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Sarcopenic obesity: Myokines as potential diagnostic biomarkers and therapeutic targets?
Abstract
Sarcopenic obesity (SO) is a condition characterized by the occurrence of both sarcopenia and obesity and imposes a heavy burden on the health of the elderly. Controversies and challenges regarding the definition, diagnosis and treatment of SO still remain because of its complex pathogenesis and limitations. Over the past few decades, numerous studies have revealed that myokines secreted from skeletal muscle play significant roles in the regulation of muscle mass and function as well as metabolic homeostasis. Abnormalities in myokines may trigger and promote the pathogenesis underlying age-related and metabolic diseases, including obesity, sarcopenia, type 2 diabetes (T2D), and SO. This review mainly focuses on the role of myokines as potential biomarkers for the early diagnosis and therapeutic targets in SO.
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“Hormones were identified and subsequently leveraged for use as therapeutics throughout the 20th century but it is only in more recent times that numerous families of secreted signaling molecules bearing the suffix “‐kines” such as myokines, 243 osteokines, adipokines, 244 and hepatokines 245 have been identified. 242”
From The role of the androgen receptor in the pathogenesis of obesity and its utility as a target for obesity treatments (2022) · cites this paper as [243]
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1 retracted
THIS ARTICLE HAS BEEN RETRACTED Exercise induces interleukin‐8 expression in human skeletal muscle
Akerstrom, T. C. A., Steensberg, A., Keller, P., Keller, C., Penkowa, M., & Pedersen, B. K. (2004) · The Journal of Physiology · doi:10.1113/jphysiol.2004.077610 · Cited by 130
RetractedAbarca-Gómez, L., Abdeen, Z. A., Hamid, Z. A., Abu-Rmeileh, N. M., Acosta-Cazares, B., Acuin, C., Adams, R. J., Aekplakorn, W., Afsana, K., Aguilar-Salinas, C. A., et al. (2017) · The Lancet · doi:10.1016/s0140-6736(17)32129-3 · Cited by 7,482
Interleukin-10 and the Interleukin-10 Receptor
Moore, K. W., de Waal Malefyt, R., Coffman, R. L., & O'Garra, A. (2001) · Annual Review of Immunology · doi:10.1146/annurev.immunol.19.1.683 · Cited by 6,737
Obesity: global epidemiology and pathogenesis
Blüher, M. (2019) · Nature Reviews Endocrinology · doi:10.1038/s41574-019-0176-8 · Cited by 5,126
A PGC1-α-dependent myokine that drives brown-fat-like development of white fat and thermogenesis
Boström, P., Wu, J., Jedrychowski, M. P., Korde, A., Ye, L., Lo, J. C., Rasbach, K. A., Boström, E. A., Choi, J. H., Long, J. Z., et al. (2012) · Nature · doi:10.1038/nature10777 · Cited by 4,810
Cruz-Jentoft, A. J., & Sayer, A. A. (2019) · The Lancet · doi:10.1016/s0140-6736(19)31138-9 · Cited by 3,905
Muscles, exercise and obesity: skeletal muscle as a secretory organ
Pedersen, B. K., & Febbraio, M. A. (2012) · Nature Reviews Endocrinology · doi:10.1038/nrendo.2012.49 · Cited by 2,909
Kanda, H. (2006) · Journal of Clinical Investigation · doi:10.1172/jci26498 · Cited by 2,682
Interleukin-8 as a macrophage-derived mediator of angiogenesis
Koch, A. E., Polverini, P. J., Kunkel, S. L., Harlow, L. A., DiPietro, L. A., Elner, V. M., Elner, S. G., & Strieter, R. M. (1992) · Science · doi:10.1126/science.1281554 · Cited by 2,135
Research works printed but not linked: 4
- Batsis, 2018, Sarcopenic obesity in older adults: aetiology, epidemiology and treatment strategies, Nat. Rev. Endocrinol., 14, 513, 10.1038/s41574-018-0062-9 · DOI · Paper page
- Di Meo, 2017, Skeletal muscle insulin resistance: role of mitochondria and other ROS sources, J. Endocrinol., 233, R15, 10.1530/JOE-16-0598 · DOI · Paper page
- Kostrominova, 2016, Role of myokines in the maintenance of whole-body metabolic homeostasis, Minerva Endocrinol., 41, 403
- Lipina, 2017, Lipid modulation of skeletal muscle mass and function, J. Cachexia. Sarcopenia Muscle, 8, 190, 10.1002/jcsm.12144 · DOI · Paper page
Cited by
Sorted by citations
Bilski, J., Pierzchalski, P., Szczepanik, M., Bonior, J., & Zoladz, J. A. (2022) · Cells · doi:10.3390/cells11010160 · Cited by 271
“Disorders in myokine secretion may play a role in the pathogenesis of age-related and metabolic diseases, including obesity, T2D, sarcopenia, and SO [111,243,244].”
