The DOI matches its Crossref record; 43 of the 43 references it cites were found in a registry or an index.
Impaired Mitochondrial Biogenesis in Adipose Tissue in Acquired Obesity
Abstract
Low mitochondrial number and activity have been suggested as underlying factors in obesity, type 2 diabetes, and metabolic syndrome. However, the stage at which mitochondrial dysfunction manifests in adipose tissue after the onset of obesity remains unknown. Here we examined subcutaneous adipose tissue (SAT) samples from healthy monozygotic twin pairs, 22.8–36.2 years of age, who were discordant (ΔBMI >3 kg/m2, mean length of discordance 6.3 ± 0.3 years, n = 26) and concordant (ΔBMI <3 kg/m2, n = 14) for body weight, and assessed their detailed mitochondrial metabolic characteristics: mitochondrial-related transcriptomes with dysregulated pathways, mitochondrial DNA (mtDNA) amount, mtDNA-encoded transcripts, and mitochondrial oxidative phosphorylation (OXPHOS) protein levels. We report global expressional downregulation of mitochondrial oxidative pathways with concomitant downregulation of mtDNA amount, mtDNA-dependent translation system, and protein levels of the OXPHOS machinery in the obese compared with the lean co-twins. Pathway analysis indicated downshifting of fatty acid oxidation, ketone body production and breakdown, and the tricarboxylic acid cycle, which inversely correlated with adiposity, insulin resistance, and inflammatory cytokines. Our results suggest that mitochondrial biogenesis, oxidative metabolic pathways, and OXPHOS proteins in SAT are downregulated in acquired obesity, and are associated with metabolic disturbances already at the preclinical stage.
Overview
Integrity signals
Registry
Cites
Statistics
Verification
Claims the paper makes
Claims other papers make about this one
Each is checked against this paper’s own text: does it say what the citing paper says it does?
In the citing paper
“Ultimately, this dysfunction leads to decreased mitochondrial content, decreased genetic material, and decreased rate of OXPHOS [19, 20].”
From Mitochondrial Adaptation in Skeletal Muscle: Impact of Obesity, Caloric Restriction, and Dietary Compounds (2024) · cites this paper as [20]
Citations
Cites
limma powers differential expression analyses for RNA-sequencing and microarray studies
Ritchie, M. E., Phipson, B., Wu, D., Hu, Y., Law, C. W., Shi, W., & Smyth, G. K. (2015) · Nucleic Acids Research · doi:10.1093/nar/gkv007 · Cited by 40,458
Bioconductor: open software development for computational biology and bioinformatics
Gentleman, R. C., Carey, V. J., Bates, D. M., Bolstad, B., Dettling, M., Dudoit, S., Ellis, B., Gautier, L., Ge, Y., Gentry, J., et al. (2004) · Genome biology · doi:10.1186/gb-2004-5-10-r80 · Cited by 12,082
Causal analysis approaches in Ingenuity Pathway Analysis
Krämer, A., Green, J., Pollard, J., & Tugendreich, S. (2014) · Bioinformatics · doi:10.1093/bioinformatics/btt703 · Cited by 5,724
Mitochondria: In Sickness and in Health
Nunnari, J., & Suomalainen, A. (2012) · Cell · doi:10.1016/j.cell.2012.02.035 · Cited by 3,479
Self-citationPuigserver, P., & Spiegelman, B. M. (2003) · Endocrine Reviews · doi:10.1210/er.2002-0012 · Cited by 2,076
A Mitochondrial Protein Compendium Elucidates Complex I Disease Biology
Pagliarini, D. J., Calvo, S. E., Chang, B., Sheth, S. A., Vafai, S. B., Ong, S.-E., Walford, G. A., Sugiana, C., Boneh, A., Chen, W. K., et al. (2008) · Cell · doi:10.1016/j.cell.2008.06.016 · Cited by 1,994
Attardi, G. M., & Schatz, G. (1988) · Annual Review of Cell Biology · doi:10.1146/annurev.cb.04.110188.001445 · Cited by 1,392
Rao, J. N. K., & Scott, A. J. (1984) · The Annals of Statistics · doi:10.1214/aos/1176346391 · Cited by 1,286
Weyer, C., Foley, J. E., Bogardus, C., Tataranni, P. A., & Pratley, R. E. (2000) · Diabetologia · doi:10.1007/s001250051560 · Cited by 799
DNA replication and transcription in mammalian mitochondria.
Falkenberg, M., Larsson, N., & Gustafsson, C. (2007) · Annual Review of Biochemistry · doi:10.1146/annurev.biochem.76.060305.152028 · Cited by 686
Flagged first, then by citations
Cited by
Sorted by citations
Metabolic Control of Longevity
López-Otín, C., Galluzzi, L., Freije, J. M. P., Madeo, F., & Kroemer, G. (2016) · Cell · doi:10.1016/j.cell.2016.07.031 · Cited by 753
Obesity and cardiovascular disease: revisiting an old relationship
Koliaki, C. C., Liatis, S., & Kokkinos, A. D. (2018) · Metabolism · doi:10.1016/j.metabol.2018.10.011 · Cited by 771
Targeting adipose tissue in the treatment of obesity-associated diabetes
Kusminski, C. M., Bickel, P. E., & Scherer, P. E. (2016) · Nature Reviews Drug Discovery · doi:10.1038/nrd.2016.75 · Cited by 678
PGC-1 α , Inflammation, and Oxidative Stress: An Integrative View in Metabolism
Rius‐Pérez, S., Torres-Cuevas, I., Millán, I., Ortega, Á., & Pérez, S. (2020) · Oxidative Medicine and Cellular Longevity · doi:10.1155/2020/1452696 · Cited by 671
“One striking finding was that hypermethylation has been observed in the body of the PGC-1α gene at two CpG sites in obese co-twins, which correlates with low PGC-1α expression [161].”
