Casazza F, Ferrari F, Finocchiaro G, Hartwig J, Piccone U, Tramarin R, Morpurgo M
Br Heart J. 1986 Apr;55(4):400-4. doi: 10.1136/hrt.55.4.400.
Nine patients with hypertrophic cardiomyopathy associated with Friedreich's ataxia were treated with the calcium antagonist verapamil, which is known to reduce myocardial hypertrophy and improve diastolic function in patients with idiopathic hypertrophic cardiomyopathy. Daily oral doses of 7 mg/kg were given for a mean (SD) of 24 (8) months. M mode echocardiography performed at the start of the study and at the end of follow up showed no significant difference between the treated group and an untreated control group of nine patients. Verapamil produced no changes in left ventricular wall thickness, mass index, left ventricular internal diameter, fractional shortening, peak normalised lengthening rate, peak rate of septal and posterior wall thinning, and time from minimum ventricular cavity dimension to mitral valve opening. Myocardial calcium overload has been suggested as a cause of cardiac disease in Friedreich's ataxia; however, verapamil had no beneficial effect on these patients with established myocardial hypertrophy.
9例伴有弗里德赖希共济失调的肥厚型心肌病患者接受了钙拮抗剂维拉帕米治疗,已知该药物可减轻特发性肥厚型心肌病患者的心肌肥厚并改善舒张功能。每日口服剂量为7mg/kg,平均(标准差)服用24(8)个月。在研究开始时和随访结束时进行的M型超声心动图显示,治疗组与9例未治疗的对照组患者之间无显著差异。维拉帕米对左心室壁厚度、质量指数、左心室内径、缩短分数、峰值标准化延长率、室间隔和后壁变薄峰值速率以及从最小心室腔尺寸到二尖瓣开放的时间均无影响。心肌钙超载被认为是弗里德赖希共济失调心脏病的一个病因;然而,维拉帕米对这些已出现心肌肥厚的患者并无有益作用。