Exercise as a Modulator of Biological Age: The Role of Epigenetic Clocks in Assessing Exercise-Induced Rejuvenation – A Narrative Review
DOI:
https://doi.org/10.12775/QS.2026.76.76073Keywords
biological age, epigenetic clocs, DNA methylation, physical activity, exercise, healthy agingAbstract
Background: Biological age is increasingly recognized as a valuable indicator of the aging process. Compared with chronological age, it may provide a more accurate representation of an individual’s health status and disease risk. DNA methylation–based epigenetic clocks are among the most widely used biomarkers of biological aging.
Aim: This narrative review aimed to summarize the current evidence on the association between physical activity and epigenetic aging and to evaluate the potential role of exercise as a modulator of biological age.
Materials and methods: PubMed and Embase databases were searched from their inception through July 2026 using a combination of relevant keywords. A total of 79 studies were included in the review.
Results: Current evidence indicates that higher levels of physical activity and physical fitness are generally associated with a lower rate of epigenetic aging and more favorable biological aging profiles. Aerobic exercise is the most extensively studied modality and demonstrates the most consistent associations with slower biological aging. Resistance training, high-intensity interval training, and multicomponent exercise programs may also exert beneficial effects through mechanisms involving mitochondrial function, regulation of inflammation, metabolic adaptation, and epigenetic remodeling. However, the findings remain heterogeneous due to differences in study populations, exercise protocols, follow-up durations, and the epigenetic clocks employed.
Conclusions: Physical activity appears to be a promising, modifiable factor influencing biological aging. Accumulating evidence suggests that regular exercise may contribute to slower epigenetic aging and enhanced physiological resilience. Nevertheless, the magnitude and clinical significance of exercise-induced changes in epigenetic age remain incompletely understood. Further research is warranted.
References
1. Gianfredi, V., Nucci, D., Pennisi, F., Maggi, S., Veronese, N., & Soysal, P. (2025). Aging, longevity, and healthy aging: the public health approach. Aging clinical and experimental research, 37(1), 125. https://doi.org/10.1007/s40520-025-03021-8
2. Khan, H. T. A., Addo, K. M., & Findlay, H. (2024). Public Health Challenges and Responses to the Growing Ageing Populations. Public health challenges, 3(3), e213. https://doi.org/10.1002/puh2.213
3. Crimmins E. M. (2015). Lifespan and Healthspan: Past, Present, and Promise. The Gerontologist, 55(6), 901–911. https://doi.org/10.1093/geront/gnv130
4. Cocchi, C., Zazzara, M. B., Levati, E., Calvani, R., & Onder, G. (2025). How to promote healthy aging across the life cycle. European journal of internal medicine, 135, 5–13. https://doi.org/10.1016/j.ejim.2025.03.003
5. Mathur, A., Taurin, S., & Alshammary, S. (2024). New insights into methods to measure biological age: a literature review. Frontiers in aging, 5, 1395649. https://doi.org/10.3389/fragi.2024.1395649
6. Bafei, S. E. C., & Shen, C. (2023). Biomarkers selection and mathematical modeling in biological age estimation. npj aging, 9(1), 13. https://doi.org/10.1038/s41514-023-00110-8