BackgroundLiu, C., Wong, P. Y., Chung, Y. L., Chow, S. K., Cheung, W. H., Law, S. W., Chan, J. C. N., & Wong, R. M. Y. (2023) · Obesity Reviews · doi:10.1111/obr.13534 · Cited by 247
“The pathogenetic roles of these biomarkers in SO and SO-related diseases require further investigation to explore whether they are potential therapeutic targets.(131) Simi-”
BackgroundSkeletal muscle energy metabolism in obesity
Mengeste, A. M., Rustan, A. C., & Lund, J. (2021) · Obesity · doi:10.1002/oby.23227 · Cited by 141
“Moreover, it is quite likely that other myokines with therapeutic potential for treating obesity and associated metabolic abnormalities will be explored in the future (89).”
BackgroundExercise therapy for people with sarcopenic obesity: myokines and adipokines as effective actors
Alizadeh Pahlavani, H. (2022) · Frontiers in Endocrinology · doi:10.3389/fendo.2022.811751 · Cited by 145
“Myokines act as a mediator between skeletal muscle and other tissues (13).”
BackgroundInfluentialSarcopenia and Cognitive Function: Role of Myokines in Muscle Brain Cross-Talk
Scisciola, L., Fontanella, R. A., Surina, S., Cataldo, V., Paolisso, G., & Barbieri, M. (2021) · Life · doi:10.3390/life11020173 · Cited by 153
“It was also demonstrated that LIF, via PKB/extracellular signal-regulated-mediated c-fos induction, protects against amyloid β-induced neurotoxicity [112].”
BackgroundInterplay of skeletal muscle and adipose tissue: sarcopenic obesity.
Park, M., & Choi, K. M. (2023) · Metabolism: Clinical and Experimental · doi:10.1016/j.metabol.2023.155577 · Cited by 106
Ai, Y., Xu, R., & Liu, L. (2021) · Diabetology & Metabolic Syndrome · doi:10.1186/s13098-021-00707-7 · Cited by 129
Mechanisms by Which Skeletal Muscle Myokines Ameliorate Insulin Resistance
Balakrishnan, R., & Thurmond, D. C. (2022) · International Journal of Molecular Sciences · doi:10.3390/ijms23094636 · Cited by 143
Sarcopenic Obesity: An Emerging Public Health Problem
Ji, T., Li, Y., & Ma, L. (2022) · Aging and Disease · doi:10.14336/ad.2021.1006 · Cited by 131
“The core biological factors leading to SO are changes in body composition related to aging, hormonal changes, the interplay between metabolism and inflammation, environmental factors (unhealthy diet and lack of exercise), and chronic diseases [5, 6, 11, 44].”
