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Sarcopenia


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in people with sarcopenia compared with controls [10]. In addition, a metabolomic study conducted in a relatively large population found that carnitine, a mitochondrial lipid transporter essential for the entry of fatty acids, potential fuel and synthetic precursors for the mitochondria, as well as vitamin E, a strong antioxidant important for mitochondrial function, are underrepresented in the serum of frail compared to non‐frail individuals [85]. Indeed, randomized controlled trials are currently in the field that target mitochondrial health to prevent sarcopenia. Ultimately, the results of these studies should provide an answer of whether changes in mitochondrial function are the root causes to sarcopenia.

      Supported in part by the Intramural Research Program of the National Institute on Aging, NIH ‐ Baltimore, MD, USA.

      The authors would like to thank Miguel Aon and Sonia Cortassa for reading the manuscript and providing very useful suggestions.

      1 1. Dodds, R.M., et al., Global variation in grip strength: a systematic review and meta‐analysis of normative data. Age and Ageing, 2016. 45(2): p. 209–216.

      2 2. Moore, A.Z., et al., Difference in muscle quality over the adult life span and biological correlates in the Baltimore Longitudinal Study of Aging. Journal of the American Geriatrics Society, 2014. 62(2): p. 230–236.

      3 3. Walker, J.B., Creatine: biosynthesis, regulation, and function. Advances in Enzymology and Related Areas of Molecular Biology, 1979. 50: p. 177–242.

      4 4. Barclay, C., Energy demand and supply in human skeletal muscle. Journal of Muscle Research and Cell Motility, 2017. 38(2): p. 143–155.

      5 5. Kemp, G.J., M. Meyerspeer, and E. Moser, Absolute quantification of phosphorus metabolite concentrations in human muscle in vivo; by 31P MRS: a quantitative review. NMR in Biomedicine: An International Journal Devoted to the Development and Application of Magnetic Resonance in vivo, 2007. 20(6): p. 555–565.

      6 6. Lanza, I.R., D.E. Befroy, and J.A. Kent‐Braun, Age‐related changes in ATP‐producing pathways in human skeletal muscle in vivo. Journal of Applied Physiology, 2005. 99(5): p. 1736–1744.

      7 7. Schocke, M.F., et al., High‐energy phosphate metabolism during incremental calf exercise in humans measured by 31 phosphorus magnetic resonance spectroscopy (31P MRS). Magnetic Resonance Imaging, 2004. 22(1): p. 109–115.

      8 8. Rygiel, K.A., M. Picard, and D.M. Turnbull, The ageing neuromuscular system and sarcopenia: a mitochondrial perspective. The Journal of Physiology, 2016. 594(16): p. 4499–4512.

      9 9. Wallace, D.C., Mitochondrial genetic medicine. Nature Genetics, 2018. 50(12): p. 1642–1649.

      10 10. Migliavacca, E., et al., Mitochondrial oxidative capacity and NAD+ biosynthesis are reduced in human sarcopenia across ethnicities. Nature Communications, 2019. 10(1): p. 1–14.

      11 11. Coen, P.M., et al., Mitochondria as a target for mitigating sarcopenia. Frontiers in Physiology, 2019. 9: p. 1883.

      12 12. Menshikova, E.V., et al., Calorie restriction‐induced weight loss and exercise have differential effects on skeletal muscle mitochondria despite similar effects on insulin sensitivity. The Journals of Gerontology. Series A, Biological Sciences and Medical Sciences, 2017. 73(1): p. 81–87.

      13 13. Menshikova, E.V., et al., Effects of exercise on mitochondrial content and function in aging human skeletal muscle. The Journals of Gerontology. Series A, Biological Sciences and Medical Sciences, 2006. 61(6): p. 534–540.

      14 14. Distefano, G. and B.H. Goodpaster, Effects of exercise and aging on skeletal muscle. Cold Spring Harbor Perspectives in Medicine, 2018. 8(3): a029785. doi:10.1101/cshperspect.a029785.

      15 15. Distefano, G., et al., Chronological age does not influence ex‐vivo mitochondrial respiration and quality control in skeletal muscle. The Journals of Gerontology. Series A, Biological Sciences and Medical Sciences, 2017. 72(4): p. 535–542.