7. Li, Z., Zhang, W., Duan, Y., Niu, Y., Chen, Y., Liu, X., Dong, Z., Zheng, Y., Chen, X., Feng, Z., Wang, Y., Zhao, D., Sun, X., Cai, G., Jiang, H., & Chen, X. (2023). Progress in biological age research. Frontiers in public health, 11, 1074274. https://doi.org/10.3389/fpubh.2023.1074274
8. Akeju, O., Mens, M. M. J., Warmerdam, R., Dijkema, M., van den Biggelaar, A. H. J., Franke, L., Goudsmit, J., & Wu, J. W. (2024). Genetic Correlates of Biological Aging and the Influence on Prediction of Mortality. The journals of gerontology. Series A, Biological sciences and medical sciences, 79(4), glae024. https://doi.org/10.1093/gerona/glae024
9. Min, M., Egli, C., Dulai, A. S., & Sivamani, R. K. (2024). Critical review of aging clocks and factors that may influence the pace of aging. Frontiers in aging, 5, 1487260. https://doi.org/10.3389/fragi.2024.1487260
10. Horvath S. (2013). DNA methylation age of human tissues and cell types. Genome biology, 14(10), R115. https://doi.org/10.1186/gb-2013-14-10-r115
11. Hannum, G., Guinney, J., Zhao, L., Zhang, L., Hughes, G., Sadda, S., Klotzle, B., Bibikova, M., Fan, J. B., Gao, Y., Deconde, R., Chen, M., Rajapakse, I., Friend, S., Ideker, T., & Zhang, K. (2013). Genome-wide methylation profiles reveal quantitative views of human aging rates. Molecular cell, 49(2), 359–367. https://doi.org/10.1016/j.molcel.2012.10.016
12. Levine, M. E., Lu, A. T., Quach, A., Chen, B. H., Assimes, T. L., Bandinelli, S., Hou, L., Baccarelli, A. A., Stewart, J. D., Li, Y., Whitsel, E. A., Wilson, J. G., Reiner, A. P., Aviv, A., Lohman, K., Liu, Y., Ferrucci, L., & Horvath, S. (2018). An epigenetic biomarker of aging for lifespan and healthspan. Aging, 10(4), 573–591. https://doi.org/10.18632/aging.101414
13. Lu, A. T., Quach, A., Wilson, J. G., Reiner, A. P., Aviv, A., Raj, K., Hou, L., Baccarelli, A. A., Li, Y., Stewart, J. D., Whitsel, E. A., Assimes, T. L., Ferrucci, L., & Horvath, S. (2019). DNA methylation GrimAge strongly predicts lifespan and healthspan. Aging, 11(2), 303–327. https://doi.org/10.18632/aging.101684
14. Belsky, D. W., Caspi, A., Corcoran, D. L., Sugden, K., Poulton, R., Arseneault, L., Baccarelli, A., Chamarti, K., Gao, X., Hannon, E., Harrington, H. L., Houts, R., Kothari, M., Kwon, D., Mill, J., Schwartz, J., Vokonas, P., Wang, C., Williams, B. S., & Moffitt, T. E. (2022). DunedinPACE, a DNA methylation biomarker of the pace of aging. eLife, 11, e73420. https://doi.org/10.7554/eLife.73420
15. Grolaux, R., Jones-Freeman, B., Jacques, M., & Eynon, N. (2024). The benefits of exercise on aging: focus on muscle biomarkers. Aging, 16(15), 11482–11483. https://doi.org/10.18632/aging.206064
16. Qiu, Y., Fernández-García, B., Lehmann, H. I., Li, G., Kroemer, G., López-Otín, C., & Xiao, J. (2025). Exercise attenuates the hallmarks of aging: Novel perspectives. Journal of sport and health science, 15, 101108. Advance online publication. https://doi.org/10.1016/j.jshs.2025.101108
17. López-Otín, C., Blasco, M. A., Partridge, L., Serrano, M., & Kroemer, G. (2023). Hallmarks of aging: An expanding universe. Cell, 186(2), 243–278. https://doi.org/10.1016/j.cell.2022.11.001
18. Zhang, J., Tian, Z., Qin, C., & Momeni, M. R. (2024). The effects of exercise on epigenetic modifications: focus on DNA methylation, histone modifications and non-coding RNAs. Human cell, 37(4), 887–903. https://doi.org/10.1007/s13577-024-01057-y