BackgroundObesity phenotypes and cardiovascular risk: From pathophysiology to clinical management
Preda, A., Carbone, F., Tirandi, A., Montecucco, F., & Liberale, L. (2023) · Reviews in Endocrine and Metabolic Disorders · doi:10.1007/s11154-023-09813-5 · Cited by 114
“In addition to myostatin, sarcopenia and sarcopenic obesity are associated with a dysregulation of other myokines with important cardiometabolic functions, such as IL-6, FNDC5/ irisin, fibroblast growth factor 21 or brain-derived neurotrophic factor, which play a critical role in skeletal muscle mass and function as w…”
BackgroundSearching for the link between inflammaging and sarcopenia
Wang, T. (2022) · Ageing Research Reviews · doi:10.1016/j.arr.2022.101611 · Cited by 90
Jo, D., Yoon, G., Kim, O. Y., & Song, J. (2022) · Biomedicine & Pharmacotherapy · doi:10.1016/j.biopha.2022.112636 · Cited by 86
Małkowska, P., & Sawczuk, M. (2023) · International Journal of Molecular Sciences · doi:10.3390/ijms241311156 · Cited by 72
Ageing of skeletal muscle extracellular matrix and mitochondria: finding a potential link
Cai, L., Shi, L., Peng, Z., Sun, Y., & Chen, J. (2023) · Annals of Medicine · doi:10.1080/07853890.2023.2240707 · Cited by 63
“It is highly expressed in skeletal muscle and plays a role in enhancing muscle hypertrophy in response to physical exercise [143].”
BackgroundMinniti, G., Pescinini-Salzedas, L. M., Minniti, G. A. D. S., Laurindo, L. F., Barbalho, S. M., Sinatora, R. V., Sloan, L. A., Haber, R. S. D. A., Araújo, A. C., Quesada, K. R., et al. (2022) · International Journal of Molecular Sciences · doi:10.3390/ijms232113452 · Cited by 53
Ryan, A. S., & Li, G. (2021) · JCSM Clinical Reports · doi:10.1002/crt2.43 · Cited by 50
Sarcopenia and cachexia: molecular mechanisms and therapeutic interventions
Wang, T., Zhou, D., & Hong, Z. (2025) · MedComm · doi:10.1002/mco2.70030 · Cited by 46
Cytokines and exosomal miRNAs in skeletal muscle–adipose crosstalk
Guo, L., Quan, M., Pang, W., Yin, Y., & Li, F. (2023) · Trends in Endocrinology and Metabolism · doi:10.1016/j.tem.2023.07.006 · Cited by 51
Zamboni, M. M., Mazzali, G., Brunelli, A., Saatchi, T., Urbani, S., Giani, A., Rossi, A. P., Zoico, E., & Fantin, F. (2022) · Cells · doi:10.3390/cells11213361 · Cited by 47
“BDNF affects myogenesis through activation of satellite cells [71], especially in response to muscle injury; it has also been suggested as a regulator of neuromuscular function during the aging process, with possible implications in sarcopenia and SO [72].”
BackgroundLu, Z., Wang, Z., Zhang, X., & Ning, K. (2024) · Biomolecules · doi:10.3390/biom14101205 · Cited by 47
“…has been shown to be expressed in almost all tissues and organs of eukaryotes, with particularly high expression in skeletal muscle. for 8 weeks) bone in mice training (60 min/day, One study reported that the expression of FNDC5 was nearly 200-fold higher in muscle tissue than in adipocytes [79].”
BackgroundWong, C. J. K., Tai, Y. K., Yap, J. L. Y., Fong, C. H. H., Loo, L. S. W., Kukumberg, M., Fröhlich, J., Zhang, S., Li, J., Wang, J., et al. (2022) · Biomaterials · doi:10.1016/j.biomaterials.2022.121658 · Cited by 37
“Importantly, these muscular secretome responses are largely uncoupled in individuals that are inactive, sarcopenic, or otherwise too frail to exercise, with devastating metabolic and inflammatory repercussions [14 – 16].”
