Role of Adipokines in Sarcopenia

Sarcopenia: revised European consensus on definition and diagnosis

Cruz-Jentoft, A. J., Bahat, G., Bauer, J., Boirie, Y., Bruyère, O., Cederholm, T., Cooper, C., Landi, F., Rolland, Y., Sayer, A. A., et al. (2019) · Age and Ageing · doi:10.1093/ageing/afy169 · Cited by 13,818 · see citing works

Positional cloning of the mouse obese gene and its human homologue

Zhang, Y., Proenca, R., Maffei, M., Barone, M., Leopold, L., & Friedman, J. M. (1994) · Nature · doi:10.1038/372425a0 · Cited by 13,419 · see citing works

Asian Working Group for Sarcopenia: 2019 Consensus Update on Sarcopenia Diagnosis and Treatment

Chen, L.-K., Woo, J., Assantachai, P., Auyeung, T.-W., Chou, M.-Y., Iijima, K., Jang, H. C., Kang, L., Kim, M., Kim, S., et al. (2020) · Journal of the American Medical Directors Association · doi:10.1016/j.jamda.2019.12.012 · Cited by 7,070 · see citing works

Brown Adipose Tissue: Function and Physiological Significance

CANNON, B., & NEDERGAARD, J. (2004) · Physiological Reviews · doi:10.1152/physrev.00015.2003 · Cited by 6,433 · see citing works

The hormone resistin links obesity to diabetes

Steppan, C. M., Bailey, S. T., Bhat, S., Brown, E. J., Banerjee, R. R., Wright, C. M., Patel, H. R., Ahima, R. S., & Lazar, M. A. (2001) · Nature · doi:10.1038/35053000 · Cited by 4,755 · see citing works

Adipokines in inflammation and metabolic disease

Ouchi, N., Parker, J. L., Lugus, J. J., & Walsh, K. (2011) · Nature Reviews Immunology · doi:10.1038/nri2921 · Cited by 4,625 · see citing works

Adiponectin stimulates glucose utilization and fatty-acid oxidation by activating AMP-activated protein kinase

Yamauchi, T., Kamon, J., Minokoshi, Y., Ito, Y., Waki, H., Uchida, S., Yamashita, S., Noda, M., Kita, S., Ueki, K., et al. (2002) · Nature Medicine · doi:10.1038/nm788 · Cited by 4,238 · see citing works

A Novel Serum Protein Similar to C1q, Produced Exclusively in Adipocytes

Scherer, P. E., Williams, S. P., Fogliano, M., Baldini, G., & Lodish, H. F. (1995) · Journal of Biological Chemistry · doi:10.1074/jbc.270.45.26746 · Cited by 3,238 · see citing works

Cloning of adiponectin receptors that mediate antidiabetic metabolic effects

Yamauchi, T., Kamon, J., Ito, Y., Tsuchida, A., Yokomizo, T., Kita, S., Sugiyama, T., Miyagishi, M., Hara, K., Tsunoda, M., et al. (2003) · Nature · doi:10.1038/nature01705 · Cited by 3,176 · see citing works

Sarcopenia: origins and clinical relevance

Rosenberg, I. H. (1997) · The Journal of Nutrition · doi:10.1093/jn/127.5.990s · Cited by 2,399 · see citing works

Leptin stimulates fatty-acid oxidation by activating AMP-activated protein kinase

Minokoshi, Y., Kim, Y.-B., Peroni, O. D., Fryer, L. G. D., Müller, C., Carling, D., & Kahn, B. B. (2002) · Nature · doi:10.1038/415339a · Cited by 2,053 · see citing works

The lipocalin protein family: structure and function

FLOWER, D. R. (1996) · Biochemical Journal · doi:10.1042/bj3180001 · Cited by 1,679 · see citing works

Comparison of the Release of Adipokines by Adipose Tissue, Adipose Tissue Matrix, and Adipocytes from Visceral and Subcutaneous Abdominal Adipose Tissues of Obese Humans

Fain, J. N., Madan, A. K., Hiler, M. L., Cheema, P. S., & Bahouth, S. W. (2004) · Endocrinology · doi:10.1210/en.2003-1336 · Cited by 1,571 · see citing works

Global prevalence of sarcopenia and severe sarcopenia: a systematic review and meta‐analysis

Petermann‐Rocha, F., Balntzi, V., Gray, S. R., Lara, J., Ho, F. K., Pell, J. P., & Celis‐Morales, C. (2022) · Journal of Cachexia, Sarcopenia and Muscle · doi:10.1002/jcsm.12783 · Cited by 1,499 · see citing works

Targeted disruption of AdipoR1 and AdipoR2 causes abrogation of adiponectin binding and metabolic actions

Yamauchi, T., Nio, Y., Maki, T., Kobayashi, M., Takazawa, T., Iwabu, M., Okada-Iwabu, M., Kawamoto, S., Kubota, N., Kubota, T., et al. (2007) · Nature Medicine · doi:10.1038/nm1557 · Cited by 1,396 · see citing works

Sarcopenic obesity in older adults: aetiology, epidemiology and treatment strategies

Batsis, J. A., & Villareal, D. T. (2018) · Nature Reviews Endocrinology · doi:10.1038/s41574-018-0062-9 · Cited by 1,382 · cited 2× · see citing works

Isolation and primary structure of NGAL, a novel protein associated with human neutrophil gelatinase

Kjeldsen, L., Johnsen, A., Sengeløv, H., & Borregaard, N. (1993) · Journal of Biological Chemistry · doi:10.1016/s0021-9258(18)82217-7 · Cited by 1,286 · see citing works

Adipose Tissue Remodeling: Its Role in Energy Metabolism and Metabolic Disorders

Choe, S. S., Huh, J. Y., Hwang, I. J., Kim, J. I., & Kim, J. B. (2016) · Frontiers in Endocrinology · doi:10.3389/fendo.2016.00030 · Cited by 1,206 · see citing works

Adipokines in health and disease

Fasshauer, M., & Blüher, M. (2015) · Trends in Pharmacological Sciences · doi:10.1016/j.tips.2015.04.014 · Cited by 1,050 · see citing works

Cloning and Characterization of the cDNA Encoding a Novel Human pre-B-Cell Colony-enhancing Factor

Samal, B. B., Sun, Y., Stearns, G., Xie, C., Suggs, S. V., & McNiece, I. (1994) · Molecular and Cellular Biology · doi:10.1128/mcb.14.2.1431 · Cited by 1,025 · see citing works

Welcome to the ICD‐10 code for sarcopenia

Anker, S. D., Morley, J. E., & von Haehling, S. (2016) · Journal of Cachexia, Sarcopenia and Muscle · doi:10.1002/jcsm.12147 · Cited by 983 · see citing works

PGC-1α protects skeletal muscle from atrophy by suppressing FoxO3 action and atrophy-specific gene transcription

Sandri, M., Lin, J., Handschin, C., Yang, W., Arany, Z. P., Lecker, S. H., Goldberg, A. L., & Spiegelman, B. M. (2006) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0607795103 · Cited by 974 · see citing works

Adiponectin and AdipoR1 Regulate PGC-1α and Mitochondria by Ca2+ and AMPK/SIRT1

Iwabu, M., Yamauchi, T., Okada-Iwabu, M., Sato, K., Nakagawa, T., Funata, M., Yamaguchi, M., Namiki, S., Nakayama, R., Tabata, M., et al. (2010) · Nature · doi:10.1038/nature08991 · Cited by 971 · see citing works

Function of the myogenic regulatory factors Myf5, MyoD, Myogenin and MRF4 in skeletal muscle, satellite cells and regenerative myogenesis

Zammit, P. S. (2017) · Seminars in Cell & Developmental Biology · doi:10.1016/j.semcdb.2017.11.011 · Cited by 887 · see citing works

Macroeconomic implications of population ageing and selected policy responses

Bloom, D. E., Chatterji, S., Kowal, P., Lloyd-Sherlock, P., McKee, M., Rechel, B., Rosenberg, L., & Smith, J. P. (2015) · The Lancet · doi:10.1016/s0140-6736(14)61464-1 · Cited by 769 · see citing works

Acute stimulation of glucose metabolism in mice by leptin treatment

Kamohara, S., Burcelin, R., Halaas, J. L., Friedman, J. M., & Charron, M. J. (1997) · Nature · doi:10.1038/38717 · Cited by 708 · see citing works

Mechanisms of inflammatory responses and development of insulin resistance: how are they interlinked?