19. Etayo-Urtasun, P., Sáez de Asteasu, M. L., & Izquierdo, M. (2024). Effects of Exercise on DNA Methylation: A Systematic Review of Randomized Controlled Trials. Sports medicine (Auckland, N.Z.), 54(8), 2059–2069. https://doi.org/10.1007/s40279-024-02033-0
20. Moqri, M., Herzog, C., Poganik, J. R., Biomarkers of Aging Consortium, Justice, J., Belsky, D. W., Higgins-Chen, A., Moskalev, A., Fuellen, G., Cohen, A. A., Bautmans, I., Widschwendter, M., Ding, J., Fleming, A., Mannick, J., Han, J. J., Zhavoronkov, A., Barzilai, N., Kaeberlein, M., Cummings, S., … Gladyshev, V. N. (2023). Biomarkers of aging for the identification and evaluation of longevity interventions. Cell, 186(18), 3758–3775. https://doi.org/10.1016/j.cell.2023.08.003
21. Furrer, R., & Handschin, C. (2025). Biomarkers of aging: from molecules and surrogates to physiology and function. Physiological reviews, 105(3), 1609–1694. https://doi.org/10.1152/physrev.00045.2024
22. Horvath, S., & Raj, K. (2018). DNA methylation-based biomarkers and the epigenetic clock theory of ageing. Nature reviews. Genetics, 19(6), 371–384. https://doi.org/10.1038/s41576-018-0004-3
23. Teschendorff, A. E., & Horvath, S. (2025). Epigenetic ageing clocks: statistical methods and emerging computational challenges. Nature reviews. Genetics, 26(5), 350–368. https://doi.org/10.1038/s41576-024-00807-w
24. Moqri, M., Poganik, J. R., Horvath, S., & Gladyshev, V. N. (2025). What makes biological age epigenetic clocks tick. Nature aging, 5(3), 335–336. https://doi.org/10.1038/s43587-025-00833-1
25. Tong, H., Dwaraka, V. B., Chen, Q., Luo, Q., Lasky-Su, J. A., Smith, R., & Teschendorff, A. E. (2024). Quantifying the stochastic component of epigenetic aging. Nature aging, 4(6), 886–901. https://doi.org/10.1038/s43587-024-00600-8
26. Tomusiak, A., Floro, A., Tiwari, R., Riley, R., Matsui, H., Andrews, N., Kasler, H. G., & Verdin, E. (2024). Development of an epigenetic clock resistant to changes in immune cell composition. Communications biology, 7(1), 934. https://doi.org/10.1038/s42003-024-06609-4
27. Chen, B. H., Marioni, R. E., Colicino, E., Peters, M. J., Ward-Caviness, C. K., Tsai, P. C., Roetker, N. S., Just, A. C., Demerath, E. W., Guan, W., Bressler, J., Fornage, M., Studenski, S., Vandiver, A. R., Moore, A. Z., Tanaka, T., Kiel, D. P., Liang, L., Vokonas, P., Schwartz, J., … Horvath, S. (2016). DNA methylation-based measures of biological age: meta-analysis predicting time to death. Aging, 8(9), 1844–1865. https://doi.org/10.18632/aging.101020
28. Horvath, S., & Levine, A. J. (2015). HIV-1 Infection Accelerates Age According to the Epigenetic Clock. The Journal of infectious diseases, 212(10), 1563–1573. https://doi.org/10.1093/infdis/jiv277
29. Quach, A., Levine, M. E., Tanaka, T., Lu, A. T., Chen, B. H., Ferrucci, L., Ritz, B., Bandinelli, S., Neuhouser, M. L., Beasley, J. M., Snetselaar, L., Wallace, R. B., Tsao, P. S., Absher, D., Assimes, T. L., Stewart, J. D., Li, Y., Hou, L., Baccarelli, A. A., Whitsel, E. A., … Horvath, S. (2017). Epigenetic clock analysis of diet, exercise, education, and lifestyle factors. Aging, 9(2), 419–446. https://doi.org/10.18632/aging.101168
30. López-Otín, C., Blasco, M. A., Partridge, L., Serrano, M., & Kroemer, G. (2013). The hallmarks of aging. Cell, 153(6), 1194–1217. https://doi.org/10.1016/j.cell.2013.05.039
31. Franceschi, C., Garagnani, P., Parini, P., Giuliani, C., & Santoro, A. (2018). Inflammaging: a new immune-metabolic viewpoint for age-related diseases. Nature reviews. Endocrinology, 14(10), 576–590. https://doi.org/10.1038/s41574-018-0059-4
