The DOI matches its Crossref record; 248 of the 249 references it cites were found in a registry or an index; 90 of the 184 sources its claims cite were checked for support.
The Inflammatory Continuum of Traumatic Brain Injury and Alzheimer’s Disease
Open accessAbstract
The post-injury inflammatory response is a key mediator in long-term recovery from traumatic brain injury (TBI). Moreover, the immune response to TBI, mediated by microglia and macrophages, is influenced by existing brain pathology and by secondary immune challenges. For example, recent evidence shows that the presence of beta-amyloid and phosphorylated tau protein, two hallmark features of AD that increase during normal aging, substantially alter the macrophage response to TBI. Additional data demonstrate that post-injury microglia are "primed" and become hyper-reactive following a subsequent acute immune challenge thereby worsening recovery. These alterations may increase the incidence of neuropsychiatric complications after TBI and may also increase the frequency of neurodegenerative pathology. Therefore, the purpose of this review is to summarize experimental studies examining the relationship between TBI and development of AD-like pathology with an emphasis on the acute and chronic microglial and macrophage response following injury. Furthermore, studies will be highlighted that examine the degree to which beta-amyloid and tau accumulation as well as pre- and post-injury immune stressors influence outcome after TBI. Collectively, the studies described in this review suggest that the brain's immune response to injury is a key mediator in recovery, and if compromised by previous, coincident, or subsequent immune stressors, post-injury pathology and behavioral recovery will be altered.
Overview
AI snapshot
Written from the paper’s full text.
TL;DR
This review argues that post-traumatic brain injury (TBI) neuroinflammation, mediated by microglia and macrophages, is a malleable continuum shaped by pre-existing Alzheimer’s disease (AD)-like pathology and by pre- or post-injury immune challenges. It synthesizes experimental and clinical evidence that beta-amyloid and tau accumulation alter the macrophage response to TBI, and that transient microglial/macrophage modulation may influence recovery and AD-like pathology.
Key findings
- TBI induces a conserved microglial/macrophage response; chronic microglial and astrocytic reactivity persists in subcortical regions months to years post-injury, with human evidence of increased OX-6/CD68 mRNA at 1 year and PK-[11C](R)PK11195 binding between 11 months and 17 years post-injury.
- Pre-injury peripheral immune challenge can be protective: a single i.p. LPS dose (0.1 mg/kg) 5 days before controlled cortical impact reduced CD68, increased IL-6, decreased contusion volume, and improved behavioral recovery; LPS (1.0 mg/kg for 4 days) reduced neuronal death and lesion volume after lateral cryogenic brain injury.
- Post-injury immune challenge worsens recovery: LPS at 30 days post-injury after midline fluid percussion injury exaggerated MHC-II, IL-1β, and TNFα expression and depressive-like behavior; LPS 5 days post-injury after impact acceleration was associated with depressive-like behavior and cognitive impairments 3 months post-injury.
- Aβ and tau modify the macrophage response: TBI in APP/PS1 mice delayed peak cytokine elevations by 7 days; R1.40 AD-model mice showed a muted acute macrophage response and significant tissue loss between 3 and 120 days post-injury; hTau TBI mice showed enhanced acute macrophage response and, at 120 days post-injury, increased tau pathology and persistent macrophage response correlating with memory-task deficits. CSF1R inhibition after a chronic hippocampal lesion improved behavioral recovery and increased dendritic spines.
Methods
- Narrative review summarizing experimental and clinical studies on TBI, neuroinflammation, and AD-like pathology, with emphasis on acute and chronic microglial and macrophage responses.
- Discusses animal TBI models including controlled cortical impact, fluid percussion injury, weight drop, penetrating ballistic-brain injury, closed head injury, cryogenic injury, and a chronic hippocampal lesion model, as well as transgenic AD/tau models.
- Draws on human epidemiological, neuropathological, imaging, and cerebrospinal fluid studies; no systematic review, meta-analysis, or primary data collection is reported.
Limitations
- The paper states that global TBI reporting and categorization are not standardized; experimental models each reflect a specific TBI type and do not fully recapitulate human TBI; more than 30 phase-III clinical trials have failed to improve secondary injury outcomes; some experimental studies fail to show TBI induces or worsens AD-related pathology; transgenic AD models express mutant APP/tau at nonphysiological levels and clinical co-occurrence of TBI and APP mutation is rare; no universal repetitive TBI model exists; inter-injury macrophage changes are not defined; and the distinct roles of microglia versus monocytes remain unclear.
- The paper also states that the role of soluble Aβ oligomers and tau oligomers in post-injury pathology is understudied, and that cell-specific inflammatory profiles are not routinely performed in transgenic mice before TBI.
- Evident from the text: as a narrative review, it lacks a systematic search strategy, formal quality appraisal, or quantitative synthesis, and its conclusions rely on heterogeneous animal models, injury severities, and outcome measures.
Model-written summary. Check it against the paper before relying on it.
Integrity signals
Registry
Cites
Statistics
Verification
Claims the paper makes
90 of 184 cited sources checked · 39 supported · 1 flagged · accuracy not yet measured
Every source the paper cites for this claim was checked and supports it.
In the paper
“Several lines of evidence point to a relationship between single-incident TBI and AD (10, 11).”
§ The Inflammatory Continuum of Traumatic Brain Injury and Alzheimer’s Disease > Introduction to Traumatic Brain Injury (TBI) and Alzheimer’s Disease (AD)
What the sources say
- Supportedcites [10] Johnson, 2010, Traumatic brain injury and amyloid-β pathology: a link to Alzheimer’s disease?, Nat Rev Neurosci source
The epidemiological-link section reports that studies associate a history of TBI with later AD, while acknowledging that some studies found no association. The paper also describes AD-like pathology after TBI and explicitly examines how a single TBI may trigger such changes. (LLM, conf=0.92)
- Supportedcites [11] Johnson, 2013, Inflammation and white matter degeneration persist for years after a single traumatic brain injury, Brain source
The Introduction links TBI to increased Alzheimer’s disease incidence in epidemiological studies. The Discussion adds that survivors of a single TBI have shown amyloid plaques and neurofibrillary tangles, providing another line of evidence for the relationship. Page numbers are not available in our copy. (LLM, conf=0.92)
Tests✓ Asserted: passes✓ Checkable: passes✓ Load-bearing: passes✓ Based: passes- Supported
The cited sources support only part of this claim — read each source’s verdict below.
In the paper
“Third, accumulation of APP and extracellular deposition of the 40- to 42-amino acid Aβ peptide in senile plaques has been identified in human brain tissue soon after severe TBI (29, 30).”
§ The Inflammatory Continuum of Traumatic Brain Injury and Alzheimer’s Disease > Introduction to Traumatic Brain Injury (TBI) and Alzheimer’s Disease (AD)
What the sources say
- Partly supportedcites [29] Roberts, 1994, Beta amyloid protein deposition in the brain after severe head injury: implications for the pathogenesis of Alzheimer’s disease, J Neurol Neurosurg Psychiatry sourceExperimental — accuracy not yet measured
The Abstract reports Aβ deposits after severe head injury and increased APP immunoreactivity near those deposits. The βAPP immunoreactivity section distinguishes the early diffuse deposits from classical or senile plaques, which it says were restricted to the oldest cases. Our copy does not establish that the deposited peptide was specifically 40–42 amino acids long. (LLM, conf=0.88)
- Not checked — no full text of the sourcecites [30] DeKosky, 2007, Association of increased cortical soluble Aβ42 levels with diffuse plaques after severe brain injury in humans, Arch Neurol source
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
“Second, many animal studies show increased production and accumulation of amyloid precursor protein (APP), Aβ, and pathological tau following TBI (16, 21–28).”
§ The Inflammatory Continuum of Traumatic Brain Injury and Alzheimer’s Disease > Introduction to Traumatic Brain Injury (TBI) and Alzheimer’s Disease (AD)
What the sources say
- Partly supportedcites [16] Webster, 2015, Closed head injury in an age-related Alzheimer mouse model leads to an altered neuroinflammatory response and persistent cognitive impairment, J Neurosci sourceExperimental — accuracy not yet measured
The Results section reports increased Aβ deposition after closed head injury in APP/PS1 mice and states that TBI can increase APP levels in mice. The Introduction reports changes in amyloid or tau pathology across animal studies, but the paper does not establish increased production of APP, Aβ, and tau or specifically show accumulation of pathological tau. (LLM, conf=0.83)
- Partly supportedcites [21] Tran, 2011, Controlled cortical impact traumatic brain injury in 3xTg-AD mice causes acute intra-axonal amyloid-β accumulation and independently accelerates the development of tau abnormalities, J Neurosci sourceExperimental — accuracy not yet measured
The Results (page unavailable) show increased APP- and Aβ-stained axonal accumulations after TBI in 3xTg-AD mice, along with increased tau phosphorylation. This study therefore supports the sentence as one animal-study example, but it does not establish increased production of APP, Aβ, or tau after TBI. (LLM, conf=0.85)
- Not checked — no full text of the sourcecites [22] Shishido, 2016, Traumatic brain injury accelerates amyloid-β deposition and impairs spatial learning in the triple-transgenic mouse model of Alzheimer’s disease, Neurosci Lett source
- Partly supportedcites [23] Washington, 2014, Experimental traumatic brain injury induces rapid aggregation and oligomerization of amyloid-beta in an Alzheimer’s disease mouse model, J Neurotrauma sourceExperimental — accuracy not yet measured
The Results (page not available in our copy) report increased APP processing and Aβ production after TBI in mice, and the Discussion reports increased soluble and insoluble Aβ. The paper does not report increased production or accumulation of APP itself, or a finding about pathological tau; the tau mention found is in a reference title. (LLM, conf=0.86)
- Partly supportedcites [24] Tajiri, 2013, Traumatic brain injury precipitates cognitive impairment and extracellular Aβ aggregation in Alzheimer’s disease transgenic mice, PLoS One sourceExperimental — accuracy not yet measured
The Results report increased extracellular Aβ deposits after TBI in mice, and the Discussion reports another mouse study finding Aβ accumulation and increased phospho-tau immunoreactivity. The paper does not report increased production or accumulation of APP; its Discussion only proposes increased cleavage of APP to Aβ. It also does not establish the claim across “many” animal studies. (LLM, conf=0.85)
- Partly supportedcites [25] Tran, 2011, Distinct temporal and anatomical distributions of amyloid-β and tau abnormalities following controlled cortical impact in transgenic mice, PLoS One sourceExperimental — accuracy not yet measured
The Discussion reports post-injury APP accumulation in injured axons and this study’s Aβ accumulation and tau abnormalities in transgenic mice (pages not provided). It does not establish increased APP production after TBI, and its findings are limited to particular transgenic models rather than animal studies generally. (LLM, conf=0.83)
- Not checked — no full text of the sourcecites [26] Itoh, 2009, Expression of amyloid precursor protein after rat traumatic brain injury, Neurol Res source
- Partly supportedcites [27] Hartman, 2002, Apolipoprotein E4 influences amyloid deposition but not cell loss after traumatic brain injury in a mouse model of Alzheimer’s disease, J Neurosci sourceExperimental — accuracy not yet measured
The Discussion reports that TBI accelerated Aβ deposition in the study’s PDAPP mice expressing APOE4 and describes Aβ findings from other animal studies. It does not report increased production or accumulation of APP or pathological tau after TBI; nor does it establish increased Aβ production. (LLM, conf=0.89)
- Partly supportedcites [28] Smith, 1998, Brain trauma induces massive hippocampal neuron death linked to a surge in beta-amyloid levels in mice overexpressing mutant amyloid precursor protein, Am J Pathol sourceExperimental — accuracy not yet measured
The Aβ Tissue Levels section reports an acute rise in Aβ after injury in PDAPP mice, and the introductory passage reports APP accumulation after trauma in experimental animals. The paper does not report pathological tau in injured animals; it mentions neurofibrillary tangles in human boxers. The Histopathological Analysis section also finds no increase in Aβ plaque deposition after injury, so the claim's accumulation language does not hold for plaques in this study. Page numbers are unavailable in our copy. (LLM, conf=0.88)
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
“First, numerous population-based studies demonstrate that head injury during adulthood increases the risk of AD later in life (12–19)”
§ The Inflammatory Continuum of Traumatic Brain Injury and Alzheimer’s Disease > Introduction to Traumatic Brain Injury (TBI) and Alzheimer’s Disease (AD)
What the sources say
- Not checked — no full text of the sourcecites [12] Guo, 2000, Head injury and the risk of AD in the MIRAGE study, Neurology source
- Partly supportedcites [13] Schofield, 1997, Alzheimer’s disease after remote head injury: an incidence study, J Neurol Neurosurg Psychiatry sourceExperimental — accuracy not yet measured
The Results (page not supplied) report an increased risk of incident Alzheimer’s disease for participants who reported head injury with loss of consciousness to a physician. But the Discussion (page not supplied) describes the association cautiously, and notes that two earlier cohort studies failed to find it. This paper therefore supports an association in its cohort, not the stronger claim that numerous population-based studies demonstrate an increased risk specifically from injury during adulthood. (LLM, conf=0.88)
- Not checked — no full text of the sourcecites [14] Plassman, 2000, Documented head injury in early adulthood and risk of Alzheimer’s disease and other dementias, Neurology source
- Partly supportedcites [15] LoBue, 2017, Traumatic brain injury history is associated with earlier age of onset of Alzheimer disease, Clin Neuropsychol sourceExperimental — accuracy not yet measured
The introductory passage indexed under Abstract > Conclusions reports increased later AD risk following TBI in several case-control, meta-analytic, and chart-review studies. It also says not all studies support the association. The source therefore supports an association, but not the stronger claim that numerous population-based studies demonstrate increased risk after head injury during adulthood. (LLM, conf=0.85)
- Partly supportedcites [16] Webster, 2015, Closed head injury in an age-related Alzheimer mouse model leads to an altered neuroinflammatory response and persistent cognitive impairment, J Neurosci sourceExperimental — accuracy not yet measured
The Introduction (page not provided) says head injury is associated with increased risk of later-life dementia, including AD, and the Discussion cites epidemiological studies linking prior head injury to cognitive impairment and dementia. The paper does not specify injury during adulthood or establish that numerous population-based studies demonstrate a causal increase in AD risk. (LLM, conf=0.84)
- Partly supportedcites [17] Gilbert, 2014, The association of traumatic brain injury with rate of progression of cognitive and functional impairment in a population-based cohort of Alzheimer’s disease: the cache county dementia progression study, Int Psychogeriatr sourceExperimental — accuracy not yet measured
The Introduction reports that prior studies associate traumatic brain injury with higher AD risk, including a study of veterans and evidence about the age at injury. The References identify one cited study as population-based, but our copy does not establish that numerous studies reporting this association were population-based. This paper’s own population-based cohort examines progression after AD onset, not the risk of developing AD. (LLM, conf=0.81)
- Partly supportedcites [18] Li, 2016, Traumatic brain injury and age at onset of cognitive impairment in older adults, J Neurol sourceExperimental — accuracy not yet measured
The Discussion says previous studies found traumatic brain injury to be a risk factor for AD or non-AD dementia, supporting the broad association. The Introduction and References include population-based studies of dementia risk, but our copy does not establish that numerous population-based studies specifically demonstrated increased later-life AD risk following injury during adulthood. (LLM, conf=0.85)
- Not checked — no full text of the sourcecites [19] Yang, 2015, Accumulation of amyloid in cognitive impairment after mild traumatic brain injury, J Neurol Sci source
Tests✓ Asserted: passes✓ Checkable: passes✓ Load-bearing: passes✓ Based: passesThe 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
“Given the distinct genetic and transcriptomic profile of microglia and macrophages identified via high throughput sequencing technology (69–71), the two cell types likely maintain different roles in the injured central nervous system (CNS) (72–74).”
§ The Inflammatory Continuum of Traumatic Brain Injury and Alzheimer’s Disease > Introduction to Traumatic Brain Injury (TBI) and Alzheimer’s Disease (AD) > Relevance of Microglia and Macrophages in TBI
What the sources say
- Supportedcites [69] Gosselin, 2014, Environment drives selection and function of enhancers controlling tissue-specific macrophage identities, Cell source
The citation group (69–71) is attached to the claim about distinct genetic and transcriptomic profiles, not the later inference about roles in the injured CNS, which has separate citations. In Results (‘Environment-specific gene expression’), RNA-Seq shows substantial expression differences between microglia and other macrophage populations; the Discussion (‘Tuning enhancer landscapes and gene expression to context-specific functions’) also describes distinct active enhancer sets. (LLM, conf=0.90)
- Could not verifycites [70] Butovsky, 2014, Identification of a unique TGF-β-dependent molecular and functional signature in microglia, Nat Neurosci sourceExperimental — accuracy not yet measured
The indexed passages are labeled as corrections to other articles, including “Corrigendum: Immune surveillance in the central nervous system” (Abstract; page unavailable). Searches for microglia, their transcriptomic differences from macrophages, and roles in the injured CNS found no passage addressing the claim. The available copy therefore cannot verify it. (LLM, conf=0.74)
- Supportedcites [71] Lavin, 2014, Tissue-resident macrophage enhancer landscapes are shaped by the local microenvironment, Cell source
The Results sections on genome-wide assays and gene expression report high-throughput RNA-seq and chromatin profiling of brain microglia alongside other macrophage populations, finding distinct expression patterns. The inference about roles in the injured CNS is attached to a different citation group (72–74), so it is not attributed to this paper here. (LLM, conf=0.88)
- Supportedcites [72] Yamasaki, 2014, Differential roles of microglia and monocytes in the inflamed central nervous system, J Exp Med source
The citation to this paper is attached to the claim that the two cell types likely have different roles in the affected CNS, not to the preceding high-throughput-sequencing claim. The Abstract (page unavailable) reports that monocyte-derived macrophages initiate demyelination while microglia clear debris in EAE, supporting distinct roles in an inflamed CNS. (LLM, conf=0.91)
- Supportedcites [73] Greenhalgh, 2014, Differences in the phagocytic response of microglia and peripheral macrophages after spinal cord injury and its effects on cell death, J Neurosci source
The citation to this source is attached to the claim that microglia and peripheral macrophages have different roles in the injured CNS, not to the preceding claim about sequencing. The Abstract and Discussion describe distinct responses after spinal cord injury: microglia act early and process debris while remaining viable; peripheral macrophages predominate later and are less capable of handling CNS debris. (LLM, conf=0.92)
- Not checked — no full text of the sourcecites [74] Ajami, 2011, Infiltrating monocytes trigger EAE progression, but do not contribute to the resident microglia pool, Nat Neurosci source
Tests✓ Asserted: passes✓ Checkable: passes✓ Load-bearing: passes✓ Based: passes- Supported
Every source the paper cites for this claim was checked and supports it.