Rehman, K., & Akash, M. S. H. (2016) · Journal of Biomedical Science · doi:10.1186/s12929-016-0303-y · Cited by 685 · see citing works

Adiponectin Promotes Macrophage Polarization toward an Anti-inflammatory Phenotype

Ohashi, K., Parker, J. L., Ouchi, N., Higuchi, A., Vita, J. A., Gokce, N., Pedersen, A. A., Kalthoff, C., Tullin, S., Sams, A., et al. (2010) · Journal of Biological Chemistry · doi:10.1074/jbc.m109.088708 · Cited by 646 · see citing works

Molecular Characterization and Pattern of Tissue Expression of the Gene for Neutrophil Gelatinase-Associated Lipocalin from Humans

Cowland, J. B., & Borregaard, N. (1997) · Genomics · doi:10.1006/geno.1997.4896 · Cited by 619 · see citing works

Adipokines as novel biomarkers and regulators of the metabolic syndrome

Deng, Y., & Scherer, P. E. (2010) · Annals of the New York Academy of Sciences · doi:10.1111/j.1749-6632.2010.05875.x · Cited by 558 · see citing works

Adiponectin and its receptors are expressed in bone-forming cells

Berner, H. S., Lyngstadaas, S. P., Spahr, A., Monjo, M., Thommesen, L., Drevon, C. A., Syversen, U., & Reseland, J. E. (2004) · Bone · doi:10.1016/j.bone.2004.06.008 · Cited by 507 · see citing works

Sarcopenia: burden and challenges for public health

Beaudart, C., Rizzoli, R., Bruyère, O., Reginster, J., & Biver, E. (2014) · Archives of Public Health · doi:10.1186/2049-3258-72-45 · Cited by 498 · see citing works

Sarcopenia, sarcopenic obesity and mortality in older adults: results from the national health and nutrition examination survey III

Batsis, J. A., Mackenzie, T. A., Barre, L. K., Lopez-Jimenez, F., & Bartels, S. J. (2014) · European Journal of Clinical Nutrition · doi:10.1038/ejcn.2014.117 · Cited by 479 · see citing works

The Adipokine Lipocalin 2 Is Regulated by Obesity and Promotes Insulin Resistance

Yan, Q.-W., Yang, Q., Mody, N., Graham, T. E., Hsu, C.-H., Xu, Z., Houstis, N. E., Kahn, B. B., & Rosen, E. D. (2007) · Diabetes · doi:10.2337/db07-0007 · Cited by 471 · see citing works

A new immunometabolic perspective of intervertebral disc degeneration

Francisco, V., Pino, J., González-Gay, M. Á., Lago, F., Karppinen, J. I., Tervonen, O. A., Mobasheri, A., & Gualillo, O. (2021) · Nature Reviews Rheumatology · doi:10.1038/s41584-021-00713-z · Cited by 464 · see citing works

Maintenance of muscle stem-cell quiescence by microRNA-489

Cheung, T. H., Quach, N. L., Charville, G. W., Liu, L., Park, L., Edalati, A., Yoo, B., Hoang, P., & Rando, T. A. (2012) · Nature · doi:10.1038/nature10834 · Cited by 461 · see citing works

MC4R-dependent suppression of appetite by bone-derived lipocalin 2

Mosialou, I., Shikhel, S., Liu, J., Maurizi, A., Luo, N., He, Z., Huang, Y., Zong, H., Friedman, R. A., Barasch, J. M., et al. (2017) · Nature · doi:10.1038/nature21697 · Cited by 457 · see citing works

Lipocalin 2: an emerging player in iron homeostasis and inflammation

Xiao, X., Yeoh, B. S., & Vijay-Kumar, M. (2017) · Annual Review of Nutrition · doi:10.1146/annurev-nutr-071816-064559 · Cited by 426 · see citing works

The role of leptin/adiponectin ratio in metabolic syndrome and diabetes

López-Jaramillo, P., Gómez-Arbeláez, D., López-López, J., López-López, C., Martínez-Ortega, J., Gómez-Rodríguez, A., & Triana-Cubillos, S. (2014) · Hormone Molecular Biology and Clinical Investigation · doi:10.1515/hmbci-2013-0053 · Cited by 405 · see citing works

Fatty infiltration of skeletal muscle: mechanisms and comparisons with bone marrow adiposity

Hamrick, M. W., McGee-Lawrence, M. E., & Frechette, D. M. (2016) · Frontiers in Endocrinology · doi:10.3389/fendo.2016.00069 · Cited by 372 · see citing works

Adipokines: A treasure trove for the discovery of biomarkers for metabolic disorders

Lehr, S., Hartwig, S., & Sell, H. (2011) · PROTEOMICS - CLINICAL APPLICATIONS · doi:10.1002/prca.201100052 · Cited by 354 · see citing works

Generation of globular fragment of adiponectin by leukocyte elastase secreted by monocytic cell line THP-1

Waki, H., Yamauchi, T., Kamon, J., Kita, S., Ito, Y., Hada, Y., Uchida, S., Tsuchida, A., Takekawa, S., & Kadowaki, T. (2005) · Endocrinology · doi:10.1210/en.2004-1096 · Cited by 319 · see citing works

Role of PGC-1α Signaling in Skeletal Muscle Health and Disease

Kang, C., & Li Ji, L. (2012) · Annals of the New York Academy of Sciences · doi:10.1111/j.1749-6632.2012.06738.x · Cited by 291 · see citing works

The physiological and pathophysiological role of adiponectin and adiponectin receptors in the peripheral tissues and CNS

Kadowaki, T., Yamauchi, T., & Kubota, N. (2007) · FEBS Letters · doi:10.1016/j.febslet.2007.11.070 · Cited by 270 · see citing works

The role of adipokines as regulators of skeletal muscle fatty acid metabolism and insulin sensitivity

Dyck, D. J., Heigenhauser, G. J. F., & Bruce, C. R. (2005) · Acta Physiologica · doi:10.1111/j.1748-1716.2005.01502.x · Cited by 269 · see citing works

Cloning and Characterization of the cDNA Encoding a Novel Human pre-B-Cell Colony-enhancing Factor

Samal, B. B., Sun, Y., Stearns, G., et al. (1994) · Molecular and Cellular Biology · doi:10.1128/mcb.14.2.1431-1437.1994 · Cited by 264 · see citing works

Sarcopenic obesity: time to meet the challenge

Barazzoni, R., Bischoff, S., Boirie, Y., Busetto, L., Cederholm, T., Dicker, D., Toplak, H., Van Gossum, A., Yumuk, V., & Vettor, R. (2018) · Obesity Facts · doi:10.1159/000490361 · Cited by 244 · see citing works

Irisin, a Novel Myokine, Regulates Glucose Uptake in Skeletal Muscle Cells via AMPK

Lee, H. J., Lee, J. O., Kim, N., Kim, J. K., Kim, H. I., Lee, Y. W., Kim, S. J., Choi, J., Oh, Y., Kim, J. H., et al. (2015) · Molecular Endocrinology · doi:10.1210/me.2014-1353 · Cited by 219 · see citing works