BackgroundKim, J., Shin, S., & Kwon, E. (2023) · Molecular Nutrition & Food Research · doi:10.1002/mnfr.202200729 · Cited by 36
Exploring exercise-driven exerkines: unraveling the regulation of metabolism and inflammation
Zhou, N., Gong, L., Zhang, E., & Wang, X. (2024) · PeerJ · doi:10.7717/peerj.17267 · Cited by 35
“It plays a role in regulating metabolic homeostasis, muscle growth, in fl ammation, and premature aging ( Guo, Li & Xiao, 2020 ).”
BackgroundJurdana, M., & Čemažar, M. (2024) · Radiology and Oncology · doi:10.2478/raon-2024-0011 · Cited by 27
“37-40 This results in a decrease in oxidative capacities, mitochondrial number, atrophy of fast type II muscle fibres and neurodegeneration, decrease in protein synthesis and increase muscle protein degradation.”
BackgroundTeixeira, L. A. D. C., Soares, L. A., da Fonseca, S. F., Gonçalves, G. T., dos Santos, J. M., Viegas, Â. A., Parentoni, A. N., Figueiredo, P. H. S., Mendonça, V. A., & Lacerda, A. C. R. (2024) · Scientific Reports · doi:10.1038/s41598-024-76417-7 · Cited by 32
“The pathophysiology of sarcopenic obesity involves the infiltration and storage of intra-and intermuscular fat, increased inflammation and muscle catabolism 10,34 .”
BackgroundCrucial Regulatory Role of Organokines in Relation to Metabolic Changes in Non-Diabetic Obesity
Lőrincz, H., Somodi, S., Ratku, B., Harangi, M., & Paragh, G. (2023) · Metabolites · doi:10.3390/metabo13020270 · Cited by 26
Venkatesh, V. S., Grossmann, M., Zajac, J. D., & Davey, R. A. (2022) · Obesity Reviews · doi:10.1111/obr.13429 · Cited by 22
FGF19 protects against obesity-induced bone loss by promoting osteogenic differentiation
Guo, A., Li, K., Tian, H., Tao, B., Xiao, Q., & Jiang, D. (2021) · Biomedicine & Pharmacotherapy · doi:10.1016/j.biopha.2021.112524 · Cited by 21
Self-citationBorba, V. Z. C., & Costa, T. M. D. R. L. (2024) · Archives of Endocrinology and Metabolism · doi:10.20945/2359-4292-2024-0084 · Cited by 21
“Proinflammatory cytokines, such as interleukin (IL)-6, IL-1, and tumor necrosis factor-α (TNF-α ), play an important role in muscle homeostasis and can contribute to the pathogenesis of obesity, sarcopenia, and sarcopenic obesity by disrupting metabolic homeostasis (18).”
InfluentialResearch Progress on the Effect and Mechanism of Exercise Intervention on Sarcopenia Obesity
Chen, J., Jia, S., Guo, C., Fan, Z., Yan, W., & Dong, K. (2024) · Clinical Interventions in Aging · doi:10.2147/cia.s473083 · Cited by 22
“64 IGF-1 is a key regulator of muscle growth and regeneration.”
BackgroundUnderstanding the development of sarcopenic obesity
Gross, D. C., Cheever, C. R., & Batsis, J. A. (2023) · Expert Review of Endocrinology & Metabolism · doi:10.1080/17446651.2023.2267672 · Cited by 19
“After exercise, levels of the inflammatory markers IL-6 and TNF-α decrease, and the level of insulin-like growth factor one (IGF-1) increases [105,106].”
BackgroundMakiel, K., Suder, A., Targosz, A., Maciejczyk, M., & Haim, A. (2023) · Biomolecules · doi:10.3390/biom13050852 · Cited by 22
“All authors have read and agreed to the published version of the manuscript.”