In the paper
“These changes are directly associated with an altered and time-dependent inflammatory profile in microglia (80).”
§ The Inflammatory Continuum of Traumatic Brain Injury and Alzheimer’s Disease > Introduction to Traumatic Brain Injury (TBI) and Alzheimer’s Disease (AD) > Relevance of Microglia and Macrophages in TBI
What the sources say
- Supportedcites [80] Febinger, 2015, Time-dependent effects of CX3CR1 in a mouse model of mild traumatic brain injury, J Neuroinflammation source
The Discussion reports that, after mild TBI, CX3CR1-deficient mice show a protective M2 microglial profile during the acute phase but a pronounced inflammatory M1 profile during the chronic phase. It associates these time-dependent profiles with changes in neuronal damage. The provided passages do not give page numbers. (LLM, conf=0.90)
Tests✓ Asserted: passes✓ Checkable: passes✓ Load-bearing: passes✓ Based: passes- Supported
The cited sources support only part of this claim — read each source’s verdict below.
In the paper
“For example, APP expression increases in striatal and hippocampal axons along with cortical and thalamic neurons within the first 24 h after experimental impact and fluid percussion TBI (121–123)”
§ The Inflammatory Continuum of Traumatic Brain Injury and Alzheimer’s Disease > TBI and Amyloid-Related Pathology
What the sources say
- Partly supportedcites [121] Pierce, 1996, Immunohistochemical characterization of alterations in the distribution of amyloid precursor proteins and beta-amyloid peptide after experimental brain injury in the rat, J Neurosci sourceExperimental — accuracy not yet measured
The Discussion (page not available in our copy) reports increased APP/APLP immunoreactivity in the thalamus at 1 hour and in the striatum, hippocampus, and injured cortex by 2 hours after lateral fluid-percussion injury. This paper does not study impact injury, and the Results place increased staining in cortical and thalamic neuronal cell bodies at 48 hours or later, not within the first 24 hours. It measures APP/APLP accumulation and immunoreactivity rather than establishing increased APP expression. (LLM, conf=0.88)
- Not checked — no full text of the sourcecites [122] Bramlett, 1997, Temporal and regional patterns of axonal damage following traumatic brain injury: a beta-amyloid precursor protein immunocytochemical study in rats, J Neuropathol Exp Neurol source
- Not checked — no full text of the sourcecites [123] Van Den Heuvel, 1998, Diffuse neuronal perikaryon amyloid precursor protein immunoreactivity in a focal head impact model, Acta Neurochir Suppl source
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
“Indeed, the complex neuroanatomy and neurophysiology of the human brain, such as cortical folding, substantial white matter, and specific pathophysiology compared to the rodent brain, may facilitate distinct post-injury neuropathology (137).”
§ The Inflammatory Continuum of Traumatic Brain Injury and Alzheimer’s Disease > TBI and Amyloid-Related Pathology
What the sources say
- Supportedcites [137] Cullen, 2016, A porcine model of traumatic brain injury via head rotational acceleration, Methods Mol Biol source
Section 1.3 states that the gyrencephalic brains, substantial white matter, and pathophysiological features of humans and other large mammals may be key to specific features of trauma-induced neuropathology. The same section contrasts these features with rodent brains and explains why rodent models may not reproduce all aspects of clinical TBI. (LLM, conf=0.95)
Tests✓ Asserted: passes✓ Checkable: passes✓ Load-bearing: passes✓ Based: passes- Supported
Every source the paper cites for this claim was checked and supports it.
In the paper
“A longstanding concern with many clinical studies is reliance on self-report and use of diagnostic verbiage in medical records to identify a correlation between TBI and post-injury development of AD (32).”
§ The Inflammatory Continuum of Traumatic Brain Injury and Alzheimer’s Disease > Introduction to Traumatic Brain Injury (TBI) and Alzheimer’s Disease (AD)
What the sources say
- Supportedcites [32] Weiner, 2017, Traumatic brain injury may not increase the risk of Alzheimer disease, Neurology source
The paper states that most epidemiologic studies used self-reports to establish TBI history and relied on billing codes for clinical AD diagnoses. It identifies both practices as limitations in studying the TBI–AD relationship (passage 1, section labeled Abstract). (LLM, conf=0.93)
Strength:plain· not yet calibratedCausal:correlational· not yet calibratedTests✓ Asserted: passes✓ Checkable: passes? Load-bearing: unclear✓ Based: passes- 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
“Although Aβ deposition is apparent following rotational acceleration TBI in pigs (132, 133) and rabbits (134)”
§ The Inflammatory Continuum of Traumatic Brain Injury and Alzheimer’s Disease > TBI and Amyloid-Related Pathology
What the sources say
- Supportedcites [132] Smith, 1999, Accumulation of amyloid beta and tau and the formation of neurofilament inclusions following diffuse brain injury in the pig, J Neuropathol Exp Neurol source
This source is cited for the pig finding; the rabbit finding has a separate citation. The Results (‘Aβ in Plaques’) report Aβ-containing plaque-like profiles 3–10 days after rotational-acceleration injury in pigs, though they were found in only about one third of injured animals. (LLM, conf=0.90)
- Supportedcites [133] Chen, 2004, Long-term accumulation of amyloid-beta, beta-secretase, presenilin-1, and caspase-3 in damaged axons following brain trauma, Am J Pathol source
This source is one of the citations attached to the pig finding, not the separately cited rabbit finding. The Brain Injury section describes rotational acceleration in pigs, and the Discussion reports Aβ plaques six months after injury. (LLM, conf=0.93)
- Not checked — no full text of the sourcecites [134] Hamberger, 2003, Redistribution of neurofilaments and accumulation of beta-amyloid protein after brain injury by rotational acceleration of the head, J Neurotrauma source
Tests✓ Asserted: passes✓ Checkable: passes✓ Load-bearing: passes✓ Based: passes- Supported
- It may state two separate claims as one. 65
- The quote only partly states this claim. 1
- Probably not a substantial claim. 18
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
“Although CCI TBI induced a surge of plaque pathology in PDAPP mice soon after injury at 6 months of age, a substantial reduction in cortical and hippocampal plaque load was detected chronically (28, 40).”
§ The Inflammatory Continuum of Traumatic Brain Injury and Alzheimer’s Disease > TBI and Amyloid-Related Pathology
What the sources say
- Disputedcites [28] Smith, 1998, Brain trauma induces massive hippocampal neuron death linked to a surge in beta-amyloid levels in mice overexpressing mutant amyloid precursor protein, Am J Pathol sourceExperimental — accuracy not yet measured
The Brain Injury section says the PDAPP mice were injured at 4 months of age, not 6 months. The Histopathological Analysis section reports no discernible difference in plaque number or distribution between injured and sham mice two months later, contradicting both the claimed surge in plaques and the claimed chronic reduction. The reported acute surge was in Aβ peptide levels, not plaque pathology (Aβ Tissue Levels section); page numbers are unavailable in our copy. (LLM, conf=0.90)
Checked by a reasoning model — may be wrong.
- Not checked — no full text of the sourcecites [40] Nakagawa, 1999, Traumatic brain injury in young, amyloid-beta peptide overexpressing transgenic mice induces marked ipsilateral hippocampal atrophy and diminished Abeta deposition during aging, J Comp Neurol source
Tests✓ Asserted: passes✓ Checkable: passes✓ Load-bearing: passes✓ Based: passesIt may state two separate claims as one.
- Disputed
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
“Separate groups have shown that CCX872 and RS504393, two selective CCR2 antagonists, reduce post-injury macrophage recruitment and improve functional recovery after CCI and weight drop TBI (76, 77).”
§ The Inflammatory Continuum of Traumatic Brain Injury and Alzheimer’s Disease > Introduction to Traumatic Brain Injury (TBI) and Alzheimer’s Disease (AD) > Relevance of Microglia and Macrophages in TBI
What the sources say
- Supportedcites [76] Morganti, 2015, CCR2 antagonism alters brain macrophage polarization and ameliorates cognitive dysfunction induced by traumatic brain injury, J Neurosci source
This source supports the CCX872 portion of the two-citation sentence. The Animals section describes a CCI injury; the macrophage-accumulation results (Fig. 5c) report a 50% reduction with CCX872, and the cognitive-dysfunction results (Fig. 8) report improved learning and memory after TBI. The RS504393 and weight-drop findings are not the part attributed to this source. (LLM, conf=0.91)
- Not checked — no full text of the sourcecites [77] Liu, 2013, Chemokine CCL2 induces apoptosis in cortex following traumatic brain injury, J Mol Neurosci source
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
“Clinical studies indicate that Aβ accumulates within hours after severe TBI and is spread throughout the cerebral cortex compared to age-matched controls (29, 31).”
§ The Inflammatory Continuum of Traumatic Brain Injury and Alzheimer’s Disease > TBI and Amyloid-Related Pathology
What the sources say
- Partly supportedcites [29] Roberts, 1994, Beta amyloid protein deposition in the brain after severe head injury: implications for the pathogenesis of Alzheimer’s disease, J Neurol Neurosurg Psychiatry sourceExperimental — accuracy not yet measured
The βAP immunoreactivity results report deposits in 30% of severe-head-injury cases, including some who survived less than 24 hours, and higher positivity than in age-matched controls. They do not show that deposits were spread throughout the cerebral cortex: a positive case could have deposits in just one cortical area, and the pattern varied between cases. The copy does not establish that the patients who survived only four hours had deposits. Page numbers were not supplied for these passages. (LLM, conf=0.86)
- Not checked — no full text of the sourcecites [31] Ikonomovic, 2004, Alzheimer’s pathology in human temporal cortex surgically excised after severe brain injury, Exp Neurol source
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
“A primed microglia profile includes (1) increased basal expression of inflammatory markers and mediators, (2) decreased activation threshold to express and release pro-inflammatory molecules, and (3) exaggerated inflammatory response to immune challenge (93).”
§ The Inflammatory Continuum of Traumatic Brain Injury and Alzheimer’s Disease > Post-Injury Neuroinflammation and Aging
What the sources say
- Supportedcites [93] Norden, 2015, Microglial priming and enhanced reactivity to secondary insult in aging, and traumatic CNS injury, and neurodegenerative disease, Neuropharmacology source
The “Evidence of Microglial Priming with Age” section defines a primed profile using the same three features: higher baseline inflammatory markers and mediators, a lower threshold for switching to a pro-inflammatory state, and an exaggerated response after immune activation. The claim is a close paraphrase of that definition. (LLM, conf=0.95)
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
“Finally, accumulating evidence shows that microglia and monocytes play distinct roles in AD pathogenesis (116–119), thus implicating both the central and peripheral immune response in long-term outcome.”
§ The Inflammatory Continuum of Traumatic Brain Injury and Alzheimer’s Disease > Post-Injury Neuroinflammation and Aging > TBI, Inflammation, and AD
What the sources say
- Partly supportedcites [116] Bhaskar, 2010, Regulation of tau pathology by the microglial fractalkine receptor, Neuron sourceExperimental — accuracy not yet measured
The Introduction and Discussion (pages unavailable) link microglial signaling to AD-related pathology. The Results also show that peripheral LPS administration increases tau phosphorylation in mice. Our copy does not establish distinct roles for microglia and monocytes in AD, or show how both affect long-term outcome. (LLM, conf=0.84)
- Partly supportedcites [117] Lee, 2010, CX3CR1 deficiency alters microglial activation and reduces beta-amyloid deposition in two Alzheimer’s disease mouse models, Am J Pathol sourceExperimental — accuracy not yet measured
The Discussion reports enhanced amyloid-beta phagocytosis by microglia in the AD mouse models. The Microglial Proliferation/Migration section mentions migration of peripheral monocytes or macrophages only as a possibility; it does not establish a distinct role for them alongside microglia. The paper therefore supports a microglial role in amyloid pathology, but not the attributed distinction between the two cell populations. (LLM, conf=0.82)
- Partly supportedcites [118] Lee, 2014, Opposing effects of membrane-anchored CX3CL1 on amyloid and tau pathologies via the p38 MAPK pathway, J Neurosci sourceExperimental — accuracy not yet measured
The Introduction (page unavailable) says accumulating evidence implicates microglia-mediated neuroinflammation in AD pathogenesis, and the Discussion reports effects of altered microglial activity in APPPS1 mice. The paper does not establish distinct roles for microglia and monocytes or connect peripheral immune responses to long-term outcome; its mention of monocyte chemotactic protein 1 is not a comparison of the two cell types. (LLM, conf=0.85)
- Supportedcites [119] Martin, 2017, Distinct inflammatory phenotypes of microglia and monocyte-derived macrophages in Alzheimer’s disease models: effects of aging and amyloid pathology, Aging Cell source
The Introduction distinguishes resident microglia from monocyte-derived macrophages and describes different apparent roles in Aβ clearance. The Discussion likewise reports distinct responses in AD mouse models. The citation is attached to the distinct-roles statement; the subsequent implication for long-term outcome is the citing authors’ inference. (LLM, conf=0.88)
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
“After a single CCI TBI, Cx3cr1−/− mice have improved motor recovery and decreased neuronal loss through 15 days post-injury (DPI).”
§ The Inflammatory Continuum of Traumatic Brain Injury and Alzheimer’s Disease > Introduction to Traumatic Brain Injury (TBI) and Alzheimer’s Disease (AD) > Relevance of Microglia and Macrophages in TBI
What the sources say
- Partly supportedcites [80] Febinger, 2015, Time-dependent effects of CX3CR1 in a mouse model of mild traumatic brain injury, J Neuroinflammation sourceExperimental — accuracy not yet measured
The Results sections on neuromotor function and neuronal survival report better motor scores in injured CX3CR1−/− mice than injured wild-type mice at 24 hours, and less neuronal loss at day 15. The motor-score difference between injured groups was not significant at days 7 or 15, so improved motor recovery relative to wild-type mice throughout that period is not established. Page numbers are not provided in our copy. (LLM, conf=0.88)
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
“Many biological pathways are disrupted by experimental TBI resulting in progressive neurodegeneration including atrophy, neuronal loss, and axonal degeneration which are often associated with neuroinflammation including macrophage reactivity (82–85).”
§ The Inflammatory Continuum of Traumatic Brain Injury and Alzheimer’s Disease > Post-Injury Neuroinflammation and Aging
What the sources say
- Not checked — no full text of the sourcecites [82] Carbonell, 1998, Adaptation of the fluid percussion injury model to the mouse, J Neurotrauma source
- Not checked — no full text of the sourcecites [83] Carbonell, 1999, Regional and temporal characterization of neuronal, glial, and axonal response after traumatic brain injury in the mouse, Acta Neuropathol source
- Not checked — no full text of the sourcecites [84] Smith, 1997, Progressive atrophy and neuron death for one year following brain trauma in the rat, J Neurotrauma source
- Partly supportedcites [85] Pierce, 1998, Enduring cognitive, neurobehavioral and histopathological changes persist for up to one year following severe experimental brain injury in rats, Neuroscience 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.
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
“This strategy presents additional challenges as each animal model reflects a specific type of TBI and does not fully recapitulate primary and secondary damage evident in human TBI (45) resulting in restricted translation (46).”
§ The Inflammatory Continuum of Traumatic Brain Injury and Alzheimer’s Disease > Introduction to Traumatic Brain Injury (TBI) and Alzheimer’s Disease (AD) > Experimental Models of TBI
What the sources say
- Supportedcites [45] Saatman, 2008, Classification of traumatic brain injury for targeted therapies, J Neurotrauma source
The roundtable discussion on pathoanatomic heterogeneity and laboratory models describes animal models designed for particular focal or diffuse injuries and says they do not capture the full spectrum of injury severity or the variability of human injuries and recovery. That supports the limitation attributed to this paper. The concluding phrase about restricted translation is attached to citation (46), not this source. (LLM, conf=0.86)
- Not checked — no full text of the sourcecites [46] Margulies, 2009, Combination therapies for traumatic brain injury: prospective considerations, J Neurotrauma 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
Every source the paper cites for this claim was checked and supports it.
In the paper
“For example, myeloid cells are instrumental in maintaining CNS homeostasis; however, aging significantly alters their properties (88).”
§ The Inflammatory Continuum of Traumatic Brain Injury and Alzheimer’s Disease > Post-Injury Neuroinflammation and Aging
What the sources say
- Supportedcites [88] Harry, 2013, Microglia during development and aging, Pharmacol Ther source
The Introduction describes microglia as CNS immune cells that maintain homeostasis. It also reports age-related changes in their inflammatory activity, while section 6 describes changes in their morphology and responses to injury. (LLM, conf=0.88)
Tests✓ Asserted: passes✓ Checkable: passes✓ Load-bearing: passes✓ Based: passesIt may state two separate claims as one.
- 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
“Also, several clinical studies report that individuals with genetic predisposition to developing AD (ApoE4 risk alleles) display altered outcome after TBI making the distinction between environmental and genetic risk factors for post-injury recovery unclear (33, 34).”
§ The Inflammatory Continuum of Traumatic Brain Injury and Alzheimer’s Disease > Introduction to Traumatic Brain Injury (TBI) and Alzheimer’s Disease (AD)
What the sources say
- Supportedcites [33] Li, 2015, The association between apolipoprotein E and functional outcome after traumatic brain injury, Medicine (Baltimore) source
The Introduction identifies APOE ε4 as implicated in late-onset Alzheimer’s disease. The Discussion reports an association between APOE ε4 and unfavorable long-term functional outcome after TBI, while noting that non-genetic confounders could affect the estimated association. It found no significant association at six months. (LLM, conf=0.87)
- Not checked — no full text of the sourcecites [34] Padgett, 2016, Exploring the effect of the apolipoprotein E (APOE) gene on executive function, working memory, and processing speed during the early recovery period following traumatic brain injury, J Clin Exp Neuropsychol source
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
“The cause of microglial priming is unclear and likely results from multiple factors, including but not limited to (1) a loss of inhibitory ligand–receptor communication with aging neurons (94), (2) interactions with age-related misfolded proteins such as Aβ which promote pro-inflammatory cytokine production (95), (3) age-related exposure to increasing transforming growth factor-β which could”
§ The Inflammatory Continuum of Traumatic Brain Injury and Alzheimer’s Disease > Post-Injury Neuroinflammation and Aging
What the sources say
- Not checked — no full text of the sourcecites [94] Perry, 2014, Microglial priming in neurodegenerative disease, Nat Rev Neurol source
- Not checked — no full text of the sourcecites [95] Flanary, 2007, Evidence that aging and amyloid promote microglial cell senescence, Rejuvenation Res source
- Partly supportedcites [96] Cohen, 2014, Chronic exposure to TGFβ1 regulates myeloid cell inflammatory response in an IRF7-dependent manner, EMBO J sourceExperimental — accuracy not yet measured
The Results section on the M1-to-M2 phenotype switch reports that prolonged TGFβ1 exposure impaired microglia’s ability to adopt an anti-inflammatory phenotype. The Discussion links this effect to chronic exposure in the adult CNS, but our copy does not show that TGFβ exposure increases with age or establish it as a cause of age-related microglial priming. Page numbers were not available in the indexed passages. (LLM, conf=0.87)
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. The quote only partly states this claim.