Adiponectin Activates AMP-Activated Protein Kinase in Muscle Cells via APPL1/LKB1-Dependent and Phospholipase C/Ca2+/Ca2+/Calmodulin-Dependent Protein Kinase Kinase-Dependent Pathways

Zhou, L., Deepa, S. S., Etzler, J. C., Ryu, J., Mao, X., Fang, Q., Liu, D. D., Torres, J. M., Jia, W., Lechleiter, J. D., et al. (2009) · Journal of Biological Chemistry · doi:10.1074/jbc.m109.028357 · Cited by 212 · see citing works

Adiponectin Sensitizes Insulin Signaling by Reducing p70 S6 Kinase-mediated Serine Phosphorylation of IRS-1

Wang, C., Mao, X., Wang, L., Liu, M., Wetzel, M. D., Guan, K.-L., Dong, L. Q., & Liu, F. (2007) · Journal of Biological Chemistry · doi:10.1074/jbc.m700098200 · Cited by 210 · see citing works

Lipocalin-2 Deficiency Impairs Thermogenesis and Potentiates Diet-Induced Insulin Resistance in Mice

Guo, H., Jin, D., Zhang, Y., Wright, W. S., Bazuine, M., Brockman, D. A., Bernlohr, D., & Chen, X. (2010) · Diabetes · doi:10.2337/db09-1735 · Cited by 206 · see citing works

Resistin- and Obesity-associated Metabolic Diseases

Lazar, M. A. (2007) · Hormone and Metabolic Research · doi:10.1055/s-2007-985897 · Cited by 195 · see citing works

Resistin in Rodents and Humans

Park, H. K., & Ahima, R. S. (2013) · Diabetes & Metabolism Journal · doi:10.4093/dmj.2013.37.6.404 · Cited by 194 · see citing works

Effects of a leucine-enriched amino acid supplement on muscle mass, muscle strength, and physical function in post-stroke patients with sarcopenia: A randomized controlled trial

Yoshimura, Y., Bise, T., Shimazu, S., Tanoue, M., Tomioka, Y., Araki, M., Nishino, T., Kuzuhara, A., & Takatsuki, F. (2018) · Nutrition · doi:10.1016/j.nut.2018.05.028 · Cited by 193 · see citing works

Adipokines: New Therapeutic Target for Osteoarthritis?

Xie, C., & Chen, Q. (2019) · Current Rheumatology Reports · doi:10.1007/s11926-019-0868-z · Cited by 187 · see citing works

Effects of exercise and nutrition supplementation in community-dwelling older Chinese people with sarcopenia: a randomized controlled trial

Zhu, L.-Y., Chan, R., Kwok, T., Cheng, K. C.-C., Ha, A., & Woo, J. (2019) · Age and Ageing · doi:10.1093/ageing/afy179 · Cited by 179 · see citing works

The Adaptive Potential of Skeletal Muscle Fibers

Pette, D. (2002) · Canadian Journal of Applied Physiology · doi:10.1139/h02-023 · Cited by 178 · see citing works

Adiponectin is expressed by skeletal muscle fibers and influences muscle phenotype and function

Krause, M. P., Liu, Y., Vu, V., Chan, L., Xu, A., Riddell, M. C., Sweeney, G., & Hawke, T. J. (2008) · American Journal of Physiology-Cell Physiology · doi:10.1152/ajpcell.00030.2008 · Cited by 168 · see citing works

Regulation and phylogeny of skeletal muscle regeneration.

Baghdadi, M. B., & Tajbakhsh, S. (2018) · Developmental Biology · doi:10.1016/j.ydbio.2017.07.026 · Cited by 166 · see citing works

Leptin and the Regulation of Body Weigh

Friedman, J. M. (2011) · The Keio Journal of Medicine · doi:10.2302/kjm.60.1 · Cited by 164 · see citing works

The adipokine leptin increases skeletal muscle mass and significantly alters skeletal muscle miRNA expression profile in aged mice

Hamrick, M. W., Herberg, S., Arounleut, P., He, H.-Z., Shiver, A. L., Qi, R.-Q., Zhou, L., Isales, C. M., & Mi, Q. (2010) · Biochemical and Biophysical Research Communications · doi:10.1016/j.bbrc.2010.08.079 · Cited by 157 · see citing works

Adipose Extracellular Vesicles in Intercellular and Inter-Organ Crosstalk in Metabolic Health and Diseases

Huang, Z. P., & Xu, A. (2021) · Frontiers in Immunology · doi:10.3389/fimmu.2021.608680 · Cited by 142 · see citing works

Sarcopenic obesity and dynapenic obesity: 5-year associations with falls risk in middle-aged and older adults: Falls Risk in Sarcopenic and Dynapenic Obesity

Scott, D., Sanders, K. M., Aitken, D., Hayes, A., Ebeling, P. R., & Jones, G. (2014) · Obesity · doi:10.1002/oby.20734 · Cited by 141 · see citing works

Adipokines as regulators of muscle metabolism and insulin sensitivityThis paper is one of a selection of papers published in this Special Issue, entitled 14th International Biochemistry of Exercise Conference – Muscles as Molecular and Metabolic Machines, and has undergone the Journal’s usual peer review process.

Dyck, D. J. (2009) · Applied Physiology, Nutrition, and Metabolism · doi:10.1139/h09-037 · Cited by 136 · see citing works

Leptin Administration Favors Muscle Mass Accretion by Decreasing FoxO3a and Increasing PGC-1α in ob/ob Mice

Sáinz, N., Rodríguez, A., Catalán, V., Becerril, S., Ramírez, B., Gómez-Ambrosi, J., & Frühbeck, G. (2009) · PLoS ONE · doi:10.1371/journal.pone.0006808 · Cited by 135 · see citing works

Transcriptional pathways associated with skeletal muscle disuse atrophy in humans

Chen, Y., Gregory, C. M., Scarborough, M. T., Shi, R., Walter, G. A., & Vandenborne, K. (2007) · Physiological Genomics · doi:10.1152/physiolgenomics.00115.2006 · Cited by 134 · see citing works

Effects of 16 Weeks of Resistance Training on Muscle Quality and Muscle Growth Factors in Older Adult Women with Sarcopenia: A Randomized Controlled Trial

Seo, M.-W., Jung, S.-W., Kim, S.-W., Lee, J.-M., Jung, H. C., & Song, J.-K. (2021) · International Journal of Environmental Research and Public Health · doi:10.3390/ijerph18136762 · Cited by 130 · cited 1× · see citing works

Age-related changes in muscle architecture and metabolism in humans: The likely contribution of physical inactivity to age-related functional decline

Shur, N. F., Creedon, L., Skirrow, S., Atherton, P. J., Macdonald, I. A., Lund, J. N., & Greenhaff, P. L. (2021) · Ageing Research Reviews · doi:10.1016/j.arr.2021.101344 · Cited by 129 · see citing works

Change in Expression of GBP28/Adiponectin in Carbon Tetrachloride-Administrated Mouse Liver

Yoda-Murakami, M., Taniguchi, M., Takahashi, K., Kawamata, S., Saito, K., Choi-Miura, N.-H., & Tomita, M. (2001) · Biochemical and Biophysical Research Communications · doi:10.1006/bbrc.2001.5134 · Cited by 126 · see citing works

Effect of whey protein supplementation after resistance exercise on the muscle mass and physical function of healthy older women: A randomized controlled trial

Mori, H., & Tokuda, Y. (2018) · Geriatrics and gerontology international/Geriatrics & gerontology international · doi:10.1111/ggi.13499 · Cited by 124 · see citing works

