., Zhang, D., Cleveland, K. H., et al. (2021) · American Journal of Respiratory and Critical Care Medicine · doi:10.1164/rccm.202012-4510oc · Cited by 100
Myostatin Up-Regulation Is Associated with the Skeletal Muscle Response to Hypoxic Stimuli
Hayot, M., Rodriguez, J., Vernus, B., Carnac, G., Jean, E., Allen, D., Goret, L., Obert, P., Candau, R., & Bonnieu, A. (2011) · Molecular and Cellular Endocrinology · doi:10.1016/j.mce.2010.09.008 · Cited by 98 · cited 2×
“Its expression is increased in the quadriceps of COPD patients [176], possibly related to hypoxia [72].”
BackgroundSelf-citationGosker, H. R., LANGEN, R. C. J., Bracke, K. R., Joos, G., Brusselle, G., Steele, C. H., Ward, K. A., Wouters, E. F. �., & Schols, A. M. W. J. (2008) · American Journal of Respiratory Cell and Molecular Biology · doi:10.1165/rcmb.2008-0312oc · Cited by 97
The Mitochondrial Phenotype of Peripheral Muscle in Chronic Obstructive Pulmonary Disease
Picard, M., Godin, R., Sinnreich, M., Baril, J., Bourbeau, J., Perrault, H., Taivassalo, T., & Burelle, Y. (2008) · American Journal of Respiratory and Critical Care Medicine · doi:10.1164/rccm.200807-1005oc · Cited by 95 · cited 4×
“While some authors have found an increased COX activity in COPD patients with resting hypoxemia [96] and with exercise hypoxemia [97], others have not found any significant increase [98].”
BackgroundResultInfluentialMueller, T. C., Bachmann, J., Prokopchuk, O., Friess, H., & Martignoni, M. E. (2016) · BMC Cancer · doi:10.1186/s12885-016-2121-8 · Cited by 95 · cited 1×
“However, experimental models do not reflect the complexity of human disease, as currently illustrated in the field of cancer research [190], and are quite heterogeneous in their ability to reproduce every characteristic of COPD sarcopenia.”
BackgroundNF-κB Activation Is Required for the Transition of Pulmonary Inflammation to Muscle Atrophy
LANGEN, R. C. J., Haegens, A., Vernooy, J. H. J., Wouters, E. F. �., de Winther, M. P. J., Carlsen, H., Steele, C. H., Shoelson, S. E., & Schols, A. M. W. J. (2012) · American Journal of Respiratory Cell and Molecular Biology · doi:10.1165/rcmb.2011-0119oc · Cited by 91 · cited 2×
“LPS Intratracheal Decreased muscle mass Increased catabolism (mRNA and protein level) [204,205] Figure 2.”
BackgroundKoncarevic, A., Jackman, R. W., & Kandarian, S. C. (2007) · The FASEB Journal · doi:10.1096/fj.06-6665com · Cited by 90
Meyer, A., Zoll, J., Charles, A. L., Charloux, A., de Blay, F., Diemunsch, P., Sibilia, J., Piquard, F., & Geny, B. (2013) · Experimental Physiology · doi:10.1113/expphysiol.2012.069468 · Cited by 90 · cited 1×
“The current knowledge considers that state 3 respiration (ADP-stimulated) is impaired in COPD patients; however, contradictory data are reported regarding complex I- (CI) or complex II-, succinate dehydrogenase (CII-SDH), driven respiration states [100].”
BackgroundBarreiro, E., Gea, J., Matar, G., & Hussain, S. N. A. (2005) · American Journal of Respiratory Cell and Molecular Biology · doi:10.1165/rcmb.2005-0114oc · Cited by 89 · cited 1×
“These results point towards an impairment of the muscle energy production and are consistent with other studies showing low baseline creatine kinase and ATP concentrations [121].”
ResultSkeletal Muscle Molecular Responses to Resistance Training and Dietary Supplementation in COPD
Constantin, D., Menon, M. K., Houchen-Wolloff, L., Morgan, M. D., Singh, S. J., Greenhaff, P., & Steiner, M. C. (2013) · Thorax · doi:10.1136/thoraxjnl-2012-202764 · Cited by 88 · cited 1×
“To our knowledge, only one study has investigated the calpain expression in COPD quadriceps and reported an unchanged expression compared to that of the control group [187].”
ResultRabinovich, R. A., Drost, E., Manning, J. R., Dunbar, D. R., Díaz-Ramos, M., Lakhdar, R., Bastos, R., & MacNee, W. (2015) · Respiratory Research · doi:10.1186/s12931-014-0139-5 · Cited by 88
Cellular interplay in skeletal muscle regeneration and wasting: insights from animal models
Henrot, P., Blervaque, L., Dupin, I., Zysman, M., Estèves, P., Gouzi, F., Hayot, M., Pomiès, P., & Berger, P. (2023) · Journal of Cachexia Sarcopenia and Muscle · doi:10.1002/jcsm.13103 · Cited by 88
Self-citationBarreiro, E., & Gea, J. (2016) · Chronic Respiratory Disease · doi:10.1177/1479972316642366 · Cited by 87 · cited 2×
“In particular, inverse structural changes are usually reported in respiratory muscles, such as an increase in type I fiber proportion, capillary, and mitochondrial density; hence, this review focuses on alterations reported in peripheral muscles, as excellent reviews already address the differences between respiratory…”
BackgroundGarros, R. F., Paul, R., Connolly, M., Lewis, A., Garfield, B. E., Natanek, S. A., Bloch, S., Mouly, V., Griffiths, M. J., Polkey, M. I., et al. (2017) · American Journal of Respiratory and Critical Care Medicine · doi:10.1164/rccm.201701-0101oc · Cited by 86 · cited 1×
“In vitro data showed its implication in mitochondrial stress and transforming growth factor beta (TGF-β) canonical signaling, and an in vivo experimental study confirmed its role in muscle wasting through a decrease of mitochondrial function [160].”
BackgroundThe Ubiquitin Ligase Nedd4-1 Participates in Denervation-Induced Skeletal Muscle Atrophy in Mice
Nagpal, P., Plant, P. J., Correa, J., Bain, A., Takeda, M., Kawabe, H., Rotin, D., Bain, J. R., & Batt, J. A. E. (2012) · PLoS ONE · doi:10.1371/journal.pone.0046427 · Cited by 85 · cited 1×
“Nedd4, another muscle-specific E3-ubiquitin ligase acting through Notch1 signaling [167], has recently drawn attention because of its implication in denervation-induced muscle atrophy [168], here unrelated to Notch1 activation.”
