期刊
EUROPEAN JOURNAL OF NUTRITION
卷 60, 期 2, 页码 917-928出版社
SPRINGER HEIDELBERG
DOI: 10.1007/s00394-020-02302-4
关键词
Sarcopenia; Aging; Elderly; Hypertrophy; Lean body mass; Physical performance
资金
- Meiji Co., Ltd.
The study found that long-term ingestion of low-dose milk protein supplementation combined with low-to-moderate intensity exercise training can increase muscle mass in older adults and reduce fat mass and plasma uric acid levels.
Purpose The purpose of this study was to examine whether long-term ingestion of low-dose milk protein supplementation causes a greater increase in muscle mass and strength of older adults during low-to-moderate intensity exercise training intervention than isocaloric carbohydrate. Methods In a randomized, double-blind, and placebo-controlled design, 122 healthy older adults (60-84 year) received either an acidified milk protein drink containing 10 g of milk protein (MILK;n = 61) or an isocaloric placebo drink (PLA;n = 61) daily throughout 6 months of body weight and medicine ball exercise training. Measurements before and after the intervention included body composition, physical performance and blood biochemistry. Results Lean body mass significantly increased in the MILK group (+ 0.54 kg,p < 0.001), but did not change in the PLA group (- 0.10 kg,p = 0.534). The increases in the MILK group were significantly greater than in the PLA group (p = 0.004). Fat mass (- 0.77 kg) and plasma uric acid levels (- 0.3 mg/dL) significantly decreased only in the MILK group (p < 0.001), with a significant group difference (p = 0.002 andp < 0.001, respectively). Most of the physical performance tests significantly improved in both groups, but no group differences were found. Conclusion We conclude that low-dose milk protein supplementation (10 g of protein/day) combined with low-to-moderate intensity exercise training is associated with increased muscle mass, but not improved physical performance compared to carbohydrate combined with exercise in healthy older adults. This study was registered in the UMIN Clinical Trials Registry (UMIN000032189).
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