BackgroundMitochondrial dynamics in type 2 diabetes: Pathophysiological implications
Rovira-Llopis, S., Bañuls, C., Diaz-Morales, N., Hernandez-Mijares, A., Rocha, M., & Victor, V. M. (2017) · Redox Biology · doi:10.1016/j.redox.2017.01.013 · Cited by 657
“In fact, a downshifting of fatty acid oxidation, ketone body production and breakdown, and tricarboxylic acid cycle was observed and inversely correlated with insulin resistance, adiposity and inflammatory cytokines [42].”
BackgroundMitochondrial dysfunction in obesity
de Mello, A. H., Costa, A. B., Engel, J. D. G., & Rezin, G. T. (2018) · Life Sciences · doi:10.1016/j.lfs.2017.11.019 · Cited by 508
Metabolic adaptation and maladaptation in adipose tissue
Chouchani, E. T., & Kajimura, S. (2019) · Nature Metabolism · doi:10.1038/s42255-018-0021-8 · Cited by 405
Lu, Q., Zhu, Y., Deng, C., Liang, Z., Chen, J., Chen, Y., Wang, X., Liu, Y., Tian, Y., & Yang, Y. (2024) · Signal Transduction and Targeted Therapy · doi:10.1038/s41392-024-01756-w · Cited by 391
Lee, J. H., Park, A., Oh, K., Lee, S. C., Kim, W. K., & Bae, K. (2019) · International Journal of Molecular Sciences · doi:10.3390/ijms20194924 · Cited by 280
“One study showed that the protein levels of OXPHOS complexes III, IV, and V are also decreased in the adipose tissues of obese subjects [54].”
BackgroundObesity in Type 1 Diabetes: Pathophysiology, Clinical Impact, and Mechanisms
Corbin, K. D., Driscoll, K. A., Pratley, R. E., Smith, S. R., Maahs, D. M., Mayer-Davis, E. J., & Advancing Care for Type 1 Diabetes and Obesity Network (ACT1ON) (2018) · Endocrine Reviews · doi:10.1210/er.2017-00191 · Cited by 262
Obesity May Accelerate the Aging Process
Salvestrini, V., Sell, C., & Lorenzini, A. (2019) · Frontiers in Endocrinology · doi:10.3389/fendo.2019.00266 · Cited by 260
“In obese individuals, reduced mitochondrial biogenesis is associated withmetabolic alterations, low-grade inflammation, and insulin resistance (57).”
BackgroundWhite adipose tissue mitochondrial metabolism in health and in obesity
Heinonen, S., Jokinen, R., Rissanen, A., & Pietiläinen, K. H. (2019) · Obesity Reviews · doi:10.1111/obr.12958 · Cited by 252
“Mitochondria possess their own genome, a circular mitochondrial DNA (mtDNA), which encodes 13 proteins critical for OXPHOS and two ribosomal and 22 transfer RNAs required for mitochondrial ribosomes and translation, respectively.31,32 In addition, over one thousand mitochondrial proteins, including essential proteins…”
BackgroundResultInfluentialSelf-citationMitochondria in White, Brown, and Beige Adipocytes
Čedíková, M., Kripnerová, M., Dvořáková, J., Pitule, P., Grundmanova, M., Babuška, V., Müllerová, D., & Kuncová, J. (2016) · Stem Cells International · doi:10.1155/2016/6067349 · Cited by 249
“…findings suggest that dysregulation of mitochondrial calcium influx and efflux could be a crucial factor contributing to decreased insulin sensitivity [100] that is associated with impaired mitochondrial biogenesis and decreased expression of mitochondrial proteins in adipose tissues [101, 102].”
Obesity and aging: Molecular mechanisms and therapeutic approaches
Santos, A. L., & Sinha, S. (2021) · Ageing Research Reviews · doi:10.1016/j.arr.2021.101268 · Cited by 249
Integrative metabolism in MASLD and MASH: Pathophysiology and emerging mechanisms
Steinberg, G. R., Valvano, C. M., De Nardo, W., & Watt, M. J. (2025) · Journal of Hepatology · doi:10.1016/j.jhep.2025.02.033 · Cited by 240
The Influence of Oxidative Stress on Thyroid Diseases
Kochman, J., Jakubczyk, K., Bargiel, P., & Janda, K. (2021) · Antioxidants · doi:10.3390/antiox10091442 · Cited by 204
Adipose Tissue and Metabolic Health
An, S.-M., Cho, S.-H., & Yoon, J. C. (2023) · Diabetes & Metabolism Journal · doi:10.4093/dmj.2023.0011 · Cited by 184
“Studies have described reduced levels of mitochondrial amount or function in adipose tissues of obese human subjects [63-65].”