BackgroundAllaire, J., Maltais, F., LeBlanc, P., Simard, P., Whittom, F., Doyon, J., Simard, C., & Jobin, J. (2002) · Muscle & Nerve · doi:10.1002/mus.10039 · Cited by 85 · cited 1×
“For example, several studies have found an increased lipofuscin accumulation in COPD quadriceps [126] and higher levels of hydroxy-2-nonenal (4-HNE) in quadriceps”
BackgroundIL-15 Promotes Human Myogenesis and Mitigates the Detrimental Effects of TNFα on Myotube Development
O’Leary, M. F., Wallace, G. R., Bennett, A. J., Tsintzas, K., & Jones, S. W. (2017) · Scientific Reports · doi:10.1038/s41598-017-13479-w · Cited by 85 · cited 1×
“In vitro, IL-15 has an anabolic effect by inducing myosin chain synthesis in myotubes [52], notably in response to TNF-α stimulation [53].”
BackgroundPuig-Vilanova, E., Martínez-Llorens, J., Ausin, P., Roca, J., Gea, J., & Barreiro, E. (2015) · Clinical Science · doi:10.1042/cs20140428 · Cited by 84 · cited 1×
“Then, Puig-Vilanova and colleagues found inverse results with a local decrease of miR-1 and miR-206 and an increase in HDAC4 in COPD quadriceps (including sarcopenic and nonsarcopenic patients) [157].”
ResultChaillou1, T., & Lanner, J. T. (2016) · The FASEB Journal · doi:10.1096/fj.201600757r · Cited by 84 · cited 2×
“Hypoxia also seems to alter myonuclear turnover by affecting satellite cells’ (muscle stem cells) activity and myogenesis [76].”
BackgroundElevated Levels of IL-18 in Plasma and Skeletal Muscle in Chronic Obstructive Pulmonary Disease
Petersen, A. M. W., Penkowa, M., Iversen, M., Frydelund-Larsen, L., Andersen, J. L., Mortensen, J., Lange, P., & Pedersen, B. K. (2007) · Lung · doi:10.1007/s00408-007-9000-7 · Cited by 83 · cited 2×
“One study has found an elevation of IL-18, another proinflammatory cytokine, in the plasma and the quadriceps of COPD patients (at the mRNA level) compared to healthy controls [51].”
ResultGenetic Polymorphism and Chronic Obstructive Pulmonary Disease
Yuan, C., Chang, D., Lu, G., & Deng, X. (2017) · International Journal of Chronic Obstructive Pulmonary Disease · doi:10.2147/copd.s134161 · Cited by 83
Remels, A. H. V., Gosker, H. R., Verhees, K. J. P., Langen, R. C. J., & Schols, A. M. W. J. (2015) · Endocrinology · doi:10.1210/en.2014-1591 · Cited by 82 · cited 2×
“To our knowledge, only one study investigated HIF-1α expression and found an increased mRNA level in the quadriceps of COPD patients, related to increased TNF-α signaling [36].”
BackgroundAnti-TNF Treatment Reduces Rat Skeletal Muscle Wasting in Monocrotaline-Induced Cardiac Cachexia
Steffen, B. T., Lees, S. J., & Booth, F. W. (2008) · Journal of Applied Physiology · doi:10.1152/japplphysiol.90884.2008 · Cited by 81 · cited 2×
“Mechanistically, TNF-α plays a dual role in muscle mass regulation, possibly via differential signaling according to receptor binding (TNFR1 or TNF-R2) [32,33].”
BackgroundUnravelling the Complexity of COPD by MicroRNAs: It’s a Small World after All
Osei, E. T., Florez-Sampedro, L., Timens, W., Postma, D. S., Heijink, I. H., & Brandsma, C.-A. (2015) · European Respiratory Journal · doi:10.1183/13993003.02139-2014 · Cited by 80 · cited 1×
“Among them, miRNAs represent a growing body of interest in COPD, and they have been associated with several features of the disease in the lung [154].”
BackgroundZhang, M., Tang, J., Li, Y., Xie, Y., Hu, S., Chen, M., Zhang, J., Yang, X., Zhang, Q., & Yang, X. (2017) · Chemico-Biological Interactions · doi:10.1016/j.cbi.2017.09.018 · Cited by 80 · cited 1×
“CS + LPS Decreased myofibers’ CSA Decreased mitochondrial density, altered ultrastructure and oxidative capacity [216,217]”
BackgroundWang, Y., Welc, S. S., Wehling‐Henricks, M., & Tidball, J. G. (2018) · Aging Cell · doi:10.1111/acel.12828 · Cited by 80 · cited 1×
“TNF-α secreted by myeloid cells (CD68+ macrophages) inhibits myotubes fusion in vivo [34], supporting its catabolic role.”
BackgroundChaillou, T. (2018) · Frontiers in Physiology · doi:10.3389/fphys.2018.01450 · Cited by 80 · cited 1×
“At the structural level, hypoxia might favor a fiber-type switch in the muscle of COPD patients [69].”
BackgroundGene Expression Profiling in Vastus Lateralis Muscle During an Acute Exacerbation of COPD
Crul, T., Testelmans, D., Spruit, M., Troosters, T., Gosselink, R., Geeraerts, I., Decramer, M., & Gayan-Ramirez, G. (2010) · Cellular Physiology and Biochemistry · doi:10.1159/000303054 · Cited by 79 · cited 2×
“During exacerbations, this pathway seems to be further enhanced in the quadriceps with the upregulation of MuRF-1 and Atrogin-1 expression [104].”
BackgroundInflammatory Cells and Apoptosis in Respiratory and Limb Muscles of Patients with COPD
Barreiro, E., Ferrer, D., Sanchez, F., Minguella, J., Marin-Corral, J., Martinez-Llorens, J., Lloreta, J., & Gea, J. (2011) · Journal of Applied Physiology · doi:10.1152/japplphysiol.01017.2010 · Cited by 79 · cited 2×
“Since the early reports of Agusti and colleagues and Gosker and colleagues, who observed, respectively, an increased and unchanged myonuclear fragmentation in muscle cells [111,112], only one study reported increased terminal deoxynucleotidyl transferase mediated dUTP nick-end labeling (TUNEL)-positive cells in quadri…”
BackgroundResultRole of Autophagy in COPD Skeletal Muscle Dysfunction
Hussain, S. N. A., & Sandri, M. (2013) · Journal of Applied Physiology · doi:10.1152/japplphysiol.00893.2012 · Cited by 77 · cited 2×
“A major other proteolytic pathway is autophagy-induced lysosomal degradation, an essential process leading to the degradation of cytoplasmic portions of variable sizes in the lysosomes (see the review by [179]).”