32. Furman, D., Campisi, J., Verdin, E., Carrera-Bastos, P., Targ, S., Franceschi, C., Ferrucci, L., Gilroy, D. W., Fasano, A., Miller, G. W., Miller, A. H., Mantovani, A., Weyand, C. M., Barzilai, N., Goronzy, J. J., Rando, T. A., Effros, R. B., Lucia, A., Kleinstreuer, N., & Slavich, G. M. (2019). Chronic inflammation in the etiology of disease across the life span. Nature medicine, 25(12), 1822–1832. https://doi.org/10.1038/s41591-019-0675-0
33. Gleeson, M., Bishop, N. C., Stensel, D. J., Lindley, M. R., Mastana, S. S., & Nimmo, M. A. (2011). The anti-inflammatory effects of exercise: mechanisms and implications for the prevention and treatment of disease. Nature reviews. Immunology, 11(9), 607–615. https://doi.org/10.1038/nri3041
34. Pedersen, B. K., & Saltin, B. (2015). Exercise as medicine - evidence for prescribing exercise as therapy in 26 different chronic diseases. Scandinavian journal of medicine & science in sports, 25 Suppl 3, 1–72. https://doi.org/10.1111/sms.12581
35. Konopka, A. R., & Sreekumaran Nair, K. (2013). Mitochondrial and skeletal muscle health with advancing age. Molecular and cellular endocrinology, 379(1-2), 19–29. https://doi.org/10.1016/j.mce.2013.05.008
36. Hood, D. A., Memme, J. M., Oliveira, A. N., & Triolo, M. (2019). Maintenance of Skeletal Muscle Mitochondria in Health, Exercise, and Aging. Annual review of physiology, 81, 19–41. https://doi.org/10.1146/annurev-physiol-020518-114310
37. Egan, B., & Zierath, J. R. (2013). Exercise metabolism and the molecular regulation of skeletal muscle adaptation. Cell metabolism, 17(2), 162–184. https://doi.org/10.1016/j.cmet.2012.12.012
38. Robinson, M. M., Dasari, S., Konopka, A. R., Johnson, M. L., Manjunatha, S., Esponda, R. R., Carter, R. E., Lanza, I. R., & Nair, K. S. (2017). Enhanced Protein Translation Underlies Improved Metabolic and Physical Adaptations to Different Exercise Training Modes in Young and Old Humans. Cell metabolism, 25(3), 581–592. https://doi.org/10
39. Barrès, R., Yan, J., Egan, B., Treebak, J. T., Rasmussen, M., Fritz, T., Caidahl, K., Krook, A., O'Gorman, D. J., & Zierath, J. R. (2012). Acute exercise remodels promoter methylation in human skeletal muscle. Cell metabolism, 15(3), 405–411. https://doi.org/10.1016/j.cmet.2012.01.001
40. Radak, Z., Zhao, Z., Koltai, E., Ohno, H., & Atalay, M. (2013). Oxygen consumption and usage during physical exercise: the balance between oxidative stress and ROS-dependent adaptive signaling. Antioxidants & redox signaling, 18(10), 1208–1246. https://doi.org/10.1089/ars.2011.4498
41. Powers, S. K., & Jackson, M. J. (2008). Exercise-induced oxidative stress: cellular mechanisms and impact on muscle force production. Physiological reviews, 88(4), 1243–1276. https://doi.org/10.1152/physrev.00031.2007
42. Merry, T. L., & Ristow, M. (2016). Do antioxidant supplements interfere with skeletal muscle adaptation to exercise training?. The Journal of physiology, 594(18), 5135–5147. https://doi.org/10.1113/JP270654
43. Ristow, M., Zarse, K., Oberbach, A., Klöting, N., Birringer, M., Kiehntopf, M., Stumvoll, M., Kahn, C. R., & Blüher, M. (2009). Antioxidants prevent health-promoting effects of physical exercise in humans. Proceedings of the National Academy of Sciences of the United States of America, 106(21), 8665–8670. https://doi.org/10.1073/pnas.0903485106