Every source the paper cites for this claim was checked and supports it.
In the paper
“Interruption of CCR2 signaling through the use of Ccr2RFP/RFP mice reduces post-injury monocytic infiltration and axonal pathology but enhances cortical and hippocampal MAPT mislocalization and hyperphosphorylation soon after lateral fluid percussion TBI suggesting that monocyte sub-populations may differentially influence outcome (78).”
§ The Inflammatory Continuum of Traumatic Brain Injury and Alzheimer’s Disease > Introduction to Traumatic Brain Injury (TBI) and Alzheimer’s Disease (AD) > Relevance of Microglia and Macrophages in TBI
What the sources say
- Supportedcites [78] Gyoneva, 2015, Ccr2 deletion dissociates cavity size and tau pathology after mild traumatic brain injury, J Neuroinflammation source
Split into 2 atoms — 2 confirmed, 0 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.
- 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
“Secondary damage includes excitotoxicity (64), oxidative stress (65), and widespread neuroinflammation (63).”
§ The Inflammatory Continuum of Traumatic Brain Injury and Alzheimer’s Disease > Introduction to Traumatic Brain Injury (TBI) and Alzheimer’s Disease (AD) > Inflammation as a Mediator of Post-Injury Outcome
What the sources say
- Supportedcites [64] Dorsett, 2017, Glutamate neurotransmission in rodent models of traumatic brain injury, J Neurotrauma source
Only “excitotoxicity” is attributed to this paper by citation (64); oxidative stress and neuroinflammation have separate citations. The Introduction (page unavailable) says increased extracellular glutamate initiates secondary injury cascades and can make neuronal tissue vulnerable to excitotoxicity. (LLM, conf=0.91)
- Supportedcites [65] Hall, 2010, Antioxidant therapies for traumatic brain injury, Neurotherapeutics source
Citation (65) is attached to oxidative stress, not to excitotoxicity or neuroinflammation. The Introduction identifies oxygen radical-induced oxidative damage as a validated secondary-injury mechanism in traumatic brain injury. (LLM, conf=0.93)
- Not checked — no full text of the sourcecites [63] Simon, 2017, The far-reaching scope of neuroinflammation after traumatic brain injury, Nat Rev Neurol source
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
“While both brain-injured AD and wild-type mice had increased expression of inflammatory cytokines IL-1β, IL-6, and TNFα, peak elevations were delayed by 7 days in the AD mice but persisted in conjunction with astrocyte activation.”
§ The Inflammatory Continuum of Traumatic Brain Injury and Alzheimer’s Disease > TBI and Amyloid-Related Pathology
What the sources say
- Partly supportedcites [16] Webster, 2015, Closed head injury in an age-related Alzheimer mouse model leads to an altered neuroinflammatory response and persistent cognitive impairment, J Neurosci sourceExperimental — accuracy not yet measured
The cytokine-response Results section reports that IL-1β, IL-6, and TNFα gene expression peaked at 7 days after injury in APP/PS1 mice, later than in wild-type mice. But cytokine protein levels followed similar time courses in both groups, and the chronic-time-point Results report no injury-related increase in those cytokines at day 32. Persistent activation is supported for astrocytes, not for sustained elevation of all three cytokines. (LLM, conf=0.88)
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
“Recent studies using the same injury model confirmed that post-injury microglial depletion followed by microglial repopulation improves behavioral recovery, attenuates the lesion-induced neuroinflammatory response, and increases dendritic spin densities despite extensive neuronal loss in the hippocampus (240).”
§ The Inflammatory Continuum of Traumatic Brain Injury and Alzheimer’s Disease > Macrophage Elimination Alters Recovery Following TBI
What the sources say
- Partly supportedcites [240] Rice, 2017, Microglial repopulation resolves inflammation and promotes brain recovery after injury, Glia sourceExperimental — accuracy not yet measured
The Results sections report behavioral recovery and reduced inflammatory markers after microglial repopulation despite extensive hippocampal neuronal loss. However, the dendritic-spine Results report no significant difference in spine density between lesioned mice with and without repopulation; the reported increase was relative to uninjured controls. Page numbers are unavailable in our copy. (LLM, conf=0.90)
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
“A recent highly repetitive mouse model of TBI including 30 injuries has also been characterized (59).”
§ The Inflammatory Continuum of Traumatic Brain Injury and Alzheimer’s Disease > Post-Injury Peripheral Immune Challenge Worsens Recovery Following TBI > Repetitive TBI as a Post-Injury Immune Challenge
What the sources say
- Supportedcites [59] Winston, 2016, Dendritic spine loss and chronic white matter inflammation in a mouse model of highly repetitive head trauma, Am J Pathol source
The Discussion describes the authors' new mouse model of repetitive mild TBI, designed to deliver up to 30 head impacts. The Neuronal Architecture Changes after mTBI section reports exposing mice to 30 injuries, so the cited paper is the model the sentence identifies. (LLM, conf=0.95)
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.
- Supported
The cited sources support only part of this claim — read each source’s verdict below.
In the paper
“The co-occurrence of TBI and APP mutation in the clinical setting is rare (29) thereby restricting the results of many of these studies.”
§ The Inflammatory Continuum of Traumatic Brain Injury and Alzheimer’s Disease > TBI and Amyloid-Related Pathology
What the sources say
- Partly supportedcites [29] Roberts, 1994, Beta amyloid protein deposition in the brain after severe head injury: implications for the pathogenesis of Alzheimer’s disease, J Neurol Neurosurg Psychiatry sourceExperimental — accuracy not yet measured
In the discussion (page not available in our copy), the paper describes two pedigrees in which a person with an APP gene mutation had a history of significant head injury. It does not establish that this co-occurrence is rare in clinical settings or say that its rarity restricts the results of other studies. (LLM, conf=0.78)
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
“supporting the notion that tau oligomers are neurotoxic and contribute to tau spreading throughout the brain (180).”
§ The Inflammatory Continuum of Traumatic Brain Injury and Alzheimer’s Disease > TBI and Tau-Related Pathology
What the sources say
- Supportedcites [180] Gerson, 2016, Tau oligomers derived from traumatic brain injury cause cognitive impairment and accelerate onset of pathology in htau mice, J Neurotrauma source
The Discussion (page not provided) reports that injected TBI-derived tau oligomers caused spatial-memory deficits in mice and were detected beyond the injection site. It interprets those findings as suggesting that the oligomers may spread to other brain regions, matching the citing sentence’s hedged claim. (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
“Treatment with MW151, a small-molecule inhibitor targeting pro-inflammatory cytokines in glia, attenuated the persistent increase in pro-inflammatory cytokine expression and improved cognitive recovery in APP/PS1 mice.”
§ The Inflammatory Continuum of Traumatic Brain Injury and Alzheimer’s Disease > TBI and Amyloid-Related Pathology
What the sources say
- Supportedcites [16] Webster, 2015, Closed head injury in an age-related Alzheimer mouse model leads to an altered neuroinflammatory response and persistent cognitive impairment, J Neurosci source
The results section reports that MW151 suppressed the injury-induced pro-inflammatory cytokine response in APP/PS1 KI mice, and Figure 6 reports that treated injured mice made fewer errors than vehicle-treated injured mice. The Discussion describes the inflammatory response as extended and says treatment during that phase prevented cognitive impairment. The measured cytokine suppression was at day 10 after injury; the paper does not claim cytokines remained elevated at day 32. (LLM, conf=0.91)
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
“While CCI TBI increased soluble and insoluble cortical Aβ40 and Aβ42 within 24 h after injury, both soluble and insoluble Aβ returned to sham levels by 7 DPI (23).”
§ The Inflammatory Continuum of Traumatic Brain Injury and Alzheimer’s Disease > TBI and Amyloid-Related Pathology
What the sources say
- Supportedcites [23] Washington, 2014, Experimental traumatic brain injury induces rapid aggregation and oligomerization of amyloid-beta in an Alzheimer’s disease mouse model, J Neurotrauma source
The Results report that CCI increased soluble and insoluble Aβ40 and Aβ42 in the injured cortex of 3xTg mice at 1 day postinjury. The Discussion says the brain cleared the injury-induced Aβ accumulations within 7 days. The Results also note that a greater proportion of Aβ remained insoluble at day 7, a distinction the claim does not address. (LLM, conf=0.90)
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
“Similarly, CSF1R inhibition after a chronic hippocampal lesion model of brain injury improved behavioral recovery, reduced pro-inflammatory molecules, and increased dendritic spines (239).”
§ The Inflammatory Continuum of Traumatic Brain Injury and Alzheimer’s Disease > Macrophage Elimination Alters Recovery Following TBI
What the sources say
- Partly supportedcites [239] Rice, 2015, Elimination of microglia improves functional outcomes following extensive neuronal loss in the hippocampus, J Neurosci sourceExperimental — accuracy not yet measured
The Abstract reports that CSF1R inhibition after a 25-day hippocampal lesion improved behavioral recovery and reduced elevated pro-inflammatory molecules. The Results (‘Microglia regulate dendritic spine densities in the intact brain’) report increased spine density with microglial elimination alone, but no further increase in overall spine numbers when elimination was combined with the lesion. The claim incorrectly presents the spine increase as an outcome of post-lesion treatment. (LLM, conf=0.92)
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
“Together, these studies demonstrate that single TBI induces acute tau phosphorylation but not aggregation.”
§ The Inflammatory Continuum of Traumatic Brain Injury and Alzheimer’s Disease > TBI and Tau-Related Pathology
What the sources say
- Not checked — no full text of the sourcecites [31] Ikonomovic, 2004, Alzheimer’s pathology in human temporal cortex surgically excised after severe brain injury, Exp Neurol source
- Could not verifycites [165] Uryu, 2002, Repetitive mild brain trauma accelerates Abeta deposition, lipid peroxidation, and cognitive impairment in a transgenic mouse model of Alzheimer amyloidosis, J Neurosci sourceExperimental — accuracy not yet measured
The Histology and Discussion passages address single mild TBI in terms of tissue pathology, amyloid deposition, and lipid peroxidation, but do not report tau phosphorylation or aggregation. Searches for tau phosphorylation and neurofibrillary tangles found only a general mention of tangles as an Alzheimer’s disease hallmark, not a finding after single TBI. Page numbers were unavailable in our copy. (LLM, conf=0.76)
- Not checked — no full text of the sourcecites [166] Smith, 2003, Tau immunohistochemistry in acute brain injury, Neuropathol Appl Neurobiol source
Tests✓ 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
“In these experiments, low and moderate doses of valganciclovir reduced CD11b cell populations with no effect on axonal injury, silver staining, or APP accumulation at sub-acute post-injury time points (241).”
§ The Inflammatory Continuum of Traumatic Brain Injury and Alzheimer’s Disease > Macrophage Elimination Alters Recovery Following TBI
What the sources say
- Partly supportedcites [241] Bennett, 2014, Acute reduction of microglia does not alter axonal injury in a mouse model of repetitive concussive traumatic brain injury, J Neurotrauma sourceExperimental — accuracy not yet measured
In the subacute-effects section (21 days; page unavailable), low-dose valganciclovir reduced microglial cells, with no difference in silver staining. The paper reports unchanged APP staining and axonal injury for intermediate-dose treatment at 7 days, not 21 days. At 21 days, intermediate-dose treatment caused tissue loss, and silver staining was not quantified, so the claim extends the no-effect finding beyond the reported results. (LLM, conf=0.89)
Tests✓ Asserted: passes✓ Checkable: passes✓ Load-bearing: passes✓ Based: passesIt may state two separate claims as one.
- Partly supported
In the paper
“NFTs spread from the medial temporal lobes and hippocampus to the neocortex (9).”
§ The Inflammatory Continuum of Traumatic Brain Injury and Alzheimer’s Disease > Introduction to Traumatic Brain Injury (TBI) and Alzheimer’s Disease (AD)
What the sources say
- Not checked — no full text of the sourcecites [9] Braak, 1997, Frequency of stages of Alzheimer-related lesions in different age categories, Neurobiol Aging 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 and other studies indicate that there is a biological link between TBI and AD pathology, but the exact molecular pathways underlying this relationship are poorly understood and post-injury mechanisms that facilitate Aβ and tau pathology remain under investigation.”
§ The Inflammatory Continuum of Traumatic Brain Injury and Alzheimer’s Disease > Introduction to Traumatic Brain Injury (TBI) and Alzheimer’s Disease (AD)
Tests✓ Asserted: passes✓ Checkable: passes✓ Load-bearing: passes✓ Based: passesIt may state two separate claims as one.
In the paper
“Alzheimer’s disease is a neurodegenerative disease that progresses from mild cognitive impairment to severe dementia over time (5).”
§ The Inflammatory Continuum of Traumatic Brain Injury and Alzheimer’s Disease > Introduction to Traumatic Brain Injury (TBI) and Alzheimer’s Disease (AD)
What the sources say
- Not checked yetcites [5] Alzheimer, 1907, Uber eine eigenartige Erkrankung der Hirnrinde. Allg. Zeitschrift fur Psychiatr, Und Psych Medizin
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. 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
“This review will consider post-injury neuroinflammation as a malleable response that is closely associated with development of AD-like pathology, thereby supporting a relationship between TBI, neuroinflammation, and development of AD.”
§ The Inflammatory Continuum of Traumatic Brain Injury and Alzheimer’s Disease > Introduction to Traumatic Brain Injury (TBI) and Alzheimer’s Disease (AD)
Tests✓ Asserted: passes✓ Checkable: passes✓ Load-bearing: passes✓ Based: passesIt may state two separate claims as one.
The paper states this without a source or data behind it here, so there is nothing to check it against. The quote shows it is in the paper.
In the paper
“Indeed, TBI is recognized as an environmental risk factor for many neurodegenerative diseases such as AD, Parkinson’s disease (PD), and chronic traumatic encephalopathy (CTE).”
§ The Inflammatory Continuum of Traumatic Brain Injury and Alzheimer’s Disease > Introduction to Traumatic Brain Injury (TBI) and Alzheimer’s Disease (AD)
Tests✓ Asserted: passes✓ Checkable: passes✓ Load-bearing: passes✗ Based: failsProbably not a substantial claim. The paper may give no reason why it holds.
In the paper
“In typical cases of AD, Aβ spreads from the frontal and temporal lobes to the hippocampus and limbic system.”
§ The Inflammatory Continuum of Traumatic Brain Injury and Alzheimer’s Disease > Introduction to Traumatic Brain Injury (TBI) and Alzheimer’s Disease (AD)
What the sources say
- Not checked — no full text of the sourcecites [9] Braak, 1997, Frequency of stages of Alzheimer-related lesions in different age categories, Neurobiol Aging 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
“Collectively, the studies described in this review suggest that the brain’s immune response to injury is a key mediator in recovery, and if compromised by previous, coincident, or subsequent immune stressors, post-injury pathology and behavioral recovery”
- Also stated in: § Inflammation as a Mediator of Post-Injury Outcome · plain
“We propose that the brain’s immune response to injury is a key mediator in recovery, and if compromised by previous, coincident, or subsequent immune stressors, progressive impairments will be evident.”
§ The Inflammatory Continuum of Traumatic Brain Injury and Alzheimer’s Disease > Abstract
Tests✓ Asserted: passes✓ Checkable: passes✓ Load-bearing: passes✓ Based: passesIt may state two separate claims as one.
- Also stated in: § Inflammation as a Mediator of Post-Injury Outcome · plain
In the paper
“and intracellular aggregation of microtubule-associated protein tau (MAPT, tau) in neurofibrillary tangles (NFTs) (7).”
§ The Inflammatory Continuum of Traumatic Brain Injury and Alzheimer’s Disease > Introduction to Traumatic Brain Injury (TBI) and Alzheimer’s Disease (AD)
What the sources say
- Not checked — no full text of the sourcecites [7] Kidd, 1963, Paired helical filaments in electron microscopy of Alzheimer’s disease, Nature 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.
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 alterations may increase the incidence of neuropsychiatric complications after TBI and may also increase the frequency of neurodegenerative pathology.”
§ The Inflammatory Continuum of Traumatic Brain Injury and Alzheimer’s Disease > Abstract
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
“Moreover, the immune response to TBI, mediated by microglia and macrophages, is influenced by existing brain pathology and by secondary immune challenges.”
§ The Inflammatory Continuum of Traumatic Brain Injury and Alzheimer’s Disease > Abstract
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
“Moreover, inflammation is a malleable response to TBI that changes with aging which suggests that it could be critical in mediating post-injury outcome.”
§ The Inflammatory Continuum of Traumatic Brain Injury and Alzheimer’s Disease > Post-Injury Neuroinflammation and Aging
Tests✓ Asserted: passes✓ Checkable: passes✓ Load-bearing: passes✗ Based: failsProbably not a substantial claim. The paper may give no reason why it holds. It 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
“For example, APP accumulates in traumatized axons after all severities of TBI and has been detected many months post-injury (129–131).”
§ The Inflammatory Continuum of Traumatic Brain Injury and Alzheimer’s Disease > TBI and Amyloid-Related Pathology
What the sources say
- Not checked — no full text of the sourcecites [129] Blumbergs, 1995, Topography of axonal injury as defined by amyloid precursor protein and the sector scoring method in mild and severe closed head injury, J Neurotrauma source
- Not checked — no full text of the sourcecites [130] Blumbergs, 1994, Staining of amyloid precursor protein to study axonal damage in mild head injury, Lancet source
- Not checked — no full text of the sourcecites [131] Gentleman, 1995, Axonal injury: a universal consequence of fatal closed head injury?, Acta Neuropathol source
Tests✓ Asserted: passes✓ Checkable: passes✓ Load-bearing: passes✓ Based: passesIt may state two separate claims as one.