BackgroundMolecular pathways linking adipose innervation to insulin action in obesity and diabetes mellitus
Guilherme, A., Henriques, F. D. S., Bedard, A. H., & Czech, M. (2019) · Nature Reviews Endocrinology · doi:10.1038/s41574-019-0165-y · Cited by 179
Xia, W., Veeragandham, P., Cao, Y., Xu, Y., Rhyne, T. E., Qian, J., Hung, C.-W., Zhao, P., Jones, Y., Gao, H., et al. (2024) · Nature Metabolism · doi:10.1038/s42255-024-00978-0 · Cited by 176
“While accumulating evidence suggests that mitochondrial dysfunction is a characteristic trait of obesity in human and rodent adipocytes 16,37,38,49 , the underlying molecular mechanisms remain unknown.”
BackgroundHe, F., Huang, Y., Song, Z. Q., Zhou, H. J., Zhang, H., Perry, R. J., Shulman, G. I., & Wang, M. (2020) · The Journal of Experimental Medicine · doi:10.1084/jem.20201416 · Cited by 160
Kunz, H., Hart, C. R., Gries, K. J., Parvizi, M., LAURENTI, M. C., Man, C. D., Moore, N., Zhang, X., Ryan, Z., Polley, E. C., et al. (2021) · American Journal of Physiology-Endocrinology and Metabolism · doi:10.1152/ajpendo.00070.2021 · Cited by 170
Jukarainen, S., Heinonen, S., Rämö, J. T., Rinnankoski‐Tuikka, R., Rappou, E., Tümmers, M., Muniandy, M., Hakkarainen, A., Lundbom, J., Lundbom, N. M. I., et al. (2015) · The Journal of Clinical Endocrinology & Metabolism · doi:10.1210/jc.2015-3095 · Cited by 154
Self-citationKraja, A. T., Liu, C., Fetterman, J. L., Graff, M., Have, C. T., Gu, C. C., Yanek, L. R., Feitosa, M. F., Arking, D. E., Chasman, D. I., et al. (2018) · The American Journal of Human Genetics · doi:10.1016/j.ajhg.2018.12.001 · Cited by 146
Caturano, A., Rocco, M. P., Tagliaferri, G., Piacevole, A., Nilo, D., Lorenzo, G. D., Iadicicco, I., Donnarumma, M., Galiero, R., Acierno, C., et al. (2025) · Antioxidants · doi:10.3390/antiox14010072 · Cited by 178
Cox, F. F., Misiou, A., Vierkant, A., Ale‐Agha, N., Grandoch, M., Haendeler, J., & Altschmied, J. (2022) · Cells · doi:10.3390/cells11030342 · Cited by 154
Oxidative stress: The nexus of obesity and cognitive dysfunction in diabetes
Li, H., Ren, J. L., Li, Y., Wu, Q., & Wei, J. (2023) · Frontiers in Endocrinology · doi:10.3389/fendo.2023.1134025 · Cited by 163
“Down-regulation of mitochondrial biogenesis in obesity is associated with metabolic alterations, insulin resistance, and low-grade inflammation (67).”
BackgroundOxygenation of adipose tissue: A human perspective
Lempesis, I. G., van Meijel, R. L. J., Manolopoulos, K. N., & Goossens, G. H. (2019) · Acta Physiologica · doi:10.1111/apha.13298 · Cited by 139
Alginate derived functional oligosaccharides: Recent developments, barriers, and future outlooks
Vasudevan, U. M., Lee, O. K., & Lee, E. Y. (2021) · Carbohydrate Polymers · doi:10.1016/j.carbpol.2021.118158 · Cited by 129
Mitochondrial Dysfunction in Adipocytes as a Primary Cause of Adipose Tissue Inflammation
Woo, C.-Y., Jang, J. E., Lee, S. E., Koh, E. H., & Lee, K. (2019) · Diabetes & Metabolism Journal · doi:10.4093/dmj.2018.0221 · Cited by 128
Lapatto, H. A. K., Kuusela, M., Heikkinen, A., Muniandy, M., van der Kolk, B. W., Gopalakrishnan, S., Sandvik, M., Schmidt, M. S., Heinonen, S., Saari, S., et al. (2023) · Science Advances · doi:10.1126/sciadv.add5163 · Cited by 136
Self-citationBarazzoni, R., Deutz, N. E. P., Biolo, G., Bischoff, S., Boirie, Y., Cederholm, T., Cuerda, C., Delzenne, N., Leon Sanz, M., Ljungqvist, O., et al. (2017) · Clinical Nutrition · doi:10.1016/j.clnu.2016.09.010 · Cited by 112
“Hyperinsulinemia is a key inducer of lipogenesis and adipose tissue expansion, and selective adipose tissue insulin receptor knockout may protect from fat tissue accumulation [35,36] (Fig.”
BackgroundOkla, M., Wang, W., Kang, I., Pashaj, A., Carr, T. P., & Chung, S. (2015) · Journal of Biological Chemistry · doi:10.1074/jbc.m115.677724 · Cited by 116
“Obesity is defined as a chronic low-grade inflammatory status (meta-inflammation) wherein mitochondrial function is frequently compromised (28).”
Inflammatory Signaling and Brown Fat Activity
Omran, F., & Christian, M. (2020) · Frontiers in Endocrinology · doi:10.3389/fendo.2020.00156 · Cited by 111
“These alterations are further demonstrated by downregulation of mitochondrial biogenesis, oxidative metabolic pathways, and oxidative phosphorylation proteins in WAT in obesity, and a negative correlation with pro-inflammatory cytokines (192).”
