Physical Exercise and Myokines: Relationships with Sarcopenia and Cardiovascular Complications

Sarcopenia: revised European consensus on definition and diagnosis

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A PGC1-α-dependent myokine that drives brown-fat-like development of white fat and thermogenesis

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Sarcopenia: revised European consensus on definition and diagnosis

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Guidelines for Adult Stroke Rehabilitation and Recovery: A Guideline for Healthcare Professionals From the American Heart Association/American Stroke Association

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The anti-inflammatory effect of exercise

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Muscle as an Endocrine Organ: Focus on Muscle-Derived Interleukin-6

Pedersen, B. K., & Febbraio, M. A. (2008) · Physiological Reviews · doi:10.1152/physrev.90100.2007 · Cited by 2,388 · see citing works

FoxO3 Controls Autophagy in Skeletal Muscle In Vivo

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Sarcopenia: Aging-Related Loss of Muscle Mass and Function

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FoxO3 coordinately activates protein degradation by the autophagic/lysosomal and proteasomal pathways in atrophying muscle cells.

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Fibroblast growth factor 21 reverses hepatic steatosis, increases energy expenditure, and improves insulin sensitivity in diet-induced obese mice

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Myostatin reduces Akt/TORC1/p70S6K signaling, inhibiting myoblast differentiation and myotube size

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Sarcopenia: A Time for Action. An SCWD Position Paper

Bauer, J. M., Morley, J. E., Schols, A. M. W. J., Ferrucci, L., Cruz-Jentoft, A. J., Dent, E., Baracos, V. E., Crawford, J. A., Doehner, W., Heymsfield, S. B., et al. (2019) · Journal of Cachexia Sarcopenia and Muscle · doi:10.1002/jcsm.12483 · Cited by 739 · see citing works

The diseasome of physical inactivity – and the role of myokines in muscle–fat cross talk

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Muscle as a secretory organ

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Skeletal muscle as an endocrine organ: PGC-1α, myokines and exercise

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The exerkine apelin reverses age-associated sarcopenia

Vinel, C., Lukjanenko, L., Batut, A., Deleruyelle, S., Pradère, J.-P., Le Gonidec, S., Dortignac, A., Geoffre, N., Pereira, O., Karaz, S., et al. (2018) · Nature Medicine · doi:10.1038/s41591-018-0131-6 · Cited by 398 · see citing works

Physical Exercise-Induced Myokines and Muscle-Adipose Tissue Crosstalk: A Review of Current Knowledge and the Implications for Health and Metabolic Diseases

Leal, L. G., Lopes, M. A., & Batista, M. L. (2018) · Frontiers in Physiology · doi:10.3389/fphys.2018.01307 · Cited by 382 · cited 1× · see citing works

Sarcopenia and sarcopenic obesity

Choi, K. M. (2016) · The Korean Journal of Internal Medicine · doi:10.3904/kjim.2016.193 · Cited by 344 · see citing works

FGF21 as Modulator of Metabolism in Health and Disease

Tezze, C., Romanello, V., & Sandri, M. (2019) · Frontiers in Physiology · doi:10.3389/fphys.2019.00419 · Cited by 313 · see citing works

Irisin: A Hope in Understanding and Managing Obesity and Metabolic Syndrome

Arhire, L. I., Mihalache, L., & Covașă, M. (2019) · Frontiers in Endocrinology · doi:10.3389/fendo.2019.00524 · Cited by 306 · see citing works

Irisin promotes osteoblast proliferation and differentiation via activating the MAP kinase signaling pathways

Qiao, X., Nie, Y., Ma, Y., Chen, Y., Cheng, R., Yin, W., Hu, Y., Xu, W., & Xu, L. (2016) · Scientific Reports · doi:10.1038/srep18732 · Cited by 291 · see citing works

The Ever-Expanding Myokinome: Discovery Challenges and Therapeutic Implications

Whitham, M., & Febbraio, M. A. (2016) · Nature Reviews Drug Discovery · doi:10.1038/nrd.2016.153 · Cited by 279 · see citing works

Resistance Exercise Training as a Primary Countermeasure to Age-Related Chronic Disease

Mcleod, J. C., Stokes, T., & Phillips, S. M. (2019) · Frontiers in Physiology · doi:10.3389/fphys.2019.00645 · Cited by 254 · see citing works