In the paper
“Secondary damage develops hours and days after the primary damage, but is not necessarily dependent on the primary injury itself.”
§ The Inflammatory Continuum of Traumatic Brain Injury and Alzheimer’s Disease > Introduction to Traumatic Brain Injury (TBI) and Alzheimer’s Disease (AD) > Inflammation as a Mediator of Post-Injury Outcome
What the sources say
- Not checked — no full text of the sourcecites [3] Maas, 2008, Moderate and severe traumatic brain injury in adults, Lancet Neurol source
Load-bearingStrength:plain· not yet calibratedTests✓ 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
“TBI induces a widespread neuroinflammatory response that can promote recovery if controlled for a defined time period.”
§ The Inflammatory Continuum of Traumatic Brain Injury and Alzheimer’s Disease > Post-Injury Neuroinflammation and Aging > TBI, Inflammation, and AD
Tests✓ Asserted: passes✓ Checkable: passes✓ Load-bearing: passes✓ Based: passesIt may state two separate claims as one.
The paper states this without a source or data behind it here, so there is nothing to check it against. The quote shows it is in the paper.
In the paper
“These PDAPP transgenic mice display age-related cognitive impairment, synaptic dysfunction, Aβ accumulation, and tau phosphorylation.”
§ The Inflammatory Continuum of Traumatic Brain Injury and Alzheimer’s Disease > TBI and Amyloid-Related Pathology
Tests✓ Asserted: passes✓ Checkable: passes✓ Load-bearing: passes✓ Based: passesIt may state two separate claims as one.
In the paper
“Consequently, age-related immune changes and those that occur during AD share many similarities and the distinction between the two processes remains unclear (89).”
§ The Inflammatory Continuum of Traumatic Brain Injury and Alzheimer’s Disease > Post-Injury Neuroinflammation and Aging
What the sources say
- Not checked — no full text of the sourcecites [89] Heneka, 2010, Neuroinflammatory processes in Alzheimer’s disease, J Neural Transm 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.
In the paper
“Subsequent work by a separate group confirms these results and demonstrates that CX3CR1 deficiency results in early protection but chronic worsening of CCI TBI-induced deficits due in part to a decrease in anti-inflammatory cytokines on CD11b+ sorted cells at 28 DPI (81).”
§ The Inflammatory Continuum of Traumatic Brain Injury and Alzheimer’s Disease > Introduction to Traumatic Brain Injury (TBI) and Alzheimer’s Disease (AD) > Relevance of Microglia and Macrophages in TBI
What the sources say
- Not checked — no full text of the sourcecites [81] Zanier, 2016, Fractalkine receptor deficiency is associated with early protection but late worsening of outcome following brain trauma in mice, J Neurotrauma source
Tests✓ Asserted: passes✓ Checkable: passes✓ Load-bearing: passes✓ Based: passesIt may state two separate claims as one.
The paper states this without a source or data behind it here, so there is nothing to check it against. The quote shows it is in the paper.
In the paper
“Monomeric Aβ aggregates to form oligomers, protofibrils, and fibrils that accumulate in the characteristic Aβ plaque of AD.”
§ The Inflammatory Continuum of Traumatic Brain Injury and Alzheimer’s Disease > TBI and Amyloid-Related Pathology
Strength:plain· not yet calibratedCausal:direct· 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.
The paper states this without a source or data behind it here, so there is nothing to check it against. The quote shows it is in the paper.
In the paper
“Similarly, microglia and astrocyte reactivity increases within days post-injury, but altered and reactive morphology diminishes by 10–14 days post-injury.”
§ The Inflammatory Continuum of Traumatic Brain Injury and Alzheimer’s Disease > Introduction to Traumatic Brain Injury (TBI) and Alzheimer’s Disease (AD) > Experimental Models of TBI
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 paper states this without a source or data behind it here, so there is nothing to check it against. The quote shows it is in the paper.
In the paper
“In normal physiological conditions, the BBB prevents entry of peripheral monocytes into the brain parenchyma.”
§ The Inflammatory Continuum of Traumatic Brain Injury and Alzheimer’s Disease > Introduction to Traumatic Brain Injury (TBI) and Alzheimer’s Disease (AD) > Relevance of Microglia and Macrophages in TBI
Tests✓ Asserted: passes✓ Checkable: passes✓ Load-bearing: passes✗ Based: failsProbably not a substantial claim. The paper may give no reason why it holds.
The paper states this without a source or data behind it here, so there is nothing to check it against. The quote shows it is in the paper.
In the paper
“For example, after TBI, microglia and monocyte-derived macrophages adopt a similar morphology, upregulate similar inflammatory surface markers, and increase production of similar inflammatory cytokines.”
§ The Inflammatory Continuum of Traumatic Brain Injury and Alzheimer’s Disease > Introduction to Traumatic Brain Injury (TBI) and Alzheimer’s Disease (AD) > Relevance of Microglia and Macrophages in TBI
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
“It is necessary to acknowledge that post-injury inflammation poses both beneficial and detrimental consequences that need to be balanced.”
§ The Inflammatory Continuum of Traumatic Brain Injury and Alzheimer’s Disease > Introduction to Traumatic Brain Injury (TBI) and Alzheimer’s Disease (AD) > Inflammation as a Mediator of Post-Injury Outcome
Tests✓ Asserted: passes✓ Checkable: passes✓ Load-bearing: passes✓ Based: passesProbably not a substantial claim. 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
“Collectively, these results suggest that chronic post-injury neuroinflammation may be sufficient to induce or facilitate AD-related pathology.”
§ The Inflammatory Continuum of Traumatic Brain Injury and Alzheimer’s Disease > Post-Injury Neuroinflammation and Aging > TBI, Inflammation, and AD
Tests✓ Asserted: passes✓ Checkable: passes✓ Load-bearing: passes✓ Based: passesIt may state two separate claims as one.
The paper states this without a source or data behind it here, so there is nothing to check it against. The quote shows it is in the paper.
In the paper
“Accumulating data indicate that pre- and post-injury immune challenges may influence the microglial and macrophage response to brain injury and influence post-injury pathology and behavioral recovery.”
§ The Inflammatory Continuum of Traumatic Brain Injury and Alzheimer’s Disease > Introduction to Traumatic Brain Injury (TBI) and Alzheimer’s Disease (AD) > Inflammation as a Mediator of Post-Injury Outcome
Tests✓ Asserted: passes✓ Checkable: passes✓ Load-bearing: passes? Based: unclearIt 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
“Finally, several experimental studies have failed to show that TBI induces or worsens AD-related pathology (38, 39) with some even reporting a reduction in post-injury Aβ accumulation in transgenic mice (40, 41).”
§ The Inflammatory Continuum of Traumatic Brain Injury and Alzheimer’s Disease > Introduction to Traumatic Brain Injury (TBI) and Alzheimer’s Disease (AD)
What the sources say
- Not checked — no full text of the sourcecites [38] Kokiko-Cochran, 2016, Altered Neuroinflammation and behavior after traumatic brain injury in a mouse model of Alzheimer’s disease, J Neurotrauma source
- Not checked — no full text of the sourcecites [39] Collins, 2015, The effect of focal brain injury on beta-amyloid plaque deposition, inflammation and synapses in the APP/PS1 mouse model of Alzheimer’s disease, Exp Neurol source
- Not checked — no full text of the sourcecites [40] Nakagawa, 1999, Traumatic brain injury in young, amyloid-beta peptide overexpressing transgenic mice induces marked ipsilateral hippocampal atrophy and diminished Abeta deposition during aging, J Comp Neurol source
- Not checked — no full text of the sourcecites [41] Nakagawa, 2000, Brain trauma in aged transgenic mice induces regression of established abeta deposits, Exp Neurol 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
“First, microglia, monocytes, and astrocytes as well as inflammatory cytokines and chemokines are elevated in the AD brain (108).”
§ The Inflammatory Continuum of Traumatic Brain Injury and Alzheimer’s Disease > Post-Injury Neuroinflammation and Aging > TBI, Inflammation, and AD
What the sources say
- Not checked — no full text of the sourcecites [108] Minter, 2016, The contribution of neuroinflammation to amyloid toxicity in Alzheimer’s disease, J Neurochem source
Tests✓ Asserted: passes✓ Checkable: passes✓ Load-bearing: passes✓ 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
“Post-injury neuroinflammation is characterized by activation of brain-resident microglia, infiltration of peripheral immune cells, astrogliosis, and increased synthesis and release of pro- and anti-inflammatory molecules which can persist for months to years after the initial insult (106, 107).”
§ The Inflammatory Continuum of Traumatic Brain Injury and Alzheimer’s Disease > Post-Injury Neuroinflammation and Aging > TBI, Inflammation, and AD
What the sources say
- Not checked — no full text of the sourcecites [106] Başkaya, 1997, The biphasic opening of the blood-brain barrier in the cortex and hippocampus after traumatic brain injury in rats, Neurosci Lett source
- Not checked — no full text of the sourcecites [107] Morganti-Kossmann, 2007, Modulation of immune response by head injury, Injury 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
“Inflammation following TBI is a complex and dynamic response of both the central and peripheral nervous systems, which is influenced by age, sex, injury location and severity, secondary injury cascades, and genetics (63).”
§ The Inflammatory Continuum of Traumatic Brain Injury and Alzheimer’s Disease > Introduction to Traumatic Brain Injury (TBI) and Alzheimer’s Disease (AD) > Inflammation as a Mediator of Post-Injury Outcome
What the sources say
- Not checked — no full text of the sourcecites [63] Simon, 2017, The far-reaching scope of neuroinflammation after traumatic brain injury, Nat Rev Neurol 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.
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 both sets of experiments, the reduction in Aβ pathology was accompanied by increased neuronal death and memory impairment, ultimately bringing into question the neurotoxic properties of Aβ alone.”
§ The Inflammatory Continuum of Traumatic Brain Injury and Alzheimer’s Disease > TBI and Amyloid-Related Pathology
Tests✓ Asserted: passes✓ Checkable: passes✓ Load-bearing: passes✓ Based: passesIt may state two separate claims as one.
In the paper
“Similarly, post-injury macrophage recruitment substantially decreases in Ccr2−/− mice following CCI TBI and correlates with improved behavioral outcome (75).”
§ The Inflammatory Continuum of Traumatic Brain Injury and Alzheimer’s Disease > Introduction to Traumatic Brain Injury (TBI) and Alzheimer’s Disease (AD) > Relevance of Microglia and Macrophages in TBI
What the sources say
- Not checked — no full text of the sourcecites [75] Hsieh, 2014, CCR2 deficiency impairs macrophage infiltration and improves cognitive function after traumatic brain injury, J Neurotrauma source
Tests✓ Asserted: passes✓ Checkable: passes✓ Load-bearing: passes✓ Based: passesIt may state two separate claims as one.
The paper states this without a source or data behind it here, so there is nothing to check it against. The quote shows it is in the paper.
In the paper
“While no single model recapitulates all aspects of human TBI, the neuroinflammatory response to injury occurs in a temporally distinct manner.”
§ The Inflammatory Continuum of Traumatic Brain Injury and Alzheimer’s Disease > Introduction to Traumatic Brain Injury (TBI) and Alzheimer’s Disease (AD) > Experimental Models of TBI
Strength:plain· 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.
The paper states this without a source or data behind it here, so there is nothing to check it against. The quote shows it is in the paper.
In the paper
“Inflammatory cytokines and chemokines are immediately release after moderate TBI and peak within hours post-injury.”
§ The Inflammatory Continuum of Traumatic Brain Injury and Alzheimer’s Disease > Introduction to Traumatic Brain Injury (TBI) and Alzheimer’s Disease (AD) > Experimental Models of TBI
Strength:plain· not yet calibratedCausal:direct· not yet calibratedTests✓ Asserted: passes✓ Checkable: passes? Load-bearing: unclear? Based: unclearIt may state two separate claims as one.
In the paper
“Genetic deletion of CC ligand-2 (CCL2), the cognate ligand for CCR2, attenuates lesion volume, reduces macrophage recruitment and astrogliosis, and improves functional outcome compared to controls after CHI (60).”
§ The Inflammatory Continuum of Traumatic Brain Injury and Alzheimer’s Disease > Introduction to Traumatic Brain Injury (TBI) and Alzheimer’s Disease (AD) > Relevance of Microglia and Macrophages in TBI
What the sources say
- Not checked — no full text of the sourcecites [60] Semple, 2010, Role of CCL2 (MCP-1) in traumatic brain injury (TBI): evidence from severe TBI patients and CCL2-/- mice, J Cereb Blood Flow Metab source
Tests✓ Asserted: passes✓ Checkable: passes✓ Load-bearing: passes✓ Based: passesIt may state two separate claims as one.
The paper states this without a source or data behind it here, so there is nothing to check it against. The quote shows it is in the paper.
In the paper
“Disruption and dysfunction of the BBB after TBI facilities monocyte infiltration though.”
§ The Inflammatory Continuum of Traumatic Brain Injury and Alzheimer’s Disease > Introduction to Traumatic Brain Injury (TBI) and Alzheimer’s Disease (AD) > Relevance of Microglia and Macrophages in TBI
Tests✓ Asserted: passes✓ Checkable: passes✓ Load-bearing: passes✗ Based: failsProbably not a substantial claim. The paper may give no reason why it holds.
In the paper
“For example, LPS treatment 1 day after repetitive mild TBI (3 TBI’s, 5 days apart) increased macrophage reactivity but decreased production of inflammatory cytokines and reduced neuronal injury (235).”
§ The Inflammatory Continuum of Traumatic Brain Injury and Alzheimer’s Disease > Post-Injury Peripheral Immune Challenge Worsens Recovery Following TBI > Repetitive TBI as a Post-Injury Immune Challenge
What the sources say
- Not checked — no full text of the sourcecites [235] Corrigan, 2017, Toll like receptor 4 activation can be either detrimental or beneficial following mild repetitive traumatic brain injury depending on timing of activation, Brain Behav Immun 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
“the presence or absence of tau phosphorylation alone is not sufficient to define tau pathology and may represent a transient effect of TBI.”
§ The Inflammatory Continuum of Traumatic Brain Injury and Alzheimer’s Disease > TBI and Tau-Related Pathology
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
“the cumulative effect of aging and TBI in microglial priming remains unknown”
§ The Inflammatory Continuum of Traumatic Brain Injury and Alzheimer’s Disease > Post-Injury Peripheral Immune Challenge Worsens Recovery Following TBI
Load-bearingStrength:plain· not yet calibratedTests✓ Asserted: passes✓ Checkable: passes✓ Load-bearing: passes✓ Based: passesProbably not a substantial claim.
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
“Both Aβ and tau phosphorylation are reported in normal aging and could, therefore, influence the brain’s response to TBI without causing AD.”
§ The Inflammatory Continuum of Traumatic Brain Injury and Alzheimer’s Disease > Conclusion
Tests✓ Asserted: passes✓ Checkable: passes✓ Load-bearing: passes✓ Based: passesIt may state two separate claims as one.
- Rests on an assumption: Aβ and tau phosphorylation are reported in normal aging.
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
“Based on recent evidence, the presence of these low-molecular weight aggregates may substantially alter the neuroinflammatory environment and influence outcome following TBI.”
§ The Inflammatory Continuum of Traumatic Brain Injury and Alzheimer’s Disease > TBI and Amyloid-Related Pathology
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
“may be critical in determining the relationship between TBI and development of age-related neurodegenerative disease such as AD.”
§ The Inflammatory Continuum of Traumatic Brain Injury and Alzheimer’s Disease > Post-Injury Peripheral Immune Challenge Worsens Recovery Following TBI
Tests✓ Asserted: passes✓ Checkable: passes✓ Load-bearing: passes✗ Based: failsProbably not a substantial claim. 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
“Alternatively, a common mechanism may mediate post-injury amyloid and tau pathology in a temporally distinct manner which may vary between transgenic and non-transgenic rodent models.”
§ The Inflammatory Continuum of Traumatic Brain Injury and Alzheimer’s Disease > TBI and Combined Effect of Amyloid and Tau-Related Pathology
Strength:hedged· not yet calibratedCausal:conditional· not yet calibratedTests✗ Asserted: fails✓ Checkable: passes✗ Load-bearing: fails✗ Based: failsProbably not a substantial claim. The authors may not put it forward as true. The paper’s conclusions may not depend on it. The paper may give no reason why it holds. 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
“Nonetheless, these studies highlight the potential therapeutic relevance of targeting microglia and macrophages to modulate post-injury outcome and further indicate that neuroinflammation is a critical mediator of post-injury pathology.”
§ The Inflammatory Continuum of Traumatic Brain Injury and Alzheimer’s Disease > Macrophage Elimination Alters Recovery Following TBI
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
“Although these studies indicate that TBI induces an acute increase in oligomeric Aβ, the long-term consequences of this increase and the effect on specific cell types or brain region pathology remains unknown.”
§ The Inflammatory Continuum of Traumatic Brain Injury and Alzheimer’s Disease > TBI and Amyloid-Related Pathology
Tests✓ Asserted: passes✓ Checkable: passes✓ Load-bearing: passes✓ Based: passesProbably not a substantial claim. It may state two separate claims as one.
The paper states this without a source or data behind it here, so there is nothing to check it against. The quote shows it is in the paper.
In the paper
“the role of amyloid is underexplored in experimental models of repetitive TBI, which is predominantly characterized by tau pathology.”
§ The Inflammatory Continuum of Traumatic Brain Injury and Alzheimer’s Disease > Post-Injury Peripheral Immune Challenge Worsens Recovery Following TBI > Repetitive TBI as a Post-Injury Immune Challenge
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
“Certainly, there is a specific cascade of inflammatory events that occur after TBI, but these studies indicate that subtle alterations in this response are possible and can influence outcome.”
§ The Inflammatory Continuum of Traumatic Brain Injury and Alzheimer’s Disease > Conclusion
Tests✓ Asserted: passes✓ Checkable: passes✓ Load-bearing: passes✓ Based: passesIt may state two separate claims as one.
- Rests on an assumption: There is a specific cascade of inflammatory events that occur after TBI.
In the paper
“Delayed LPS treatment 5 days after repetitive TBI increased inflammatory cytokines, worsened neuronal damage including phosphorylation and aggregation of tau, and impaired behavioral recovery (235).”
