Petnikota Harish, Madhuri Vrisha, Gangadharan Sangeet, Agarwal Indira, Antonisamy Belavendra
Department of Paediatric Orthopaedics, CMC, Vellore, Tamil Nadu, India.
Department of Child Health, CMC, Vellore, Tamil Nadu, India.
Indian J Orthop. 2016 Sep;50(5):551-557. doi: 10.4103/0019-5413.189609.
Muscular dystrophies are inherited myogenic disorders characterized by progressive muscle wasting and weakness of variable distribution and severity. They are a heterogeneous group characterized by variable degree of skeletal and cardiac muscle involvement. The most common and the most severe form of muscular dystrophy is DMD. Currently, there is no curative treatment for muscular dystrophies. Several drugs have been studied to retard the progression of the muscle weakness. There is much controversy about steroid usage in muscular dystrophy with respect to regimen, adverse effects, and whether long term benefits outweigh side effects. This study is to assess steroid efficacy in children with muscular dystrophy.
All children with diagnosed muscular dystrophy by muscle biopsy, immunohistochemistry and/or genetic test were enrolled in the study. They were started on either prednisolone (0.75 mg/kg/day) or deflazacort 0.9 mg/kg/day based on affordability. All were followed up every 6 months with clinical assessment, quality of life questionnaire and clinical and laboratory assessment of side effects. Outcome measures of children on deflazacort and prednisolone at 1 year followup were summarized as numbers and percentages and were compared using Fisher's exact test.
Twenty two children with muscular dystrophy were included (prednisolone group: 10 and deflazacort group: 12). The mean age was 7.7 years at an average followup of 26.4 months. Twenty children were diagnosed to have Duchenne's; one had Becker's muscular dystrophy while one had sarcoglycanopathy by Type 2C. All children from prednisolone group maintained their ambulatory status at 2 and 4 years followups while three on deflazacort lost their ability to walk at an average age of 11.3 years. All activities of daily living were found to be better in prednisolone group. Muscle function and time taken to walk improved in prednisolone group. Weight gain in children on prednisolone was three times more.
Prednisolone is more beneficial than deflazacort at doses of 0.75 mg/kg/day and 0.9 mg/kg/day, respectively, however it is associated with adverse effects.
肌营养不良症是遗传性肌源性疾病,其特征为进行性肌肉萎缩以及分布和严重程度各异的肌无力。它们是一组异质性疾病,其特征是骨骼肌和心肌受累程度不同。最常见且最严重的肌营养不良症形式是杜氏肌营养不良症(DMD)。目前,尚无治愈肌营养不良症的疗法。已对几种药物进行研究以延缓肌无力的进展。关于肌营养不良症中使用类固醇,在用药方案、不良反应以及长期益处是否超过副作用方面存在诸多争议。本研究旨在评估类固醇对患有肌营养不良症儿童的疗效。
所有经肌肉活检、免疫组织化学和/或基因检测确诊为肌营养不良症的儿童均纳入本研究。根据经济承受能力,他们开始服用泼尼松龙(0.75毫克/千克/天)或地夫可特(0.9毫克/千克/天)。所有儿童每6个月接受一次随访,进行临床评估、生活质量问卷调查以及副作用的临床和实验室评估。在1年随访时,将服用地夫可特和泼尼松龙的儿童的结果指标总结为数字和百分比,并使用Fisher精确检验进行比较。
纳入了22名患有肌营养不良症的儿童(泼尼松龙组:10名,地夫可特组:12名)。平均年龄为7.7岁,平均随访时间为26.4个月。20名儿童被诊断为杜氏肌营养不良症;1名患有贝氏肌营养不良症,1名通过2C型被诊断为肌聚糖病。在2年和4年随访时,泼尼松龙组的所有儿童均保持了行走能力,而地夫可特组有3名儿童在平均11.3岁时失去了行走能力。发现泼尼松龙组的所有日常生活活动情况更好。泼尼松龙组的肌肉功能和行走所需时间有所改善。服用泼尼松龙的儿童体重增加是前者的三倍。
在分别为0.75毫克/千克/天和0.9毫克/千克/天的剂量下,泼尼松龙比地夫可特更有益,但它会带来不良反应。