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高剂量每周口服泼尼松可改善杜氏肌营养不良男孩的肌力。

High dose weekly oral prednisone improves strength in boys with Duchenne muscular dystrophy.

作者信息

Connolly Anne M, Schierbecker Jeanine, Renna Renee, Florence Julaine

机构信息

Department of Neurology, Saint Louis Children's Hospital, Washington University School of Medicine, Box 8111, 660 S. Euclid Avenue, Saint Louis, MO 63110, USA.

出版信息

Neuromuscul Disord. 2002 Dec;12(10):917-25. doi: 10.1016/s0960-8966(02)00180-3.

Abstract

Daily prednisone improves strength in boys with Duchenne muscular dystrophy, but side effects are almost universal. We used a different dosing regimen of prednisone to determine if benefit to boys with Duchenne muscular dystrophy might be maintained with fewer side effects. Twice weekly oral prednisone was given each Friday and Saturday (5mg/kg/dose). This total dose is twice as high as the daily low dosage prednisone regimen (0.75 mg/kg/day). Twenty boys (8.0+/-1.2 years) were treated. Historical control groups included 18 untreated boys (6.1+/-1.6 years) and four boys (7.3+/-0.6 years) treated with daily prednisone. Strength (using a hand-held manometer and grip meter) and timed functional testing were measured. There was an improvement in upper extremity strength for 95% of boys (n=20) at 6 months using quantitative strength testing. Improvement in lower extremity strength occurred in all boys with antigravity quadriceps strength (17/17). The improvement (P=0.001 for proximal upper extremities; P=0.002 for grip; and P<0.0001 for proximal lower extremities) was significant compared to untreated boys. Sixteen boys were treated continuously for more than 12 months (22+/-1.5 months). Of these, 15 remained significantly stronger than prior to treatment and 8/16 showed additional gains in strength after six months of treatment. Six boys were on the weekly prednisolone 2 years or longer without interruption. All six had upper and lower extremity strength at follow-up that was as good or better than at baseline. Functional testing improved in boys less than 8 years without contractures. Three boys without antigravity quadriceps strength at the start of treatment lost the ability to walk unassisted within 6 months. Eight other boys lost the ability to ambulate unassisted between 12 and 24 months of treatment. In each, progressive contractures developed. Linear growth was maintained in all boys on weekly treatment. Obesity rates did not differ from untreated boys. Twice weekly prednisone improved strength over 6-12 months in the majority of boys, but did not slow contracture development. Sustained benefit beyond 12 months is possible with fewer side effects compared to daily prednisone.

摘要

每日服用泼尼松可增强杜氏肌营养不良症男孩的肌力,但副作用几乎普遍存在。我们采用了不同的泼尼松给药方案,以确定能否在减少副作用的情况下,维持对杜氏肌营养不良症男孩的疗效。每周两次口服泼尼松,于每周五和周六服用(5毫克/千克/剂量)。该总剂量是每日低剂量泼尼松方案(0.75毫克/千克/天)的两倍。对20名男孩(8.0±1.2岁)进行了治疗。历史对照组包括18名未接受治疗的男孩(6.1±1.6岁)和4名接受每日泼尼松治疗的男孩(7.3±0.6岁)。测量了肌力(使用手持式压力计和握力计)和定时功能测试。在6个月时,使用定量肌力测试,95%的男孩(n = 20)上肢肌力有所改善。所有具有抗重力股四头肌力量的男孩(17/17)下肢肌力均有改善。与未接受治疗的男孩相比,改善情况显著(近端上肢P = 0.001;握力P = 0.002;近端下肢P < 0.0001)。16名男孩连续治疗超过12个月(22±1.5个月)。其中,15名男孩的肌力仍显著强于治疗前,16名中有8名在治疗6个月后肌力进一步增强。6名男孩连续服用泼尼松龙2年或更长时间且未中断。随访时,所有6名男孩的上肢和下肢肌力与基线时一样好或更好。8岁以下无挛缩的男孩功能测试有所改善。3名在治疗开始时无抗重力股四头肌力量的男孩在6个月内失去了独立行走的能力。另外8名男孩在治疗12至24个月之间失去了独立行走的能力。在每个病例中,均出现了进行性挛缩。每周接受治疗的所有男孩线性生长均得以维持。肥胖率与未接受治疗的男孩无差异。每周两次服用泼尼松在6至12个月内可增强大多数男孩的肌力,但并未减缓挛缩的发展。与每日服用泼尼松相比,有可能在副作用较少的情况下获得超过12个月的持续疗效。

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