BackgroundKumari, M., & Khanna, A. (2022) · Annals of Geriatric Medicine and Research · doi:10.4235/agmr.22.0081 · Cited by 17
Inflammatory Biomarkers in Older Women with Obesity, Sarcopenia, and Sarcopenic Obesity
Teixeira, L. A. D. C., de Avelar, N. C. P., Parentoni, A. N., dos Santos, J. M., Leopoldino, A. A. O., Costa, S. P., Arrieiro, A. N., Soares, L. A., Nobre, J. N. P., Brant, F. P., et al. (2023) · Journal of the American Medical Directors Association · doi:10.1016/j.jamda.2023.05.022 · Cited by 15
Jin, H., Oh, H., Kim, J., Lee, K., Han, X., Lee, O., & Lee, B.-Y. (2021) · Journal of Functional Foods · doi:10.1016/j.jff.2021.104511 · Cited by 15
Lim, G., Lee, H., & Lim, Y. (2022) · Biomedicines · doi:10.3390/biomedicines10102529 · Cited by 16
“Many studies have examined myokines as potential biomarkers that reflect whole-body metabolism homeostasis [28].”
BackgroundLosasso, M. R., Parussolo, M. L. C., Silva, A. O., Direito, R., Quesada, K. R., Detregiachi, C. R. P., Bechara, M. D., Méndez‐Sánchez, N., Abenavoli, L., Araújo, A. C., et al. (2025) · International Journal of Molecular Sciences · doi:10.3390/ijms26104673 · Cited by 14
Sharma, A. R., Chatterjee, S., Lee, Y., & Lee, S. (2023) · Aging and Disease · doi:10.14336/ad.2023.00903 · Cited by 15
“Sarcopenia, Type 2 diabetes, and obesity are some metabolic diseases associated with age [76-78].”
BackgroundStudy on the comorbid mechanisms of sarcopenia and late-life depression
Wu, J., Tang, J., Huang, D., Wang, Y., Zhou, E., Ru, Q., Xu, G., Chen, L., & Wu, Y. (2025) · Behavioural Brain Research · doi:10.1016/j.bbr.2025.115538 · Cited by 12
“IL-6 has a dual role: it can promote muscle hypertrophy by regulating satellite cells[227] and activate anti-inflammatory pathways, including IL-10, to suppress TNF-α expression[228].”
LeDrew, M., Sadri, P., Peil, A., & Farahnak, Z. (2025) · Nutrients · doi:10.3390/nu17172758 · Cited by 13
“In summary, myostatin is recognized not only as a potential biomarker for muscle status but also as a promising therapeutic target for managing muscle degenerative diseases [10,18].”
InfluentialPossible Mechanisms Linking Obesity, Steroidogenesis, and Skeletal Muscle Dysfunction
Sheptulina, A. F., Antyukh, K. Y., Kiselev, A. R., Mitkovskaya, N. P., & Drapkina, O. M. (2023) · Life · doi:10.3390/life13061415 · Cited by 11
“Currently, they are extensively studied as potential prognostic markers and therapeutic targets [20,21].”
BackgroundImmune activation induced by dysregulated lipid metabolism in the pathogenesis of type 2 diabetes
Yang, H., Yu, W., Mao, Q., & Zhao, L. (2025) · World Journal of Diabetes · doi:10.4239/wjd.v16.i12.114395 · Cited by 11
Immunogenetic Aspects of Sarcopenic Obesity
Mazurkiewicz, Ł., Czernikiewicz, K., & Grygiel‐Górniak, B. (2024) · Genes · doi:10.3390/genes15020206 · Cited by 11
“Some of them (like IL-6) have anti-inflammatory activity in the physiological state, while they gain pro-inflammatory properties in the obesity state [10].”
BackgroundInfluentialSarcopenic obesity and brain health: A critical appraisal of the current evidence
Booranasuksakul, U., Guan, Z., Macdonald, I. A., Tsintzas, K., Stephan, B. C. M., & Siervo, M. (2025) · Nutrition Bulletin · doi:10.1111/nbu.12725 · Cited by 10
Kim, N. Y., & Choi, Y. (2023) · Journal of Clinical Medicine · doi:10.3390/jcm12113676 · Cited by 11
Rauen, M., Hao, D., Müller, A., Mückter, E., Bollheimer, L. C., & Nourbakhsh, M. (2021) · Biology · doi:10.3390/biology10121318 · Cited by 10
“The high level of systemic inflammatory proteins was suggested to play a key role in the development of human sarcopenic obesity; however, it has been difficult to clarify which proteins are clinically relevant [21,22,24].”