Nutrition, Inflammation, and Leptin Levels in Aging and Frailty

Hubbard, R. E., O'Mahony, M. S., Calver, B. L., & WOODHOUSE, K. W. (2008) · Journal of the American Geriatrics Society · doi:10.1111/j.1532-5415.2007.01548.x · Cited by 117 · see citing works

Globular and full-length forms of adiponectin mediate specific changes in glucose and fatty acid uptake and metabolism in cardiomyocytes

PALANIVEL, R., FANG, X., PARK, M., EGUCHI, M., PALLAN, S., DEGIROLAMO, S., LIU, Y., WANG, Y., XU, A., & SWEENEY, G. (2007) · Cardiovascular Research · doi:10.1016/j.cardiores.2007.04.011 · Cited by 117 · see citing works

Enhanced Skeletal Muscle for Effective Glucose Homeostasis

Yang, J. (2014) · Progress in molecular biology and translational science · doi:10.1016/b978-0-12-800101-1.00005-3 · Cited by 116 · see citing works

Distinct Effects of Leptin and a Melanocortin Receptor Agonist Injected Into Medial Hypothalamic Nuclei on Glucose Uptake in Peripheral Tissues

Toda, C., Shiuchi, T., Lee, S. P., Yamato-Esaki, M., Fujino, Y., Suzuki, A., Okamoto, S., & Minokoshi, Y. (2009) · Diabetes · doi:10.2337/db09-0638 · Cited by 114 · see citing works

Cellular and molecular mechanisms of sarcopenia: The S100B perspective

Riuzzi, F., Sorci, G., Arcuri, C., Giambanco, I., Bellezza, I., Minelli, A., & Donato, R. (2018) · Journal of Cachexia Sarcopenia and Muscle · doi:10.1002/jcsm.12363 · Cited by 114 · see citing works

Regulation of fatty acid uptake and metabolism in L6 skeletal muscle cells by resistin

Palanivel, R., & Sweeney, G. (2005) · FEBS Letters · doi:10.1016/j.febslet.2005.08.011 · Cited by 111 · see citing works

Sarcopenic obesity, weight loss, and mortality: the english longitudinal study of ageing

Hamer, M., & O’Donovan, G. (2017) · The American Journal of Clinical Nutrition · doi:10.3945/ajcn.117.152488 · Cited by 110 · see citing works

The Adipokine Network in Rheumatic Joint Diseases

Carrión, M., Frommer, K., Pérez‐García, S., Müller‐Ladner, U., Gomariz, R. P., & Neumann, E. (2019) · International Journal of Molecular Sciences · doi:10.3390/ijms20174091 · Cited by 105 · see citing works

Leptin in Sarcopenic Visceral Obesity: Possible Link between Adipocytes and Myocytes

Kohara, K., Ochi, M., Tabara, Y., Nagai, T., Igase, M., & Miki, T. (2011) · PLoS ONE · doi:10.1371/journal.pone.0024633 · Cited by 99 · see citing works

Adiponectin Action: A Combination of Endocrine and Autocrine/Paracrine Effects

Dadson, K., Liu, Y., & Sweeney, G. (2011) · Frontiers in Endocrinology · doi:10.3389/fendo.2011.00062 · Cited by 97 · see citing works

Regulatory role of leptin in glucose and lipid metabolism in skeletal muscle

Minokoshi, Y., Toda, C., & Okamoto, S. (2012) · Indian Journal of Endocrinology and Metabolism · doi:10.4103/2230-8210.105573 · Cited by 93 · see citing works

Smooth muscle myosin heavy chain isoforms and their role in muscle physiology

Babu, G. J., Warshaw, D. M., & Periasamy, M. (2000) · Microscopy Research and Technique · doi:10.1002/1097-0029(20000915)50:6 · Cited by 92 · see citing works

Effects of branched‐chain amino acids and vitamin D supplementation on physical function, muscle mass and strength, and nutritional status in sarcopenic older adults undergoing hospital‐based rehabilitation: A multicenter randomized controlled trial

Takeuchi, I., Yoshimura, Y., Shimazu, S., Jeong, S., Yamaga, M., & Koga, H. (2018) · Geriatrics and gerontology international/Geriatrics & gerontology international · doi:10.1111/ggi.13547 · Cited by 91 · see citing works

Exercise restores muscle stem cell mobilization, regenerative capacity and muscle metabolic alterations via adiponectin/AdipoR1 activation in SAMP10 mice

Inoue, A., Cheng, X. W., Huang, Z., Hu, L., Kikuchi, R., Jiang, H., Piao, L., Sasaki, T., Itakura, K., Wu, H., et al. (2017) · Journal of Cachexia Sarcopenia and Muscle · doi:10.1002/jcsm.12166 · Cited by 89 · see citing works

Leptin receptors in human skeletal muscle

Guerra, B., Santana, A., Fuentes, T., Delgado‐Guerra, S., Cabrera‐Socorro, A., Dorado, C., & Calbet, J. A. L. (2007) · Journal of Applied Physiology · doi:10.1152/japplphysiol.01313.2006 · Cited by 88 · see citing works

Description of a local cardiac adiponectin system and its deregulation in dilated cardiomyopathy

Skurk, C., Wittchen, F., Suckau, L., Witt, H., Noutsias, M., Fechner, H., Schultheiss, H.-P., & Poller, W. C. (2008) · European Heart Journal · doi:10.1093/eurheartj/ehn136 · Cited by 86 · see citing works

Leptin and UCP1 Genes are Reciprocally Regulated in Brown Adipose Tissue

Cancello, R., Zingaretti, M. C., Sarzani, R., Ricquier, D., & Cinti, S. (1998) · Endocrinology · doi:10.1210/endo.139.11.6434 · Cited by 78 · see citing works

Role of the Cytokine-like Hormone Leptin in Muscle-bone Crosstalk with Aging

Hamrick, M. W. (2017) · Journal of Bone Metabolism · doi:10.11005/jbm.2017.24.1.1 · Cited by 77 · see citing works

Systemic and Metabolic Signature of Sarcopenia in Community-Dwelling Older Adults

Lu, Y., Karagounis, L. G., Ng, T. P., Carré, C., Narang, V., Wong, G. C. L., Tan, C. T. Y., Nyunt, M. S. Z., Gao, Q., Abel, B., et al. (2019) · The Journals of Gerontology Series A · doi:10.1093/gerona/glz001 · Cited by 73 · see citing works

An extensive review regarding the adipokines in the pathogenesis and progression of osteoarthritis.

Tu, C., He, J.-Y., Wu, B., Wang, W.-C., & Li, Z.-H. (2019) · Cytokine · doi:10.1016/j.cyto.2018.06.019 · Cited by 71 · see citing works

Globular adiponectin induces differentiation and fusion of skeletal muscle cells

Fiaschi, T., Cirelli, D., Comito, G., Gelmini, S., Ramponi, G., Serio, M., & Chiarugi, P. (2009) · Cell Research · doi:10.1038/cr.2009.39 · Cited by 70 · see citing works

Obese subcutaneous adipose tissue impairs human myogenesis, particularly in old skeletal muscle, via resistin-mediated activation of NFκB

O’Leary, M. F., Wallace, G. R., Davis, E. T., Murphy, D. P., Nicholson, T. A., Bennett, A. J., Tsintzas, K., & Jones, S. W. (2018) · Scientific Reports · doi:10.1038/s41598-018-33840-x · Cited by 70 · see citing works

Adiponectin as a tissue regenerating hormone: More than a metabolic function

Fiaschi, T., Magherini, F., Gamberi, T., Modesti, P. A., & Modesti, A. (2014) · Cellular and Molecular Life Sciences · doi:10.1007/s00018-013-1537-4 · Cited by 66 · see citing works

The Adiponectin Paradox in the Elderly: Associations With Body Composition, Physical Functioning, and Mortality