The role of exercise-induced myokines in regulating metabolism

Huh, J. Y. (2018) · Archives of Pharmacal Research · doi:10.1007/s12272-017-0994-y · Cited by 242 · see citing works

Secreted proteins from adipose tissue and skeletal muscle – adipokines, myokines and adipose/muscle cross-talk

Trayhurn, P., Drevon, C. A., & Eckel, J. (2011) · Archives of Physiology and Biochemistry · doi:10.3109/13813455.2010.535835 · Cited by 214 · see citing works

Browning of White Fat: Novel Insight Into Factors, Mechanisms, and Therapeutics: FAT BROWNING AND THEIR POTENTIAL AS THERAPEUTICS

Jeremic, N., Chaturvedi, P., & Tyagi, S. C. (2017) · Journal of Cellular Physiology · doi:10.1002/jcp.25450 · Cited by 211 · see citing works

The myokine decorin is regulated by contraction and involved in muscle hypertrophy

Kanzleiter, T., Rath, M., Görgens, S. W., Jensen, J., Tangen, D. S., Kolnes, A. J., Kolnes, K. J., Lee, S., Eckel, J., Schürmann, A., et al. (2014) · Biochemical and Biophysical Research Communications · doi:10.1016/j.bbrc.2014.06.123 · Cited by 209 · see citing works

Usability Issues of Clinical and Research Applications of Virtual Reality in Older People: A Systematic Review

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Identification and Validation of Novel Contraction-Regulated Myokines Released from Primary Human Skeletal Muscle Cells

Raschke, S., Eckardt, K., Bjørklund Holven, K., Jensen, J., & Eckel, J. (2013) · PLoS ONE · doi:10.1371/journal.pone.0062008 · Cited by 199 · see citing works

FGF21 as a Hepatokine, Adipokine, and Myokine in Metabolism and Diseases

Itoh, N. (2014) · Frontiers in Endocrinology · doi:10.3389/fendo.2014.00107 · Cited by 198 · see citing works

Exercise-Induced Myokines With Therapeutic Potential for Muscle Wasting

Piccirillo, R. (2019) · Frontiers in Physiology · doi:10.3389/fphys.2019.00287 · Cited by 190 · see citing works

Myonectin Is an Exercise-Induced Myokine That Protects the Heart From Ischemia-Reperfusion Injury

Otaka, N., Shibata, R., Ohashi, K., Uemura, Y., Kambara, T., Enomoto, T., Ogawa, H., Ito, M., Kawanishi, H., Maruyama, S., et al. (2018) · Circulation Research · doi:10.1161/circresaha.118.313777 · Cited by 189 · see citing works

Osteosarcopenia is more than sarcopenia and osteopenia alone

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Therapeutic impact of follistatin-like 1 on myocardial ischemic injury in preclinical models

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Disrupted Skeletal Muscle Mitochondrial Dynamics, Mitophagy, and Biogenesis during Cancer Cachexia: A Role for Inflammation

VanderVeen, B. N., Fix, D. K., & Carson, J. A. (2017) · Oxidative Medicine and Cellular Longevity · doi:10.1155/2017/3292087 · Cited by 182 · see citing works

Evolution of sarcopenia research

Janssen, I. (2010) · Applied Physiology, Nutrition, and Metabolism · doi:10.1139/h10-067 · Cited by 181 · see citing works

Factors associated with sarcopenia: A cross-sectional analysis using UK Biobank

Petermann-Rocha, F., Chen, M., Gray, S. R., Ho, F. K., Pell, J. P., & Celis-Morales, C. (2020) · Maturitas · doi:10.1016/j.maturitas.2020.01.004 · Cited by 172 · see citing works

Impact of Skeletal Muscle Mass on Metabolic Health

Kim, G., & Kim, J. H. (2020) · Endocrinology and Metabolism · doi:10.3803/enm.2020.35.1.1 · Cited by 171 · see citing works

Ectopic Expression of Myostatin Induces Atrophy of Adult Skeletal Muscle by Decreasing Muscle Gene Expression

Durieux, A., Amirouche, A., Banzet, S., Koulmann, N., Bonnefoy, R., Pasdeloup, M., Mouret, C., Bigard, X. A., Peinnequin, A., & Freyssenet, D. G. (2007) · Endocrinology · doi:10.1210/en.2006-1500 · Cited by 162 · see citing works