BackgroundCigarette smoke-induced oxidative stress in skeletal muscles of mice
Barreiro, E., del Puerto‐Nevado, L., Puig‐Vilanova, E., Pérez-Rial, S., Martín‐Sánchez, F. J., Martínez-Galán, L., Rivera, S. E., Gea, J., González‐Mangado, N., & Peces‐Barba, G. (2012) · Respiratory Physiology & Neurobiology · doi:10.1016/j.resp.2012.02.001 · Cited by 77
Majmundar, A. J., Skuli, N., Mesquita, R. C., Kim, M. N., Yodh, A. G., Nguyen-McCarty, M., & Simon, M. C. (2011) · Molecular and Cellular Biology · doi:10.1128/mcb.05857-11 · Cited by 76 · cited 1×
“In an experimental model of hindlimb ischemia, hypoxia induced a reduced protein expression of the skeletal-muscle differentiation markers (myogenic differentiation 1 (MyoD) and myogenin) [78].”
BackgroundExercise intolerance and systemic manifestations of pulmonary emphysema in a mouse model
Lüthje, L., Raupach, T., Michels, H., Unsöld, B. W., Hasenfuss, G. P., Kögler, H., & Andreas, S. (2009) · Respiratory Research · doi:10.1186/1465-9921-10-7 · Cited by 74 · cited 1×
“Elastase Intratracheal (1X to 5X) Decreased muscle mass and endurance Decreased myofibers’ CSA (type I), fiber-type switch [201,202]”
MethodTuran, N., Kalko, S., Stincone, A., Clarke, K., Sabah, A., Howlett, K., Curnow, S. J., Rodriguez, D. A., Cascante, M., O'Neill, L., et al. (2011) · PLoS Computational Biology · doi:10.1371/journal.pcbi.1002129 · Cited by 74 · cited 1×
“Hypoxia seems to play a prominent role in the skeletal muscle wasting of COPD patients, as suggested by a network-analysis transcriptomic studies evidencing upregulation of four histone deacetylase in the muscle of COPD patients (HDAC 9 and 4, SIRT 2 and 3) compared to that of healthy subjects and correlated with oxyg…”
BackgroundShieh, J., Tseng, H., Jung, F., Yang, S., & Lin, J. (2019) · Mediators of Inflammation · doi:10.1155/2019/7947596 · Cited by 74 · cited 1×
“Bleomycin Intratracheal Decreased myofibers’ CSA Increased catabolism (protein level) [206]”
BackgroundPomiès, P., Blaquière, M., Maury, J., Mercier, J., Gouzi, F., & Hayot, M. (2016) · PLOS ONE · doi:10.1371/journal.pone.0160092 · Cited by 70 · cited 1×
“However, several studies point towards a direct relationship between oxidative stress, atrophy, and the ubiquitin–proteasome pathway [131], including data obtained in experimental models [132].”
BackgroundSelf-citationDecline in muscle strength and running endurance in klotho deficient C57BL/6 mice
Phelps, M., Pettan-Brewer, C., Ladiges, W., & Yablonka‐Reuveni, Z. (2013) · Biogerontology · doi:10.1007/s10522-013-9447-2 · Cited by 69 · cited 1×
“Klotho−/− Decreased grip strength and endurance [209]”
Lewis, A., Lee, J. Y., Donaldson, A. V., Natanek, S. A., Vaidyanathan, S., Man, W. D. ‐., Hopkinson, N. S., Sayer, A. A., Patel, H. P., Cooper, C., et al. (2016) · Journal of Cachexia, Sarcopenia and Muscle · doi:10.1002/jcsm.12078 · Cited by 68 · cited 1×
“An increase in the maternally imprinted miR675 was found in the quadriceps of COPD patients with a low fat-free mass index (FFMI), and this was associated with an inhibition of myoblast proliferation in vitro [159].”
BackgroundHIF modulation of Wnt signaling regulates skeletal myogenesis in vivo
Majmundar, A. J., Lee, D. S. M., Skuli, N., Mesquita, R. C., Kim, M. N., Yodh, A. G., Nguyen-McCarty, M., Li, B., & Simon, M. C. (2015) · Development · doi:10.1242/dev.123026 · Cited by 67 · cited 1×
“In C2C12 myoblasts, HIF-1α inhibits the canonical Wnt signaling known to promote muscle regeneration [74].”
BackgroundTLR4 Activation Is Required for IL-17–Induced Multiple Tissue Inflammation and Wasting in Mice
Tang, H., Pang, S., Wang, M., Xiao, X., Rong, Y., Wang, H., & Zang, Y. Q. (2010) · The Journal of Immunology · doi:10.4049/jimmunol.0903664 · Cited by 63 · cited 1×
“Two studies outside the COPD context also point towards a prominent role of the Toll-like receptor (TLR)-4 pathway in muscle wasting, via the activation of the p38-MAPK atrophy pathway [63,64].”
BackgroundPomiès, P., Rodriguez, J., Blaquière, M., Sedraoui, S., Gouzi, F., Carnac, G., Laoudj‐Chenivesse, D., Mercier, J., Préfaut, C., & Hayot, M. (2015) · Journal of Cellular and Molecular Medicine · doi:10.1111/jcmm.12390 · Cited by 61 · cited 3×
“tissue [87,127], as well as in cultured myotubes from COPD patients [128].”
BackgroundSelf-citationMoresi, V., Garcia-Alvarez, G., Pristerà, A., Rizzuto, E., Albertini, M. C., Rocchi, M., Marazzi, G., Sassoon, D., Adamo, S., & Coletti, D. (2009) · PLoS ONE · doi:10.1371/journal.pone.0005570 · Cited by 60 · cited 1×
“Surprisingly, few data are available to date in COPD despite the fact that caspase-induced apoptosis is a known contributor of muscle wasting [114].”
BackgroundChronic obstructive pulmonary disease and obstructive sleep apnoea-the overlap syndrome.
McNicholas, W. T. (2016) · PubMed Central · doi:10.3978/j.issn.2072-1439.2016.01.52 · Cited by 60 · cited 1×
“Finally, a recent study pointed out a possible role of intermittent hypoxia (such as the nocturnal hypoxemia seen in obstructive sleep apnea disorder, frequent among COPD patients [83]) in skeletal muscle wasting, driven by mitochondrial dysfunction and a lower activity [84].”
BackgroundContribution of the Mitochondria to Locomotor Muscle Dysfunction in Patients with COPD
Taivassalo, T., & Hussain, S. N. A. (2016) · Chest · doi:10.1016/j.chest.2015.11.021 · Cited by 59 · cited 1×
“Thus, it is not surprising that mitochondria appear to be at the center of sarcopenia pathophysiology [85,86].”
BackgroundHernandez Cordero, A. I., Gonzales, N. M., Parker, C. C., Sokolof, G., Vandenbergh, D. J., Cheng, R., Abney, M., Sko, A., Douglas, A., Palmer, A. A., et al. (2019) · The American Journal of Human Genetics · doi:10.1016/j.ajhg.2019.10.014 · Cited by 59 · cited 1×
“Recently, a GWAS performed simultaneously on humans and mice allowed the identification of 23 loci associated with appendicular lean mass [148].”