§ The Inflammatory Continuum of Traumatic Brain Injury and Alzheimer’s Disease > Post-Injury Peripheral Immune Challenge Worsens Recovery Following TBI > Repetitive TBI as a Post-Injury Immune Challenge
What the sources say
- Not checked — no full text of the sourcecites [235] Corrigan, 2017, Toll like receptor 4 activation can be either detrimental or beneficial following mild repetitive traumatic brain injury depending on timing of activation, Brain Behav Immun 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
“These results highlight the temporal immune response to TBI and indicate that delayed post-injury immune challenges are detrimental to outcome.”
§ The Inflammatory Continuum of Traumatic Brain Injury and Alzheimer’s Disease > Post-Injury Peripheral Immune Challenge Worsens Recovery Following TBI > Repetitive TBI as a Post-Injury Immune Challenge
Tests✓ Asserted: passes✓ Checkable: passes✓ Load-bearing: passes✓ Based: passesIt may state two separate claims as one.
In the paper
“Macrophage reactivity was only reported in 1 of these 4 studies, and indicated that repetitive TBI in aged hTau mice resulted in increased CD45 immunoreactivity in the cortex, corpus callosum, and hippocampus 3 weeks post-injury (153).”
§ The Inflammatory Continuum of Traumatic Brain Injury and Alzheimer’s Disease > Post-Injury Peripheral Immune Challenge Worsens Recovery Following TBI > Repetitive TBI as a Post-Injury Immune Challenge
What the sources say
- Not checked — no full text of the sourcecites [153] Ojo, 2013, Repetitive mild traumatic brain injury augments tau pathology and glial activation in aged hTau mice, J Neuropathol Exp Neurol source
Strength:hedged· not yet calibratedCausal:direct· 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 first TBI is the priming event and subsequent brain injuries cause an exaggerated inflammatory response that promotes pathology.”
§ The Inflammatory Continuum of Traumatic Brain Injury and Alzheimer’s Disease > Post-Injury Peripheral Immune Challenge Worsens Recovery Following TBI > Repetitive TBI as a Post-Injury Immune Challenge
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
“Repetitive post-injury immune challenge (dotted blue line), similar to what is observed in repetitive TBI, increases macrophage-related neuroinflammation and correlates with the advanced neuropathology.”
§ The Inflammatory Continuum of Traumatic Brain Injury and Alzheimer’s Disease > Conclusion
Tests✓ Asserted: passes✓ Checkable: passes✓ Load-bearing: passes✓ Based: passesIt may state two separate claims as one.
The paper states this without a source or data behind it here, so there is nothing to check it against. The quote shows it is in the paper.
In the paper
“Indeed, many of these models express mutant APP at higher levels than endogenous APP and maintain genetic risk variants that cause familial AD which is fairly uncommon.”
§ The Inflammatory Continuum of Traumatic Brain Injury and Alzheimer’s Disease > TBI and Amyloid-Related Pathology
Load-bearingStrength:plain· not yet calibratedTests✓ 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
“This could be due, in part, to intrinsic differences between human and rodent APP and tau.”
§ The Inflammatory Continuum of Traumatic Brain Injury and Alzheimer’s Disease > Conclusion
Tests✓ Asserted: passes✓ Checkable: passes✓ Load-bearing: passes✗ Based: failsProbably not a substantial claim. The paper may give no reason why it holds.
In the paper
“Animal models of repetitive mild TBI are described in a recent review, which includes references to development of post-injury Aβ and tau pathology (232).”
§ The Inflammatory Continuum of Traumatic Brain Injury and Alzheimer’s Disease > Post-Injury Peripheral Immune Challenge Worsens Recovery Following TBI > Repetitive TBI as a Post-Injury Immune Challenge
What the sources say
- Not checked — no full text of the sourcecites [232] Edwards, 2017, Amyloid-beta and tau pathology following repetitive mild traumatic brain injury, Biochem Biophys Res Commun 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.
In the paper
“demonstrate that the glial response to TBI is altered in the presence of Aβ and correlates with altered functional recovery (38).”
§ The Inflammatory Continuum of Traumatic Brain Injury and Alzheimer’s Disease > TBI and Amyloid-Related Pathology
What the sources say
- Not checked — no full text of the sourcecites [38] Kokiko-Cochran, 2016, Altered Neuroinflammation and behavior after traumatic brain injury in a mouse model of Alzheimer’s disease, J Neurotrauma 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
“Second, accumulation of Aβ and tau phosphorylation are routinely considered primary dependent variables in experimental studies, but these pathological features do not often correlate with neuronal loss or behavioral impairment.”
§ The Inflammatory Continuum of Traumatic Brain Injury and Alzheimer’s Disease > Conclusion
Tests✓ Asserted: passes✓ Checkable: passes✓ Load-bearing: passes? Based: unclearIt may state two separate claims as one.
The paper relies on this without support.
The molecular mechanisms that link TBI to development of neurodegenerative disease remain underexplored and few studies account for age-specific pathological response to and recovery from brain injury.
“The molecular mechanisms that link TBI to development of neurodegenerative disease remain underexplored and few studies account for age-specific pathological response to and recovery from brain injury.”
The paper relies on this without support.
The roles of monocyte sub-populations in mediating outcome from TBI remain unknown without detailed follow-up studies.
“Without detailed follow-up studies, the roles of monocyte sub-populations in mediating outcome from TBI remain unknown.”
The paper relies on this without support.
The role of soluble Aβ oligomers in post-injury pathology has received limited attention.
“Surprisingly, the role of soluble Aβ oligomers in post-injury pathology has received limited attention.”
The paper relies on this without support.
No single experimental TBI model recapitulates all aspects of human TBI.
“While no single model recapitulates all aspects of human TBI, the neuroinflammatory response to injury occurs in a temporally distinct manner.”
The paper relies on this without support.
Findings from rodent models of TBI and AD are informative about human TBI-AD pathology.
“the relevance of these abnormal proteins as mediators of response to and recovery from TBI remains applicable.”
The paper relies on this without support.
The presence of Aβ and tau pathology in animal models is relevant to human AD.
“the relevance of these abnormal proteins as mediators of response to and recovery from TBI remains applicable.”
The paper relies on this without support.
Both TBI and AD are complex neurodegenerative pathologies that elicit a central and peripheral immune response.
“Both TBI and AD are complex neurodegenerative pathologies that elicit a central and peripheral immune response.”
The paper relies on this without support.
There is a specific cascade of inflammatory events that occur after TBI.
“Certainly, there is a specific cascade of inflammatory events that occur after TBI, but these studies indicate that subtle alterations in this response are possible and can influence outcome.”
The paper relies on this without support.
The severity of repetitive TBI is typically referred to as 'mild,' but the number of injuries varies from 2 to 10 across several days or weeks.
“While severity of repetitive TBI is typically referred to as “mild,” the number of injuries varies from 2 to 10 across several days or weeks.”
The paper relies on this without support.
Aβ and tau phosphorylation are reported in normal aging.
“Both Aβ and tau phosphorylation are reported in normal aging and could, therefore, influence the brain’s response to TBI without causing AD.”
The paper relies on this without support.
Multiple mouse models of AD display an altered inflammatory response to TBI.
“Given that multiple mouse models of AD display an altered inflammatory response to TBI, it is possible that accumulation of pathological proteins alters the neuroinflammatory environment in a way influences the brain’s response to injury.”
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.
Study year conflicts with its reference
MinorThe text calls reference 142 a 2013 study, while the reference entry dates it to 2012.
“a 2013 study revealed that peripheral administration of Aβ42 and Aβ40 attenuates paralysis and reduces neuroinflammation in multiple mouse models of experimental autoimmune encephalomyelitis (EAE) (142).”
“142. Grant JL Ghosn EEB Axtell RC Herges K Kuipers HF Woodling NS Reversal of paralysis and reduced inflammation from peripheral administration of β-amyloid in TH1 and TH17 versions of experimental autoimmune encephalomyelitis. Sci Transl Med (2012) 4: 145ra105”
Rat-study description cites a mouse study
MinorThe text groups reference 186 among studies reporting these findings in rats, but reference 186 identifies its subjects as mice.
“Both fluid percussion and moderate CCI TBI induce Aβ and tau pathology at acute (3 and 7 DPI) and chronic (6 months post-injury) time points in rats (177, 185, 186)”
“186. Yu F Zhang Y Chuang D-M Lithium reduces BACE1 overexpression, beta amyloid accumulation, and spatial learning deficits in mice with traumatic brain injury.”
Citations
Cites
Amyloid oligomers exacerbate tau pathology in a mouse model of tauopathy
Selenica, M.-L. B., Brownlow, M., Jimenez, J. P., Lee, D. C., Pena, G., Dickey, C. A., Gordon, M. N., & Morgan, D. (2013) · Neurodegenerative Diseases · doi:10.1159/000337230 · Cited by 10,359
Corder, E. H., Saunders, A. M., Strittmatter, W. J., Schmechel, D. E., Gaskell, P. C., Small, G. W., Roses, A. D., Haines, J. L., & Pericak-Vance, M. A. (1993) · Science · doi:10.1126/science.8346443 · Cited by 9,429
Glenner, G. G., & Wong, C. W. (1984) · Biochemical and Biophysical Research Communications · doi:10.1016/s0006-291x(84)80190-4 · Cited by 5,404
Meta-Analysis of 74,046 Individuals Identifies 11 New Susceptibility Loci for Alzheimer’s Disease
(EADI), E. A. D. I., Lambert, J.-C., (GERAD), G. A. E. R. I. A. D., Alzheimer's Disease Genetic Consortium (ADGC), (CHARGE), C. F. H. A. A. R. I. G. E., Ibrahim-Verbaas, C. A., Harold, D., Naj, A. C., Sims, R., Bellenguez, C., et al. (2013) · Nature Genetics · doi:10.1038/ng.2802 · Cited by 4,336
Strittmatter, W. J., Saunders, A. M., Schmechel, D., Pericak-Vance, M., Enghild, J., Salvesen, G. S., & Roses, A. D. (1993) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.90.5.1977 · Cited by 4,268
TREM2 Variants in Alzheimer's Disease
Guerreiro, R., Wojtas, A., Bras, J., Carrasquillo, M., Rogaeva, E., Majounie, E., Cruchaga, C., Sassi, C., Kauwe, J. S. K., Younkin, S., et al. (2013) · New England Journal of Medicine · doi:10.1056/nejmoa1211851 · Cited by 3,020
Weıntraub, S. (1990) · Archives of Neurology · doi:10.1001/archneur.1990.00530120075013 · Cited by 3,018
Variant of TREM2 Associated with the Risk of Alzheimer's Disease
Jonsson, T., Stefansson, H., Steinberg, S., Jonsdottir, I., Jonsson, P. V., Snaedal, J., Bjornsson, S., Huttenlocher, J., Levey, A. I., Lah, J. J., et al. (2013) · New England Journal of Medicine · doi:10.1056/nejmoa1211103 · Cited by 2,558
Identification of a unique TGF-β–dependent molecular and functional signature in microglia
Butovsky, O., Jedrychowski, M. P., Moore, C. S., Cialic, R., Lanser, A. J., Gabriely, G., Koeglsperger, T., Dake, B., Wu, P. M., Doykan, C. E., et al. (2014) · Nature Neuroscience · doi:10.1038/nn.3599 · Cited by 2,543
Chronic traumatic encephalopathy in athletes: Progressive tauopathy after repetitive head injury
McKee, A. C., Cantu, R. C., Nowinski, C. J., Hedley-Whyte, E. T., Gavett, B. E., Budson, A. E., Santini, V. E., Lee, H.-S., Kubilus, C. A., & Stern, R. A. (2009) · Journal of Neuropathology & Experimental Neurology · doi:10.1097/nen.0b013e3181a9d503 · Cited by 2,295
Tau-mediated neurodegeneration in Alzheimer’s disease and related disorders
Ballatore, C., Lee, V. M.-Y., & Trojanowski, J. Q. (2007) · Nature Reviews Neuroscience · doi:10.1038/nrn2194 · Cited by 2,174
Tissue-Resident Macrophage Enhancer Landscapes Are Shaped by the Local Microenvironment
Lavin, Y., Winter, D., Blecher-Gonen, R., David, E., Keren-Shaul, H., Merad, M., Jung, S., & Amit, I. (2014) · Cell · doi:10.1016/j.cell.2014.11.018 · Cited by 2,167
Moderate and severe traumatic brain injury in adults
Maas, A. I., Stocchetti, N., & Bullock, R. (2008) · The Lancet Neurology · doi:10.1016/s1474-4422(08)70164-9 · Cited by 2,123
Initiative, T. A. D. N., Hollingworth, P., CHARGE consortium, EADI1 consortium, Harold, D., Sims, R., Gerrish, A., Lambert, J.-C., Carrasquillo, M. M., Abraham, R., et al. (2011) · Nature Genetics · doi:10.1038/ng.803 · Cited by 1,997
The ageing systemic milieu negatively regulates neurogenesis and cognitive function
Villeda, S. A., Luo, J., Mosher, K. I., Zou, B., Britschgi, M., Bieri, G., Stan, T. M., Fainberg, N., Ding, Z., Eggel, A., et al. (2011) · Nature · doi:10.1038/nature10357 · Cited by 1,763
Frequency of Stages of Alzheimer-Related Lesions in Different Age Categories
Braak, H., & Braak, E. (1997) · Neurobiology of Aging · doi:10.1016/s0197-4580(97)00056-0 · Cited by 1,656
Changing patterns in the epidemiology of traumatic brain injury
Roozenbeek, B., Maas, A. I. R., & Menon, D. K. (2013) · Nature Reviews Neurology · doi:10.1038/nrneurol.2013.22 · Cited by 1,405
Strittmatter, W. J., Weisgraber, K. H., Huang, D. Y., Dong, L. M., Salvesen, G. S., Pericak-Vance, M., Schmechel, D., Saunders, A. M., Goldgaber, D., & Roses, A. D. (1993) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.90.17.8098 · Cited by 1,363
Gosselin, D., Link, V. M., Romanoski, C. E., Fonseca, G. J., Eichenfield, D. Z., Spann, N. J., Stender, J. D., Chun, H. B., Garner, H., Geissmann, F., et al. (2014) · Cell · doi:10.1016/j.cell.2014.11.023 · Cited by 1,307
A new model of diffuse brain injury in rats
Marmarou, A., Foda, M. A. A.-E., van den Brink, W., Campbell, J., Kita, H., & Demetriadou, K. (1994) · Journal of neurosurgery · doi:10.3171/jns.1994.80.2.0291 · Cited by 1,244
Katzman, R., Terry, R., DeTeresa, R., Brown, T., Davies, P., Fuld, P., Renbing, X., & Peck, A. (1988) · Annals of Neurology · doi:10.1002/ana.410230206 · Cited by 1,225
A systematic review of brain injury epidemiology in Europe
Tagliaferri, F., Compagnone, C., Koršič, M., Servadei, F., & Kraus, J. F. (2005) · Acta Neurochirurgica · doi:10.1007/s00701-005-0651-y · Cited by 1,223
The far-reaching scope of neuroinflammation after traumatic brain injury
Simon, D. W., McGeachy, M. J., Bayır, H., Clark, R. S. B., Loane, D. J., & Kochanek, P. M. (2017) · Nature Reviews Neurology · doi:10.1038/nrneurol.2017.13 · Cited by 1,190 · cited 4×
“Multiple other reviews eloquently describe this inflammatory process and provide insight into cell types and molecular pathways involved in the response (48, 63, 66, 67).”
