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线粒体肌病的运动训练:一项随机对照试验。

Exercise training in mitochondrial myopathy: a randomized controlled trial.

作者信息

Cejudo Pilar, Bautista Juan, Montemayor Teodoro, Villagómez Rafael, Jiménez Luis, Ortega Francisco, Campos Yolanda, Sánchez Hildegard, Arenas Joaquín

机构信息

Chest Department, Hospital Universitario Virgen del Rocío, 41013 Seville, Spain.

出版信息

Muscle Nerve. 2005 Sep;32(3):342-50. doi: 10.1002/mus.20368.

Abstract

Patients with mitochondrial myopathies (MM) usually suffer from exercise intolerance due to their impaired oxidative capacity and physical deconditioning. We evaluated the effects of a 12-week supervised randomized rehabilitation program involving endurance training in patients with MM. Twenty MM patients were assigned to a training or control group. For three nonconsecutive days each week, patients combined cycle exercise at 70% of their peak work rate with three upper-body weight-lifting exercises performed at 50% of maximum capacity. Training increased maximal oxygen uptake (28.5%), work output (15.5%), and minute ventilation (40%), endurance performance (62%), walking distance in shuttle walking test (+95 m), and peripheral muscle strength (32%-62%), and improved Nottingham Health Profile scores (21.47%) and clinical symptoms. Control MM patients did not change from baseline. Results show that our exercise program is an adequate training strategy for patients with mitochondrial myopathy.

摘要

线粒体肌病(MM)患者通常因氧化能力受损和身体机能下降而存在运动不耐受的情况。我们评估了一项为期12周的有监督的随机康复计划对MM患者进行耐力训练的效果。20名MM患者被分为训练组或对照组。每周有三天,患者将以其峰值工作率70%的强度进行自行车运动与以最大容量50%的强度进行三项上肢举重运动相结合。训练使最大摄氧量提高了28.5%、工作输出提高了15.5%、分钟通气量提高了40%、耐力表现提高了62%、穿梭步行试验中的步行距离增加了95米、外周肌肉力量提高了32%-62%,并改善了诺丁汉健康状况评分(21.47%)以及临床症状。对照组的MM患者与基线相比没有变化。结果表明,我们的运动计划是线粒体肌病患者的一种合适的训练策略。

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