Exercise-Released Myokines in the Control of Energy Metabolism

Laurens, C., Bergouignan, A., & Moro, C. (2020) · Frontiers in Physiology · doi:10.3389/fphys.2020.00091 · Cited by 159 · see citing works

New insights into the pathogenesis and treatment of sarcopenia in chronic heart failure

Yin, J., Lü, X., Qian, Z., Xu, W., & Zhou, X. (2019) · Theranostics · doi:10.7150/thno.33000 · Cited by 155 · see citing works

Fibroblast growth factor 21 and browning of white adipose tissue

Cuevas-Ramos, D., Mehta, R., & Aguilar-Salinas, C. A. (2019) · Frontiers in Physiology · doi:10.3389/fphys.2019.00037 · Cited by 149 · see citing works

Sarcopenia, Frailty, and Diabetes in Older Adults

Jang, H. C. (2016) · Diabetes & Metabolism Journal · doi:10.4093/dmj.2016.40.3.182 · Cited by 138 · see citing works

Myokines in skeletal muscle physiology and metabolism: Recent advances and future perspectives

Das, D. K., Graham, Z. A., & Cardozo, C. P. (2020) · Acta Physiologica · doi:10.1111/apha.13367 · Cited by 129 · see citing works

Motoneuron Loss Is Associated With Sarcopenia

Drey, M., Krieger, B., Sieber, C. C., Bauer, J. M., Hettwer, S., Bertsch, T., Dahinden, P., Mäder, A., Vrijbloed, J. W., Schuster, G. M., et al. (2014) · Journal of the American Medical Directors Association · doi:10.1016/j.jamda.2014.02.002 · Cited by 126 · see citing works

A Key Role for Leukemia Inhibitory Factor in C26 Cancer Cachexia

Seto, D. N., Kandarian, S. C., & Jackman, R. W. (2015) · Journal of Biological Chemistry · doi:10.1074/jbc.m115.638411 · Cited by 123 · see citing works

The role of PGC‐1 coactivators in aging skeletal muscle and heart

Dillon, L. M., Rebelo, A. P., & Moraes, C. T. (2012) · IUBMB Life · doi:10.1002/iub.608 · Cited by 116 · see citing works

Serum myostatin levels and skeletal muscle wasting in chronic obstructive pulmonary disease

Ju, C., & Chen, R. (2011) · Respiratory Medicine · doi:10.1016/j.rmed.2011.07.016 · Cited by 114 · see citing works

An Overview of the Beneficial Effects of Exercise on Health and Performance

Krämer, A. (2020) · Advances in experimental medicine and biology · doi:10.1007/978-981-15-1792-1_1 · Cited by 114 · see citing works

No pain, no gain? The effects of pain-promoting neuropeptides and neurotrophins on fracture healing

Sun, S., Diggins, N. H., Gunderson, Z. J., Fehrenbacher, J. C., White, F. A., & Kacena, M. A. (2019) · Bone · doi:10.1016/j.bone.2019.115109 · Cited by 106 · see citing works

On the Definition of Sarcopenia in the Presence of Aging and Obesity—Initial Results from UK Biobank

Linge, J., Heymsfield, S. B., & Dahlqvist Leinhard, O. (2020) · The Journals of Gerontology: Series A · doi:10.1093/gerona/glz229 · Cited by 103 · see citing works

Sustained Elevation of Circulating Growth and Differentiation Factor-15 and a Dynamic Imbalance in Mediators of Muscle Homeostasis Are Associated With the Development of Acute Muscle Wasting Following Cardiac Surgery*

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Role of myokines in the development of skeletal muscle insulin resistance and related metabolic defects in type 2 diabetes

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Sarcopenia and cardiovascular risk indices in patients with chronic kidney disease on conservative and replacement therapy

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Prevalência e fatores associados à sarcopenia, dinapenia e sarcodinapenia em idosos residentes no Município de São Paulo - Estudo SABE

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Sarcopenia and physical function are associated with inflammation and arteriosclerosis in community-dwelling people: The Yakumo study

Hida, T., Imagama, S., Ando, K., Kobayashi, K., Muramoto, A., Ito, K., Ishikawa, Y., Tsushima, M., Nishida, Y., Ishiguro, N., et al. (2017) · Modern Rheumatology · doi:10.1080/14397595.2017.1349058 · Cited by 84 · see citing works

