Zatz M, Betti R T, Frota-Pessoa O
Am J Med Genet. 1986 Jul;24(3):549-66. doi: 10.1002/ajmg.1320240322.
A controlled, double-blind therapeutic trial with the drug mazindol, a growth hormone inhibitor, was performed in a pair of 7 1/2 year-old monozygotic twins, with Duchenne muscular dystrophy (DMD). The rationale for this trial was based on a patient (reported previously) affected simultaneously with DMD and growth hormone (GH) deficiency, who is showing a benign course of the dystrophic process and is still walking at 18 years. One of the twins received 2 mg of mazindol daily, while the other received a placebo. The assessment, repeated every 2 months, included weight and height measurements, functional and motor ability tests, ergometry and determinations of serum enzymes and GH levels. After one year of trial the code was broken and it was seen that the twin under placebo treatment was strikingly worse than his brother, the progression of whose condition was practically arrested. These results strongly suggest that treatment with a GH inhibitor is beneficial for DMD patients.
对一对患有杜氏肌营养不良症(DMD)的7岁半同卵双胞胎进行了一项使用生长激素抑制剂马吲哚的对照双盲治疗试验。该试验的依据是一名先前报道的同时患有DMD和生长激素(GH)缺乏症的患者,其营养不良过程呈良性,18岁时仍能行走。其中一个双胞胎每天服用2毫克马吲哚,另一个服用安慰剂。每2个月重复进行一次评估,包括体重和身高测量、功能和运动能力测试、测力计测试以及血清酶和GH水平测定。试验一年后密码被破解,发现接受安慰剂治疗的双胞胎比他的兄弟明显更差,而他兄弟的病情进展实际上已停止。这些结果强烈表明,用GH抑制剂治疗对DMD患者有益。