Brooke M H, Fenichel G M, Griggs R C, Mendell J R, Moxley R T, Miller J P, Kaiser K K, Florence J M, Pandya S, Signore L
Arch Neurol. 1987 Aug;44(8):812-7. doi: 10.1001/archneur.1987.00520200016010.
We investigated the effect of high-dose prednisone therapy in 33 boys with Duchenne muscular dystrophy. The drug was given daily in doses of 1.5 mg/kg of body weight (to a maximum of 80 mg) for six months. Muscle strength, joint contractures, timed functional tests, functional ability, and pulmonary function were measured at the beginning and end of the treatment period. The trial was designed using natural history controls, and the power of the study was 0.80 to detect a slowing of 50% in the rate of progression. During the period of the trial, muscle strength, functional grades, timed functional tests, and pulmonary function improved. Contractures followed the expected natural history of the illness.
我们研究了大剂量泼尼松疗法对33名杜氏肌营养不良症男孩的影响。药物按每日1.5毫克/千克体重的剂量给予(最大剂量为80毫克),持续六个月。在治疗期开始和结束时测量肌肉力量、关节挛缩、定时功能测试、功能能力和肺功能。该试验采用自然病史对照设计,研究效能为0.80,以检测进展速度减缓50%的情况。在试验期间,肌肉力量、功能分级、定时功能测试和肺功能均有所改善。挛缩遵循疾病预期的自然病史。