Baker, J. F., Newman, A. B., Kanaya, A. M., Leonard, M. B., Zemel, B. S., Miljkovic, I., Long, J., Weber, D. R., & Harris, T. B. (2018) · The Journals of Gerontology Series A · doi:10.1093/gerona/gly017 · Cited by 65 · see citing works

Serum Leptin Concentration is Associated with Incident Frailty in Older Adults

Lana, A., Valdés-Bécares, A., Soto, A. B., Rodríguez‐Artalejo, F., & López‐García, E. (2017) · Aging and Disease · doi:10.14336/ad.2016.0819 · Cited by 62 · see citing works

The Role of Anti-Inflammatory Adipokines in Cardiometabolic Disorders: Moving beyond Adiponectin

Jung, H. N., & Jung, C. H. (2021) · International Journal of Molecular Sciences · doi:10.3390/ijms222413529 · Cited by 59 · see citing works

Involvement of adiponectin in the pathogenesis of dystrophinopathy

Abou-Samra, M., Lecompte, S., Schakman, O., Noel, L., Many, M. C., Gailly, P., & Brichard, S. M. (2015) · Skeletal Muscle · doi:10.1186/s13395-015-0051-9 · Cited by 55 · see citing works

Globular adiponectin reverses osteo-sarcopenia and altered body composition in ovariectomized rats

China, S. P., Pal, S., Chattopadhyay, S., Porwal, K., Kushwaha, S., Bhattacharyya, S., Mittal, M., Gurjar, A. A., Barbhuyan, T. K., Singh, A. K., et al. (2017) · Bone · doi:10.1016/j.bone.2017.08.005 · Cited by 53 · see citing works

Adiponectin and Skeletal Muscle

Jortay, J., Senou, M., Abou-Samra, M., Noel, L., Robert, A., Many, M.-C., & Brichard, S. M. (2012) · The American Journal of Pathology · doi:10.1016/j.ajpath.2012.03.035 · Cited by 52 · see citing works

Consequences of OX40-OX40 ligand interactions in Langerhans cell function: enhanced contact hypersensitivity responses in OX40L-transgenic mice

Sato, T., Ishii, N., Murata, K., Kikuchi, K., Nakagawa, S., Ndhlovu, L. C., & Sugamura, K. (2002) · European Journal of Immunology · doi:10.1002/1521-4141(200211)32:11 · Cited by 51 · see citing works

Leptin Administration Downregulates the Increased Expression Levels of Genes Related to Oxidative Stress and Inflammation in the Skeletal Muscle ofob/obMice

Sáinź, N., Rodrı́guez, A., Catalán, V., Becerril, S., Ramírez, B., Gómez‐Ambrosi, J., & Frühbeck, G. (2010) · Mediators of Inflammation · doi:10.1155/2010/784343 · Cited by 51 · see citing works

Absence of Functional Leptin Receptor Isoforms in the POUND (Leprdb/lb) Mouse Is Associated with Muscle Atrophy and Altered Myoblast Proliferation and Differentiation

Arounleut, P., Bowser, M., Upadhyay, S. K., Shi, X., Fulzele, S., Johnson, M. H., Stranahan, A. M., Hill, W., Isales, C. M., & Hamrick, M. W. (2013) · PLoS ONE · doi:10.1371/journal.pone.0072330 · Cited by 49 · see citing works

Loss of the adipokine lipocalin-2 impairs satellite cell activation and skeletal muscle regeneration

Rebalka, I. A., Monaco, C. M. F., Varah, N. E., Berger, T., D’Souza, D. M., Zhou, S., Mak, T. W., & Hawke, T. J. (2018) · American Journal of Physiology-Cell Physiology · doi:10.1152/ajpcell.00195.2017 · Cited by 48 · see citing works

Gender-specific association of body composition with inflammatory and adipose-related markers in healthy elderly Europeans from the NU-AGE study

Santoro, A., Guidarelli, G., Ostan, R., Giampieri, E., Fabbri, C., Bertarelli, C., Nicoletti, C., Kadi, F., de Groot, C. P. G. M., Feskens, E. J. M., et al. (2019) · European Radiology · doi:10.1007/s00330-018-5973-2 · Cited by 48 · see citing works

Novel Biomolecules in the Pathogenesis of Gestational Diabetes Mellitus

Ruszała, M., Niebrzydowska-Tatus, M., Pilszyk, A., Kimber-Trojnar, Ż., Trojnar, M. P., & Leszczyńska‐Gorzelak, B. (2021) · International Journal of Molecular Sciences · doi:10.3390/ijms222111578 · Cited by 46 · see citing works

The effect of bone morphogenetic protein-2 expression on the early fate of skeletal muscle-derived cells

Musgrave, D. S., Pruchnic, R., Wright, V., Bosch, P., Ghivizzani, S. C., Robbins, P. D., & Huard, J. (2001) · Bone · doi:10.1016/s8756-3282(01)00413-6 · Cited by 45 · see citing works

Local induction of adiponectin reduces lipopolysaccharide-triggered skeletal muscle damage

Jortay, J., Senou, M., Delaigle, A., Noel, L., Funahashi, T., Maeda, N., Many, M. C., & Brichard, S. M. (2010) · Endocrinology · doi:10.1210/en.2009-1462 · Cited by 44 · see citing works

Adipocytokines and disease progression in endometrial cancer: a systematic review

Ray, I., Meira, L. B., Michael, A., & Ellis, P. E. (2021) · Cancer and Metastasis Reviews · doi:10.1007/s10555-021-10002-6 · Cited by 44 · see citing works

Sarcopenia in older people

Yu, S., Umapathysivam, K., & Visvanathan, R. (2014) · International Journal of Evidence-Based Healthcare · doi:10.1097/xeb.0000000000000018 · Cited by 43 · see citing works

Small molecule adiponectin receptor agonist GTDF protects against skeletal muscle atrophy

Singh, A. K., Shree, S., Chattopadhyay, S., Kumar, S., Gurjar, A., Kushwaha, S., Kumar, H., Trivedi, A. K., Chattopadhyay, N., Maurya, R., et al. (2017) · Molecular and Cellular Endocrinology · doi:10.1016/j.mce.2016.09.013 · Cited by 42 · see citing works

Induction of glucose uptake in skeletal muscle by central leptin is mediated by muscle β2-adrenergic receptor but not by AMPK

Shiuchi, T., Toda, C., Okamoto, S., Coutinho, E. A., Saito, K., Miura, S., Ezaki, O., & Minokoshi, Y. (2017) · Scientific Reports · doi:10.1038/s41598-017-15548-6 · Cited by 42 · see citing works

Novel Biomolecules in the Pathogenesis of Gestational Diabetes Mellitus 2.0

Ruszała, M., Pilszyk, A., Niebrzydowska-Tatus, M., Kimber-Trojnar, Ż., Trojnar, M. P., & Leszczyńska‐Gorzelak, B. (2022) · International Journal of Molecular Sciences · doi:10.3390/ijms23084364 · Cited by 39 · see citing works

Globular Adiponectin Activates Motility and Regenerative Traits of Muscle Satellite Cells

Fiaschi, T., Giannoni, E., Taddei, M. L., & Chiarugi, P. (2012) · PLoS ONE · doi:10.1371/journal.pone.0034782 · Cited by 37 · see citing works

Caloric restriction improves diabetes-induced cognitive deficits by attenuating neurogranin-associated calcium signaling in high-fat diet-fed mice

Kim, H., Kang, H., Heo, R. W., Jeon, B. T., Yi, C., Shin, H. J., Kim, J., Jeong, S., Kwak, W., Kim, W., et al. (2015) · Journal of Cerebral Blood Flow & Metabolism · doi:10.1177/0271678x15606724 · Cited by 37 · see citing works

