A Systematic Review investigating the Effectiveness of Exercise training in Glycogen Storage Diseases.

Therapeutic advances in rare disease Pub Date : 2022-02-23 eCollection Date: 2022-01-01 DOI:10.1177/26330040221076497
Claire Bordoli, Elaine Murphy, Ian Varley, Graham Sharpe, Philip Hennis
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引用次数: 3

Abstract

Introduction: Glycogen storage diseases (GSDs) are rare inborn errors of carbohydrate metabolism typically with skeletal muscle and liver involvement. In those with skeletal muscle involvement, the majority display symptoms of exercise intolerance which can cause profound exercise limitation and impair everyday living and quality of life (QoL). There are no curative treatments for GSDs, thus therapeutic options, such as exercise training, are aimed at improving QoL by alleviating signs and symptoms. In order to investigate the effectiveness of exercise training in adults with GSDs, we systematically reviewed the literature.

Methods: In this review we conducted searches within SCOPUS and MEDLINE to identify potential papers for inclusion. These papers were independently assessed for inclusion and quality by two authors. We identified 23 studies which included aerobic training, strength training or respiratory muscle training in patients with McArdles (n = 41) and Pompe disease (n = 139).

Results: In McArdle disease, aerobic exercise training improved aerobic capacity (VO2 peak) by 14-111% with further benefits to functional capacity and well-being. Meanwhile, strength training increased muscle peak power by 100-151% and reduced disease severity. In Pompe disease, a combination of aerobic and strength training improved VO2 peak by 9-10%, muscle peak power by 64%, functional capacity and well-being. Furthermore, respiratory muscle training (RMT) improved respiratory muscular strength [maximum inspiratory pressure (MIP) increased by up to 65% and maximum expiratory pressure (MEP) by up to 70%], with additional benefits shown in aerobic capacity, functional capacity and well-being.

Conclusion: This adds to the growing body of evidence which suggests that supervised exercise training is safe and effective in improving aerobic capacity and muscle function in adults with McArdle or Pompe disease. However, the literature base is limited in quality and quantity with a dearth of literature regarding exercise training in other GSD subtypes.

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研究糖原储存性疾病运动训练有效性的系统综述。
引言:糖原储存性疾病(GSDs)是一种罕见的先天性碳水化合物代谢错误,通常与骨骼肌和肝脏有关。在骨骼肌受累的患者中,大多数表现出运动不耐受的症状,这可能会导致严重的运动限制,并损害日常生活和生活质量(QoL)。GSD没有治疗方法,因此运动训练等治疗选择旨在通过减轻体征和症状来改善生活质量。为了研究运动训练对患有GSD的成年人的有效性,我们系统地回顾了文献。方法:在这篇综述中,我们在SCOPUS和MEDLINE中进行了搜索,以确定潜在的纳入论文。两位作者对这些论文的收录和质量进行了独立评估。我们确定了23项研究,包括有氧训练、力量训练或呼吸肌训练对McArdles(n = 41)和庞贝病(n = 结果:在McArdle病中,有氧运动训练使有氧能力(VO2峰值)提高了14-111%,对功能能力和幸福感有进一步的益处。同时,力量训练使肌肉峰值力量增加了100-151%,并降低了疾病的严重程度。在庞贝病中,有氧和力量训练相结合可使VO2峰值提高9-10%,肌肉峰值功率提高64%,功能能力和幸福感得到改善。此外,呼吸肌训练(RMT)提高了呼吸肌强度[最大吸气压力(MIP)增加了65%,最大呼气压力(MEP)增加了70%],有氧能力显示出额外的好处,结论:越来越多的证据表明,有监督的运动训练在改善患有McArdle或Pompe病的成年人的有氧能力和肌肉功能方面是安全有效的。然而,文献基础在质量和数量上都是有限的,缺乏关于其他GSD亚型运动训练的文献。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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