44. Levine, B., & Kroemer, G. (2019). Biological Functions of Autophagy Genes: A Disease Perspective. Cell, 176(1-2), 11–42. https://doi.org/10.1016/j.cell.2018.09.048
45. Kaushik, S., Tasset, I., Arias, E., Pampliega, O., Wong, E., Martinez-Vicente, M., & Cuervo, A. M. (2021). Autophagy and the hallmarks of aging. Ageing research reviews, 72, 101468. https://doi.org/10.1016/j.arr.2021.101468
46. He, C., Sumpter, R., Jr, & Levine, B. (2012). Exercise induces autophagy in peripheral tissues and in the brain. Autophagy, 8(10), 1548–1551. https://doi.org/10.4161/auto.21327
47. He, C., Bassik, M. C., Moresi, V., Sun, K., Wei, Y., Zou, Z., An, Z., Loh, J., Fisher, J., Sun, Q., Korsmeyer, S., Packer, M., May, H. I., Hill, J. A., Virgin, H. W., Gilpin, C., Xiao, G., Bassel-Duby, R., Scherer, P. E., & Levine, B. (2012). Exercise-induced BCL2-regulated autophagy is required for muscle glucose homeostasis. Nature, 481(7382), 511–515. https://doi.org/10.1038/nature10758
48. Zoila, F., Filannino, F. M., Panaro, M. A., Sannicandro, I., Cianciulli, A., & Porro, C. (2025). Enhancing active aging through exercise: a comparative study of high-intensity interval training and continuous aerobic training benefits. Frontiers in aging, 6, 1493827.
49. Campisi J. (2013). Aging, cellular senescence, and cancer. Annual review of physiology, 75, 685–705. https://doi.org/10.1146/annurev-physiol-030212-183653
50. Campisi, J., & d'Adda di Fagagna, F. (2007). Cellular senescence: when bad things happen to good cells. Nature reviews. Molecular cell biology, 8(9), 729–740. https://doi.org/10.1038/nrm2233
51. Muñoz-Espín, D., & Serrano, M. (2014). Cellular senescence: from physiology to pathology. Nature reviews. Molecular cell biology, 15(7), 482–496. https://doi.org/10.1038/nrm3823
52. Denham, J., O'Brien, B. J., & Charchar, F. J. (2016). Telomere Length Maintenance and Cardio-Metabolic Disease Prevention Through Exercise Training. Sports medicine (Auckland, N.Z.), 46(9), 1213–1237. https://doi.org/10.1007/s40279-016-0482-4
53. Voisin, S., Eynon, N., Yan, X., & Bishop, D. J. (2015). Exercise training and DNA methylation in humans. Acta physiologica (Oxford, England), 213(1), 39–59. https://doi.org/10.1111/apha.12414
54. Garcia, L. A., Zapata-Bustos, R., Day, S. E., Campos, B., Hamzaoui, Y., Wu, L., Leon, A. D., Krentzel, J., Coletta, R. L., De Filippis, E., Roust, L. R., Mandarino, L. J., & Coletta, D. K. (2022). Can Exercise Training Alter Human Skeletal Muscle DNA Methylation?. Metabolites, 12(3), 222. https://doi.org/10.3390/metabo12030222
55. Seaborne, R. A., Strauss, J., Cocks, M., Shepherd, S., O'Brien, T. D., Someren, K. A. V., Bell, P. G., Murgatroyd, C., Morton, J. P., Stewart, C. E., Mein, C. A., & Sharples, A. P. (2018). Methylome of human skeletal muscle after acute & chronic resistance exercise training, detraining & retraining. Scientific data, 5, 180213. https://doi.org/10.1038/sdata.2018.213
56. Nitert, M. D., Dayeh, T., Volkov, P., Elgzyri, T., Hall, E., Nilsson, E., Yang, B. T., Lang, S., Parikh, H., Wessman, Y., Weishaupt, H., Attema, J., Abels, M., Wierup, N., Almgren, P., Jansson, P. A., Rönn, T., Hansson, O., Eriksson, K. F., Groop, L., … Ling, C. (2012). Impact of an exercise intervention on DNA methylation in skeletal muscle from first-degree relatives of patients with type 2 diabetes. Diabetes, 61(12), 3322–3332. https://doi.org/10.2337/db11-1653