BackgroundFaiz, H., Heiston, E. M., & Malin, S. K. (2023) · Journal of Diabetes Research · doi:10.1155/2023/4618215 · Cited by 8
“BAIBA has been implicated as a potential target for lowering T2D risk [29].”
BackgroundMyokines and Biomarkers of Frailty in Older Inpatients with Undernutrition: A Prospective Study
Liu, H., Li, W., Zhu, M., Wen, X., Jin, J., Wang, H., Lv, D., Zhao, S., Wu, X., & Jiao, J. (2024) · The Journal of Frailty & Aging · doi:10.14283/jfa.2024.9 · Cited by 11
“From embryonic development to adulthood, MSTN negatively regulates mass, impairs muscle synthesis, and increases muscle catabolism (44-46).”
Lack of association between serum myonectin levels and sarcopenia in older Asian adults
Ji, S., Park, S. J., Lee, J. Y., Baek, J. Y., Jung, H., Kim, K., Yoo, H. J., Jang, I., & Kim, B. (2023) · Experimental Gerontology · doi:10.1016/j.exger.2023.112229 · Cited by 8
Mückter, E., Lozoya, M., Müller, A., Weissig, V., & Nourbakhsh, M. (2022) · Biology · doi:10.3390/biology11050701 · Cited by 7
Li, W., Hu, M., Yin, Q., Liu, Y., Chen, L., Ru, Q., Xu, G., & Wu, Y. (2025) · Frontiers in Physiology · doi:10.3389/fphys.2025.1616874 · Cited by 8
“Myostatin, also known as growth differentiation factor 8, is primarily expressed in skeletal muscle(Baczeketal.,2020)andactsasanegativeregulatorofmuscle mass and development (Guo et al., 2020).”
Hart, D. A., Zernicke, R. F., & Shrive, N. G. (2022) · International Journal of Molecular Sciences · doi:10.3390/ijms23179949 · Cited by 6
Lin, W. W., Su, H., Lan, X. Y., Ni, Q. Y., Wang, X. Y., Cui, K. Y., & Zhang, L. (2024) · Science & Sports · doi:10.1016/j.scispo.2023.09.002 · Cited by 5
Muthukrishnan, R., Alzaabi, A. M. M. A., Ismail, M., Kandakurthi, P. K., Durairaj, S., Sukumar, S., & Gopal, K. (2025) · Journal of Medicine and Life · doi:10.25122/jml-2024-0277 · Cited by 5
Qi, D. E. N. G., Huang, J., Wang, C., & Liang, J. (2026) · International Journal of Molecular Sciences · doi:10.3390/ijms27062746 · Cited by 4
“Notably, independent centenarians exhibit significantly elevated serum IL-15 concentrations, implying a protective effect against aging-related debility [98].”
Laboratory markers of osteosarcopenic obesity
Гриценко, О. В., Gruzdeva, O. V., Chumakova, G. A., & Барбараш, О. Л. (2023) · Russian Journal of Cardiology · doi:10.15829/1560-4071-2023-5563 · Cited by 4
Ai, Y., Xu, R., & Liu, L. (2021) · Research Square · doi:10.21203/rs.3.rs-717363/v1 · Cited by 4
Jiang, H., Zhang, Y., Luo, Z., Tang, X., 赫一佑, & Hao, G. (2026) · Frontiers in Immunology · doi:10.3389/fimmu.2026.1808488 · Cited by 5
“Speci fi cally, IL-10, as a powerful anti-in fl ammatory cytokine, directly inhibits macrophage M1 polarization and the release of pro-in fl ammatory factors like TNF-a and IL-2, improving the pro-in fl ammatory microenvironment of muscle (137).”
