School of Allied Health Professions, Keele University, Keele, Staffordshire, UK
Faculty of Health and Social Sciences, Bournemouth University, Bournemouth, UK.
J Neurol Neurosurg Psychiatry. 2024 Apr 12;95(5):442-453. doi: 10.1136/jnnp-2023-331988.
Management of muscular dystrophies (MD) relies on conservative non-pharmacological treatments, but evidence of their effectiveness is limited and inconclusive.
To investigate the effectiveness of conservative non-pharmacological interventions for MD physical management.
This systematic review and meta-analysis followed Preferred Reporting Items for Systematic Reviews and Meta-Analyses (PRISMA) guidelines and searched Medline, CINHAL, Embase, AMED and Cochrane Central Register of Controlled Trial (inception to August 2022). Effect size (ES) and 95% Confidence Interval (CI) quantified treatment effect.
Of 31,285 identified articles, 39 studies (957 participants), mostly at high risk of bias, were included. For children with Duchenne muscular dystrophy (DMD), trunk-oriented strength exercises and usual care were more effective than usual care alone in improving distal upper-limb function, sitting and dynamic reaching balance (ES range: 0.87 to 2.29). For adults with Facioscapulohumeral dystrophy (FSHD), vibratory proprioceptive assistance and neuromuscular electrical stimulation respectively improved maximum voluntary isometric contraction and reduced pain intensity (ES range: 1.58 to 2.33). For adults with FSHD, Limb-girdle muscular dystrophy (LGMD) and Becker muscular dystrophy (BMD), strength-training improved dynamic balance (sit-to-stand ability) and self-perceived physical condition (ES range: 0.83 to 1.00). A multicomponent programme improved perceived exertion rate and gait in adults with Myotonic dystrophy type 1 (DM1) (ES range: 0.92 to 3.83).
Low-quality evidence suggests that strength training, with or without other exercise interventions, may improve perceived exertion, distal upper limb function, static and dynamic balance, gait and well-being in MD. Although more robust and larger studies are needed, current evidence supports the inclusion of strength training in MD treatment, as it was found to be safe.
肌肉萎缩症(MD)的治疗依赖于保守的非药物治疗,但这些治疗的有效性证据有限且不确定。
研究保守的非药物干预措施对 MD 身体管理的效果。
本系统评价和荟萃分析遵循系统评价和荟萃分析的首选报告项目(PRISMA)指南,并检索了 Medline、CINHAL、Embase、AMED 和 Cochrane 对照试验中心注册库(从建立到 2022 年 8 月)。效应量(ES)和 95%置信区间(CI)量化了治疗效果。
在 31285 篇鉴定的文章中,纳入了 39 项研究(957 名参与者),这些研究大多存在高偏倚风险。对于患有杜氏肌营养不良症(DMD)的儿童,躯干定向力量训练和常规护理比单纯常规护理更有效地改善远端上肢功能、坐姿和动态平衡(ES 范围:0.87 至 2.29)。对于患有面肩肱型肌营养不良症(FSHD)的成年人,振动本体感觉辅助和神经肌肉电刺激分别改善了最大自主等长收缩和降低了疼痛强度(ES 范围:1.58 至 2.33)。对于患有 FSHD、肢带型肌营养不良症(LGMD)和 Becker 肌营养不良症(BMD)的成年人,力量训练改善了动态平衡(从坐姿到站立能力)和自我感知的身体状况(ES 范围:0.83 至 1.00)。一项多组分方案改善了 1 型肌强直性营养不良(DM1)成年患者的感知用力率和步态(ES 范围:0.92 至 3.83)。
低质量证据表明,力量训练,无论是否结合其他运动干预,可能改善 MD 患者的感知用力、远端上肢功能、静态和动态平衡、步态和整体健康状况。尽管需要更强大和更大规模的研究,但现有证据支持将力量训练纳入 MD 治疗,因为它已被证明是安全的。