BackgroundPerivascular Adipose Tissue as a Relevant Fat Depot for Cardiovascular Risk in Obesity
da Costa, R. M., Neves, K. B., Tostes, R. C., & Lobato, N. S. (2018) · Frontiers in Physiology · doi:10.3389/fphys.2018.00253 · Cited by 108
“…been associated with numerous local consequences, including inflammation (Apovian et al., 2008), fibrosis (Henegar et al., 2008), hypoxia (Jiang et al., 2011), dysregulated adipokine secretion (Jernås et al., 2006; Skurk et al., 2007), and disrupted mitochondrial function (Heinonen et al., 2015).”
BackgroundMitophagy and mitochondrial dynamics in type 2 diabetes mellitus treatment
Shan, Z., Fa, W. H., Tian, C. R., Yuan, C. S., & Ning, J. (2022) · Aging · doi:10.18632/aging.203969 · Cited by 107
Loss of mitochondrial protease ClpP protects mice from diet‐induced obesity and insulin resistance
Bhaskaran, S., Pharaoh, G. A., Ranjit, R., Murphy, A., Matsuzaki, S., Nair, B. C., Forbes, B., Gispert, S., Auburger, G. W. J., Humphries, K. M., et al. (2018) · EMBO Reports · doi:10.15252/embr.201745009 · Cited by 107
“The importance of WAT mitochondria in metabolism is highlighted by the fact that a reduction in mitochondrial number, respiration, or antioxidant levels is associated with metabolic disease conditions in mice and humans [54,55].”
Jokinen, R., Pirnes-Karhu, S., Pietiläinen, K. H., & Pirinen, E. (2017) · Redox Biology · doi:10.1016/j.redox.2017.02.011 · Cited by 103
Self-citationAnti-Inflammatory Strategies Targeting Metaflammation in Type 2 Diabetes
Kuryłowicz, A., & Koźniewski, K. (2020) · Molecules · doi:10.3390/molecules25092224 · Cited by 104
“Recent evidence suggests that mitochondria are essential for maintaining metabolic homeostasis in adipocytes, and their dysfunction in the course of obesity (reflected by downregulation of cellular pathways involved in fatty acid oxidation, ketone body production and breakdown, and the tricarboxylic acid cycle) is dir…”
BackgroundEvidence of Flavonoids on Disease Prevention
Li, M., Qian, M., Jiang, Q., Tan, B., Yin, Y., & Han, X. (2023) · Antioxidants · doi:10.3390/antiox12020527 · Cited by 103
Bean, C., Audano, M., Varanita, T., Favaretto, F., Medaglia, M., Gerdol, M., Pernas, L. F., Stasi, F., Giacomello, M., Herkenne, S., et al. (2021) · Nature Metabolism · doi:10.1038/s42255-021-00497-2 · Cited by 101
Self-citationMitochondrial Dysfunction as a Hallmark of Environmental Injury
Tête, A., Brial, F., Benoit, L., Koual, M., Tomkiewicz, C., Kim, M. J., Blanc, É., Coumoul, X., & Bortoli, S. (2021) · Cells · doi:10.3390/cells11010110 · Cited by 99
“In adipocytes of obese patients, a reduction of mitochondrial oxidative capacity (oxygen consumption rate) is observed [17] and is associated with a decrease of mitochondrial biogenesis [18].”
BackgroundHeinonen, S., Muniandy, M., Buzková, J., Mardinoğlu, A., Rodríguez, A., Frühbeck, G., Hakkarainen, A., Lundbom, J., Lundbom, N. M. I., Kaprio, J. A., et al. (2016) · Diabetologia · doi:10.1007/s00125-016-4121-2 · Cited by 97
“In our previous study with 26 BMI-discordant pairs [7], we reported reduced expression of mitochondrial ribosomal protein subunit transcripts in the heavier co-twins’ adipose tissue.”
BackgroundMethodResultInfluentialSelf-citationTinkov, A. A., Bjørklund, G., Skalny, A. V., Holmgren, A., Геннадиевна, С. М., Chirumbolo, S., & Aaseth, J. (2018) · Cellular and Molecular Life Sciences · doi:10.1007/s00018-018-2745-8 · Cited by 94
“Examination twin pairs revealed a significant (+ 30%) up-regulation of TrxR1 in subcutaneous adipose tissue of obese twins in comparison to the lean ones [94].”
The Role of Mitochondria in Diabetic Kidney Disease
Hallan, S. I., & Sharma, K. (2016) · Current Diabetes Reports · doi:10.1007/s11892-016-0748-0 · Cited by 93
Lemos, V., de Oliveira, R. M., Naia, L., Szegő, É. M., Ramos, E., Pinho, S., Magro, F., Cavadas, C., Rego, A. C., Costa, V., et al. (2017) · Human Molecular Genetics · doi:10.1093/hmg/ddx298 · Cited by 94
Hao, Z., Zhang, Z., Lu, D., Ding, B., Shu, L., Zhang, Q., & Wang, C. (2019) · Chemical Research in Toxicology · doi:10.1021/acs.chemrestox.9b00058 · Cited by 94
Cavaliere, G., Cimmino, F., Trinchese, G., Catapano, A., Petrella, L., D’Angelo, M., Lucchin, L., & Mollica, M. P. (2023) · Antioxidants · doi:10.3390/antiox12061172 · Cited by 104
Obesity-Driven Metabolic Disorders: The Interplay of Inflammation and Mitochondrial Dysfunction
Choi, W., Woo, G. H., Kwon, T., & Jeon, J. (2025) · International Journal of Molecular Sciences · doi:10.3390/ijms26199715 · Cited by 120
“For example, one classic study found that muscle biopsies from insulin-resistant offspring of T2DM patients had ~38% lower mitochondrial density compared with controls [49].”