Effects of 12 Weeks Resistance Training on Serum Irisin in Older Male Adults

Zhao, J., Su, Z., Qu, C., & Dong, Y. (2017) · Frontiers in Physiology · doi:10.3389/fphys.2017.00171 · Cited by 82 · see citing works

Circulating Irisin and Myostatin as Markers of Muscle Strength and Physical Condition in Elderly Subjects

Planella-Farrugia, C., Comas, F., Sabater, M., Moreno, M., Moreno‐Navarrete, J. M., Rovira, O., Ricart, W., & Fernández‐Real, J. M. (2019) · Frontiers in Physiology · doi:10.3389/fphys.2019.00871 · Cited by 74 · see citing works

Adropin and irisin in arterial hypertension, diabetes mellitus and chronic kidney disease

Maciorkowska, M., Musiałowska, D., & Małyszko, J. (2019) · Advances in Clinical and Experimental Medicine · doi:10.17219/acem/104551 · Cited by 72 · see citing works

Iron Metabolism of the Skeletal Muscle and Neurodegeneration

Hałoń, M., Borkowska, A., Herman-Antosiewicz, A., & Antosiewicz, J. (2019) · Frontiers in Neuroscience · doi:10.3389/fnins.2019.00165 · Cited by 69 · see citing works

If my muscle could talk: Myokines as a biomarker of frailty

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Serum and muscle interleukin-15 levels decrease in aging mice: Correlation with declines in soluble interleukin-15 receptor alpha expression

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Musclin, A Myokine Induced by Aerobic Exercise, Retards Muscle Atrophy During Cancer Cachexia in Mice

Re Cecconi, A. D., Forti, M., Chiappa, M., Zhu, Z., Zingman, L. V., Cervo, L., Beltrame, L., Marchini, S., & Piccirillo, R. (2019) · Cancers · doi:10.3390/cancers11101541 · Cited by 66 · see citing works

Interval exercise training increases LIF expression and prevents myocardial infarction-induced skeletal muscle atrophy in rats

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Myokines as possible therapeutic targets in cancer cachexia

Manole, E., Ceafalan, L. C., Popescu, B. O., Dumitru, C., & Bastian, A. E. (2018) · Journal of Immunology Research · doi:10.1155/2018/8260742 · Cited by 60 · see citing works

Serum myostatin levels are independently associated with skeletal muscle wasting in patients with heart failure

Furihata, T., Kinugawa, S., Fukushima, A., Takada, S., Homma, T., Masaki, Y., Abe, T., Yokota, T., Oba, K., Okita, K., et al. (2016) · International Journal of Cardiology · doi:10.1016/j.ijcard.2016.06.231 · Cited by 59 · see citing works

Inhibition of the myostatin/Smad signaling pathway by short decorin-derived peptides

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Myostatin and Insulin-Like Growth Factor 1 Are Biomarkers of Muscle Strength, Muscle Mass, and Mortality in Patients on Hemodialysis

Delanaye, P., Bataille, S., Quinonez, K., Buckinx, F., Warling, X., Krzesinski, J.-M., Pottel, H., Burtey, S., Bruyère, O., & Cavalier, E. (2019) · Journal of Renal Nutrition · doi:10.1053/j.jrn.2018.11.010 · Cited by 54 · see citing works

Growth Differentiation Factor-15 (GDF-15) Is a Biomarker of Muscle Wasting and Renal Dysfunction in Preoperative Cardiovascular Surgery Patients

Nakajima, T., Shibasaki, I., Sawaguchi, T., Haruyama, A., Kaneda, H., Nakajima, T., Hasegawa, T., Arikawa, T., Obi, S., Sakuma, M., et al. (2019) · Journal of Clinical Medicine · doi:10.3390/jcm8101576 · Cited by 52 · see citing works

The prevalence of sarcopenia and subtypes in cardiovascular diseases, and a new diagnostic approach

Sasaki, K., Kakuma, T., Sasaki, M., Ishizaki, Y., Fukami, A., Enomoto, M., Adachi, H., Matsuse, H., Shiba, N. N., Ueno, T., et al. (2020) · Journal of Cardiology · doi:10.1016/j.jjcc.2020.03.004 · Cited by 50 · see citing works

Lower irisin levels in coronary artery disease: a meta-analysis

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Sarcopenic obesity in fatty liver