BackgroundHaji, G., Wiegman, C. H., Michaeloudes, C., Patel, M. S., Curtis, K., Bhavsar, P., Polkey, M. I., Adcock, I. M., Chung, K. F., & on behalf of the COPDMAP consortium (2020) · Respiratory Research · doi:10.1186/s12931-020-01527-5 · Cited by 58 · cited 3×
“A recent study evidenced a decreased in SOD2 quadriceps expression only in severe (GOLD III–IV) COPD patients [89].”
BackgroundEpigenetic Control of Skeletal Muscle Fibre Type
Baar, K. (2010) · Acta Physiologica · doi:10.1111/j.1748-1716.2010.02121.x · Cited by 57 · cited 1×
“Epigenetic modifications are believed to control muscle fiber type, and can be influenced by external factors such as nutrition [153].”
BackgroundKook, S., Son, Y., Lee, K., Lee, H., Chung, W., Choi, K., & Lee, J. (2008) · Cell Biology International · doi:10.1016/j.cellbi.2008.03.017 · Cited by 57 · cited 1×
“These observations were in line with that already shown in vitro [79].”
ResultEliason, G., Abdel-Halim, S. M., Piehl-Aulin, K., & Kadi, F. (2010) · Respiratory Research · doi:10.1186/1465-9921-11-97 · Cited by 57
Time course of cigarette smoke-induced changes of systemic inflammation and muscle structure
Krüger, K., Dischereit, G., Seimetz, M., Wilhelm, J., Weißmann, N., & Mooren, F. C. (2015) · American Journal of Physiology-Lung Cellular and Molecular Physiology · doi:10.1152/ajplung.00074.2015 · Cited by 56
Zhang, Y., Cao, J., Chen, Y., Chen, P., Peng, H., Cai, S., Luo, H., & Wu, S. (2012) · Experimental Lung Research · doi:10.3109/01902148.2012.745910 · Cited by 56 · cited 9×
“A study showed that exercise training improved functional capacity in both normoxemic and hypoxemic COPD patients, however the structural improvements (increased mitochondrial density, capillary-to-fiber ratio, and fibers’ CSA) occurred only in the normoxemic ones [80].”
InfluentialRole of Protein Carbonylation in Skeletal Muscle Mass Loss Associated with Chronic Conditions
Barreiro, E. (2016) · Proteomes · doi:10.3390/proteomes4020018 · Cited by 56
Gavriilidis, C., Laredj, L., Solinhac, R., Messaddeq, N., Viaud, J., Laporte, J., Sumara, I., & Hnia, K. (2018) · Nature Cell Biology · doi:10.1038/s41556-017-0024-9 · Cited by 56 · cited 1×
“The ubiquitin–proteasome system plays a major role in protein content turnover by degrading misfolded or defective proteins [163,164].”
BackgroundKneppers, A. E. M., Langen, R. C. J., Gosker, H. R., Verdijk, L. B., Cebron Lipovec, N., Leermakers, P. A., Kelders, M. C. J. M., de Theije, C. C., Omersa, D., Lainscak, M., et al. (2017) · Journal of the American Medical Directors Association · doi:10.1016/j.jamda.2017.04.016 · Cited by 55 · cited 3×
“Finally, another study reported an increase in the phosphoULK1/ULK1 ratio—ULK1 is a kinase protein essential for autophagy initiation and progression [183].”
BackgroundFerrari, R., Caram, L., Faganello, M. M., Sanchez, F. F., Tanni, S. É., & Godoy, I. (2015) · International Journal of COPD · doi:10.2147/copd.s85954 · Cited by 54 · cited 1×
“Classically, circulating TNF-α is reported to be higher in COPD patients than controls and negatively correlated to lean mass [23,24], as well as to muscle strength, including upper muscles [25].”
BackgroundP38β MAPK Upregulates Atrogin1/MAFbx by Specific Phosphorylation of C/EBPβ
Zhang, G., & Li, Y.-P. (2012) · Skeletal Muscle · doi:10.1186/2044-5040-2-20 · Cited by 53 · cited 1×
“Ultimately, p38-MAPK upregulation could directly lead to increased proteasome-related catabolism, as shown in mice [173].”
BackgroundLeermakers, P. A., Schols, A. M. W. J., Kneppers, A. E. M., Kelders, M. C. J. M., de Theije, C. C., Lainscak, M., & Gosker, H. R. (2018) · Scientific Reports · doi:10.1038/s41598-018-33471-2 · Cited by 53 · cited 2×
“Only one study investigated dynamin-1-like protein DNML1 (also known as DRP1, a GTPase regulating mitochondrial fission) expression in COPD quadriceps and found a decreased protein level [88].”
BackgroundMAPK Signaling in the Quadriceps of Patients with Chronic Obstructive Pulmonary Disease
Lemire, B. B., Debigaré, R., Dubé, A., Thériault, M.-E., Côté, C. H., & Maltais, F. (2012) · Journal of Applied Physiology · doi:10.1152/japplphysiol.01518.2011 · Cited by 51 · cited 1×
“One study reported evidence of the activation of MAPK p38 and ERK1/2 in the quadriceps [171].”
BackgroundPuente-Maestu, L., Tejedor, A., Lázaro, A., de Miguel, J., ÁLvarez-Sala, L., González-Aragoneses, F., Simón, C., & Agustí, A. (2012) · American Journal of Respiratory Cell and Molecular Biology · doi:10.1165/rcmb.2011-0382oc · Cited by 51 · cited 3×
“Puente-Maestu and colleagues have reported an enhanced susceptibility to mPTP opening by common triggers (including Ca2+ and H2O2) in isolated mitochondria of COPD muscle cells [85].”
BackgroundQuadriceps Myostatin Expression in COPD
D-C. Man, W., Natanek, S. A., Riddoch-Contreras, J., Lewis, A., Marsh, G. S., Kemp, P. R., & Polkey, M. I. (2010) · European Respiratory Journal · doi:10.1183/09031936.00032510 · Cited by 48 · cited 1×
“Its expression is increased in the quadriceps of COPD patients [176], possibly related to hypoxia [72].”
BackgroundCostes, F., Gosker, H., Feasson, L., Desgeorges, M., Kelders, M., Castells, J., Schols, A., & Freyssenet, D. (2015) · Journal of Applied Physiology · doi:10.1152/japplphysiol.00557.2014 · Cited by 48 · cited 1×
“A study showed that exercise training improved functional capacity in both normoxemic and hypoxemic COPD patients, however the structural improvements (increased mitochondrial density, capillary-to-fiber ratio, and fibers’ CSA) occurred only in the normoxemic ones [80].”