57. Shan, J., Tay, J. H., Wang, W., Tan, R., Joshi, R., Maier, A. B., & Feng, L. (2026). Physical activity and biological age measured by DNA methylation clocks: a systematic review and meta-analysis. The lancet. Healthy longevity, 7(4), 100835. https://doi.org/10.1016/j.lanhl.2026.100835
58. Wu, Y. R., & Lin, W. Y. (2025). Associations between lifestyle factors, physiological conditions, and epigenetic age acceleration in an Asian population. Biogerontology, 26(2), 51. https://doi.org/10.1007/s10522-025-10195-1
59. Hernandez Cordero, A. I., Peters, C., Li, X., Yang, C. X., Ambalavanan, A., MacIsaac, J. L., Kobor, M. S., Fonseca, G. J., Doiron, D., Tan, W., Bourbeau, J., Jensen, D., Sin, D. D., Koelwyn, G. J., Stickland, M. K., Duan, Q., Leung, J. M., & CanCOLD Collaborative Research Group (2024). Younger epigenetic age is associated with higher cardiorespiratory fitness in individuals with airflow limitation. iScience, 27(10), 110934. https://doi.org/10.1016/j.isci.2024.110934
60. Kawamura, T., Radak, Z., Tabata, H., Akiyama, H., Nakamura, N., Kawakami, R., Ito, T., Usui, C., Jokai, M., Torma, F., Kim, H. K., Miyachi, M., Torii, S., Suzuki, K., Ishii, K., Sakamoto, S., Oka, K., Higuchi, M., Muraoka, I., McGreevy, K. M., … Tanisawa, K. (2024). Associations between cardiorespiratory fitness and lifestyle-related factors with DNA methylation-based ageing clocks in older men: WASEDA'S Health Study. Aging cell, 23(1), e13960. https://doi.org/10.1111/acel.13960
61. Yang, Y., Zhu, F., & Chen, A. (2026). Effects of exercise on peripheral blood DNA methylation and related epigenetic markers: a systematic review of human trials. Clinical epigenetics, 18(1), 123. https://doi.org/10.1186/s13148-026-02123-y
62. Kriebs A. (2026). Systematic review assesses link between physical activity and epigenetic age. Nature aging, 6(6), 1198. https://doi.org/10.1038/s43587-026-01155-6
63. Wyss-Coray, T., & Topol, E. J. (2026). Biological aging clocks in health and disease. Nature medicine, 32(7), 2383–2394. https://doi.org/10.1038/s41591-026-04495-3
64. Hawley, J. A., Hargreaves, M., Joyner, M. J., & Zierath, J. R. (2014). Integrative biology of exercise. Cell, 159(4), 738–749. https://doi.org/10.1016/j.cell.2014.10.029
65. Sillanpää, E., Ollikainen, M., Kaprio, J., Wang, X., Leskinen, T., Kujala, U. M., & Törmäkangas, T. (2019). Leisure-time physical activity and DNA methylation age-a twin study. Clinical epigenetics, 11(1), 12. https://doi.org/10.1186/s13148-019-0613-5
66. Zhou, B., Wu, D., Chen, S., Zhang, S., Ge, X., Li, J., Zhu, L., Zhou, S., Chang, N., Zhou, B., Zhang, L., & Meng, H. (2026). Body mass index, physical activity, and epigenetic aging: a cross-population study. Clinical epigenetics, 18(1), 127. https://doi.org/10.1186/s13148-026-02149-2
67. Peterson, M. D., Sen, A., & Gordon, P. M. (2011). Influence of resistance exercise on lean body mass in aging adults: a meta-analysis. Medicine and science in sports and exercise, 43(2), 249–258. https://doi.org/10.1249/MSS.0b013e3181eb6265
68. Fragala, M. S., Cadore, E. L., Dorgo, S., Izquierdo, M., Kraemer, W. J., Peterson, M. D., & Ryan, E. D. (2019). Resistance Training for Older Adults: Position Statement From the National Strength and Conditioning Association. Journal of strength and conditioning research, 33(8), 2019–2052. https://doi.org/10.1519/JSC.0000000000003230
69. Coffey, V. G., & Hawley, J. A. (2007). The molecular bases of training adaptation. Sports medicine (Auckland, N.Z.), 37(9), 737–763. https://doi.org/10.2165/00007256-200737090-00001