Merli, M., Lattanzi, B., & Aprile, F. (2019) · Current Opinion in Clinical Nutrition & Metabolic Care · doi:10.1097/mco.0000000000000558 · Cited by 48 · see citing works

Effect of exercise intensity on circulating hepatokine concentrations in healthy men

Willis, S. A., Sargeant, J. A., Thackray, A. E., Yates, T. E., Stensel, D. J., Aithal, G. P., & King, J. A. (2019) · Applied Physiology, Nutrition, and Metabolism · doi:10.1139/apnm-2018-0818 · Cited by 48 · see citing works

Association of Sarcopenia with Metabolic Syndrome in Korean Population Using 2009–2010 Korea National Health and Nutrition Examination Survey

Park, S., Ryu, S. Y., Park, J., & Choi, S.-W. (2019) · Metabolic Syndrome and Related Disorders · doi:10.1089/met.2019.0059 · Cited by 48 · see citing works

Organokines in disease

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Apelin promotes hepatic fibrosis through ERK signaling in LX-2 cells

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The role of decorin in cardiovascular diseases: more than just a decoration

Vu, T. T., Marquez, J. C., Long, L. T., Nguyen, A. T. T., Kim, H. K., & Han, J. (2018) · Free Radical Research · doi:10.1080/10715762.2018.1516285 · Cited by 44 · see citing works

Protective Roles of Adipocytokines and Myokines in Cardiovascular Disease

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Targeting mitochondrial quality control for treating sarcopenia: lessons from physical exercise

Picca, A., Calvani, R., Leeuwenburgh, C., Coelho‐Júnior, H. J., Bernabei, R., Landi, F., & Marzetti, E. (2018) · Expert Opinion on Therapeutic Targets · doi:10.1080/14728222.2019.1559827 · Cited by 42 · see citing works

Prestroke Sarcopenia and Stroke Severity in Elderly Patients with Acute Stroke

Nozoe, M., Kanai, M., Kubo, H., Yamamoto, M., Shimada, S., & Mase, K. (2019) · Journal of Stroke and Cerebrovascular Diseases · doi:10.1016/j.jstrokecerebrovasdis.2019.05.001 · Cited by 42 · see citing works

Angiogenin and Osteoprotegerin are type II muscle specific myokines protecting pancreatic beta-cells against proinflammatory cytokines

Rütti, S., Dusaulcy, R., Hansen, J. S., Howald, C., Dermitzakis, E. T., Pedersen, B. K., Pinget, M., Plomgaard, P., & Bouzakri, K. (2018) · Scientific Reports · doi:10.1038/s41598-018-28117-2 · Cited by 41 · see citing works

The Timed Up and Go test and the ageing heart: Findings from a national health screening of 1,084,875 community-dwelling older adults

Chun, S., Shin, D. W., Han, K., Jung, J., Kim, B., Jung, H., Son, K. Y., Lee, S., & Lee, S. (2019) · European Journal of Preventive Cardiology · doi:10.1177/2047487319882118 · Cited by 41 · see citing works

The brown bear as a translational model for sedentary lifestyle‐related diseases

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Exercise-induced myokines: a brief review of controversial issues of this decade

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Sarcopenia and sarcopenic obesity as prognostic predictors in hospitalized elderly patients with acute myocardial infarction

Santana, N. D. M., Mendes, R. M. L., da Silva, N. F., & Pinho, C. P. S. (2019) · Einstein (São Paulo) · doi:10.31744/einstein_journal/2019ao4632 · Cited by 37 · see citing works

Role of irisin in androgen-deficient muscle wasting and osteopenia in mice

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Association between reduced brain-derived neurotrophic factor concentration & coronary heart disease

Šustar, A., Perkovic, M. N., Erjavec, G. N., Strac, D. S., & Pivac, N. (2019) · The Indian Journal of Medical Research · doi:10.4103/ijmr.ijmr_1566_17 · Cited by 37 · see citing works

Updated concept of sarcopenia based on muscle–bone relationship

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Exercise and Cardiovascular Protection

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Relación entre los niveles de actividad física y la condición física autopercibida en una muestra de estudiantes universitarios en Bogotá, Colombia

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Muskeltraining – ein universelles Medikament

Laube, W. (2021) · Manuelle Medizin · doi:10.1007/s00337-021-00801-x · Cited by 8 · see citing works