BackgroundAltered skeletal muscle mitochondrial phenotype in COPD: disease vs. disuse
Gifford, J. R., Trinity, J. D., Kwon, O.-S., Layec, G., Garten, R. S., Park, S., Nelson, A. D., & Richardson, R. S. (2017) · Journal of Applied Physiology · doi:10.1152/japplphysiol.00788.2017 · Cited by 48 · cited 1×
“A recent study explored the possibility of the reduced mitochondrial density being due to deconditioning by matching COPD patients to control subjects for objectively measured physical activity [93].”
BackgroundD’Ercole, C., D’Angelo, P., Ruggieri, V., Proietti, D., Virtanen, L., Parisi, C., Riera, C. S., Renzini, A., Macone, A., Marzullo, M., et al. (2022) · Cell Reports · doi:10.1016/j.celrep.2022.111861 · Cited by 48
Barreiro, E., & Sznajder, J. I. (2013) · Journal of Applied Physiology · doi:10.1152/japplphysiol.01027.2012 · Cited by 47 · cited 1×
“Epigenetic modifications, whether methylation, acetylation, or muscle-specific microRNAs (myomiRNAs) play essential roles in muscle physiology, including embryogenesis and adaptation to environmental factors (for a comprehensive review, see [152]).”
BackgroundSystemic effects of cigarette smoke exposure in the guinea pig
Ardite, E., Peinado, V. I., Rabinovich, R., Fernández-Checa, J. C., Roca, J., & Barberà, J. A. (2005) · Respiratory Medicine · doi:10.1016/j.rmed.2005.10.023 · Cited by 47 · cited 1×
“Guinea Pig CS Acute exposure (24 h) Decreased skeletal muscle glutathioneIncreased plasma lipid peroxidation [219]”
Konokhova, Y., Spendiff, S., Jagoe, R. T., Aare, S., Kapchinsky, S., MacMillan, N. J., Rozakis, P., Picard, M., Aubertin-Leheudre, M., Pion, C. H., et al. (2016) · Skeletal Muscle · doi:10.1186/s13395-016-0083-9 · Cited by 46 · cited 4×
“tissue [87,127], as well as in cultured myotubes from COPD patients [128].”
BackgroundInfluentialAttaway, A. H., Bellar, A., Mishra, S., Karthikeyan, M., Sekar, J., Welch, N., Musich, R., Singh, S. S., Kumar, A., Menon, A., et al. (2023) · The Journal of Physiology · doi:10.1113/jp283700 · Cited by 45 · cited 1×
“Finally, a recent study pointed out a possible role of intermittent hypoxia (such as the nocturnal hypoxemia seen in obstructive sleep apnea disorder, frequent among COPD patients [83]) in skeletal muscle wasting, driven by mitochondrial dysfunction and a lower activity [84].”
BackgroundSepsis in mice stimulates muscle proteolysis in the absence of IL-6
Williams, A., Wang, J. J., Wang, L., Sun, X., Fischer, J. E., & Hasselgren, P.-O. (1998) · American Journal of Physiology-Regulatory, Integrative and Comparative Physiology · doi:10.1152/ajpregu.1998.275.6.r1983 · Cited by 44 · cited 1×
“prevent sarcopenia in a sepsis mouse model [48].”
BackgroundNogueira, L., Trisko, B. M., Lima‐Rosa, F. L., Jackson, J., Lund‐Palau, H., Yamaguchi, M., & Breen, E. C. (2018) · The Journal of Physiology · doi:10.1113/jp275888 · Cited by 44 · cited 1×
“Two other studies performed in CS-exposed mice evidenced impaired calcium signaling, notably a decreased sarcoplasmic reticulum calcium uptake [141,142].”
Uncoupling Protein-3 Content Is Decreased in Peripheral Skeletal Muscle of Patients with COPD
Gosker, H. R., Schrauwen, P., Hesselink, M. K. C., Schaart, G., van der Vusse, G. J., Wouters, E. F. M., & Schols, A. M. W. J. (2003) · European Respiratory Journal · doi:10.1183/09031936.03.00089802 · Cited by 42 · cited 3×
“Since the early reports of Agusti and colleagues and Gosker and colleagues, who observed, respectively, an increased and unchanged myonuclear fragmentation in muscle cells [111,112], only one study reported increased terminal deoxynucleotidyl transferase mediated dUTP nick-end labeling (TUNEL)-positive cells in quadri…”
BackgroundResultWillis-Owen, S. A. G., Thompson, A., Kemp, P. R., Polkey, M. I., Cookson, W. O. C. M., Moffatt, M. F., & Natanek, S. A. (2018) · Scientific Reports · doi:10.1038/s41598-018-29789-6 · Cited by 42 · cited 2×
“Indeed, one study reported an increase in the COPD quadriceps of SLC22A3, a metabolic stress gene involved in AA transportation and histamine clearance [94].”
BackgroundGifford, J. R., Trinity, J. D., Layec, G., Garten, R. S., Park, S.-Y., Rossman, M. J., Larsen, S., Dela, F., & Richardson, R. S. (2015) · Journal of Applied Physiology · doi:10.1152/japplphysiol.00460.2015 · Cited by 40 · cited 1×
“Finally, Gifford and colleagues observed a reduction in state 3:CI+CII respiration in COPD patients compared to healthy controls [101].”
BackgroundSugiyama, Y., Asai, K., Yamada, K., Kureya, Y., Ijiri, N., Watanabe, T., Kanazawa, H., & Hirata, K. (2017) · International Journal of COPD · doi:10.2147/copd.s126233 · Cited by 40 · cited 1×
“Other myokines can also play a role in the control of muscle mass, most of which having not been thoroughly investigated in COPD, such as IL-4 (promoting myoblast fusion in vitro) [61], IL-7, which secretion by skeletal muscle gradually decreases with age [20], or irisin, known to decrease oxidant-induced apoptosis in…”
BackgroundNetwork Modules Uncover Mechanisms of Skeletal Muscle Dysfunction in COPD Patients
Tényi, Á., Cano, I., Marabita, F., Kiani, N., Kalko, S. G., Barreiro, E., de Atauri, P., Cascante, M., Gomez-Cabrero, D., & Roca, J. (2018) · Journal of Translational Medicine · doi:10.1186/s12967-018-1405-y · Cited by 40 · cited 3×
“Another recent study [56], using microarrays and gene ontology algorithms to detect network modules in COPD and healthy quadriceps, identified abnormalities in creatine metabolism and calcium homeostasis, which were significantly associated with exercise capacity.”
BackgroundInfluentialTNF-α Is Associated with Loss of Lean Body Mass Only in Already Cachectic COPD Patients
Eagan, T. M., Gabazza, E. C., D’Alessandro-Gabazza, C., Gil-Bernabe, P., Aoki, S., Hardie, J. A., Bakke, P. S., & Wagner, P. D. (2012) · Respiratory Research · doi:10.1186/1465-9921-13-48 · Cited by 39 · cited 1×
“However, this correlation seems to be consistent only in cachectic patients [26].”