Mitochondrial oxidative injury: a key player in nonalcoholic fatty liver disease
Dornas, W., & Schuppan, D. (2020) · American Journal of Physiology-Gastrointestinal and Liver Physiology · doi:10.1152/ajpgi.00121.2020 · Cited by 89
“In human obesity, mitochondrial biogenesis is downregulated in subcutaneous adipose tissue (SAT), where reduction in the expression of both mitochondrial- and nuclear-encoded mitochondrial genes leads to impaired mitochondrial biogenesis that correlates with whole body insulin resistance and inflammation (45).”
BackgroundLaiglesia, L. M., Lorente-Cebrián, S., Prieto-Hontoria, P. L., Fernández-Galilea, M., Ribeiro, S. M. R., Sáinz, N., Martínez, J. A., & Moreno-Aliaga, M. J. (2016) · The Journal of Nutritional Biochemistry · doi:10.1016/j.jnutbio.2016.07.019 · Cited by 85
Obesity as a premature aging phenotype — implications for sarcopenic obesity
Nunan, E. L., Wright, C. L., Semola, O. A., Subramanian, M., Balasubramanian, P., Lovern, P. C., Fancher, I. S., & Butcher, J. T. (2022) · GeroScience · doi:10.1007/s11357-022-00567-7 · Cited by 83
Tang, C., Wang, Y., Chen, D., Zhang, M., Xu, J., Chen, X., Liu, J., Kan, J., & Jin, C. (2023) · Food Research International · doi:10.1016/j.foodres.2023.113192 · Cited by 89
Frühbeck, G., Fernández-Quintana, B., Paniagua, M., Hernández‐Pardos, A. W., Valentí, V., Moncada, R., Catalán, V., Becerril, S., Gómez‐Ambrosi, J., Portincasa, P., et al. (2020) · Metabolism · doi:10.1016/j.metabol.2020.154261 · Cited by 80
FoxO transcription factors in mitochondrial homeostasis
Cheng, Z. (2022) · Biochemical Journal · doi:10.1042/bcj20210777 · Cited by 81
Rappou, E., Jukarainen, S., Rinnankoski‐Tuikka, R., Kaye, S. M., Heinonen, S., Hakkarainen, A., Lundbom, J., Lundbom, N. M. I., Saunavaara, V., Rissanen, A., et al. (2016) · The Journal of Clinical Endocrinology & Metabolism · doi:10.1210/jc.2015-3054 · Cited by 79
Self-citationLundgren, S., Kuitunen, S., Pietiläinen, K. H., Hurme, M., Kähönen, M. A. P., Männistö, S., Perola, M., Lehtimäki, T. J., Raitakari, O. T., Kaprio, J. A., et al. (2022) · Journal of Internal Medicine · doi:10.1111/joim.13528 · Cited by 84
Self-citationFrom Obesity to Hippocampal Neurodegeneration: Pathogenesis and Non-Pharmacological Interventions
Lee, T. H.-Y., & Yau, S. (2020) · International Journal of Molecular Sciences · doi:10.3390/ijms22010201 · Cited by 78
Miao, Z., Alvarez, M., Ko, A., Bhagat, Y. V., Rahmani, E., Jew, B., Heinonen, S., Muñóz-Hernández, L. L., Herrera-Hernández, M. F., Aguilar-Salinas, C. A., et al. (2020) · PLoS Genetics · doi:10.1371/journal.pgen.1009018 · Cited by 74
“It has been shown previously that a high BMI associates with adipose MT activity [48].”
BackgroundSelf-citationAdipose tissue macrophages: Regulators of adipose tissue immunometabolism during obesity
Nance, S. A., Muir, L. A., & Lumeng, C. N.-K. (2022) · Molecular Metabolism · doi:10.1016/j.molmet.2022.101642 · Cited by 75
Stinkens, R., Brouwers, B., Jocken, J. W. E., Blaak, E. E., Teunissen-Beekman, K. F. M., Hesselink, M. K. C., van Baak, M. A., Schrauwen, P., & Goossens, G. H. (2018) · Journal of Applied Physiology · doi:10.1152/japplphysiol.00496.2018 · Cited by 72
van der Kolk, B. W., Saari, S., Lovrić, A., Arif, M., Alvarez, M., Ko, A., Miao, Z., Sahebekhtiari, N., Muniandy, M., Heinonen, S., et al. (2021) · Cell Reports Medicine · doi:10.1016/j.xcrm.2021.100226 · Cited by 72
Self-citationFinnTwin16: A Longitudinal Study from Age 16 of a Population-Based Finnish Twin Cohort
Kaidesoja, M., Aaltonen, S., Bogl, L. H., Heikkila, K. V., Kaartinen, S., Kujala, U. M., Kärkkäinen, U., Masip, G., Mustelin, L., Palviainen, T., et al. (2019) · Twin Research and Human Genetics · doi:10.1017/thg.2019.106 · Cited by 69
“…been that a key process associated with the development of metabolic derangements in obesity is mitochondrial downregulation in the adipose tissue (Heinonen et al., 2015; Naukkarinen et al., 2014, Muniandy et al., 2017) and adipocytes (Heinonen et al., 2017); in particular, a reduction in…”
BackgroundSelf-citationPodolak, A., Wocławek-Potocka, I., & Łukaszuk, K. (2022) · Cells · doi:10.3390/cells11050797 · Cited by 68
“Mitochondrial insufficiency was also reported to result from obesity [64,65].”