Alterations in the Myokine Concentrations in Relation to Sarcopenia and Sleep Disturbances: A Narrative Review

Knapik, M., Kuna, J., Chmielewski, G., Jaśkiewicz, Ł., & Krajewska–Włodarczyk, M. (2025) · Journal of Clinical Medicine · doi:10.3390/jcm14186527 · Cited by 7 · see citing works

Organokine-Mediated Crosstalk: A Systems Biology Perspective on the Pathogenesis of MASLD—A Narrative Review

Barbalho, S. M., Laurindo, L. F., Valenti, V. E., Méndez‐Sánchez, N., Ramírez-Mejía, M. M., & Goulart, R. D. Á. (2025) · International Journal of Molecular Sciences · doi:10.3390/ijms262311547 · Cited by 7 · see citing works

Comparison irisin peptide serum level in pregnant women with and without gestational diabetes mellitus: A case–control study

Khorasani, Z. M., Besharat, M., Mehrad‐Majd, H., Mohammadi, S. A., & Mahmoudinia, M. (2022) · Endocrinology Diabetes & Metabolism · doi:10.1002/edm2.370 · Cited by 7 · see citing works

Sarcopenia predicts cardiovascular disease in chronic kidney disease at advanced stage and associated risks

Xuan, Y., Pang, S., Xie, W., He, R., Li, Q., & Yuan, J. (2023) · Medicine · doi:10.1097/md.0000000000035976 · Cited by 6 · see citing works

Total and Regional Changes in Body Composition in Metastatic Hormone-sensitive Prostate Cancer Patients Randomized to Receive Androgen Deprivation + Enzalutamide ± Zoledronic Acid. The BONENZA Study

Buffoni, M., Volta, A. D., Valcamonico, F., Bergamini, M., Caramella, I., D'Apollo, D., Zivi, A., Procopio, G., Sepe, P., Conte, G. D., et al. (2025) · European Urology Oncology · doi:10.1016/j.euo.2025.02.006 · Cited by 6 · see citing works

Eight Weeks of Aerobic Exercise Training Improves Fitness, Metabolic Health, Inflammation, and Intestinal Barrier Integrity in Overweight and Obese Women of Different Age Groups

Lee, T., Lee, H.-I., Roh, H., & Cho, S.-Y. (2025) · Life · doi:10.3390/life15111752 · Cited by 6 · see citing works

Progress in the Identification and Management of Protein-Energy Wasting and Sarcopenia in Chronic Kidney Disease

Workeneh, B., Kalantar‐Zadeh, K., & Moore, L. W. (2021) · Journal of Renal Nutrition · doi:10.1053/j.jrn.2021.04.004 · Cited by 6 · see citing works

Anthropometric, muscle and serum myokine levels effects of physical exercise with an online platform in female patients with obesity

Primo, D., Izaola, O., Gómez, J. J. L., & de Luis, D. A. (2023) · Endocrinología Diabetes y Nutrición · doi:10.1016/j.endinu.2023.04.002 · Cited by 6 · see citing works

Yangxinshi tablet protects against myocardial injury and increases skeletal muscle exercise capacity by regulating mitochondrial bioenergetics

Song, H., Liu, C., Yang, Z., Liu, D., Li, J., Mei, Z., Xu, J., Pan, J., Zhang, X., Yan, C., et al. (2025) · Phytomedicine · doi:10.1016/j.phymed.2025.156990 · Cited by 5 · see citing works

Der Muskulatur mehr Aufmerksamkeit schenken!

Laube, W. (2021) · Manuelle Medizin · doi:10.1007/s00337-021-00821-7 · Cited by 5 · see citing works

Systematic training in master swimmer athletes increases serum insulin growth factor-1 and decreases myostatin and irisin levels

Curiel-Cervantes, V., Solís‐S, J. C., Camacho-Barrón, M., Aguilar-Galarza, A., Valencia, M. E., & Anaya‐Loyola, M. A. (2022) · Growth Factors · doi:10.1080/08977194.2022.2049262 · Cited by 5 · see citing works

Sarcopenia and cardiovascular disease in patients with and without kidney disease: what do we know?