BackgroundGouzi, F., Maury, J., Héraud, N., Molinari, N., Bertet, H., Ayoub, B., Blaquière, M., Bughin, F., De Rigal, P., Poulain, M., et al. (2019) · Oxidative Medicine and Cellular Longevity · doi:10.1155/2019/5496346 · Cited by 38 · cited 1×
“Moreover, a combination of oral antioxidant supplementation has also shown interesting results on muscle strength with an excellent tolerance [135].”
BackgroundSelf-citationInhibition of AMPK expression in skeletal muscle by systemic inflammation in COPD rats
Qi, Y., Shang, J., Ma, L., Sun, B., Hu, X., Liu, B., & Zhang, G. (2014) · Respiratory Research · doi:10.1186/s12931-014-0156-4 · Cited by 37
Passey, S. L., Bozinovski, S., Vlahos, R., Anderson, G. P., & Hansen, M. J. (2016) · PLoS ONE · doi:10.1371/journal.pone.0146882 · Cited by 37 · cited 1×
“In vitro, it can be induced in C2C12 myotubes by serum amyloid A, which is increased during COPD exacerbations [35].”
BackgroundBasic, V., Roxlau, E. T., Elmabsout, A. A., Yao, H., Rahman, I., Sirsjö, A., & Abdel‐Halim, S. M. (2012) · American Journal of Physiology-Lung Cellular and Molecular Physiology · doi:10.1152/ajplung.00007.2012 · Cited by 35
Balnis, J., Korponay, T. C., Vincent, C. E., Singer, D. V., Adam, A. P., Lacomis, D., Lee, C. G., Elias, J. A., Singer, H. A., & Jaitovich, A. (2019) · Journal of Applied Physiology · doi:10.1152/japplphysiol.00627.2019 · Cited by 35 · cited 1×
“IL-13+/+ Decreased muscle mass, grip strength and contractility Decreased myofibers’ CSA Increased catabolism (mRNA level) [208]”
BackgroundZhang, D., Cao, L., Wang, Z., Feng, H., Xu, C., Xu, M., Li, M., Yu, N. H., Yin, Y., Wang, W., et al. (2019) · Bioscience Reports · doi:10.1042/bsr20190440 · Cited by 35
Hansen, M. J., Chen, H., Jones, J. E. C., Langenbach, S. Y., Vlahos, R., Gualano, R. C., Morris, M. J., & Anderson, G. P. (2013) · PLoS ONE · doi:10.1371/journal.pone.0080471 · Cited by 34
de Theije, C. C., Schols, A. M. W. J., Lamers, W. H., Ceelen, J., van Gorp, R. H., Hermans, J. J. R., Köhler, E. S., & LANGEN, R. C. J. (2017) · Endocrinology · doi:10.1210/en.2017-00603 · Cited by 33 · cited 1×
“Intricate mechanisms with malnutrition could also compete, since exposing mice to hypoxia leads to a loss of appetite [81].”
BackgroundSkeletal muscle interleukin 15 promotes CD8+ T-cell function and autoimmune myositis
Huang, P.-L., Hou, M.-S., Wang, S.-W., Chang, C.-L., Liou, Y.-H., & Liao, N. (2015) · Skeletal Muscle · doi:10.1186/s13395-015-0058-2 · Cited by 32 · cited 1×
“Furthermore, IL-15 possibly promotes the effector function of memory CD8+ T cells [55].”
BackgroundStrle, K., McCusker, R. H., Johnson, R. W., Zunich, S. M., Dantzer, R., & Kelley, K. W. (2008) · American Journal of Physiology-Endocrinology and Metabolism · doi:10.1152/ajpendo.00662.2007 · Cited by 32 · cited 1×
“It bears potent anabolic effects by inhibiting the atrophy signaling induced by TNF-α in myotubes [59].”
BackgroundNatanek, S. A., Riddoch-Contreras, J., Marsh, G. S., Hopkinson, N. S., Moxham, J., Man, W. D.-C., Kemp, P. R., & Polkey, M. I. (2013) · COPD: Journal of Chronic Obstructive Pulmonary Disease · doi:10.3109/15412555.2013.781577 · Cited by 32 · cited 1×
“Of note, some studies have failed to report a significant difference between COPD patients and healthy subjects [166], possibly due to the timing of the assessment.”
ResultSkeletal muscle mitophagy in chronic disease
Leermakers, P. A., & Gosker, H. R. (2016) · Current Opinion in Clinical Nutrition & Metabolic Care · doi:10.1097/mco.0000000000000319 · Cited by 31 · cited 1×
“Data are more scarce in skeletal muscles, but the potential role of mitophagy in skeletal muscle wasting has been recently reviewed [107].”
BackgroundReduced HDAC2 in Skeletal Muscle of COPD Patients
To, M., Swallow, E. B., Akashi, K., Haruki, K., Natanek, S. A., Polkey, M. I., Ito, K., & Barnes, P. J. (2017) · Respiratory Research · doi:10.1186/s12931-017-0588-8 · Cited by 31 · cited 1×
“Finally, a recent study has found that the downregulation of histone deacetylase 2 (HDAC2) by RNA interference in cultured primary myotubes increased TNF-α production and cell apoptosis [37].”
BackgroundImpaired Exercise Capacity and Skeletal Muscle Function in a Mouse Model of Pulmonary Inflammation
Tang, K., Murano, G., Wagner, H., Nogueira, L., Wagner, P. D., Tang, A., Dalton, N. D., Gu, Y., Peterson, K. L., & Breen, E. C. (2013) · Journal of Applied Physiology · doi:10.1152/japplphysiol.00607.2012 · Cited by 30 · cited 2×
“Moreover, an overexpression of TNF-α in the lung leads to an increased muscle fatigue, decreased muscle mass and mitochondrial content, and increased catabolism (mostly in male mice) [42].”
BackgroundBarreiro, E., Puig-Vilanova, E., Salazar-Degracia, A., Pascual-Guardia, S., Casadevall, C., & Gea, J. (2018) · Journal of Applied Physiology · doi:10.1152/japplphysiol.00798.2017 · Cited by 30 · cited 1×
“For future therapeutic prospects, roflumilast, an inhibitor of phosphodiesterase-4 (PDE-4) which exerts antioxidant effects, has shown promising results in a proof-of-concept study on cultured myotubes from COPD patients [134].”