BackgroundResultInfluentialClassification of traumatic brain injury for targeted therapies
Saatman, K. E., Duhaime, A.-C., Bullock, R., Maas, A. I. R., Valadka, A., & Manley, G. T. (2008) · Journal of Neurotrauma · doi:10.1089/neu.2008.0586 · Cited by 1,141
A controlled cortical impact model of traumatic brain injury in the rat
Edward Dixon, C., Clifton, G. L., Lighthall, J. W., Yaghmai, A. A., & Hayes, R. L. (1991) · Journal of Neuroscience Methods · doi:10.1016/0165-0270(91)90104-8 · Cited by 1,141
Microglial priming in neurodegenerative disease
Perry, V. H., & Holmes, C. (2014) · Nature Reviews Neurology · doi:10.1038/nrneurol.2014.38 · Cited by 1,127
Debris clearance by microglia: an essential link between degeneration and regeneration
Neumann, H., Kotter, M. R., & Franklin, R. J. M. (2008) · Brain · doi:10.1093/brain/awn109 · Cited by 1,111
Age-dependent dysregulation of innate immunity
Shaw, A. C., Goldstein, D. R., & Montgomery, R. R. (2013) · Nature Reviews Immunology · doi:10.1038/nri3547 · Cited by 1,061
Infiltrating monocytes trigger EAE progression, but do not contribute to the resident microglia pool
Ajami, B., Bennett, J. L., Krieger, C., McNagny, K. M., & Rossi, F. M. V. (2011) · Nature Neuroscience · doi:10.1038/nn.2887 · Cited by 1,061
Inflammation and white matter degeneration persist for years after a single traumatic brain injury
Johnson, V. E., Stewart, J. E., Begbie, F. D., Trojanowski, J. Q., Smith, D. H., & Stewart, W. (2013) · Brain · doi:10.1093/brain/aws322 · Cited by 1,045
A fluid percussion model of experimental brain injury in the rat
Dixon, C. E., Lyeth, B. G., Povlishock, J. T., Findling, R. L., Hamm, R. J., Marmarou, A., Young, H. F., & Hayes, R. L. (1987) · Journal of neurosurgery · doi:10.3171/jns.1987.67.1.0110 · Cited by 1,038
Paired Helical Filaments in Electron Microscopy of Alzheimer's Disease
KIDD, M. (1963) · Nature · doi:10.1038/197192b0 · Cited by 1,012
Inflammation after trauma: Microglial activation and traumatic brain injury
Ramlackhansingh, A. F., Brooks, D. J., Greenwood, R. J., Bose, S. K., Turkheimer, F. E., Kinnunen, K. M., Gentleman, S., Heckemann, R. A., Gunanayagam, K., Gelosa, G., et al. (2011) · Annals of Neurology · doi:10.1002/ana.22455 · Cited by 999
Kumar, D. K. V., Choi, S. H., Washicosky, K. J., Eimer, W. A., Tucker, S., Ghofrani, J., Lefkowitz, A., McColl, G., Goldstein, L. E., Tanzi, R. E., et al. (2016) · Science Translational Medicine · doi:10.1126/scitranslmed.aaf1059 · Cited by 971
Goldstein, L. E., Fisher, A. M., Tagge, C. A., Zhang, X.-L., Velisek, L., Sullivan, J. A., Upreti, C., Kracht, J. M., Ericsson, M., Wojnarowicz, M. W., et al. (2012) · Science Translational Medicine · doi:10.1126/scitranslmed.3003716 · Cited by 958
Clinical trials in head injury
Narayan, R. K., Michel, M. E., Ansell, B., Baethmann, A., Biegon, A., Bracken, M. B., Bullock, M. R., Choi, S. C., Clifton, G. L., Contant, C. F., et al. (2002) · Journal of Neurotrauma · doi:10.1089/089771502753754037 · Cited by 913
Documented head injury in early adulthood and risk of Alzheimer’s disease and other dementias
Plassman, B. L., Havlik, R. J., Steffens, D. C., Helms, M. J., Newman, T. N., Drosdick, D., Phillips, C., Gau, B. A., Welsh–Bohmer, K. A., Burke, J. R., et al. (2000) · Neurology · doi:10.1212/wnl.55.8.1158 · Cited by 896
the TBI/CTE group, McKee, A. C., Cairns, N. J., Dickson, D. W., Folkerth, R. D., Dirk Keene, C., Litvan, I., Perl, D. P., Stein, T. D., Vonsattel, J.-P., et al. (2016) · Acta Neuropathologica · doi:10.1007/s00401-015-1515-z · Cited by 885
Differential roles of microglia and monocytes in the inflamed central nervous system
Yamasaki, R., Lu, H., Butovsky, O., Ohno, N., Rietsch, A. M., Cialic, R., Wu, P. M., Doykan, C. E., Lin, J., Cotleur, A. C., et al. (2014) · Journal of Experimental Medicine · doi:10.1084/jem.20132477 · Cited by 856
Godbout, J. P., Chen, J., Abraham, J., Richwine, A. F., Berg, B. M., Kelley, K. W., & Johnson, R. W. (2005) · The FASEB Journal · doi:10.1096/fj.05-3776fje · Cited by 813
Self-citationNeuroimmunology of Traumatic Brain Injury: Time for a Paradigm Shift
Jassam, Y. N., Izzy, S., Whalen, M., McGavern, D. B., & El Khoury, J. (2017) · Neuron · doi:10.1016/j.neuron.2017.07.010 · Cited by 799
Lee, J. W., Lee, Y. K., Yuk, D. Y., Choi, D. Y., Ban, S. B., Oh, K. W., & Hong, J. T. (2008) · Journal of Neuroinflammation · doi:10.1186/1742-2094-5-37 · Cited by 772
Cunningham, C., Wilcockson, D. C., Campion, S., Lunnon, K., & Perry, V. H. (2005) · The Journal of Neuroscience · doi:10.1523/jneurosci.2614-05.2005 · Cited by 768
Streit, W. J., Braak, H., Xue, Q.-S., & Bechmann, I. (2009) · Acta Neuropathologica · doi:10.1007/s00401-009-0556-6 · Cited by 727
Dystrophic microglia in the aging human brain
Streit, W. J., Sammons, N. W., Kuhns, A. J., & Sparks, D. L. (2004) · Glia · doi:10.1002/glia.10319 · Cited by 705
Kitazawa, M., Oddo, S., Yamasaki, T. R., Green, K. N., & LaFerla, F. M. (2005) · The Journal of Neuroscience · doi:10.1523/jneurosci.2868-05.2005 · Cited by 697
Spangenberg, E. E., Lee, R. J., Najafi, A. R., Rice, R. A., Elmore, M. R. P., Blurton-Jones, M., West, B. L., & Green, K. N. (2016) · Brain · doi:10.1093/brain/aww016 · Cited by 695
Blennow, K., Brody, D. L., Kochanek, P. M., Levin, H. S., McKee, A. C., Ribbers, G. M., Yaffe, K. S., & Zetterberg, H. (2016) · Nature Reviews Disease Primers · doi:10.1038/nrdp.2016.84 · Cited by 693
Association of apolipoprotein E polymorphism with outcome after head injury
Teasdale, G. M., Nicoll, J. A. R., Murray, G. D., & Fiddes, M. (1997) · The Lancet · doi:10.1016/s0140-6736(97)04318-3 · Cited by 683
A new model of diffuse brain injury in rats. Part II: Morphological characterization.
Foda, M. A. A.-E., & Marmarou, A. (1994) · Journal of Neurosurgery · doi:10.3171/jns.1994.80.2.0301 · Cited by 673
Identification of normal and pathological aging in prospectively studied nondemented elderly humans
Dickson, D. W., Crystal, H. A., Mattiace, L. A., Masur, D. M., Blau, A. D., Davies, P., Yen, S.-H., & Aronson, M. K. (1992) · Neurobiology of Aging · doi:10.1016/0197-4580(92)90027-u · Cited by 643
Regulation of Tau Pathology by the Microglial Fractalkine Receptor
Bhaskar, K., Konerth, M., Kokiko-Cochran, O. N., Cardona, A., Ransohoff, R. M., & Lamb, B. T. (2010) · Neuron · doi:10.1016/j.neuron.2010.08.023 · Cited by 639
Self-citationTau oligomers impair memory and induce synaptic and mitochondrial dysfunction in wild-type mice
Lasagna-Reeves, C. A., Castillo-Carranza, D. L., Sengupta, U., Clos, A. L., Jackson, G. R., & Kayed, R. (2011) · Molecular Neurodegeneration · doi:10.1186/1750-1326-6-39 · Cited by 633
Widespread tau and amyloid-beta pathology many years after a single traumatic brain injury in humans
Johnson, V. E., Stewart, W., & Smith, D. H. (2012) · Brain Pathology · doi:10.1111/j.1750-3639.2011.00513.x · Cited by 620
Demonstration of amyloid deposits and neurofibrillary changes in whole brain sections
Braak, H., & Braak, E. (1991) · Brain Pathology · doi:10.1111/j.1750-3639.1991.tb00661.x · Cited by 598
Traumatic brain injury and amyloid-β pathology: a link to Alzheimer's disease?
Johnson, V. E., Stewart, W., & Smith, D. H. (2010) · Nature Reviews Neuroscience · doi:10.1038/nrn2808 · Cited by 587
Roberts, G. W., Gentleman, S. M., Lynch, A., Murray, L., Landon, M., & Graham, D. I. (1994) · Journal of Neurology, Neurosurgery & Psychiatry · doi:10.1136/jnnp.57.4.419 · Cited by 569
Epidemiology of traumatic brain injury
Faul, M., & Coronado, V. G. (2015) · Handbook of clinical neurology · doi:10.1016/b978-0-444-52892-6.00001-5 · Cited by 543
Olmos-Alonso, A., Schetters, S. T. T., Sri, S., Askew, K., Mancuso, R., Vargas-Caballero, M., Holscher, C., Perry, V. H., & Gomez-Nicola, D. (2016) · Brain · doi:10.1093/brain/awv379 · Cited by 532
Microglia during development and aging
Harry, G. J. (2013) · Pharmacology & Therapeutics · doi:10.1016/j.pharmthera.2013.04.013 · Cited by 524
Lee, S., Varvel, N. H., Konerth, M. E., Xu, G., Cardona, A. E., Ransohoff, R. M., & Lamb, B. T. (2010) · The American Journal of Pathology · doi:10.2353/ajpath.2010.100265 · Cited by 522
Gram-negative bacterial molecules associate with Alzheimer disease pathology
Zhan, X., Stamova, B., Jin, L.-W., DeCarli, C., Phinney, B., & Sharp, F. R. (2016) · Neurology · doi:10.1212/wnl.0000000000003391 · Cited by 521
Head injury and the risk of AD in the MIRAGE study
Guo, Z., Cupples, L. A., Kurz, A., Auerbach, S. H., Volicer, L., Chui, H., Green, R. C., Sadovnick, A. D., Duara, R., DeCarli, C., et al. (2000) · Neurology · doi:10.1212/wnl.54.6.1316 · Cited by 506
Dagher, N. N., Najafi, A. R., Kayala, K. M. N., Elmore, M. R. P., White, T. E., Medeiros, R., West, B. L., & Green, K. N. (2015) · Journal of Neuroinflammation · doi:10.1186/s12974-015-0366-9 · Cited by 505
Loane, D. J., Kumar, A., Stoica, B. A., Cabatbat, R., & Faden, A. I. (2014) · Journal of Neuropathology & Experimental Neurology · doi:10.1097/nen.0000000000000021 · Cited by 498
Stalning af amyloid percursor protein to study axonal damage in mild head Injury
Blumbergs, P. C., Scott, G., Manavis, J., Wainwright, H., Simpson, D. A., & McLean, A. J. (1994) · The Lancet · doi:10.1016/s0140-6736(94)91712-4 · Cited by 454
The contribution of neuroinflammation to amyloid toxicity in Alzheimer's disease
Minter, M. R., Taylor, J. M., & Crack, P. J. (2016) · Journal of Neurochemistry · doi:10.1111/jnc.13411 · Cited by 451
Antibody against early driver of neurodegeneration cis P-tau blocks brain injury and tauopathy
Kondo, A., Shahpasand, K., Mannix, R., Qiu, J., Moncaster, J., Chen, C.-H., Yao, Y., Lin, Y.-M., Driver, J. A., Sun, Y., et al. (2015) · Nature · doi:10.1038/nature14658 · Cited by 445
The Aβ oligomer hypothesis for synapse failure and memory loss in Alzheimer’s disease
Ferreira, S. T., & Klein, W. L. (2011) · Neurobiology of Learning and Memory · doi:10.1016/j.nlm.2011.08.003 · Cited by 442
Progressive atrophy and neuron death for one year following brain trauma in the rat
Smith, D. H., Chen, X.-H., Pierce, J. E. S., Wolf, J. A., Trojanowski, J. Q., Graham, D. I., & McIntosh, T. K. (1997) · Journal of Neurotrauma · doi:10.1089/neu.1997.14.715 · Cited by 440
Apolipoprotein E-ε4 genotype predicts a poor outcome in survivors of traumatic brain injury
Friedman, G., Froom, P., Sazbon, L., Grinblatt, I., Shochina, M., Tsenter, J., Babaey, S., Yehuda, A. B., & Groswasser, Z. (1999) · Neurology · doi:10.1212/wnl.52.2.244 · Cited by 437
Neuroinflammatory processes in Alzheimer’s disease
Heneka, M. T., O’Banion, M. K., Terwel, D., & Kummer, M. P. (2010) · Journal of Neural Transmission · doi:10.1007/s00702-010-0438-z · Cited by 433
Chen, Z., Jalabi, W., Shpargel, K. B., Farabaugh, K. T., Dutta, R., Yin, X., Kidd, G. J., Bergmann, C. C., Stohlman, S. A., & Trapp, B. D. (2012) · The Journal of Neuroscience · doi:10.1523/jneurosci.0730-12.2012 · Cited by 432
Norden, D. M., Muccigrosso, M. M., & Godbout, J. P. (2015) · Neuropharmacology · doi:10.1016/j.neuropharm.2014.10.028 · Cited by 413
Self-citationModulation of immune response by head injury
Morganti-Kossmann, M. C., Satgunaseelan, L., Bye, N., & Kossmann, T. (2007) · Injury · doi:10.1016/j.injury.2007.10.005 · Cited by 412
Chen, J., Buchanan, J. B., Sparkman, N. L., Godbout, J. P., Freund, G. G., & Johnson, R. W. (2007) · Brain Behavior and Immunity · doi:10.1016/j.bbi.2007.08.014 · Cited by 407
Self-citationAlzheimer's pathology in human temporal cortex surgically excised after severe brain injury
Ikonomovic, M. D., Uryu, K., Abrahamson, E. E., Ciallella, J. R., Trojanowski, J. Q., Lee, V. M.-Y., Clark, R. S., Marion, D. W., Wisniewski, S. R., & DeKosky, S. T. (2004) · Experimental Neurology · doi:10.1016/j.expneurol.2004.06.011 · Cited by 399
Microglial senescence: does the brain's immune system have an expiration date?
Streit, W. J. (2006) · Trends in Neurosciences · doi:10.1016/j.tins.2006.07.001 · Cited by 397
Antioxidant Therapies for Traumatic Brain Injury
Hall, E. D., Vaishnav, R. A., & Mustafa, A. G. (2010) · Neurotherapeutics · doi:10.1016/j.nurt.2009.10.021 · Cited by 390 · cited 1×
“Secondary damage includes excitotoxicity (64), oxidative stress (65), and widespread neuroinflammation (63).”
BackgroundSheng, J. (2003) · Neurobiology of Disease · doi:10.1016/s0969-9961(03)00069-x · Cited by 388
Pierce, J. E. S., Smith, D. H., Trojanowski, J. Q., & McIntosh, T. K. (1998) · Neuroscience · doi:10.1016/s0306-4522(98)00142-0 · Cited by 385
Soares, H., Hicks, R., Smith, D., & McIntosh, T. (1995) · The Journal of Neuroscience · doi:10.1523/jneurosci.15-12-08223.1995 · Cited by 379
Semple, B. D., Bye, N., Rancan, M., Ziebell, J. M., & Morganti-Kossmann, M. C. (2010) · Journal of Cerebral Blood Flow & Metabolism · doi:10.1038/jcbfm.2009.262 · Cited by 358 · cited 5×
“Singleincident mild CHI TBI in aged hTau transgenic mice that express all six isoforms of hTau in absence of murine tau did not worsen 8 Kokiko-Cochran and Godbout Inflammatory Continuum of Brain Injury Frontiers in Immunology | www.frontiersin.org April 2018 | Volume 9 | Article 672 tau phosphorylation or induce tau…”
BackgroundInfluentialGyoneva, S., & Ransohoff, R. M. (2015) · Trends in Pharmacological Sciences · doi:10.1016/j.tips.2015.04.003 · Cited by 351
Mizutani, M., Pino, P. A., Saederup, N., Charo, I. F., Ransohoff, R. M., & Cardona, A. E. (2012) · The Journal of Immunology · doi:10.4049/jimmunol.1100421 · Cited by 346
Conde, J. R., & Streit, W. J. (2006) · Journal of Neuropathology and Experimental Neurology · doi:10.1097/01.jnen.0000202887.22082.63 · Cited by 344
BLUMBERGS, P. C., SCOTT, G., VIS, J. M., WAINWRIGHT, H., SIMPSON, D. A., & McLEAN, A. J. (1995) · Journal of Neurotrauma · doi:10.1089/neu.1995.12.565 · Cited by 342
Mouzon, B., Bachmeier, C. J., Ferro, A., Ojo, J., Crynen, G. C., Acker, C. M., Davies, P., MULLAN, M. J., Stewart, W. B., Jr., & Crawford, F. (2013) · Annals of Neurology · doi:10.1002/ana.24064 · Cited by 341
Uryu, K., Laurer, H., McIntosh, T., Praticò, D., Martinez, D., Leight, S., Lee, V. M.-Y., & Trojanowski, J. Q. (2002) · The Journal of Neuroscience · doi:10.1523/jneurosci.22-02-00446.2002 · Cited by 337
Başkaya, M. K., Muralikrishna Rao, A., Doğan, A., Donaldson, D., & Dempsey, R. J. (1997) · Neuroscience Letters · doi:10.1016/s0304-3940(97)00239-5 · Cited by 332
mRNA up-regulation of MHC II and pivotal pro-inflammatory genes in normal brain aging
Frank, M. G., Barrientos, R. M., Biedenkapp, J. C., Rudy, J. W., Watkins, L. R., & Maier, S. F. (2006) · Neurobiology of Aging · doi:10.1016/j.neurobiolaging.2005.03.013 · Cited by 327
Microglial neuroinflammation contributes to tau accumulation in chronic traumatic encephalopathy
Cherry, J. D., Tripodis, Y., Alvarez, V. E., Huber, B. R., Kiernan, P. T., Daneshvar, D. H., Mez, J., Montenigro, P. H., Solomon, T. M., Alosco, M. L., et al. (2016) · Acta Neuropathologica Communications · doi:10.1186/s40478-016-0382-8 · Cited by 304
Godbout, J. P., Moreau, M., Lestage, J., Chen, J., Sparkman, N. L., Connor, J. O., Castanon, N., Kelley, K. W., Dantzer, R., & Johnson, R. W. (2008) · Neuropsychopharmacology · doi:10.1038/sj.npp.1301649 · Cited by 299
Self-citationGreenhalgh, A. D., & David, S. (2014) · The Journal of Neuroscience · doi:10.1523/jneurosci.4912-13.2014 · Cited by 296
Axonal injury: a universal consequence of fatal closed head injury?
Gentleman, S. M., Roberts, G. W., Gennarelli, T. A., Maxwell, W. L., Adams, J. H., Kerr, S., & Graham, D. I. (1995) · Acta Neuropathologica · doi:10.1007/bf00571509 · Cited by 296
Amyloid-β Dynamics Correlate with Neurological Status in the Injured Human Brain
Brody, D. L., Magnoni, S., Schwetye, K. E., Spinner, M. L., Esparza, T. J., Stocchetti, N., Zipfel, G. J., & Holtzman, D. M. (2008) · Science · doi:10.1126/science.1161591 · Cited by 295
Traumatic brain injury and time to onset of Alzheimer’s disease: a population-based study
Nemetz, P. N., Leibson, C., Naessens, J. M., Beard, M., Kokmen, E., Annegers, J. F., & Kurland, L. T. (1999) · American Journal of Epidemiology · doi:10.1093/oxfordjournals.aje.a009724 · Cited by 295
Clinical trials in traumatic brain injury: past experience and current developments
Maas, A. I. R., Roozenbeek, B., & Manley, G. T. (2010) · Neurotherapeutics · doi:10.1016/j.nurt.2009.10.022 · Cited by 291
A Spatial Gradient of Tau Protein Phosphorylation in Nascent Axons
Mandell, J. W., & Banker, G. A. (1996) · Journal of Neuroscience · doi:10.1523/jneurosci.16-18-05727.1996 · Cited by 283
Fenn, A. M., Gensel, J. C., Huang, Y., Popovich, P. G., Lifshitz, J., & Godbout, J. P. (2014) · Biological Psychiatry · doi:10.1016/j.biopsych.2013.10.014 · Cited by 283
Self-citationEvidence That Aging And Amyloid Promote Microglial Cell Senescence
Flanary, B. E., Sammons, N. W., Nguyen, C., Walker, D., & Streit, W. J. (2007) · Rejuvenation Research · doi:10.1089/rej.2006.9096 · Cited by 272
Tau-based therapies in neurodegeneration: opportunities and challenges
Li, C., & Götz, J. (2017) · Nature Reviews Drug Discovery · doi:10.1038/nrd.2017.155 · Cited by 272
Chen, X.-H., Siman, R., Iwata, A., Meaney, D. F., Trojanowski, J. Q., & Smith, D. H. (2004) · The American Journal of Pathology · doi:10.1016/s0002-9440(10)63303-2 · Cited by 271
Rice, R. A., Spangenberg, E. E., Yamate-Morgan, H., Lee, R. J., Arora, R. P. S., Hernandez, M. X., Tenner, A. J., West, B. L., & Green, K. N. (2015) · Journal of Neuroscience · doi:10.1523/jneurosci.0336-15.2015 · Cited by 270 · cited 1×
“Similarly, CSF1R inhibition after a chronic hippocampal lesion model of brain injury improved behavioral recovery, reduced pro-inflammatory molecules, and increased dendritic spines (239).”