Güngör, Ö., Sevinç, M., Sena Memnune, U. L. U., & Kocyigit, I. D. (2022) · International Urology and Nephrology · doi:10.1007/s11255-022-03393-0 · Cited by 5 · see citing works

Low Lean Tissue Index and Muscle Strength Combined with High Fat Tissue Index Are Associated with Cardiovascular Disease-Related Hospitalisation in Patients on Haemodialysis

Tian, M., Lan, Q., Yuan, J., He, P., Yu, F., Long, C., & Zha, Y. (2023) · Cardiorenal Medicine · doi:10.1159/000534399 · Cited by 5 · see citing works

The Role of Sarcopenia in Heart Failure with Depression

Wang, R., Duan, J., Liu, W., Huang, K., Chen, Z., Yang, C., & Yang, L. (2022) · Reviews in Cardiovascular Medicine · doi:10.31083/j.rcm2309296 · Cited by 5 · see citing works

State-of-the-art insights into myokines as biomarkers of sarcopenia: a literature review

Moussaoui, O. R. (2025) · International Journal of Physiology Pathophysiology and Pharmacology · doi:10.62347/rneq8696 · Cited by 4 · see citing works

Cardioprotective and hypotensive mechanistic insights of hydroethanolic extract of Cucumis melo L. kernels in isoprenaline-induced cardiotoxicity based on metabolomics and in silico electrophysiological models

Wahid, M., Saqib, F., Abbas, G., Shah, S., Alshammari, A., Albekairi, T. H., Ali, A., Khurm, M., & Mubarak, M. S. (2024) · Frontiers in Pharmacology · doi:10.3389/fphar.2023.1277594 · Cited by 4 · see citing works

The effect of different exercise types on migraine frequency in individuals with migraine: A pilot study

Meydanal, Y. E., Şenışık, S., & ŞİRİN, H. (2025) · Headache The Journal of Head and Face Pain · doi:10.1111/head.14951 · Cited by 4 · see citing works

Vasodilator Dysfunction in Human Obesity: Established and Emerging Mechanisms

Schinzari, F., Tesauro, M., & Cardillo, C. (2021) · Journal of Cardiovascular Pharmacology · doi:10.1097/fjc.0000000000001108 · Cited by 5 · see citing works

Free fatty acids are associated with muscle dysfunction in Chinese adults with type 2 diabetes

Fu, J., Sun, L., Mu, Z., & Xiu, S. (2022) · Endocrine · doi:10.1007/s12020-022-03053-4 · Cited by 4 · see citing works

Teil 2: Muskeldysfunktionen – mit Training gegen Schmerz

Laube, W. (2022) · Man and medicine · doi:10.1007/s00337-022-00887-x

How Sarcopenia, Muscle Mass, Strength, and Performance Relate to Non-Alcoholic Fatty Liver Disease: A Systematic Review

Rigor, J., Monteiro‐Soares, M., Barata, P., & Martins‐Mendes, D. (2024) · Sci · doi:10.3390/sci6040059 · Cited by 4 · see citing works

Effect of Dynamic and Static Load on the Concentration of Myokines in the Blood Plasma and Content of Sodium and Potassium in Mouse Skeletal Muscles

Кироненко, Т. А., Милованова, К. Г., Zakharova, A. N., Sidorenko, S. V., Климанова, Е. А., Dyakova, E. Y., Орлова, А. А., Negodenko, E. S., Kalinnikova, J. G., Orlov, S. N., et al. (2021) · Biochemistry (Moscow) · doi:10.1134/s0006297921030123 · Cited by 4 · see citing works

Impact of simple equation for estimating appendicular skeletal muscle mass in patients with stable coronary artery disease undergoing percutaneous coronary intervention

Nishio, R., Dohi, T., Fukase, T., Takeuchi, M., Takahashi, N., Endo, H., Doi, S., Okai, I., Iwata, H., Okazaki, S., et al. (2022) · IJC Heart & Vasculature · doi:10.1016/j.ijcha.2022.101163 · Cited by 6 · see citing works

Research trends and hotspot evolution of exercise-regulated myokines: a bibliometric analysis from 2003 to 2023

Sun, Z., Wu, Z., Zhu, L., Li, X., Xu, D., Tian, X., & Mao, D. (2024) · Frontiers in Physiology · doi:10.3389/fphys.2024.1410068 · Cited by 5 · see citing works

Association Between Appendicular Skeletal Muscle Mass and Myocardial Glucose Uptake Measured by 18F-FDG PET