Impact of adiposity on muscle function and clinical events among elders with dynapenia, presarcopenia and sarcopenia: a community-based cross-sectional study

Kao, T., Peng, T., Chen, W., Han, D., Chen, C., & Yang, W. (2021) · Aging · doi:10.18632/aging.202581 · Cited by 37 · see citing works

Activation of autophagy by globular adiponectin is required for muscle differentiation

Gamberi, T., Modesti, A., Magherini, F., D’Souza, D. M., Hawke, T. J., & Fiaschi, T. (2016) · Biochimica et Biophysica Acta (BBA) - Molecular Cell Research · doi:10.1016/j.bbamcr.2016.01.016 · Cited by 35 · see citing works

Skeletal muscle secretome in Duchenne muscular dystrophy: A pivotal anti-inflammatory role of adiponectin

Lecompte, S., Abou-Samra, M., Boursereau, R., Noel, L., & Brichard, S. M. (2017) · Cellular and Molecular Life Sciences · doi:10.1007/s00018-017-2465-5 · Cited by 34 · see citing works

Higher Leptin and Adiponectin Concentrations Predict Poorer Performance-based Physical Functioning in Midlife Women: the Michigan Study of Women’s Health Across the Nation

Karvonen-Gutierrez, C. A., Zheng, H. T., Mancuso, P., & Harlow, S. D. (2015) · The Journals of Gerontology Series A · doi:10.1093/gerona/glv123 · Cited by 33 · see citing works

Examining the Association Between Serum Leptin and Sarcopenic Obesity

Yang, Z., & Chen, W. (2021) · Journal of Inflammation Research · doi:10.2147/jir.s320445 · Cited by 33 · see citing works

The Role of Osteokines in Sarcopenia: Therapeutic Directions and Application Prospects

Lu, W., Xiao, W., Xie, W., Fu, X., Pan, L., Jin, H., Yu, Y., Zhang, Y., & Li, Y. (2021) · Frontiers in Cell and Developmental Biology · doi:10.3389/fcell.2021.735374 · Cited by 33 · see citing works

Adiponectin and insulin cross talk: The microvascular connection

Zhao, L., Fu, Z., & Liu, Z. (2014) · Trends in Cardiovascular Medicine · doi:10.1016/j.tcm.2014.08.001 · Cited by 32 · see citing works

Human Resistin Inhibits Myogenic Differentiation and Induces Insulin Resistance in Myocytes

Sheng, C. H., Du, Z. W., Song, Y., Wu, X. D., Zhang, Y. C., Wu, M., Wang, Q., & Zhang, G. Z. (2013) · BioMed Research International · doi:10.1155/2013/804632 · Cited by 31 · see citing works

A New Leptin-Mediated Mechanism for Stimulating Fatty Acid Oxidation: A Pivotal Role for Sarcolemmal FAT/CD36

Momken, I., Chabowski, A., Dirkx, E., Nabben, M., Jain, S. S., McFarlan, J. T., Glatz, J. F. C., Luiken, J. J. F. P., & Bonen, A. (2017) · Biochemical Journal · doi:10.1042/bcj20160804 · Cited by 30 · see citing works

Effects of Exercise Alone or in Combination with High-Protein Diet on Muscle Function, Aerobic Capacity, and Physical Function in Middle-Aged Obese Adults: A Randomized Controlled Trial

Hsu, K., Chien, K., Tsai, S.-C., Tsai, Y.-S., Liao, Y. H., Chen, J. J., Chen, Y.-R., & Chen, C. (2021) · The journal of nutrition health & aging · doi:10.1007/s12603-021-1599-1 · Cited by 30 · see citing works

The adipokine leptin mediates muscle- and liver-derived IGF-1 in aged mice

Hamrick, M. W., Dukes, A., Arounleut, P., Davis, C. L., Periyasamy‐Thandavan, S., Mork, S., Herberg, S., Johnson, M. H., Isales, C. M., Hill, W., et al. (2015) · Experimental Gerontology · doi:10.1016/j.exger.2015.07.014 · Cited by 29 · see citing works

Adipokines as Immune Cell Modulators in Multiple Sclerosis

Rijnsburger, M., Djuric, N., Mulder, I. A., & de Vries, H. E. (2021) · International Journal of Molecular Sciences · doi:10.3390/ijms221910845 · Cited by 27 · see citing works

Higher Serum Leptin Levels are Associated with a Reduced Risk of Sarcopenia but a Higher Risk of Dynapenia Among Older Adults

Kao, T., Peng, T., Chen, W., Chi, Y., Chen, C., & Yang, W. (2021) · Journal of Inflammation Research · doi:10.2147/jir.s335694 · Cited by 25 · see citing works

Lipocalin 2 increases after high‐intensity exercise in humans and influences muscle gene expression and differentiation in mice

Ponzetti, M., Aielli, F., Ucci, A., Cappariello, A., Lombardi, G., Teti, A. M., & Rucci, N. (2021) · Journal of Cellular Physiology · doi:10.1002/jcp.30501 · Cited by 23 · see citing works

Sarcojoint®, the branched-chain amino acid-based supplement, plus resistance exercise improved muscle mass in adults aged 50 years and older: A double-blinded randomized controlled trial

Peng, L., Yu, P.-C., Hsu, C., Tseng, S., Lee, W., Lin, M., Hsiao, F., & Chen, L. (2021) · Experimental Gerontology · doi:10.1016/j.exger.2021.111644 · Cited by 23 · see citing works

Inflammation et régénération musculaire

Dufresne, S. S., Frenette, J., & Dumont, N. A. (2016) · médecine/sciences · doi:10.1051/medsci/20163206022 · Cited by 22 · see citing works

Skeletal Lipocalin-2 Is Associated with Iron-Related Oxidative Stress in ob/ob Mice with Sarcopenia

Choi, E. B., Jeong, J. H., Jang, H. M., Ahn, Y. J., Kim, K. H., An, H. S., Lee, J. Y., Jeong, E. A., Lee, J., Shin, H. J., et al. (2021) · Antioxidants · doi:10.3390/antiox10050758 · Cited by 22 · see citing works

In Vivo and ex Vivo Regulation of Visfatin Production by Leptin in Human and Murine Adipose Tissue: Role of Mitogen-Activated Protein Kinase and Phosphatidylinositol 3-Kinase Signaling Pathways

Tan, B. K., Chen, J., Brown, J. E. P., Adya, R., Ramanjaneya, M., Menon, V., Bailey, C. J., Lehnert, H., & Randeva, H. S. (2009) · Endocrinology · doi:10.1210/en.2008-1655 · Cited by 21 · see citing works

Local Biomarkers Involved in the Interplay between Obesity and Breast Cancer

Holm, J. B., Rosendahl, A. H., & Borgquist, S. (2021) · Cancers · doi:10.3390/cancers13246286 · Cited by 20 · see citing works

Effects of Milk or Soy Milk Combined with Mild Resistance Exercise on the Muscle Mass and Muscle Strength in Very Old Nursing Home Residents with Sarcopenia

Chiang, F.-Y., Chen, J., Lee, W., & Yang, S. (2021) · Foods · doi:10.3390/foods10112581 · Cited by 18 · see citing works

A Leptin Receptor Antagonist Attenuates Adipose Tissue Browning and Muscle Wasting in Infantile Nephropathic Cystinosis-Associated Cachexia

Gonzalez, A., Cheung, W. W., Perens, E. A., OLIVEIRA, E. A., Gertler, A., & MAK, R. H. K. (2021) · Cells · doi:10.3390/cells10081954 · Cited by 16 · see citing works

Leptin—A Potential Bridge between Fat Metabolism and the Brain’s Vulnerability to Neuropsychiatric Disorders: A Systematic Review

de Assis, G. G., & Murawska‐Ciałowicz, E. (2021) · Journal of Clinical Medicine · doi:10.3390/jcm10235714 · Cited by 15 · see citing works

Adiponectin overexpression in C2C12 myocytes increases lipid oxidation and myofiber transition

Lopez‐Yus, M., Lopez-Perez, R., García-Sobreviela, M. P., del Moral, R., Lorente‐Cebrián, S., & Arbonés-Mainar, J. M. (2021) · Journal of Physiology and Biochemistry · doi:10.1007/s13105-021-00836-7 · Cited by 13 · see citing works

Association between sarcopenia and cognitive impairment in community-dwelling population

Zhu, H., Li, H.-D., Feng, B., Zhang, L., Zheng, Z., Zhang, Y., Wang, D., Xiong, Z., Kang, J., Jin, J.-C., et al. (2020) · Chinese Medical Journal · doi:10.1097/cm9.0000000000001310 · Cited by 12 · see citing works

Assessment of leptin-to-adiponectin ratio in prediction of insulin resistance and nutrition status in a geriatric female population.