Backgroundde Theije, C. C., Schols, A. M. W. J., Lamers, W. H., Neumann, D., Köhler, E., & LANGEN, R. C. J. (2018) · PLoS ONE · doi:10.1371/journal.pone.0203630 · Cited by 30
TNFα receptor genotype influences smoking-induced muscle-fibre-type shift and atrophy in mice
De Paepe, B., Brusselle, G. G., Maes, T., Creus, K. K., D’hose, S., D’Haese, N., Bracke, K. R., D’hulst, A. I., Joos, G. F., & De Bleecker, J. L. (2008) · Acta Neuropathologica · doi:10.1007/s00401-008-0348-4 · Cited by 29 · cited 2×
“Mechanistically, TNF-α plays a dual role in muscle mass regulation, possibly via differential signaling according to receptor binding (TNFR1 or TNF-R2) [32,33].”
BackgroundGouzi, F., Blaquière, M., Catteau, M., Bughin, F., Maury, J., Passerieux, E., Ayoub, B., Mercier, J., Hayot, M., & Pomiès, P. (2018) · Journal of Cellular Physiology · doi:10.1002/jcp.26868 · Cited by 29 · cited 2×
“Moreover, it has also been reported that increased autophagy was directly linked to oxidative stress, as treatment with an antioxidant molecule decreased autophagy levels in cultured myotubes [184].”
BackgroundSelf-citationSu, J., Li, J., Lu, Y., Li, N., Li, P., Wang, Z., Wu, W., & Liu, X. (2020) · BMC Pulmonary Medicine · doi:10.1186/s12890-020-1109-y · Cited by 29
Oxidative Stress Causes Muscle Structural Alterations via P38 MAPK Signaling in COPD Mouse Model
Mano, Y., Tsukamoto, M., Wang, K.-Y., Nabeshima, T., Kosugi, K., Tajima, T., Yamanaka, Y., Suzuki, H., Kawasaki, M., Nakamura, E., et al. (2022) · Journal of Bone and Mineral Metabolism · doi:10.1007/s00774-022-01371-1 · Cited by 29 · cited 1×
“Oxidative stress is increased both at the systemic and muscular levels in COPD [10,89,116].”
BackgroundReducción de la masa muscular mediada por miostatina en un modelo experimental de enfisema pulmonar
Fermoselle, C., Sanchez, F., & Barreiro, E. (2011) · Archivos de Bronconeumología · doi:10.1016/j.arbres.2011.07.008 · Cited by 28 · cited 1×
“However, several studies point towards a direct relationship between oxidative stress, atrophy, and the ubiquitin–proteasome pathway [131], including data obtained in experimental models [132].”
BackgroundIFN-γ does not mimic the catabolic effects of TNF-α
Smith, M. A., Moylan, J. S., Smith, J. D., Li, W. S., & Reid, M. B. (2007) · American Journal of Physiology-Cell Physiology · doi:10.1152/ajpcell.00269.2007 · Cited by 28 · cited 1×
“In vitro, IFN-γ does not activate catabolic pathways on C2C12 myoblasts [57] but induces the expression of proangiogenic factors such as angiopoietin-2 in primary human myoblasts [58].”
BackgroundInteraction between Physical Activity and Smoking on Lung, Muscle, and Bone in Mice
Cielen, N., Maes, K., Heulens, N., Troosters, T., Carmeliet, G., Janssens, W., & Gayan‐Ramirez, G. (2015) · American Journal of Respiratory Cell and Molecular Biology · doi:10.1165/rcmb.2015-0181oc · Cited by 28
Reduction of Muscle Mass Mediated by Myostatin in an Experimental Model of Pulmonary Emphysema
Fermoselle, C., Sanchez, F., & Barreiro, E. (2011) · Archivos de Bronconeumología · doi:10.1016/j.arbr.2011.11.002 · Cited by 28
Deaccelerated Myogenesis and Autophagy in Genetically Induced Pulmonary Emphysema
Balnis, J., Drake, L. A., Singer, D. V., Vincent, C. E., Korponay, T. C., D’Armiento, J., Lee, C. G., Elias, J. A., Singer, H. A., & Jaitovich, A. (2022) · American Journal of Respiratory Cell and Molecular Biology · doi:10.1165/rcmb.2021-0351oc · Cited by 27 · cited 1×
“In that work, autophagy seemed to be correlated to satellite cell dysfunction contributing to the pathogenesis of emphysema in a transgenic mouse model [185].”
BackgroundSin, D. D., & Man, S. F. P. (2008) · Chest · doi:10.1378/chest.07-2085 · Cited by 25
Mao, J., Li, Y., Li, S., Li, J., Tian, Y., Feng, S., Liu, X., Bian, Q., Li, J., Hu, Y., et al. (2019) · Evidence-based Complementary and Alternative Medicine · doi:10.1155/2019/1216305 · Cited by 25 · cited 1×
“CS + Klebsiella pneumonia CS: whole body 20 weeks Klebsiella pneumonia instillations, every 5 days for the first 8 weeks Increased tissular apoptosis and decreased oxidative phosphorylation [215]”
MethodPersson, H. L., Sioutas, A., Kentson, M., Jacobson, P., Lundberg, P., Dahlqvist Leinhard, O., & Forsgren, M. F. (2022) · Journal of Inflammation Research · doi:10.2147/jir.s366204 · Cited by 25 · cited 1×
“Adipose tissue infiltration has also been reported in COPD muscle, in a similar way to senescent muscle in the aging population, particularly in the obese sarcopenic phenotype where adipose inflammation leads to the redistribution of fat to the intra-abdominal area and skeletal muscle tissue [16,17] (Figure 1).”
BackgroundTsukamoto, M., Mori, T., Wang, K., Okada, Y., Fukuda, H., Naito, K., Yamanaka, Y., Sabanai, K., Nakamura, E., Yatera, K., et al. (2018) · Bone · doi:10.1016/j.bone.2018.10.017 · Cited by 24 · cited 1×
“Elastase Intratracheal (1X to 5X) Decreased muscle mass and endurance Decreased myofibers’ CSA (type I), fiber-type switch [201,202]”
MethodCeelen, J., Schols, A. M. W. J., Kneppers, A. E. M., Rosenbrand, R. P. H. A., Drożdż, M. M., van Hoof, S. J., de Theije, C. C., KELDERS, M. C. J. M., Verhaegen, F., & LANGEN, R. C. J. (2018) · Scientific Reports · doi:10.1038/s41598-018-28579-4 · Cited by 23 · cited 1×
“Elastase + LPS x3 each Decreased muscle mass and grip strength Slightly increased catabolism (whole tissue protein) [203]”
BackgroundKneppers, A. E. M., Haast, R. A. M., LANGEN, R. C. J., Verdijk, L. B., Leermakers, P. A., Gosker, H. R., van Loon, L. J. C., Lainščak, M., & Schols, A. M. W. J. (2019) · Journal of Cachexia Sarcopenia and Muscle · doi:10.1002/jcsm.12370 · Cited by 23 · cited 1×
“Cues might come from a vast transcriptional analysis in the muscle identifying distinct molecular signatures among COPD patients, associated to specific profiles, for example in response to pulmonary rehabilitation [222].”