Kim, Y., Kim, D., Kim, J., Yun, M., & Kang, E. S. (2024) · ESC Heart Failure · doi:10.1002/ehf2.15086 · Cited by 3 · see citing works

Bioinformatics analysis based on microarray data reveals molecular crosstalk and immune relationship between sarcopenia and atherosclerosis

Yang, J., Zhong, J., Du, Y., Liu, J., Li, Z., & Liu, Y. (2025) · Experimental Gerontology · doi:10.1016/j.exger.2025.112811 · Cited by 3 · see citing works

Exercise as a protagonist in muscle plasticity and in the muscle as an endocrine organ: implications in chronic diseases

Vargas-Pacheco, A., & Correa-López, L. E. (2021) · Revista de la Facultad de Medicina Humana · doi:10.25176/rfmh.v22i1.4129 · Cited by 3 · see citing works

Resistance Band Exercise: An Effective Strategy to Reverse Cardiometabolic Disorders in Women With Osteosarcopenic Obesity

Banitalebi, E., Banitalebi, E., Ghahfarrokhi, M. M., Rahimi, M., Laher, I., & Davison, K. (2023) · Journal of Aging and Physical Activity · doi:10.1123/japa.2022-0241 · Cited by 3 · see citing works

Sarcopenia and Cardiovascular Diseases in Individuals With Diabetes or Prediabetes

Wang, X., Zeng, Q., Yu, X., & Li, S. (2025) · Journal of Clinical Hypertension · doi:10.1111/jch.70024 · Cited by 3 · see citing works

Metabolic Syndrome and Metabolic Dysfunction‐Associated Fatty Liver Disease

Koo, B. K., & Lim, S. K. (2022) · Wiley eBooks · doi:10.1002/9781119695257.ch13 · Cited by 3 · see citing works

Exercise interventions for mitigating the persistent side effects of COVID-19

Gupta, S., Liu, K. R., Sandhu, S., & Gupta, A. (2024) · Sport Sciences for Health · doi:10.1007/s11332-024-01269-7 · Cited by 2 · see citing works

Veränderungen der Struktur der autochtonen Muskulatur bei Personen mit einem „low back pain“: ein systematisches Review mit Metaanalyse

Laube, W. (2024) · Manuelle Medizin · doi:10.1007/s00337-024-01117-2 · Cited by 2 · see citing works

Exercise-induced changes in systemic inflammatory biomarkers in overweight and obese populations: a bibliometric analysis and umbrella review of meta-analyses

Chen, L., Li, A., Zhou, X., Chen, W., Zhou, Y., Wang, R., Kou, Y., & Zhou, J. (2026) · Frontiers in Immunology · doi:10.3389/fimmu.2026.1838118 · Cited by 2 · see citing works

Modifikatoren der Wirkungen eines systematischen sensomotorischen Trainings bei chronischem „low back pain“

Laube, W. (2026) · Manuelle Medizin · doi:10.1007/s00337-026-01254-w · Cited by 2 · see citing works

Comparison of the Two Algorithms of Skeletal Muscle Mass Index: An Observational Study in a Large Cohort of Chinese Adults

Sui, Y., Huang, Z., Dong, S.-Y., & Zheng, Y. (2022) · Health · doi:10.4236/health.2022.148063 · Cited by 2 · see citing works

Sarcopenia and myokines profile as risk factors in cardiovascular diseases?

Ciołkiewicz, M., Kuryliszyn-Moskal, A., Hryniewicz, A., & Kamiński, K. A. (2019) · Postępy Higieny i Medycyny Doświadczalnej · doi:10.5604/01.3001.0013.5442 · Cited by 1 · see citing works

Myokines in Aging Muscle

Brown, K., Persinger, A., & Puppa, M. (2019) · CRC Press eBooks · doi:10.1201/9780429155260-7

Myokine, a key cytokine for physical exercise to alleviate sarcopenic obesity

Zhang, L., Lv, J., Wang, C., Ren, Y., & Ming, Y. (2022) · Molecular Biology Reports · doi:10.1007/s11033-022-07821-3 · Cited by 32 · see citing works

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

Myokine Regulation as Marker of Sarcopenia in Elderly

Aryana, I. G. P. S., Hapsari, A. A. A. R., & Kuswardhani, R. A. T. (2018) · Molecular and Cellular Biomedical Sciences · doi:10.21705/mcbs.v2i2.32 · Cited by 18 · see citing works