Biercewicz, M., Ślusarz, R., Kędziora–Kornatowska, K., Filipska, K., Bielawski, K., & Ruszkowska-Ciastek, B. (2020) · PubMed · doi:10.26402/jpp.2020.1.02 · Cited by 11 · see citing works

Elevated serum leptin levels are associated with low muscle strength and muscle quality in male patients undergoing chronic hemodialysis

Hsu, B., Wang, C., Lai, Y.-H., Kuo, C., & Lin, Y. (2020) · Tzu Chi Medical Journal · doi:10.4103/tcmj.tcmj_20_20 · Cited by 9 · see citing works

AMPK/FOXO1 signaling pathway is indispensable in visfatin-regulated myosin heavy chain expression in C2C12 myotubes

Zhou, L. N., Lin, Y. N., Gu, C. J., Zhou, J., Sun, X. W., Cai, X. T., Du, J., & Li, Q. Y. (2019) · Life Sciences · doi:10.1016/j.lfs.2019.03.060 · Cited by 7 · see citing works

Introduction to the Thematic Review Series: Adipose Biology

Gupta, R. K., & Attie, A. (2019) · Journal of Lipid Research · doi:10.1194/jlr.in119000337 · Cited by 4 · see citing works

Muscle in Endocrinology: From Skeletal Muscle Hormone Regulation to Myokine Secretion and Its Implications in Endocrine–Metabolic Diseases

Iglesias, P. (2025) · Journal of Clinical Medicine · doi:10.3390/jcm14134490 · Cited by 76 · see citing works

Exercise-Induced Muscle–Fat Crosstalk: Molecular Mediators and Their Pharmacological Modulation for the Maintenance of Metabolic Flexibility in Aging

Tero-Vescan, A., Degens, H., Matsakas, A., Ștefănescu, R., Ősz, B. E., & Slevin, M. (2025) · Pharmaceuticals · doi:10.3390/ph18081222 · Cited by 44 · see citing works

Association of metabolic syndrome and sarcopenia with all-cause and cardiovascular mortality: a prospective cohort study based on the NHANES

Huang, W., Deng, S., Liu, S. M., Ma, Q., Cao, L., Liu, L., Wan, H., & Shen, J. (2024) · Frontiers in Endocrinology · doi:10.3389/fendo.2024.1346669 · Cited by 18 · see citing works

Adipose-derived exosomes ameliorate skeletal muscle atrophy via miR-146a-5p/IGF-1R signaling

Qin, M., Zhu, J., Xing, L., Fan, Y., Luo, J., Sun, J., Chen, T., Zhang, Y., & Xi, Q. (2024) · Journal of Nanobiotechnology · doi:10.1186/s12951-024-02983-7 · Cited by 15 · see citing works

Exerkines and myokines in aging sarcopenia

Wang, H., He, W., Chen, P., Wang, H., Wang, H., Zhu, L., & Liu, X. (2025) · Frontiers in Endocrinology · doi:10.3389/fendo.2025.1592491 · Cited by 14 · see citing works

Association of visceral adiposity index with sarcopenia based on NHANES data

Li, J., Lin, Y., Deng, H., Su, X., Feng, W., Shao, Q., & Zou, K. (2024) · Scientific Reports · doi:10.1038/s41598-024-72218-0 · Cited by 14 · see citing works

Coix seed oil alleviates collagen-induced arthritis-associated muscle atrophy and functional decline by modulating gut microbiota dysbiosis

Bai, Y., Zhang, X., Ouyang, F., Wu, Y., Wang, Y., Zhang, J., Meng, F., & Ren, S. (2025) · Phytomedicine · doi:10.1016/j.phymed.2025.157134 · Cited by 11 · see citing works

Endocrinological aspects of sarcopenic obesity

Minnetti, M., Poggiogalle, E., Frigerio, F., Piciocchi, C., Pierantozzi, G., Vincenzo, O. D., Pinto, A., Gianfrilli, D., Isidori, A. M., Migliaccio, S., et al. (2026) · Annals of Medicine · doi:10.1080/07853890.2026.2626085 · Cited by 11 · see citing works

The Adipokine Axis in Heart Failure: Linking Obesity, Sarcopenia and Cardiac Dysfunction in HFpEF

Komić, L., Komic, J., Pavlović, N., Kumrić, M., Bukić, J., Tomić, I. J., & Božić, J. (2026) · International Journal of Molecular Sciences · doi:10.3390/ijms27020612 · Cited by 7 · see citing works

Sex-stratified handgrip strength and adipose-derived inflammatory biomarkers in sarcopenia – a systematic review and meta-analysis

Vithran, D. T. A., Hassan, M. H. Y., Rahmati, M., Boyer, L., Wehliye, A. A., Mahamat, E. O., Xiao, W., Xiao, Y., & Li, Y. (2025) · BMC Geriatrics · doi:10.1186/s12877-025-06777-w · Cited by 6 · see citing works

Low, non-psychedelic doses of psilocybin as a novel treatment for MASLD, obesity and type 2 diabetes via 5-HT2B receptor-dependent mechanisms

Colognesi, M., Gabbia, D., Signor, A., Sarill, M., Centofanti, L., Rinaldi, A., Cascione, L., Nunziata, S., Banzato, M., Mattarei, A., et al. (2025) · Pharmacological Research · doi:10.1016/j.phrs.2025.108080 · Cited by 7 · see citing works

Bridging the Gap: Supplements Strategies from Experimental Research to Clinical Applications in Sarcopenic Obesity

Vîrgolici, B., Dobre, M.-Z., & Stefan, D. C. A. (2024) · Current Issues in Molecular Biology · doi:10.3390/cimb46120800 · Cited by 4 · see citing works

Association between IL-17 and sarcopenia in older adults

Robello, E. C., Cipolli, G. C., Lima, N. A., Nonato, I. F., Yassuda, M. S., Assunção, D. M. X., Mamoni, R. L., Pain, A. D. O., Kemp, A. M., Voshaar, R. C. O., et al. (2025) · Archives of Gerontology and Geriatrics Plus · doi:10.1016/j.aggp.2025.100200 · Cited by 4 · see citing works

Research Progress on the Association Between Sarcopenic Obesity and Atherosclerosis: Current Status and Challenges

Yang, K., Yang, W., Si, S.-C., Liu, J., Ma, Y.-X., & Zhao, H. (2025) · Journal of Clinical Medicine · doi:10.3390/jcm14228148 · Cited by 3 · see citing works

Preparing the soil: Adjusting the metabolic health of patients with chronic wounds and musculoskeletal diseases

da Fonseca, L. F., Santos, G. S., Azzini, G. O. M., Mosaner, T., Jorge, D. D. M. F., de Macedo, A. P., Huber, S. C., Sobreiro, P., Dallo, I., Jeyaraman, M., et al. (2024) · International Wound Journal · doi:10.1111/iwj.70056 · Cited by 3 · see citing works