BackgroundPafili, K., Kahl, S., Mastrototaro, L., Strassburger, K., Pesta, D., Herder, C., Pützer, J., Dewidar, B., Hendlinger, M., Granata, C., et al. (2022) · Journal of Hepatology · doi:10.1016/j.jhep.2022.08.010 · Cited by 67
“In the absence of a single validated gold-standard, the present study employed 3 independent parameters, CSA, mtDNA and protein levels of OXPHOS CI-CV, as a proxy for mitochondrial content, as previously suggested.(24,25,29,30) While reduced CSA was reported in SAT and omental AT of obese humans,(25) the present study…”
ResultMitochondrially-targeted treatment strategies
Bozi, L. H. M., Campos, J. C., Zambelli, V. O., Ferreira, N. D., & Ferreira, J. C. B. (2019) · Molecular Aspects of Medicine · doi:10.1016/j.mam.2019.100836 · Cited by 67
Khalil, M., Shanmugam, H., Abdallah, H., JohnBritto, J. S., Galerati, I., Gómez‐Ambrosi, J., Frühbeck, G., & Portincasa, P. (2022) · Nutrients · doi:10.3390/nu14153112 · Cited by 70
“Mitochondrial biogenesis, mitochondrial oxidative phosphorylation, and oxidative metabolic pathways in subcutaneous adipose tissue are downregulated in obese subjects, when compared to lean subjects [15].”
BackgroundPonnusamy, S., Tran, Q. T., Harvey, I. C., Smallwood, H. S., Thiyagarajan, T., Banerjee, S., Johnson, D. L., Dalton, J. T., Sullivan, R. D., Miller, D. D., et al. (2016) · The FASEB Journal · doi:10.1096/fj.201600787rr · Cited by 65
“One of the hallmarks of energy expenditure is an increase in mitochondrial activity (60).”
BackgroundObesity and Diabetes Mediated Chronic Inflammation: A Potential Biomarker in Alzheimer’s Disease
Khan, M. S. H., & Hegde, V. K. (2020) · Journal of Personalized Medicine · doi:10.3390/jpm10020042 · Cited by 71
Protective role of mitoquinone against impaired mitochondrial homeostasis in metabolic syndrome
Yang, J., Suo, H., & Song, J. (2020) · Critical Reviews in Food Science and Nutrition · doi:10.1080/10408398.2020.1809344 · Cited by 65
Ezquerro, S., Méndez-Giménez, L., Becerril, S., Moncada, R., Valentí, V., Catalán, V., Gómez‐Ambrosi, J., Frühbeck, G., & Rodrı́guez, A. (2016) · Scientific Reports · doi:10.1038/srep39942 · Cited by 64
Relationships Between Ion Channels, Mitochondrial Functions and Inflammation in Human Aging
Strickland, M., Yacoubi‐Loueslati, B., Bouhaouala‐Zahar, B., Pender, S. L. F., & Larbi, A. (2019) · Frontiers in Physiology · doi:10.3389/fphys.2019.00158 · Cited by 64
Effects of visceral adiposity on glycerol pathways in gluconeogenesis
Neeland, I. J., Hughes, C., Ayers, C. R., Malloy, C. R., & Jin, E. S. (2016) · Metabolism · doi:10.1016/j.metabol.2016.11.008 · Cited by 61
“[35] Heinonen S, Buzkova J, Muniandy M, Kaksonen R, Ollikainen M, Ismail K, et al.”
BackgroundZhang, H., Zhang, W., Yun, D., Li, L., Zhao, W., Li, Y., Liu, X., & Liu, Z. (2020) · The Journal of Nutritional Biochemistry · doi:10.1016/j.jnutbio.2020.108403 · Cited by 60
Traish, A. M., & Zitzmann, M. (2015) · Reviews in Endocrine and Metabolic Disorders · doi:10.1007/s11154-015-9323-2 · Cited by 57
Kobayashi, M., Deguchi, Y., Nozaki, Y., & Higami, Y. (2021) · International Journal of Molecular Sciences · doi:10.3390/ijms22116025 · Cited by 63
“Similarly, human studies have shown that obesity attenuates PGC-1α expression in WAT [63,64,66,67].”
BackgroundMediterranean diet and mitochondria: New findings
Pollicino, F., Veronese, N., Dominguez, L. J., & Barbagallo, M. (2023) · Experimental Gerontology · doi:10.1016/j.exger.2023.112165 · Cited by 59
Liao, J., He, W., Li, L., Wang, J., Gong, L., Zhang, Q., & Lin, Z. (2025) · Cell Biomaterials · doi:10.1016/j.celbio.2025.100016 · Cited by 63
Gómez‐Serrano, M., Camafeita, E., López, J. A., Rubio, M. Á., Lesmes, I. B., García‐Consuegra, I., García‐Santos, E., Lago, J., Sánchez-Pernaute, A., Torres, A., et al. (2016) · Redox Biology · doi:10.1016/j.redox.2016.12.013 · Cited by 60
“Earlier studies in subcutaneous adipose tissue also reported the down-regulation of mitochondrial complex III, IV and V in obesityassociated IR [59], in agreement with our results.”
