The effect of aerobic exercise on muscle tissue in patients with severe heart failure and normal body weight
https://doi.org/10.15829/1560-4071-2020-3670
Abstract
Aim. To assess the response of skeletal muscle and myocardium to original aerobic exercise (AE) program in patients with heart failure (HF) with reduced ejection fraction (HFrEF); to assess morphometric changes in skeletal muscle fiber after AE.
Material and methods. The study included 100 patients with class III HFrEF (age — 52±5,2 years; body mass index (BMI) — 23,5±2,8 kg/m2). At baseline and after 6 months of AE, an echocardiogram, peak oxygen uptake (VO2peak), exercise tolerance and quality of life (QOL) were evaluated. Lactate dehydrogenase (LDH) and alkaline phosphatase (ALP) activity were evaluated in biopsy material of lower leg muscles.
Results. After 6 months of AE, the left ventricular ejection fraction (LVEF) increased by 10,5±2,3%, QOL — by 24,8±3,5 points, exercise tolerance — by 9,7±0,5 points, VO2peak — by 5,2±0,5 ml/min/kg (p1,2,3,4< 0,05). In 6 patients, the diameter of muscle fiber decreased slightly. The activity of ALP (initially — 0,33±0,09 D) increased by 24,2% (p< 0,05); LDH in glycolytic fibers was initially 0,213±0,08 D, in oxidative fibers — 0,083±0,04, and after 6 months of AE, decreased by 24,4% and 6,0%, respectively (p1 <0,05, p2 >0,05). A positive relationship was found between the dynamics of HF class and fiber diameter (r=0,4, p=0,05); an increase in сardiopulmonary exercise test was associated with ALP activity (r=0,5, p=0,05).
Conclusion. 1. Dosed aerobic exercise in patients with stable class III HFrEF, normal BMI, based on reaching the lactate threshold, had a positive effect on LVEF, QOL, exercise tolerance and VO2peak. 2. With exercise training, a decrease in fiber diameter and LDH activity in both oxidative and glycolytic fibers, an increase in ALP activity were revealed. 3. The functional relationship between the increase in exercise tolerance and ALP content in muscle tissue was revealed.
About the Authors
V. L. GalenkoRussian Federation
St. Petersburg
T. A. Lelyavina
Russian Federation
St. Petersburg
M. Yu. Sitnikova
Russian Federation
St. Petersburg
G. Yu. Yukina
Russian Federation
St. Petersburg
M. A. Bortsova
Russian Federation
St. Petersburg
R. I. Dmitrieva
St. Petersburg
References
1. Аrutyunov GP, Kolesnikova EA, Begrambekova YuL, et al. Recommendations for the appointment of physical training for patients with chronic heart failure. Russian Heart Failure Journal. 2017;18(1):41-66. (In Russ.) doi:10.18087/rhfj.2017.1.2339.
2. von Haehling S, Ebner N, Dos Santos MR, et al. Muscle wasting and cachexia in heart failure: mechanisms and therapies. Nat Rev Cardiol. 2017 Jun;14(6):323-41. doi:10.1038/nrcardio.2017.51.
3. Saitoh M, Ishida J, Doehner W, et al. Sarcopenia, cachexia, and muscle performance in heart failure: Review update 2016. Int J Cardiol. 2017 Jul 1;238:5-11. doi:10.1016/j.ijcard.2017.03.155.
4. Belloum Y, Rannou-Bekono F, Favier FB. Cancer-induced cardiac cachexia: Pathogenesis and impact of physical activity (Review). Oncol Rep. 2017 May;37(5):2543-52. doi:10.3892/or.2017.5542.
5. Carbone S, Lavie CJ, Arena R. Obesity and Heart Failure: Focus on the Obesity Paradox. Mayo Clin Proc. 2017 Feb;92(2):266-79. doi:10.1016/j.mayocp.2016.11.001.
6. Lelyavina TA, Sitnikova MY, Galenko VL, et al. The role of muscle tissue in the pathogenesis of chronic heart failure — the potential of exposure (FORMA study). Russian Journal of Cardiology. 2019;(10):58-65. (In Russ.) doi:10.15829/1560-4071-2019-10-58-65.
7. Coats AJ, Adamopoulos S, Meyer TE, Conway J, Sleight P. Effects of physical training in chronic heart failure. Lancet. 1990;335(8681):63-6. doi:10.1016/0140-6736(90)90536-e.
8. Belardinelli R, Georgiou D, Cianci G, et al. Randomized, controlled trial of long-term moderate exercise training in chronic heart failure: effects on functional capacity, quality of life, and clinical outcome. Circulation. 1999;99(9):1173-82. doi:10.1161/01.cir.99.9.1173.
9. Lelyavina TA, Sitnikova MYu, Galenko V. The Effects of Individualized Physical Rehabilitation Program. International Journal of Engineering Research & Science (IJOER). 2016:2,9:1-7.
10. Lavine KJ, Sierra OL. Skeletal muscle inflammation and atrophy in heart failure. Heart Fail Rev. 2017 March;22(2):179-89. doi:10.1007/s10741-016-9593-0.
11. Dmitrieva RI, Lelyavina TA, Komarova MY, et al. Skeletal muscle resident progenitor cells coexpress mesenchymal and myogenic markers and are not affected by chronic heart failure-induced disregulations. Stem cells international. 2019; article ID 5690345, doi:10.1155/2019/5690345.
12. Souza RWA, Piedade WP, Soares LC, et al. Aerobic exercise training prevents heart failureinduced skeletal muscle atrophy by anti-catabolic, but not anabolic actions. PLos ONE. 2014;9(10):e110020. doi:10.137/journal.pone.0110020.
13. Larsen AI, Lindal S, Aukrust P, et al. Effect of exercise training on skeletal muscle fibre characteristics in men with chronic heart failure. Correlation between skeletal muscle alterations, cytokines and exercise capacity. Int J Cardiol. 2002 Apr;83(1):25-32. doi:10.1016/s0167-5273(02)00014-1.
14. Ventura-Clapier R, Bertrand M, Bigard X. Beneficial effects of endurance training on cardiac and skeletal muscle energy metabolism in heart failure. Cardiovascular research. 2007;73:10-8. doi:10.1016/j.cardiores.2006.09003.
Review
For citations:
Galenko V.L., Lelyavina T.A., Sitnikova M.Yu., Yukina G.Yu., Bortsova M.A., Dmitrieva R.I. The effect of aerobic exercise on muscle tissue in patients with severe heart failure and normal body weight. Russian Journal of Cardiology. 2020;25(6):3670. (In Russ.) https://doi.org/10.15829/1560-4071-2020-3670