Leptin’s potential mechanisms in ICU-acquired weakness

Li, M., Yang, L., Li, T., Miao, Y., Yang, J., Chen, S., Ma, X., & Xie, P. (2025) · Lipids in Health and Disease · doi:10.1186/s12944-025-02748-7 · Cited by 1 · see citing works

Clinical, laboratory and instrumental aspects of sarcopenia diagnostics

Станиславовна, Ж. А., Belaya, Z. E., Omelchenko, K. A., & Airapetov, G. A. (2026) · Osteoporosis and Bone Diseases · doi:10.14341/osteo13206 · Cited by 1 · see citing works

Cellular senescence and senescence biomarkers: pathophysiological significance, molecular mechanisms, and clinical perspectives

Borukaeva, I. K., Хараева, З. Ф., Tkhabisimova, I. K., Барасбиевич, Х. А., Алимбекович, У. Т., Shogenov, B. M., & Kunizhev, A. M. (2026) · Бюллетень Восточно-Сибирского научного центра Сибирского отделения Российской академии медицинских наук · doi:10.29413/abs.2026-11.1.11 · Cited by 1 · see citing works

Targeting MuRF1 to Combat Skeletal Muscle Wasting in Cardiac Cachexia: Mechanisms and Therapeutic Prospects

Liu, X., Wen, Y., & Lu, Y. (2024) · Medical Science Monitor · doi:10.12659/msm.945211 · Cited by 1 · see citing works

Association Between Body Roundness Index and Sarcopenia in Older Adults: Evidence from a Prospective Cohort Study Using CHARLSPreprint

Xu, Z., Zhao, Q., Wang, F., Zhang, D., Xu, L., Li, X., He, C., Guan, R., Gao, W., Zhou, M., et al. (2025) · Research Square · doi:10.21203/rs.3.rs-6435227/v1

Mechanical stretch improves high glucose-induced leptin resistance thus promoting glucose uptake of C2C12 myoblasts

Fu, S., Peng, J., & Wang, X. (2025) · Peptides · doi:10.1016/j.peptides.2025.171424

Association of adiponectin and nutritional indices with sarcopenia in elderly diabetic patients

Raju, A., Fredrick, J., Hazra, A., Munshi, B. D., & Roy, D. G. (2025) · Journal of Basic and Clinical Physiology and Pharmacology · doi:10.1515/jbcpp-2025-0128

Single-nucleus RNA sequencing and metabolomics reveal evolutionary divergence in muscle fiber programming between Equus caballus and Equus asinus

Li, C., Qin, X., Han, J., Li, N. N., Wang, Z., Yang, Q., Jafari, H., Lei, C., & Dang, R. (2026) · Journal of Integrative Agriculture · doi:10.1016/j.jia.2026.02.014

Comprehensive quantitative analysis of muscle cross-sectional area and intramuscular fat infiltration of hip using modified DIXON MRI based on chemical shift encoding technique

Jia, D., Wang, M., Yu, H., Zhang, Y., Wang, Y., Sun, Y., & Wu, M. (2026) · Frontiers in Aging · doi:10.3389/fragi.2026.1726714

Sarcopenia in patients with non-alcoholic fatty liver disease: pathogenesis, diagnosis and treatment (expert opinion)

Ilchenko, L. Y., Ахмедов, В. А., Vinnitskaya, E. V., Иванович, Д. Е., Myazin, R. G., Nikitin, I. G., Tikhomirova, A. S., Khoroshilov, I., Myazin, R. G., Александровна, Э. О., et al. (2026) · Экспериментальная и клиническая гастроэнтерология · doi:10.31146/1682-8658-ecg-236-4-3-36

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Castillo, R. L., Jofré‐Saldía, E., Cáceres-Vergara, D., Renard, G. M., & Figueroa, E. G. (2026) · Biomedicines · doi:10.3390/biomedicines14040875

Correlation between ZJU index and sarcopenia in elderly inpatients and its predictive value

Liu, F., 韩华洁, Wang, L., Tan, B., Liu, P., Yang, Y., Ding, Y., & Teng, R.-L. (2026) · Frontiers in Medicine · doi:10.3389/fmed.2026.1790722

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Minnetti, M., Poggiogalle, E., Vincenzo, O. D., Migliaccio, S., & Donini, L. M. (2026) · Endocrinology · doi:10.1007/978-3-030-71067-5_22-1

Novel biomarkers for sarcopenia: a narrative review

Chen, X., Wu, F., Shi, S., Xia, L., Wang, Y., Wei, Y., Wang, J., Li, J., Zhu, M., Zhang, X. W., et al. (2026) · Journal of Orthopaedic Surgery and Research · doi:10.1186/s13018-026-06880-7

The inverse association between skeletal muscle mass to visceral fat ratio (SVR) and sleep disturbance: the mediating role of inflammation and aging acceleration

Zhang, L., Yang, Q., Wu, X., Hu, Y., & Yu, J. (2026) · BMC Psychiatry · doi:10.1186/s12888-026-08248-x

Lymphatic dysfunction and impaired interstitial clearance in sarcopenic obesity: a hypothesis-generating review

Yu, C., Zou, X., Dai, R., & Yang, Y. (2026) · Frontiers in Endocrinology · doi:10.3389/fendo.2026.1876993

Rheumatoid arthritis complicated by osteosarcopenia: Dual burden of sarcopenia and bone loss

Pan, C., Xu, H., & Qian, J. (2026) · Chinese Medical Journal · doi:10.1097/cm9.0000000000004258

Circadian clock-driven inter-organ crosstalk in cardiovascular-kidney-metabolic (CKM) syndrome: Molecular mechanisms, pathological progression, and chronotherapeutic strategies

Cai, Y., Qin, Y., Zhu, M., Cheng, X., Liu, Y., & Liu, Y. (2026) · Metabolism · doi:10.1016/j.metabol.2026.156781

Bridging the Translational Gap in Sarcopenia: Integrating Novel Biologics with Established Lifestyle Interventions

Travieso, S. G., Ortiz, G. U., Viliod, M. C. D. L., & de Freitas, E. C. (2026) · ACS Nutrition Science · doi:10.1021/acsnutrsci.6c00069

Myokines and adipokines in sarcopenia: understanding cross-talk between skeletal muscle and adipose tissue and the role of exercise

Paris, M. T., Bell, K. E., & Mourtzakis, M. (2020) · Current Opinion in Pharmacology · doi:10.1016/j.coph.2020.06.003 · Cited by 62 · see citing works

Research progress on the role of adipokines in the pathogenesis of sarcopenia in the elderly

DANG Caihong, L. W. (2023) · DOAJ (DOAJ: Directory of Open Access Journals) · doi:10.16352/j.issn.1001-6325.2023.04.0695

A Possible Role of Skeletal Muscle‐Derived Adiponectin in the Regulation of Skeletal Muscle Mass

Goto, K., Ito, R., Higa, M., Yokoyama, S., Sugiura, T., Miyata, H., Ohira, Y., & Yoshioka, T. (2017) · The FASEB Journal · doi:10.1096/fasebj.31.1_supplement.lb776

The role and mechanisms of adipokines in skeletal muscle atrophy

Wen-Jun, F. A. N. G., Wang, H., Meng-Qian, L. I., Hao, W. A. N. G., Hao-Zhe, W. A. N. G., Lin, Z. H. U., & Liu, X. (2026) · Shengming kexue · doi:10.3724/cbls.2026084

Adipose tissue in older individuals: a contributing factor to sarcopenia

Wang, T., Zhou, D., & Hong, Z. (2024) · Metabolism · doi:10.1016/j.metabol.2024.155998 · Cited by 35 · see citing works