ResultWu, N., Zheng, W., Zhou, Y., Tian, Y., Tang, M., Feng, X., Ashrafizadeh, M., Wang, Y. Z., Niu, X., Tambuwala, M. M., et al. (2024) · Ageing Research Reviews · doi:10.1016/j.arr.2024.102428 · Cited by 59
Vink, R., Roumans, N. J. T., Fazelzadeh, P., Tareen, S. H. K., Boekschoten, M. V., van Baak, M. A., & Mariman, E. C. M. (2016) · International Journal of Obesity · doi:10.1038/ijo.2016.201 · Cited by 55
Datta, S., He, G., Tomilov, A. A., Sahdeo, S., Denison, M. S., & Cortopassi, G. A. (2017) · Environmental Health Perspectives · doi:10.1289/ehp1404 · Cited by 55
“2011), obesity (Heinonen et al. 2015), Alzheimer’s disease, Parkinson’s disease (Yan et al.”
BackgroundVisceral Adipose Tissue Accumulation and Residual Cardiovascular Risk
Jemtel, T. H. L., Samson, R., Milligan, G. P., Jaiswal, A., & Oparil, S. (2018) · Current Hypertension Reports · doi:10.1007/s11906-018-0880-0 · Cited by 56
Omega-3 Fatty Acids Attenuate Brain Alterations in High-Fat Diet-Induced Obesity Model
de Mello, A. H., Schraiber, R. D. B., Goldim, M. P. D. S., Garcez, M. L., Gomes, M. L., Silveira, G. D. B., Zaccaron, R. P., Schuck, P. F., Budni, J., Silveira, P. C. L., et al. (2018) · Molecular Neurobiology · doi:10.1007/s12035-018-1097-6 · Cited by 56
Kaye, S. M., Lokki, A. I., Hanttu, A. M., Nissilä, E., Heinonen, S., Hakkarainen, A., Lundbom, J., Lundbom, N. M. I., Saarinen, L., Tynninen, O., et al. (2017) · Frontiers in Immunology · doi:10.3389/fimmu.2017.00545 · Cited by 53
“RNA was prepared from frozen fat tissue (26).”
MethodSelf-citationCruz, M. M., Lopes, A. B., Crisma, A. R., de Sá, R. D. C. C., Kuwabara, W. M. T., Curi, R., de Andrade, P. B. M., & Alonso‐Vale, M. I. C. (2018) · Lipids in Health and Disease · doi:10.1186/s12944-018-0710-z · Cited by 52
Ngo, D. T. M., Sverdlov, A. L., Karki, S., Macartney-Coxson, D. P., Stubbs, R. S., Farb, M. G., Carmine, B. J., Hess, D. T., Colucci, W. S., & Gokce, N. (2018) · American Journal of Physiology-Endocrinology and Metabolism · doi:10.1152/ajpendo.00227.2018 · Cited by 51
van der Kolk, B. W., Muniandy, M., Kamińska, D., Alvarez, M., Ko, A., Miao, Z., Valsesia, A., Langin, D., Vaittinen, M., Pääkkönen, M., et al. (2021) · The Journal of Clinical Endocrinology & Metabolism · doi:10.1210/clinem/dgab072 · Cited by 52
“SAT mitochondrial oxidative metabolism is diminished in obesity (8-10)—a phenomenon that likely associates with both the persistence of the obesity phenotype and the development of obesity-related metabolic diseases (11).”
BackgroundSelf-citationEffect of Dietary Bioactive Compounds on Mitochondrial and Metabolic Flexibility
Serrano, J. C. E., Cassanyé, A., Martin‐Garí, M., Granado‐Serrano, A. B., & Portero‐Otín, M. (2016) · Diseases · doi:10.3390/diseases4010014 · Cited by 53
“Diverse mitochondrial parameters vary between insulin-resistant and insulin-sensitive subjects, such as mitochondrial number and structure [4].”
BackgroundShrestha, D., Ouidir, M., Workalemahu, T., Zeng, X., & Ayele, F. T. (2020) · International Journal of Obesity · doi:10.1038/s41366-020-0546-2 · Cited by 56
Fouad, G. I. (2020) · Neurochemical Research · doi:10.1007/s11064-020-02996-2 · Cited by 51
Katsouda, A., Valakos, D., Dionellis, V. S., Bibli, S., Akoumianakis, I., Karaliota, S., Zuhra, K., Fleming, I., Nagahara, N., Havaki, S., et al. (2022) · The Journal of Experimental Medicine · doi:10.1084/jem.20211894 · Cited by 49
“…inflammation and oxidative stress (Fern´andez-S´anchez et al., 2011; Gao et al., 2010; Sutherland et al., 2008; Valerio et al., 2006), and observations linking obesity to reduced expression levels of the genes that code for respiratory chain proteins (Fischer et al., 2015; Heinonen et al., 2015).”
Xu, J., Chen, S., Wang, W., Lam, S. M., Xu, Y., Zhang, S., Pan, H., Liang, J., Huang, X., Wang, Y., et al. (2021) · 中国科学通报:英文版 · doi:10.1016/j.scib.2021.10.014 · Cited by 49
Ahn, C., Ryan, B. J., Schleh, M. W., Varshney, P., Ludzki, A. C., Gillen, J. B., Pelt, D. W. V., Pitchford, L. M., Howton, S. M., Rode, T., et al. (2022) · The Journal of Physiology · doi:10.1113/jp282371 · Cited by 50
“Mitochondrial biogenesis and function are often compromised in aSAT in obesity, which has been associated with metabolic disturbances (Hammarstedt et al. 2003; Semple et al. 2004;Heinonen et al. 2015).”