Kim, J. J., Bressel, E., Kim, M., Kim, T., Koh, S.-H., & Kim, D. (2025) · Journal of Clinical Medicine · doi:10.3390/jcm14144981 · Cited by 2
“IL-15 is abundantly expressed in skeletal muscle and plays a key role in promoting muscle hypertrophy by increasing in response to exercise [9].”
Oropharyngeal cancer associated with sarcopenic obesity and sarcopenic weight loss
Manjusha, M., & Saravanan, M. (2022) · Oral Oncology · doi:10.1016/j.oraloncology.2022.106101 · Cited by 2
Habib, S. S., Bashir, S., & Habib, S. H. (2020) · Khyber Medical University Journal · doi:10.35845/kmuj.2020.20254 · Cited by 2
Underlying mechanisms of sarcopenic obesity
Rauen, M., Bollheimer, L. C., & Nourbakhsh, M. (2021) · Elsevier eBooks · doi:10.1016/b978-0-12-822146-4.00005-3 · Cited by 2
Obesity, Myokines, and Metabolic Health
Malandrino, N., & Ahima, R. S. (2023) · Springer eBooks · doi:10.1007/978-3-031-40116-9_56 · Cited by 2
Song, G. Y. (2025) · Korean Journal of Geriatrics & Gerontology · doi:10.15656/kjgg.2025.26.1.9 · Cited by 1
Tata, R. K., Rao, A. R., Poonia, Y., Chatterjee, P., Mehta, P. K., & Chakrawarty, A. (2026) · BMC Geriatrics · doi:10.1186/s12877-026-07098-2 · Cited by 2
“These were not assessed in our study and warrant further investigation in larger prospective cohorts [38].”
Jouzi, Z., & Omidi, M. (2023) · Modern Care Journal · doi:10.5812/mcj-142039 · Cited by 1
Teixeira, L. A. D. C., Soares, L. A., Costa, H. S., Nobre, J. N. P., Viegas, Â. A., de Avelar, N. C. P., Figueiredo, P. H. S., Parentoni, A. N., Mendonça, V. A., & Lacerda, A. C. R. (2025) · Scientific Reports · doi:10.1038/s41598-025-95368-1 · Cited by 1
“…encourage studies with biomarkers 3,40–42 , and advances in research point to possible diagnostic markers 3,32,41–43 , diagnostic accuracy studies with inflammatory mediators are relatively recent and scarce, and a marker with an established cutoff point has not been found either 6,10,11,22,44 .”
Obesity, Myokines, and Metabolic Health
Malandrino, N., & Ahima, R. S. (2023) · Springer eBooks · doi:10.1007/978-3-319-12125-3_56-1
Kukes, V. G., Furalyov, V. A., Амырхановна, Г. А., Parfenova, O. K., Grishin, D. V., & Sidorov, N. G. (2023) · Current Bioactive Compounds · doi:10.2174/0115734072273072231017104102
Kim, C.-Y., & Byun, Y.-H. (2025) · Exercise Science · doi:10.15857/ksep.2025.00108
ENDOCRINE FUNCTION OF SKELETAL MUSCLES
Vadzyuk, S. N., & Tabas, P. S. (2025) · Fìzìologìčnij žurnal · doi:10.15407/fz71.03.120
Du, X., Chenhang, Y., Huang, R., Zeng, Y., & Mao, S. (2025) · Journal of Science in Sport and Exercise · doi:10.1007/s42978-026-00375-x
Circulating cytokine profile in patients with obesity depending on the sarcopenia presence
Мамутовна, М. Э., Sheptulina, A. F., Valeeva, D. L., Yafarova, A. A., Timofeev, J. S., Metelskaya, V. A., & Drapkina, O. M. (2025) · Russian Journal of Preventive Medicine · doi:10.17116/profmed20252811166
Ai, Y., Xu, R., & Liu, L. (2021) · Figshare · doi:10.6084/m9.figshare.16570255
Ai, Y., Xu, R., & Liu, L. (2021) · Figshare · doi:10.6084/m9.figshare.16570258
Ai, Y., Xu, R., & Liu, L. (2021) · Figshare · doi:10.6084/m9.figshare.16570252
Sarcopenic Obesity and Hormones: A Narrative Review
Yu, D., & Zhou, B. (2025) · Journal of Biosciences and Medicines · doi:10.4236/jbm.2025.1312003
Kopylov, A. E., Агарков, Н. М., & Abramov, A. A. (2025) · Russian Annals of Ophthalmology · doi:10.17116/oftalma202514106122
Xu, Y., 石龙凯, Chen, L., Liu, J., & Ding, W. (2025) · Scientific Reports · doi:10.1038/s41598-025-28449-w
“Studies have shown that exercise can upregulate anti-inflammatory cytokines such as IL-10, thereby counteracting the inhibitory effect of TNF-α on muscle protein synthesis and alleviating inflammation and oxidative stress in skeletal muscle 32,33 .”