BackgroundHow Do Immune Cells Support and Shape the Brain in Health, Disease, and Aging?
Schwartz, M., Kipnis, J., Rivest, S., & Prat, A. (2013) · Journal of Neuroscience · doi:10.1523/jneurosci.3241-13.2013 · Cited by 269
Smith, D. H., Chen, X.-H., Nonaka, M., Trojanowski, J. Q., Lee, V.-Y., Saatman, K. E., Leoni, M. J., Xu, B.-N., Wolf, J. A., & Meaney, D. F. (1999) · Journal of Neuropathology & Experimental Neurology · doi:10.1097/00005072-199909000-00008 · Cited by 260
Alzheimer’s disease after remote head injury: an incidence study
Schofield, P. W., Tang, M., Marder, K., Bell, K., Dooneief, G., Chun, M., Sano, M., Stern, Y., & Mayeux, R. (1997) · Journal of Neurology, Neurosurgery & Psychiatry · doi:10.1136/jnnp.62.2.119 · Cited by 260
Tran, H. T., LaFerla, F. M., Holtzman, D. M., & Brody, D. L. (2011) · Journal of Neuroscience · doi:10.1523/jneurosci.0858-11.2011 · Cited by 255
Morganti, J. M., Jopson, T. D., Liu, S., Riparip, L.-K., Guandique, C. K., Gupta, N., Ferguson, A. R., & Rosi, S. (2015) · The Journal of Neuroscience · doi:10.1523/jneurosci.2405-14.2015 · Cited by 253 · cited 2×
“Use of CX3CR1GFP/+CCR2RFP/+ reporter mice provides insight into the role of microglia and macrophages following TBI (76); however, it is still unclear if myeloid cells associated with chronic injury lesions are CX3CR1+ microglia or a mixture of CX3CR1+ microglia and CX3CR1+ peripheral macrophages that downregulated CC…”
BackgroundMethodImmunosenescence of microglia and macrophages: impact on the ageing central nervous system
Rawji, K. S., Mishra, M. K., Michaels, N. J., Rivest, S., Stys, P. K., & Yong, V. W. (2016) · Brain · doi:10.1093/brain/awv395 · Cited by 252
Kumar, A., Stoica, B. A., Sabirzhanov, B., Burns, M. P., Faden, A. I., & Loane, D. J. (2013) · Neurobiology of Aging · doi:10.1016/j.neurobiolaging.2012.11.013 · Cited by 244
Pierce, J., Trojanowski, J., Graham, D., Smith, D., & McIntosh, T. (1996) · The Journal of Neuroscience · doi:10.1523/jneurosci.16-03-01083.1996 · Cited by 239 · cited 1×
“Although Aβ deposition is apparent following rotational acceleration TBI in pigs (132, 133) and rabbits (134), a majority of rodent studies fail to show this association in non-transgenic animals using CCI, FPI, and weight drop models (121, 122, 124, 125, 135).”
BackgroundPathobiology of traumatically induced axonal injury in animals and man
Povlishock, J. T. (1993) · Annals of Emergency Medicine · doi:10.1016/s0196-0644(05)82738-6 · Cited by 236 · cited 1×
“Traumatic axonal injury (TAI) is an additional source of accumulating APP (127, 128).”
BackgroundPriming the Inflammatory Pump of the CNS after Traumatic Brain Injury
Witcher, K. G., Eiferman, D. S., & Godbout, J. P. (2015) · Trends in Neurosciences · doi:10.1016/j.tins.2015.08.002 · Cited by 234
Self-citationTraumatic Brain Injury in the Rat: Characterization of a Midline Fluid-Percussion Model
McIntosh, T. K., Noble‐Haeusslein, L. J., Andrews, B. T., & Faden, A. I. (1987) · Central Nervous System Trauma · doi:10.1089/cns.1987.4.119 · Cited by 231
Microglial repopulation resolves inflammation and promotes brain recovery after injury: RICE et al.
Rice, R. A., Pham, J., Lee, R. J., Najafi, A. R., West, B. L., & Green, K. N. (2017) · Glia · doi:10.1002/glia.23135 · Cited by 228 · cited 1×
“Recent studies using the same injury model confirmed that post-injury microglial depletion followed by microglial repopulation improves behavioral recovery, attenuates the lesion-induced neuroinflammatory response, and increases dendritic spin densities despite extensive neuronal loss in the hippocampus (240).”
BackgroundBarrientos, R. M., Frank, M. G., Hein, A. M., Higgins, E. A., Watkins, L. R., Rudy, J. W., & Maier, S. F. (2009) · Brain, Behavior, and Immunity · doi:10.1016/j.bbi.2008.07.002 · Cited by 226
BRAMLETT, H. M., KRAYDIEH, S., GREEN, E. J., & DIETRICH, W. D. (1997) · Journal of Neuropathology and Experimental Neurology · doi:10.1097/00005072-199710000-00007 · Cited by 225
Amyloid beta 1-42 and tau in cerebrospinal fluid after severe traumatic brain injury
Franz, G., Beer, R., Kampfl, A., Engelhardt, K., Schmutzhard, E., Ulmer, H., & Deisenhammer, F. (2003) · Neurology · doi:10.1212/01.wnl.0000063313.57292.00 · Cited by 217
The neuroinflammatory response in humans after traumatic brain injury
Smith, C., Gentleman, S. M., Leclercq, P. D., Murray, L. S., Griffin, W. S. T., Graham, D. I., & Nicoll, J. A. R. (2012) · Neuropathology and Applied Neurobiology · doi:10.1111/nan.12008 · Cited by 213
The association between APOE ε4, age and outcome after head injury: a prospective cohort study
Teasdale, G. M., Murray, G. D., & Nicoll, J. A. R. (2005) · Brain · doi:10.1093/brain/awh595 · Cited by 211
Inflammation Induced by Infection Potentiates Tau Pathological Features in Transgenic Mice
Sy, M., Kitazawa, M., Medeiros, R., Whitman, L., Cheng, D., Lane, T. E., & LaFerla, F. M. (2011) · The American Journal of Pathology · doi:10.1016/j.ajpath.2011.02.012 · Cited by 210
Ishizawa, K., & Dickson, D. W. (2001) · Journal of Neuropathology & Experimental Neurology · doi:10.1093/jnen/60.6.647 · Cited by 209
CNS-specific T cells shape brain function via the choroid plexus
Baruch, K., & Schwartz, M. (2013) · Brain Behavior and Immunity · doi:10.1016/j.bbi.2013.04.002 · Cited by 200
Lee, Y. K., Yuk, D. Y., Lee, J. W., Lee, S. Y., Ha, T. Y., Oh, K. W., Yun, Y. P., & Hong, J. T. (2008) · Brain Research · doi:10.1016/j.brainres.2008.10.012 · Cited by 186
Exacerbated glial response in the aged mouse hippocampus following controlled cortical impact injury
Sandhir, R., Onyszchuk, G., & Berman, N. E. J. (2008) · Experimental Neurology · doi:10.1016/j.expneurol.2008.06.013 · Cited by 183
Ziebell, J. M., Taylor, S. E., Cao, T., Harrison, J. L., & Lifshitz, J. (2012) · Journal of Neuroinflammation · doi:10.1186/1742-2094-9-247 · Cited by 182
Prolonged Activation of NF-κB Following Traumatic Brain Injury in Rats
NONAKA, M., CHEN, X.-H., PIERCE, J. E. S., LEONI, M. J., McINTOSH, T. K., WOLF, J. A., & SMITH, D. H. (1999) · Journal of Neurotrauma · doi:10.1089/neu.1999.16.1023 · Cited by 176
Amyloid beta 1-42 and tau in cerebrospinal fluid after severe traumatic brain injury
Blennow, K., & Nellgård, B. (2004) · Neurology · doi:10.1212/wnl.62.1.159 · Cited by 176
Hsieh, C. L., Niemi, E. C., Wang, S. H., Lee, C. C., Bingham, D., Zhang, J., Cozen, M. L., Charo, I., Huang, E. J., Liu, J., et al. (2014) · Journal of Neurotrauma · doi:10.1089/neu.2013.3252 · Cited by 174
In vivo imaging of microglial activation with [11C](R)‐PK11195 PET in progressive supranuclear palsy
Gerhard, A., Trender‐Gerhard, I., Turkheimer, F., Quinn, N. P., Bhatia, K. P., & Brooks, D. J. (2006) · Movement Disorders · doi:10.1002/mds.20668 · Cited by 171
Luteolin Reduces Alzheimer’s Disease Pathologies Induced by Traumatic Brain Injury
Sawmiller, D. R., Li, S., Shahaduzzaman, M., de Smith, A. J., Obregon, D. F., Giunta, B. N., Borlongan, C. V., Sanberg, P. R., & Tan, J. (2014) · International Journal of Molecular Sciences · doi:10.3390/ijms15010895 · Cited by 170
Coughlin, J. M., Wang, Y., Minn, I., Bienko, N., Ambinder, E. B., Xu, X., Peters, M. E., Dougherty, J. W., Vranešić, M., Koo, S. M., et al. (2016) · JAMA Neurology · doi:10.1001/jamaneurol.2016.3764 · Cited by 168
Treatment of traumatic brain injury with anti-inflammatory drugs
Bergold, P. J. (2015) · Experimental Neurology · doi:10.1016/j.expneurol.2015.05.024 · Cited by 167
Repetitive mild traumatic brain injury augments tau pathology and glial activation in aged hTau mice
Ojo, J.-O., Mouzon, B., Greenberg, M. B., Bachmeier, C., Mullan, M., & Crawford, F. (2013) · Journal of Neuropathology & Experimental Neurology · doi:10.1097/nen.0b013e3182814cdf · Cited by 166
Conte, V., Uryu, K., Fujimoto, S., Yao, Y., Rokach, J., Longhi, L., Trojanowski, J. Q., Lee, V. M., McIntosh, T. K., & Praticò, D. (2004) · Journal of Neurochemistry · doi:10.1111/j.1471-4159.2004.02560.x · Cited by 164
Kumar, R. G., Diamond, M. L., Boles, J. A., Berger, R. P., Tisherman, S. A., Kochanek, P. M., & Wagner, A. K. (2014) · Brain Behavior and Immunity · doi:10.1016/j.bbi.2014.12.021 · Cited by 163
Glutamate neurotransmission in rodent models of traumatic brain injury
Dorsett, C. R., McGuire, J. L., DePasquale, E. A. K., Gardner, A. E., Floyd, C. L., & McCullumsmith, R. E. (2017) · Journal of Neurotrauma · doi:10.1089/neu.2015.4373 · Cited by 163 · cited 1×
“Secondary damage includes excitotoxicity (64), oxidative stress (65), and widespread neuroinflammation (63).”
BackgroundMaxwell, W. L., Watt, C., Graham, D. I., & Gennarelli, T. A. (1993) · Acta Neuropathologica · doi:10.1007/bf00334880 · Cited by 161 · cited 1×
“Traumatic axonal injury (TAI) is an additional source of accumulating APP (127, 128).”
BackgroundHuber, B. R., Meabon, J. S., Martin, T. J., Mourad, P. D., Bennett, R., Kraemer, B. C., Černak, I., Petrie, E. C., Emery, M. J., Swenson, E. R., et al. (2013) · Journal of Alzheimer s Disease · doi:10.3233/jad-130182 · Cited by 160
Erratum: The far-reaching scope of neuroinflammation after traumatic brain injury
Simon, D. W., McGeachy, M. J., Bayır, H., Clark, R. S. B., Loane, D. J., & Kochanek, P. M. (2017) · Nature Reviews Neurology · doi:10.1038/nrneurol.2017.116 · Cited by 160
Sodium selenate reduces hyperphosphorylated tau and improves outcomes after traumatic brain injury
Shultz, S. R., Wright, D. K., Zheng, P., Stuchbery, R., Liu, S.-J., Sashindranath, M., Medcalf, R. L., Johnston, L. A., Hovens, C. M., Jones, N. C., et al. (2015) · Brain · doi:10.1093/brain/awv053 · Cited by 159
Neural Stem Cells Improve Memory in an Inducible Mouse Model of Neuronal Loss
Yamasaki, T. R., Blurton-Jones, M. M., Morrissette, D. A., Kitazawa, M., Oddo, S., & LaFerla, F. M. (2007) · Journal of Neuroscience · doi:10.1523/jneurosci.1627-07.2007 · Cited by 158
A review of neuroprotection pharmacology and therapies in patients with acute traumatic brain injury
McConeghy, K. W., Hatton, J., Hughes, L., & Cook, A. M. (2012) · CNS Drugs · doi:10.2165/11634020-000000000-00000 · Cited by 158
Adaptation of the fluid percussion injury model to the mouse
CARBONELL, W. S., MARIS, D. O., McCALL, T., & GRADY, M. S. (1998) · Journal of Neurotrauma · doi:10.1089/neu.1998.15.217 · Cited by 157
Invited review: Prion‐like transmission and spreading of tau pathology
Clavaguera, F., Hench, J., Goedert, M., & Tolnay, M. (2015) · Neuropathology and Applied Neurobiology · doi:10.1111/nan.12197 · Cited by 156
Martin, E., Boucher, C., Fontaine, B., & Delarasse, C. (2017) · Aging Cell · doi:10.1111/acel.12522 · Cited by 156
Žilka, N., Kazmerova, Z., Jadhav, S., Neradil, P., Maďari, A., Obetkova, D., Bugos, O., & Novák, M. (2012) · Journal of Neuroinflammation · doi:10.1186/1742-2094-9-47 · Cited by 153
Rapid Accumulation of Endogenous Tau Oligomers in a Rat Model of Traumatic Brain Injury
Hawkins, B. E., Krishnamurthy, S., Castillo‐Carranza, D. L., Sengupta, U., Prough, D. S., Jackson, G. R., DeWitt, D. S., & Kayed, R. (2013) · Journal of Biological Chemistry · doi:10.1074/jbc.m113.472746 · Cited by 153
Neuroprotection in traumatic brain injury: a complex struggle against the biology of nature
Schouten, J. W. (2007) · Current Opinion in Critical Care · doi:10.1097/mcc.0b013e3280895d5c · Cited by 152
DeKosky, S. T., Abrahamson, E. E., Ciallella, J. R., Paljug, W. R., Wisniewski, S. R., Clark, R. S. B., & Ikonomovic, M. D. (2007) · Archives of Neurology · doi:10.1001/archneur.64.4.541 · Cited by 152
Animal models of traumatic brain injury
Johnson, V. E., Meaney, D. F., Cullen, D. K., & Smith, D. H. (2015) · Handbook of clinical neurology · doi:10.1016/b978-0-444-52892-6.00008-8 · Cited by 151
Ontogeny and Functions of Central Nervous System Macrophages
Katsumoto, A., Lu, H., Miranda, A. S., & Ransohoff, R. M. (2014) · The Journal of Immunology · doi:10.4049/jimmunol.1400716 · Cited by 149
Muccigrosso, M. M., Ford, J., Benner, B., Moussa, D., Burnsides, C., Fenn, A. M., Popovich, P. G., Lifshitz, J., Walker, F. R., Eiferman, D. S., et al. (2016) · Brain, Behavior, and Immunity · doi:10.1016/j.bbi.2016.01.009 · Cited by 146 · cited 11×
“This supports other studies showing increased CD68+ microglia in the brains of American football players, which partially mediated coincident tau pathology (231).”
BackgroundInfluentialSelf-citationNSAIDs and incident Alzheimer’s disease. The Rotterdam study
In ’t Veld, B. A., Launer, L. J., Hoes, A. W., Ott, A., Hofman, A., Breteler, M. M. B., & Stricker, B. H. C. (1998) · Neurobiology of Aging · doi:10.1016/s0197-4580(98)00096-7 · Cited by 145 · cited 1×
“Second, retrospective studies demonstrate that sustained NSAID treatment during mid-life significantly decreases the risk of AD (109, 110).”
BackgroundIn vivo imaging of microglial activation with [11C](R)‐PK11195 PET in corticobasal degeneration
Gerhard, A., Watts, J., Trender‐Gerhard, I., Turkheimer, F., Banati, R. B., Bhatia, K. P., & Brooks, D. J. (2004) · Movement Disorders · doi:10.1002/mds.20162 · Cited by 145
Smith, D. H., Nakamura, M., McIntosh, T. K., Wang, J., Rodríguez, A., Chen, X.-H., Raghupathi, R., Saatman, K. E., Clemens, J., Schmidt, M. L., et al. (1998) · The American Journal of Pathology · doi:10.1016/s0002-9440(10)65643-x · Cited by 143 · cited 1×
“Although CCI TBI induced a surge of plaque pathology in PDAPP mice soon after injury at 6 months of age, a substantial reduction in cortical and hippocampal plaque load was detected chronically (28, 40).”
BackgroundChronic exposure to TGFβ1 regulates myeloid cell inflammatory response in an IRF7-dependent manner
Cohen, M., Matcovitch, O., David, E., Barnett‐Itzhaki, Z., Keren‐Shaul, H., Blecher‐Gonen, R., Jaitin, D. A., Sica, A., Amit, I., & Schwartz, M. (2014) · The EMBO Journal · doi:10.15252/embj.201489293 · Cited by 142
Zhao, C., Li, W.-W., & Franklin, R. J. M. (2006) · Neurobiology of Aging · doi:10.1016/j.neurobiolaging.2005.06.008 · Cited by 142 · cited 1×
“org April 2018 | Volume 9 | Article 672 matter demyelination injury provokes a reduced macrophage response in older rodents compared to younger controls (102).”
