High-intensity interval training in chronic kidney disease: A randomized pilot study

被引:25
|
作者
Beetham, Kassia S. [1 ,2 ]
Howden, Erin J. [3 ]
Fassett, Robert G. [2 ]
Petersen, Aaron [4 ]
Trewin, Adam J. [4 ]
Isbel, Nicole M. [5 ,6 ]
Coombes, Jeff S. [2 ]
机构
[1] Australian Catholic Univ, Sch Behav & Hlth Sci, Brisbane, Qld, Australia
[2] Univ Queensland, Sch Human Movement & Nutr Sci, Brisbane, Qld, Australia
[3] Baker Heart & Diabet Inst, Melbourne, Vic, Australia
[4] Victoria Univ, Inst Hlth & Sport, Melbourne, Vic, Australia
[5] Univ Queensland, Sch Med, Brisbane, Qld, Australia
[6] Princess Alexandra Hosp, Dept Nephrol, Brisbane, Qld, Australia
关键词
high-volume training; intermittent training; muscle atrophy; muscle wasting; nephrology; renal; MUSCLE ATROPHY; HEART-FAILURE; FUNCTIONAL-CAPACITY; EXERCISE CAPACITY; AEROBIC EXERCISE; SKELETAL-MUSCLE; RISK; INTERVENTION; EXPRESSION; FITNESS;
D O I
10.1111/sms.13436
中图分类号
G8 [体育];
学科分类号
04 ; 0403 ;
摘要
Introduction High-intensity interval training (HIIT) increases mitochondrial biogenesis and cardiorespiratory fitness in chronic disease populations, however has not been studied in people with chronic kidney disease (CKD). The aim of this study was to compare the feasibility, safety, and efficacy of HIIT with moderate-intensity continuous training (MICT) in people with CKD. Methods Fourteen individuals with stage 3-4 CKD were randomized to 3 supervised sessions/wk for 12 weeks, of HIIT (n = 9, 4 x 4 minute intervals, 80%-95% peak heart rate [PHR]) or MICT (n = 5, 40 minutes, 65% PHR). Feasibility was assessed via session attendance and adherence to the exercise intensity. Safety was examined by adverse event reporting. Efficacy was determined from changes in cardiorespiratory fitness (VO(2)peak), exercise capacity (METs), and markers of mitochondrial biogenesis (PGC1 alpha protein levels), muscle protein catabolism (MuRF1), and muscle protein synthesis (p-P70S6k (Thr389)). Results Participants completed a similar number of sessions in each group (HIIT = 33.0[7.0] vs MICT = 33.5[3.3] sessions), and participants adhered to the target heart rates. There were no adverse events attributable to exercise training. There was a significant time effect for exercise capacity (HIIT = +0.8 +/- 1.2; MICT = +1.3 +/- 1.6 METs; P = 0.01) and muscle protein synthesis (HIIT = +0.6 +/- 1.1; MICT = +1.4 +/- 1.7 au; P = 0.04). However, there were no significant (P > 0.05) group x time effects for any outcomes. Conclusion This pilot study demonstrated that HIIT is a feasible and safe option for people with CKD, and there were similar benefits of HIIT and MICT on exercise capacity and skeletal muscle protein synthesis. These data support a larger trial to further evaluate the effectiveness of HIIT.
引用
收藏
页码:1197 / 1204
页数:8
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