BackgroundUnderstanding Adipose Tissue Dysfunction
Blüher, M. (2024) · Journal of Obesity & Metabolic Syndrome · doi:10.7570/jomes24013 · Cited by 55
Peripheral Determinants of Oxygen Utilization in Heart Failure With Preserved Ejection Fraction
Zamani, P. L., Proto, E. A., Mazurek, J. A., Prenner, S. B., Margulies, K. B., Townsend, R. R., Kelly, D. P., Arany, Z. P., Poole, D. C., Wagner, P. D., et al. (2020) · JACC Basic to Translational Science · doi:10.1016/j.jacbts.2020.01.003 · Cited by 45
“Obesity is associated with impairments in skeletal muscle fuel utilization (30–32), mitochondrial content (33,34), and an increase in inflammation and reactive oxygen species (3,35,36), which can also decrease mitochondrial function.”
BackgroundBorja-Magno, A. I., Furuzawa‐Carballeda, J., Guevara‐Cruz, M., Arias, C., Granados, J., Bourges, H., Tovar, A. R., Sears, B., Noriega, L. G., & Gómez, F. E. (2023) · The Journal of Nutritional Biochemistry · doi:10.1016/j.jnutbio.2023.109415 · Cited by 45
Zhang, J., Jiang, H., & Chen, J. (2016) · Oncotarget · doi:10.18632/oncotarget.10915 · Cited by 46
“And recent studies showed mitochondrial dysfunction was involved in obese-metabolic related diseases, as manifested in down regulation of mitochondrial biogenesis, oxidative metabolic pathways and OXPHOS proteins [38].”
BackgroundBollepalli, S., Kaye, S. M., Heinonen, S., Kaprio, J. A., Rissanen, A., Virtanen, K. A., Pietiläinen, K. H., & Ollikainen, M. (2017) · International Journal of Obesity · doi:10.1038/ijo.2017.245 · Cited by 45
Self-citationMoore, T. M., Cheng, L., Wolf, D. M., Ngo, J., Segawa, M., Zhu, X., Strumwasser, A. R., Cao, Y., Clifford, B. L., Ma, A., et al. (2022) · Nature Communications · doi:10.1038/s41467-022-34468-2 · Cited by 49
Pedersen, J. S., Rygg, M. O., Chrøis, K. M., Sustarsic, E. G., Gerhart‐Hines, Z., Albrechtsen, N. J. W., Serizawa, R., Kristiansen, V. B., Basse, A. L., Boilesen, A. E. B., et al. (2022) · Nature Communications · doi:10.1038/s41467-022-30629-5 · Cited by 42
Metadata
- Authors
- Heinonen, S., Buzkova, J., Muniandy, M., Kaksonen, R., Ollikainen, M., Ismail, K., Hakkarainen, A., Lundbom, J., Lundbom, N., Vuolteenaho, K., Moilanen, E., Kaprio, J., Rissanen, A., Suomalainen, A., & Pietiläinen, K. H.
- Affiliations
- University of Helsinki (FI)
- Research Programs Unit, Molecular Neurology, Biomedicum-Helsinki, University of Helsinki, Helsinki, Finland
- Tampere University Hospital (FI)
- Corresponding author
- Pietiläinen, Kirsi H.
- ORCID
- Venue
- Diabetes
- Publisher
- American Diabetes Association
- Published
- 2015-05-13
- Volume
- 64
- Issue
- 9
- Pages
- 3135-3145
- ISSN
- 0012-1797 (ISSN-L)
- 1939-327X
- OpenAlex
- W2168209245
- Cited by
- 362
- References
- 42
- Citations by year
- 2026: 25 · 2025: 39 · 2024: 39 · 2023: 45 · 2022: 44 · 2021: 38 · 2020: 34 · 2019: 29 · 2018: 20 · 2017: 20 · 2016: 21 · 2015: 8
- FWCI
- 16.92
- Type
- journal article
- Language
- en
- Open access
- closed
- Locations
- Diabetes (publishedVersion)
- PubMed (publishedVersion)
- STM:n Hallinnonalan avoin julkaisuarkisto (Julkari) (submittedVersion)
- Funders
- Academy of Finland
- Orion Foundation
- Finnish Foundation for Cardiovascular Research
- European Research Council
- University of Helsinki
- Sigrid Jusélius Foundation
- Novo Nordisk Foundation
- Helsinki University Hospital Research Funds
- Jalmari and Rauha Ahokas Foundation
- Diabetes Research Foundation
- Topics
- Health Sciences › Medicine › Physiology (medical) › Adipose Tissue and Metabolism
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Mitochondrial Function and Pathology
- Health Sciences › Medicine › Endocrinology, Diabetes and Metabolism › Adipokines, Inflammation, and Metabolic Diseases
- Keywords
- mitochondrial biogenesis, subcutaneous adipose tissue, monozygotic twin discordance, mitochondrial DNA, oxidative phosphorylation, fatty acid oxidation, ketone body metabolism, TCA cycle, insulin resistance, inflammatory cytokines, mitochondrial transcriptome, type 2 diabetes, metabolic syndrome
- MeSH terms
- Adult, Citric Acid Cycle, DNA, Mitochondrial, Fatty Acids, Female, Gene Expression Regulation, Humans, Inflammation, Insulin Resistance, Ketone Bodies, Male, Mitochondria, Obesity, Oxidative Phosphorylation, Twins, Monozygotic, Case-Control Studies, Cytokines, Gene Expression Profiling, Subcutaneous Fat, Mitochondrial Turnover
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.
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