BackgroundA porcine model of traumatic brain injury via head rotational acceleration
Cullen, D. K., Harris, J. P., Browne, K. D., Wolf, J. A., Duda, J. E., Meaney, D. F., Margulies, S. S., & Smith, D. H. (2016) · Methods in Molecular Biology · doi:10.1007/978-1-4939-3816-2_17 · Cited by 142 · cited 1×
“Indeed, the complex neuroanatomy and neurophysiology of the human brain, such as cortical folding, substantial white matter, and specific pathophysiology compared to the rodent brain, may facilitate distinct post-injury neuropathology (137).”
BackgroundAssociations between Neighborhood SES and Functional Brain Network Development
Tooley, U. A., Mackey, A. P., Ćirić, R., Ruparel, K., Moore, T. M., Gur, R. C., Gur, R. E., Satterthwaite, T. D., & Bassett, D. S. (2019) · Cerebral Cortex · doi:10.1093/cercor/bhz066 · Cited by 142
Yoshiyama, Y., Uryu, K., Higuchi, M., Longhi, L., Hoover, R., Fujimoto, S., McIntosh, T., Lee, V. M.-Y., & Trojanowski, J. Q. (2005) · Journal of Neurotrauma · doi:10.1089/neu.2005.22.1134 · Cited by 133 · cited 1×
“Similarly, only transgenic tau mouse models [T44 (one mouse), hTau] displayed NFT pathology following repetitive TBI (153, 234).”
BackgroundVanGuilder, H. D., Bixler, G. V., Brucklacher, R. M., Farley, J. A., Yan, H., Warrington, J. P., Sonntag, W. E., & Freeman, W. M. (2011) · Journal of Neuroinflammation · doi:10.1186/1742-2094-8-138 · Cited by 132
Lee, Y., Choi, D., Choi, I. S., Kim, K. H., Kim, Y. H., Kim, H. M., Lee, K., Cho, W. G., Jung, J. K., Han, S., et al. (2012) · Journal of Neuroinflammation · doi:10.1186/1742-2094-9-35 · Cited by 131
Cleaved-Tau: A Biomarker of Neuronal Damage after Traumatic Brain Injury
Gabbita, S., Scheff, S., Menard, R. M., Roberts, K. N., Fugaccia, I., & Zemlan, F. (2005) · Journal of Neurotrauma · doi:10.1089/neu.2005.22.83 · Cited by 127
Williams, A. J., Hartings, J. A., Lu, X. M., Rolli, M. L., & Tortella, F. C. (2006) · Journal of Neurotrauma · doi:10.1089/neu.2006.23.1828 · Cited by 124
Opposing Effects of Membrane-Anchored CX3CL1 on Amyloid and Tau Pathologies via the p38 MAPK Pathway
Lee, S., Xu, G., Jay, T. R., Bhatta, S., Kim, K.-W., Jung, S., Landreth, G. E., Ransohoff, R. M., & Lamb, B. T. (2014) · The Journal of Neuroscience · doi:10.1523/jneurosci.0853-14.2014 · Cited by 123
Rodent Aβ Modulates the Solubility and Distribution of Amyloid Deposits in Transgenic Mice
Jankowsky, J. L., Younkin, L. H., Gonzales, V., Fadale, D. J., Slunt, H. H., Lester, H. A., Younkin, S. G., & Borchelt, D. R. (2007) · Journal of Biological Chemistry · doi:10.1074/jbc.m611050200 · Cited by 122 · cited 1×
“For example, multiple reports indicate that there are endogenous differences in rodent and human APP (136), which could significantly alter the production on Aβ after TBI.”
BackgroundHartman, R. E., Laurer, H., Longhi, L., Bales, K. R., Paul, S. M., McIntosh, T. K., & Holtzman, D. M. (2002) · The Journal of Neuroscience · doi:10.1523/jneurosci.22-23-10083.2002 · Cited by 115
Beard, C. M., Waring, S. C., O'Brien, P. C., Kurland, L. T., & Kokmen, E. (1998) · Mayo Clinic Proceedings · doi:10.4065/73.10.951 · Cited by 114
Time-dependent effects of CX3CR1 in a mouse model of mild traumatic brain injury
Febinger, H. Y., Thomasy, H. E., Pavlova, M. N., Ringgold, K. M., Barf, P. R., George, A. M., Grillo, J. N., Bachstetter, A. D., Garcia, J. A., Cardona, A. E., et al. (2015) · Journal of Neuroinflammation · doi:10.1186/s12974-015-0386-5 · Cited by 110 · cited 1×
“These changes are directly associated with an altered and timedependent inflammatory profile in microglia (80).”
BackgroundTau immunohistochemistry in acute brain injury
Smith, C., Graham, D. I., Murray, L. S., & Nicoll, J. A. R. (2003) · Neuropathology and Applied Neurobiology · doi:10.1046/j.1365-2990.2003.00488.x · Cited by 110 · cited 1×
“Severe TBI resulting in death induces sporadic phosphorylated tau and tau-positive glia but no difference in NFT pathology compared to age-matched controls (165, 166).”
Carbonell, W. S., & Grady, M. S. (1999) · Acta Neuropathologica · doi:10.1007/s004010051100 · Cited by 110
Yu, F., Zhang, Y., & Chuang, D. (2012) · Journal of Neurotrauma · doi:10.1089/neu.2012.2449 · Cited by 110
Washington, P. M., Morffy, N., Parsadanian, M., Zapple, D. N., & Burns, M. P. (2014) · Journal of Neurotrauma · doi:10.1089/neu.2013.3017 · Cited by 103 · cited 1×
“While CCI TBI increased soluble and insoluble cortical Aβ40 and Aβ42 within 24 h after injury, both soluble and insoluble Aβ returned to sham levels by 7 DPI (23).”
BackgroundClinical appraisal of chronic traumatic encephalopathy: current perspectives and future directions
Gavett, B. E., Cantu, R. C., Shenton, M., Lin, A. P., Nowinski, C. J., McKee, A. C., & Stern, R. A. (2011) · Current Opinion in Neurology · doi:10.1097/wco.0b013e32834cd477 · Cited by 101
MURAKAMI, N., YAMAKI, T., IWAMOTO, Y., SAKAKIBARA, T., KOBORI, N., FUSHIKI, S., & UEDA, S. (1998) · Journal of Neurotrauma · doi:10.1089/neu.1998.15.993 · Cited by 100
Long-lasting protection in brain trauma by endotoxin preconditioning
Longhi, L. G., Gesuete, R., Perego, C., Ortolano, F., Sacchi, N., Villa, P., Stocchetti, N., & Simoni, M. G. D. (2011) · Journal of Cerebral Blood Flow & Metabolism · doi:10.1038/jcbfm.2011.42 · Cited by 99
Sheffield, L. G., Marquis, J. G., & Berman, N. E. J. (2000) · Neuroscience Letters · doi:10.1016/s0304-3940(00)01037-5 · Cited by 96
Amyloid-beta and tau pathology following repetitive mild traumatic brain injury
Edwards, G., Moreno-Gonzalez, I., & Soto, C. (2017) · Biochemical and Biophysical Research Communications · doi:10.1016/j.bbrc.2016.07.123 · Cited by 96
Juengst, S. B., Kumar, R. G., Arenth, P. M., & Wagner, A. K. (2014) · Brain Behavior and Immunity · doi:10.1016/j.bbi.2014.05.020 · Cited by 95
Ccr2 deletion dissociates cavity size and tau pathology after mild traumatic brain injury
Gyoneva, S., Kim, D., Katsumoto, A., Kokiko-Cochran, O. N., Lamb, B. T., & Ransohoff, R. M. (2015) · Journal of Neuroinflammation · doi:10.1186/s12974-015-0443-0 · Cited by 95 · cited 1×
“Interruption of CCR2 signaling through the use of Ccr2RFP/RFP mice reduces post-injury monocytic infiltration and axonal pathology but enhances cortical and hippocampal MAPT mislocalization and hyperphosphorylation soon after lateral fluid percussion TBI suggesting that monocyte sub-populations may differentially infl…”
BackgroundSelf-citationCollins-Praino, L. E., & Corrigan, F. (2017) · Brain, Behavior, and Immunity · doi:10.1016/j.bbi.2016.09.027 · Cited by 95
Ciallella, J. R., Ikonomovic, M. D., Paljug, W. R., Wilbur, Y. I., Dixon, C. E., Kochanek, P. M., Marion, D. W., & DeKosky, S. T. (2002) · Journal of Neurotrauma · doi:10.1089/089771502762300229 · Cited by 94 · cited 1×
“Although Aβ deposition is apparent following rotational acceleration TBI in pigs (132, 133) and rabbits (134), a majority of rodent studies fail to show this association in non-transgenic animals using CCI, FPI, and weight drop models (121, 122, 124, 125, 135).”
BackgroundNeuronal and glial apoptosis in human traumatic brain injury
Dreßler, J., Hanisch, U., Kuhlisch, E., & Geiger, K. D. (2007) · International Journal of Legal Medicine · doi:10.1007/s00414-006-0126-6 · Cited by 94
Found in translation: Understanding the biology and behavior of experimental traumatic brain injury
Bondi, C. O., Semple, B. D., Noble‐Haeusslein, L. J., Osier, N. D., Carlson, S. W., Dixon, C. E., Giza, C. C., & Kline, A. E. (2014) · Neuroscience & Biobehavioral Reviews · doi:10.1016/j.neubiorev.2014.12.004 · Cited by 94
Winston, C. N., Noël, A., Neustadtl, A., Parsadanian, M., Barton, D. J., Chellappa, D., Wilkins, T. E., Alikhani, A. D., Zapple, D. N., Villapol, S., et al. (2016) · The American Journal of Pathology · doi:10.1016/j.ajpath.2015.11.006 · Cited by 94
Gerson, J., Castillo-Carranza, D. L., Sengupta, U., Bodani, R., Prough, D. S., DeWitt, D. S., Hawkins, B. E., & Kayed, R. (2016) · Journal of Neurotrauma · doi:10.1089/neu.2015.4262 · Cited by 94 · cited 1×
“Tau oligomers derived from brain injured mice subsequently caused cognitive dysfunction and the appearance of tau oligomers in hTau mice supporting the notion that tau oligomers are neurotoxic and contribute to tau spreading throughout the brain (180).”
BackgroundZanier, E. R., Marchesi, F., Ortolano, F., Perego, C., Arabian, M., Zoerle, T., Sammali, E., Pischiutta, F., & De Simoni, M.-G. (2016) · Journal of Neurotrauma · doi:10.1089/neu.2015.4041 · Cited by 94 · cited 1×
“Subsequent work by a separate group confirms these results and demonstrates that CX3CR1 deficiency results in early protection but chronic worsening of CCI TBI-induced deficits due in part to a decrease in anti-inflammatory cytokines on CD11b+ sorted cells at 28 DPI (81).”
ResultTran, H., Sanchez, L., & Brody, D. L. (2012) · Journal of Neuropathology & Experimental Neurology · doi:10.1097/nen.0b013e3182456aed · Cited by 93
Grant, J. L., Ghosn, E. E. B., Axtell, R. C., Herges, K., Kuipers, H. F., Woodling, N. S., Andreasson, K., Herzenberg, L. A., Herzenberg, L. A., & Steinman, L. (2012) · Science Translational Medicine · doi:10.1126/scitranslmed.3004145 · Cited by 92 · cited 1×
“For example, a 2013 study revealed that peripheral administration of Aβ42 and Aβ40 attenuates paralysis and reduces neuroinflammation in multiple mouse models of experimental autoimmune encephalomyelitis (EAE) (142).”
BackgroundBrain Trauma in Aged Transgenic Mice Induces Regression of Established Aβ Deposits
Nakagawa, Y., Reed, L., Nakamura, M., McIntosh, T. K., Smith, D. H., Saatman, K. E., Raghupathi, R., Clemens, J., Saido, T. C., Lee, V. M.-Y., et al. (2000) · Experimental Neurology · doi:10.1006/exnr.2000.7375 · Cited by 91 · cited 2×
“Follow-up experiments revealed that CCI TBI in aged PDAPP mice caused a regression of established Aβ deposits (41).”
Lewén, A., Li, G. L., Olsson, Y., & Hillered, L. (1996) · Brain Research · doi:10.1016/0006-8993(96)00081-9 · Cited by 90
Traumatic brain injury history is associated with earlier age of onset of Alzheimer disease
LoBue, C., Wadsworth, H., Wilmoth, K., Clem, M., Hart, J., Womack, K. B., Didehbani, N., Lacritz, L. H., Rossetti, H. C., & Cullum, C. M. (2017) · The Clinical Neuropsychologist · doi:10.1080/13854046.2016.1257069 · Cited by 90
Tran, H. T., Sanchez, L., Esparza, T. J., & Brody, D. L. (2011) · PLoS ONE · doi:10.1371/journal.pone.0025475 · Cited by 86
Gruenbaum, S. E., Zlotnik, A., Gruenbaum, B. F., Hersey, D., & Bilotta, F. (2016) · CNS Drugs · doi:10.1007/s40263-016-0355-2 · Cited by 86
Preconditioning paradigms and pathways in the brain.
Shpargel, K. B., Jalabi, W., Jin, Y., Dadabayev, A. R., Penn, M. S., & Trapp, B. D. (2008) · Cleveland Clinic Journal of Medicine · doi:10.3949/ccjm.75.suppl_2.s77 · Cited by 81
Webster, S. J., Van Eldik, L. J., Watterson, D. M., & Bachstetter, A. D. (2015) · The Journal of Neuroscience · doi:10.1523/jneurosci.0291-15.2015 · Cited by 80
Expression of amyloid precursor protein after rat traumatic brain injury
Itoh, T., Satou, T., Nishida, S., Tsubaki, M., Hashimoto, S., & Ito, H. (2009) · Neurological Research · doi:10.1179/016164108x323771 · Cited by 78
Flagged first, then by citations
1 of the 249 references couldn’t be matched to a known paper.
Research works printed but not linked: 1
- Alzheimer, 1907, Uber eine eigenartige Erkrankung der Hirnrinde. Allg. Zeitschrift fur Psychiatr, Und Psych Medizin, 64, 146
Cited by
Sorted by citations
Neuroinflammation in Alzheimer disease
Heneka, M. T., van der Flier, W. M., Jessen, F., Hoozemanns, J., Thal, D. R., Boche, D., Brosseron, F., Teunissen, C., Zetterberg, H., Jacobs, A. H., et al. (2025) · Nature Reviews Immunology · doi:10.1038/s41577-024-01104-7 · Cited by 638
“Furthermore, in a vicious cycle, the accumulation of toxic peptides and proteins associated with neurodegenerative disorders may also enhance and perpetuate glial responses to traumatic injury, leading to significantly higher secondary damage and accelerated neurodegeneration 127 .”
Promoting Successful Cognitive Aging: A Ten-Year Update
Krivanek, T. J., Gale, S. A., McFeeley, B. M., Nicastri, C. M., & Daffner, K. R. (2021) · Journal of Alzheimer s Disease · doi:10.3233/jad-201462 · Cited by 189
Gene-environment interactions in Alzheimer's disease: A potential path to precision medicine
Eid, A., Mhatre, I., & Richardson, J. R. (2019) · Pharmacology & Therapeutics · doi:10.1016/j.pharmthera.2019.03.005 · Cited by 164
Ikram, M. A., Park, T. J., Ali, T., & Kim, M. O. (2020) · Antioxidants · doi:10.3390/antiox9090902 · Cited by 151
“Another life-threatening neurodegenerative disease is traumatic brain injury, which triggers neurodegeneration and AD-like pathological conditions [14].”
BackgroundInflammation in Traumatic Brain Injury
Postolache, T. T., Wadhawan, A., Can, A., Lowry, C. A., Woodbury, M., Makkar, H., Hoisington, A. J., Scott, A. J., Potocki, E., Benros, M. E., et al. (2020) · Journal of Alzheimer s Disease · doi:10.3233/jad-191150 · Cited by 154
Metadata
- Authors
- Kokiko-Cochran, O. N., & Godbout, J. P.
- Affiliations
- The Ohio State University Wexner Medical Center (US)
- ORCID
- Godbout, Jonathan P.
- Venue
- Frontiers in Immunology
- Publisher
- Frontiers Media SA
- Published
- 2018-04-09
- Volume
- 9
- Pages
- 672-672
- ISSN
- 1664-3224 (ISSN-L)
- PMC
- PMC5900037
- OpenAlex
- W2797989008
- Cited by
- 128
- References
- 249
- Citations by year
- 2026: 8 · 2025: 11 · 2024: 18 · 2023: 17 · 2022: 19 · 2021: 20 · 2020: 16 · 2019: 15 · 2018: 4
- FWCI
- 2.17
- Type
- journal article
- Language
- en
- Open access
- gold
- doi.org
- Locations
- Frontiers in Immunology (publishedVersion, cc-by)
- Europe PMC (PubMed Central) (publishedVersion, cc-by)
- PubMed Central (publishedVersion, cc-by)
- PubMed (publishedVersion)
- DOAJ (DOAJ: Directory of Open Access Journals) (submittedVersion, cc-by-sa)
- Funders
- National Institutes of Health (R56-NS090311, R01-AG-51902)
- Topics
- Health Sciences › Medicine › Clinical Neurology › Traumatic Brain Injury and Neurovascular Disturbances
- Life Sciences › Neuroscience › Neurology › Neuroinflammation and Neurodegeneration Mechanisms
- Health Sciences › Medicine › Clinical Neurology › Traumatic Brain Injury Research
- Keywords
- traumatic brain injury, Alzheimer's disease, neuroinflammation, microglia, macrophages, amyloid-beta, tau phosphorylation, microglial priming, neurodegeneration, neuropsychiatric complications, injury recovery
- MeSH terms
- Brain Injuries, Traumatic, Aging, Alzheimer Disease, Animals, Humans, Inflammation, Macrophages, tau Proteins, Amyloidogenic Proteins
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 2026-10-30, under version 3 of the claim definition (model deepseek-v4.1-flash, prompt extract-v3).
A second model labelled each claim on 2026-10-30 (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 ›
Are you an author, or do you see a problem with this page? Request a review