Interleukin profile of patients with cataracts and sarcopenic obesity
Агарков, Н. М., Kopylov, A. E., Yablokov, M. M., & Абрамов, А. А. (2026) · Russian Ophthalmological Journal · doi:10.21516/2072-0076-2026-19-1-142-147
Yu, Y., He, Y., Wang, Y., Wu, C., Zhou, R., Chen, F., & Ma, W. (2026) · The FASEB Journal · doi:10.1096/fj.202601360r
“IL-10 deficiency leads to constitutive NF-κB activation, increased IL-6 production, and compromised muscle strength [162, 172, 173].”
Jiang, N., Wang, S., Zhang, J., & Jia, D. (2026) · Cells · doi:10.3390/cells15110981
“…against age-related metabolic diseases by improving mitochondrial dysfunction [11,12], Physiological muscle hypertrophy resulting from chronic exercise training is critically associated with a panel of skeletal muscle-secreted factors, including myokines, growth factors, and myostatin [13–16].”
Mahmood, S., Safiyah, Fatima, M., Salman, M., & Siddiqui, B. (2026) · Bangladesh Journal of Endocrinology and Metabolism · doi:10.4103/bjem.bjem_15_26
Metadata
- Authors
- Guo, A., Li, K., & Xiao, Q.
- Affiliations
- The Affiliated Yongchuan Hospital of Chongqing Medical University (CN)
- Corresponding author
- Xiao, Qian
- Venue
- Experimental Gerontology
- Publisher
- Elsevier BV
- Published
- 2020-10
- Volume
- 139
- Pages
- 111022
- ISSN
- 0531-5565 (ISSN-L)
- OpenAlex
- W3043914821
- Cited by
- 83
- References
- 286
- Citations by year
- 2026: 7 · 2025: 18 · 2024: 9 · 2023: 20 · 2022: 16 · 2021: 12 · 2020: 1
- FWCI
- 1.57
- Type
- journal article
- Language
- en
- Open access
- closed
- Locations
- Experimental Gerontology (publishedVersion)
- PubMed (publishedVersion)
- Funders
- Chongqing Medical University
- Topics
- Health Sciences › Medicine › Physiology (medical) › Nutrition and Health in Aging
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Muscle Physiology and Disorders
- Health Sciences › Medicine › Endocrinology, Diabetes and Metabolism › Adipokines, Inflammation, and Metabolic Diseases
- Keywords
- sarcopenic obesity, myokines, skeletal muscle, biomarkers, therapeutic target, sarcopenia, obesity, type 2 diabetes, aging, metabolic homeostasis, muscle mass and function
- MeSH terms
- Aged, Diabetes Mellitus, Type 2, Humans, Obesity, Biomarkers, Muscle, Skeletal, Sarcopenia
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