Pernice W, Beckmann R, Ketelsen U P, Frey M, Schmidt-Redemann B, Haap K P, Roehren R, Sauer M
Abteilung Pädiatrische Muskelerkrankungen, Universitäts-Kinderklinik, Freiburg.
Klin Wochenschr. 1988 Jul 1;66(13):565-70. doi: 10.1007/BF01720830.
The role of calcium accumulation in the pathogenesis of Duchenne muscular dystrophy (DMD) has already been discussed. Several trials with different calcium-blocking drugs have revealed no clinical benefit. In addition, the present study includes histological investigations and computer tomography to verify therapeutic effects. In a randomized placebo-controlled double-blind study, 13 DMD patients aged from 3-10 years (mean, 7 years) were treated with 5 mg/kg diltiazem daily for 1 year. Compared with before therapy, the number of calcium-positive muscular fibres was remarkably reduced in the treated DMD patients, but not in the placebo group. The evaluation of all other biochemical and clinical parameters revealed no significant effects of the diltiazem therapy. The muscular X-ray density measured by computer tomography decreased under treatment. After the evaluation of the double-blind study, the code was broken. Therapy, however, was continued in the treated group and started in the placebo group. After 3 years of diltiazem therapy the clinical status of all 26 patients of the study and 20 additional DMD patients who were treated with diltiazem was compared with 46 untreated DMD patients of the same age and stage in our department. No obvious clinical benefit of diltiazem therapy could be observed.
钙蓄积在杜氏肌营养不良症(DMD)发病机制中的作用已被讨论过。几项使用不同钙阻滞剂药物的试验均未显示出临床益处。此外,本研究包括组织学调查和计算机断层扫描以验证治疗效果。在一项随机安慰剂对照双盲研究中,13名年龄在3至10岁(平均7岁)的DMD患者每天接受5mg/kg地尔硫䓬治疗,持续1年。与治疗前相比,接受治疗的DMD患者中钙阳性肌纤维数量显著减少,而安慰剂组则未减少。对所有其他生化和临床参数的评估显示地尔硫䓬治疗无显著效果。计算机断层扫描测量的肌肉X线密度在治疗期间降低。双盲研究评估后,密码被破解。然而,治疗组继续治疗,安慰剂组开始治疗。地尔硫䓬治疗3年后,将本研究中所有26名患者以及另外20名接受地尔硫䓬治疗的DMD患者的临床状况与我们科室46名年龄和阶段相同的未治疗DMD患者进行比较。未观察到地尔硫䓬治疗有明显的临床益处。