      16 16. Trounce, I., E. Byrne, and S. Marzuki, Decline in skeletal muscle mitochondrial respiratory chain function: possible factor in ageing. The Lancet, 1989. 333(8639): p. 637–639.

      17 17. Boffoli, D., et al., Decline with age of the respiratory chain activity in human skeletal muscle. Biochimica et Biophysica Acta (BBA) ‐ Molecular Basis of Disease, 1994. 1226(1): p. 73–82.

      18 18. Tonkonogi, M., et al., Reduced oxidative power but unchanged antioxidative capacity in skeletal muscle from aged humans. Pflügers Archiv, 2003. 446(2): p. 261–269.

      19 19. Short, K.R., et al., Decline in skeletal muscle mitochondrial function with aging in humans. Proceedings of the National Academy of Sciences, 2005. 102(15): p. 5618–5623.

      20 20. Lanza, I.R. and K.S. Nair, Muscle mitochondrial changes with aging and exercise. The American Journal of Clinical Nutrition, 2009. 89(1): p. 467S–471S.

      21 21. Porter, C., et al., Mitochondrial respiratory capacity and coupling control decline with age in human skeletal muscle. American Journal of Physiology. Endocrinology and Metabolism, 2015. 309(3): p. E224–E232.

      22 22. Kauppila, T.E., J.H. Kauppila, and N.‐G. Larsson, Mammalian mitochondria and aging: an update. Cell Metabolism, 2017. 25(1): p. 57–71.

      23 23. Gonzalez‐Freire, M., et al., Skeletal muscle ex vivo; mitochondrial respiration parallels decline in vivo; oxidative capacity, cardiorespiratory fitness, and muscle strength: the Baltimore Longitudinal Study of Aging. Aging Cell, 2018. 17(2): p. e12725.

      24 24. Ubaida‐Mohien, C., et al., Discovery proteomics in aging human skeletal muscle finds change in spliceosome, immunity, proteostasis and mitochondria. Elife, 2019. 8: e49874. doi:10.7554/eLife.49874.

      25 25. Choi, S., et al., 31P magnetic resonance spectroscopy assessment of muscle bioenergetics as a predictor of gait speed in the Baltimore Longitudinal Study of Aging. The Journals of Gerontology. Series A, Biological Sciences and Medical Sciences, 2016. 71(12): p. 1638–1645.

      26 26. Coen, P.M., et al., Skeletal muscle mitochondrial energetics are associated with maximal aerobic capacity and walking speed in older adults. The Journals of Gerontology. Series A, Biological Sciences and Medical Sciences, 2013. 68(4): p. 447–455.

      27 27. Zane, A.C., et al., Muscle strength mediates the relationship between mitochondrial energetics and walking performance. Aging Cell, 2017. 16(3): p. 461–468.

      28 28. Santanasto, A.J., et al., Skeletal muscle mitochondrial function and fatigability in older adults. The Journals of Gerontology. Series A, Biological Sciences and Medical Sciences, 2015. 70(11): p. 1379–1385.

      29 29. Joseph, A.M., et al., The impact of aging on mitochondrial function and biogenesis pathways in skeletal muscle of sedentary high‐and low‐functioning elderly individuals. Aging Cell, 2012. 11(5): p. 801–809.

      30 30. Gouspillou, G., et al., Mitochondrial energetics is impaired in vivo; in aged skeletal muscle. Aging Cell, 2014. 13(1): p. 39–48.

      31 31. Fabbri, E., et al., Insulin resistance is associated with reduced mitochondrial oxidative capacity measured by 31P‐magnetic resonance spectroscopy in participants without diabetes from the Baltimore longitudinal study of aging. Diabetes, 2017. 66(1): p. 170–176.

      32 32. Standley, R.A., et al., Skeletal muscle energetics and mitochondrial function are impaired following 10 days of bed rest in older adults. The Journals of Gerontology: Series A, 2020. 75(9): p. 1744–1753.

      33 33. Ubaida‐Mohien, C., et al., Physical activity associated proteomics of skeletal muscle: being physically active in daily life may protect skeletal muscle from aging. Frontiers in Physiology, 2019. 10: p. 312.

      34 34. Rowe, G.C., A. Safdar, and Z. Arany, Running forward: new frontiers in endurance exercise biology. Circulation, 2014. 129(7): p. 798–810.

      35 35.