Messina S, Hartley L, Main M, Kinali M, Jungbluth H, Muntoni F, Mercuri E
Dubowitz Neuromuscular Centre, Department of Paediatrics, Imperial College, Hammersmith Hospital, London, UK.
Neuropediatrics. 2004 Oct;35(5):262-6. doi: 10.1055/s-2004-821173.
Several studies have documented positive effects of beta-adrenergic agonists on human skeletal muscle with regard to muscle mass and strength. The aim of this pilot study was to evaluate the effect of the beta2-agonist salbutamol (albuterol) in a group of children with central core disease and multi-minicore disease. Thirteen patients, 8 with central core disease (mean age 17.5 years) and 5 with minicore disease (mean age 13.6 years) received oral salbutamol at a dose of 2 mg four times a day. Measures of efficacy were the change from baseline at 3 and 6 months in muscle strength, assessed by MRC score, myometry, functional measures and forced vital capacity. Statistical analysis was performed using repeated measures ANOVA (significance level < 0.05). Two patients with central core disease stopped the medication after one month because they did not notice any improvement and another one with minicore disease after 4 months because of increased tremors and palpitations. The remaining ten (6 with central core and 4 with minicore disease) completed the course of salbutamol without any significant adverse effects. There were significant increases in myometry, MRC scores and forced vital capacity between baseline and the six-month assessments. For both myometry and MRC the difference was already significant at 3 months and this was associated with a significant increase in functional abilities assessed with a structured functional scale. Our results suggest that salbutamol was overall well tolerated and might be beneficial in both central core and minicore patients. Larger prospective randomised, double-blind, placebo-controlled trials with salbutamol will be needed to confirm these preliminary findings.
多项研究已证明β-肾上腺素能激动剂对人体骨骼肌的肌肉质量和力量有积极影响。这项初步研究的目的是评估β2-激动剂沙丁胺醇(舒喘灵)对一组患有中央轴空病和多微小轴空病儿童的影响。13名患者,8名患有中央轴空病(平均年龄17.5岁),5名患有微小轴空病(平均年龄13.6岁),每天4次口服2毫克沙丁胺醇。疗效指标为3个月和6个月时肌肉力量相对于基线的变化,通过医学研究委员会(MRC)评分、肌动测量法、功能指标和用力肺活量进行评估。采用重复测量方差分析进行统计分析(显著性水平<0.05)。两名患有中央轴空病的患者在1个月后停止用药,因为他们未注意到任何改善,另一名患有微小轴空病的患者在4个月后停止用药,原因是震颤和心悸加重。其余10名患者(6名患有中央轴空病,4名患有微小轴空病)完成了沙丁胺醇疗程,未出现任何明显不良反应。基线与6个月评估之间,肌动测量法、MRC评分和用力肺活量均有显著增加。对于肌动测量法和MRC,3个月时差异已很显著,这与使用结构化功能量表评估的功能能力显著提高相关。我们的结果表明,沙丁胺醇总体耐受性良好,可能对中央轴空病和微小轴空病患者均有益。需要进行更大规模的关于沙丁胺醇的前瞻性随机、双盲、安慰剂对照试验来证实这些初步发现。