BackgroundChronic exposure to cigarette smoke causes extrapulmonary abnormalities in rats
Kamiide, Y., Furuya, M., Inomata, N., & Yada, T. (2015) · Environmental Toxicology and Pharmacology · doi:10.1016/j.etap.2015.02.016 · Cited by 22
Zhang, L., Li, D., Chang, C., & Sun, Y. (2022) · International Journal of Chronic Obstructive Pulmonary Disease · doi:10.2147/copd.s377226 · Cited by 22 · cited 1×
“Ferroptosis, a newly discovered type of cell death resulting from iron-dependent lipid peroxide accumulation, has been reported to be increased both in vitro in CS-exposed C2C12 myotubes and in vivo in a mouse model of COPD [129].”
BackgroundQaisar, R., Ustrana, S., Muhammad, T., & Shah, I. (2022) · Histochemistry and Cell Biology · doi:10.1007/s00418-021-02043-3 · Cited by 21 · cited 1×
“However, a recent study reported elevated markers of sarcoplasmic reticulum stress (at the protein level) in COPD quadriceps [143].”
BackgroundBalnis, J., Drake, L. A., Vincent, C. E., Korponay, T. C., Singer, D. V., Lacomis, D., Lee, C. G., Elias, J. A., Jourd’heuil, D., Singer, H. A., et al. (2021) · American Journal of Respiratory Cell and Molecular Biology · doi:10.1165/rcmb.2020-0551oc · Cited by 19
Flagged first, then by citations
11 of the 241 references couldn’t be matched to a known paper.
Cited by
Sorted by citations
Tobacco and COPD: presenting the World Health Organization (WHO) Tobacco Knowledge Summary
Lu, W., Aarsand, R., Schotte, K., Han, J., Lebedeva, E., Tsoy, E., Maglakelidze, N., Soriano, J. B., Bill, W., Halpin, D. M. G., et al. (2024) · Respiratory Research · doi:10.1186/s12931-024-02961-5 · Cited by 86
“Inactivity is common among COPD patients and significantly contributes to many systemic issues of COPD [60], especially during exacerbations [61].”
BackgroundDual role of macrophages in skeletal muscle atrophy: Mechanisms and therapeutic strategies
Shang, T., Hong-yi, X., Yao, X., Zhao, Z., Niu, X., Shen, Y., Chen, B., & Sun, H. (2025) · Biochemical Pharmacology · doi:10.1016/j.bcp.2025.117589 · Cited by 50
Fekete, M., Csípő, T., Fazekas‐Pongor, V., Bálint, M., Csizmadia, Z., Tarantini, S., & Varga, J. T. (2023) · Nutrients · doi:10.3390/nu15183902 · Cited by 31
“Weight loss is primarily a consequence of skeletal muscle atrophy [72].”
BackgroundFurukawa, Y., Miyamoto, A., Asai, K., Tsutsumi, M., Hirai, K., Ueda, T., Toyokura, E., Nishimura, M., Sato, K., Yamada, K., et al. (2025) · Respirology · doi:10.1111/resp.70003 · Cited by 16
Abdellaoui, A., Gouzi, F., Notarnicola, C., Bourret, A., Suc, A., Laoudj‐Chenivesse, D., Héraud, N., Mercier, J. G., PREFAUT, C. G., Hayot, M., et al. (2025) · Acta Physiologica · doi:10.1111/apha.70079 · Cited by 13
Self-citation
Metadata
- Authors
- Henrot, P., Dupin, I., Schilfarth, P., Esteves, P., Blervaque, L., Zysman, M., Gouzi, F., Hayot, M., Pomiès, P., & Berger, P.
- Affiliations
- Inserm (FR)
- Centre de Recherche Cardio-Thoracique de Bordeaux, Univ. Bordeaux, U1045, F-33604 Pessac, France
- Centre National de la Recherche Scientifique (FR)
- PhyMedExp, INSERM-CNRS-Montpellier University, CHRU Montpellier, F-34090 Montpellier, France
- Corresponding author
- Henrot, Pauline
- ORCID
- Venue
- International Journal of Molecular Sciences
- Publisher
- MDPI AG
- Published
- 2023-03-29
- Volume
- 24
- Issue
- 7
- Pages
- 6454
- ISSN
- 1422-0067 (ISSN-L)
- PMC
- PMC10095391
- OpenAlex
- W4361275808
- Semantic Scholar
- 7a755f572a56107af145f93ea2c0a8207b09d9c5
- Cited by
- 85
- References
- 241
- Citations by year
- 2026: 31 · 2025: 36 · 2024: 12 · 2023: 6
- FWCI
- 6.36
- Type
- journal article
- Language
- en
- Open access
- gold
- doi.org
- Licence
- Locations
- International Journal of Molecular Sciences (publishedVersion, cc-by)
- PubMed (publishedVersion)
- HAL (Le Centre pour la Communication Scientifique Directe) (submittedVersion, cc-by)
- PubMed Central (submittedVersion, cc-by)
- Funders
- Fondation Bordeaux Université
- AVAD
- FGLMR
- Topics
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Muscle Physiology and Disorders
- Health Sciences › Medicine › Pulmonary and Respiratory Medicine › Chronic Obstructive Pulmonary Disease (COPD) Research
- Health Sciences › Medicine › Physiology (medical) › Nutrition and Health in Aging
- Keywords
- chronic obstructive pulmonary disease, skeletal muscle atrophy, muscle atrophy, muscle fiber atrophy, oxidative stress, nitrosative stress, mitochondrial dysfunction, hypoxia, hypercapnia, systemic inflammation, epigenetic modifications, disuse
- MeSH terms
- Hypoxia, Humans, Inflammation, Muscular Atrophy, Tobacco Smoke Pollution, Muscle, Skeletal, Pulmonary Disease, Chronic Obstructive
About these checks
Registry, retraction, Cites and statistics results are computed, not judged, with one exception: a printed reference that no index lists is read once by a model before it counts as a citation error. Claims are extracted by a model and kept only when their quote appears verbatim in the text; each cited source is then checked, with a model’s help, for whether it says what the claim relies on. Those verdicts can be wrong — read the claim’s quote and the cited source before relying on one.
A language model drew the claims from the paper on 2026-10-14, under version 3 of the claim definition (model deepseek-v4.1-flash, prompt extract-v3).
A second model labelled each claim on 2026-10-14 (model jev-1.13-20260917, definition revision gold-guideline-v0.2).
Cited sources are checked with a language model’s help (gpt-6-sol).
Statistics and arithmetic are recomputed, not judged.
Confidence bands are shown only for fields calibrated on our annotated test set. None is calibrated yet, so no band is shown.
What counts as a claim ›How we measure confidence ›How we check this ›
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