70. McGregor, R. A., Cameron-Smith, D., & Poppitt, S. D. (2014). It is not just muscle mass: a review of muscle quality, composition and metabolism during ageing as determinants of muscle function and mobility in later life. Longevity & healthspan, 3(1), 9. https://doi.org/10.1186/2046-2395-3-9
71. Sexton, C. L., Godwin, J. S., McIntosh, M. C., Ruple, B. A., Osburn, S. C., Hollingsworth, B. R., Kontos, N. J., Agostinelli, P. J., Kavazis, A. N., Ziegenfuss, T. N., Lopez, H. L., Smith, R., Young, K. C., Dwaraka, V. B., Frugé, A. D., Mobley, C. B., Sharples, A. P., & Roberts, M. D. (2023). Skeletal Muscle DNA Methylation and mRNA Responses to a Bout of Higher versus Lower Load Resistance Exercise in Previously Trained Men. Cells, 12(2), 263. https://doi.org/10.3390/cells12020263
72. Atakan, M. M., Li, Y., Koşar, Ş. N., Turnagöl, H. H., & Yan, X. (2021). Evidence-Based Effects of High-Intensity Interval Training on Exercise Capacity and Health: A Review with Historical Perspective. International journal of environmental research and public health, 18(13), 7201. https://doi.org/10.3390/ijerph18137201
73. Weston, K. S., Wisløff, U., & Coombes, J. S. (2014). High-intensity interval training in patients with lifestyle-induced cardiometabolic disease: a systematic review and meta-analysis. British journal of sports medicine, 48(16), 1227–1234. https://doi.org/10.1136/bjsports-2013-092576
74. MacInnis, M. J., & Gibala, M. J. (2017). Physiological adaptations to interval training and the role of exercise intensity. The Journal of physiology, 595(9), 2915–2930. https://doi.org/10.1113/JP273196
75. Izquierdo, M., Merchant, R. A., Morley, J. E., Anker, S. D., Aprahamian, I., Arai, H., Aubertin-Leheudre, M., Bernabei, R., Cadore, E. L., Cesari, M., Chen, L. K., de Souto Barreto, P., Duque, G., Ferrucci, L., Fielding, R. A., García-Hermoso, A., Gutiérrez-Robledo, L. M., Harridge, S. D. R., Kirk, B., Kritchevsky, S., … Fiatarone Singh, M. (2021). International Exercise Recommendations in Older Adults (ICFSR): Expert Consensus Guidelines. The journal of nutrition, health & aging, 25(7), 824–853. https://doi.org/10.1007/s12603-021-1665-8
76. Cadore, E. L., Rodríguez-Mañas, L., Sinclair, A., & Izquierdo, M. (2013). Effects of different exercise interventions on risk of falls, gait ability, and balance in physically frail older adults: a systematic review. Rejuvenation research, 16(2), 105–114. https://doi.org/10.1089/rej.2012.1397
77. Chou, C. H., Hwang, C. L., & Wu, Y. T. (2012). Effect of exercise on physical function, daily living activities, and quality of life in the frail older adults: a meta-analysis. Archives of physical medicine and rehabilitation, 93(2), 237–244. https://doi.org/10.1016/j.apmr.2011.08.042
78. Booth, F. W., Roberts, C. K., & Laye, M. J. (2012). Lack of exercise is a major cause of chronic diseases. Comprehensive Physiology, 2(2), 1143–1211. https://doi.org/10.1002/cphy.c110025
79. Izquierdo, M., Duque, G., & Morley, J. E. (2021). Physical activity guidelines for older people: knowledge gaps and future directions. The lancet. Healthy longevity, 2(6), e380–e383. https://doi.org/10.1016/S2666-7568(21)00079-9
Downloads
Published
How to Cite
Issue
Section
License
Copyright (c) 2026 Weronika Nowicka, Anna Kożuch, Maria Marcak, Michał Dróżdż, Emilia Rymarczyk

This work is licensed under a Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International License.
Stats
Number of views and downloads: 6
Number of citations: 0