Kuo H F, Liu P C, Shih K C, Lee T S, Ho L T
Department of Medicine, Veterans General Hospital-Taipei, Taiwan, R.O.C.
Zhonghua Min Guo Xiao Er Ke Yi Xue Hui Za Zhi. 1992 Jan-Feb;33(1):12-9.
Five prepubertal children with previously untreated growth hormone deficiency were enrolled in this trial and treated with authentic recombinant human growth hormone hGH, 0.1 IU/Kg/day, subcutaneously, for one year. All of the children markedly increased their growth rate; the height velocity increased from 3.4 +/- 0.7 cm/yr to 11.3 +/- 2.0 cm/yr during one year's treatment. The height-standard deviation score for chronological age increased from -4.03 +/- 0.52 to -2.70 +/- 0.68. The bone age increased from 5.6 +/- 1.5 year before treatment to 6.4 +/- 1.6 years after one-year treatment. Only one child acquired low titer anti-hGH antibodies during the course of treatment (1:2 to 1:6). No untoward symptoms were complained of by these children and no biochemical abnormalities occurred except transient subclinical hypothyroidism in one child during the treatment course.
五名青春期前患有未经治疗的生长激素缺乏症的儿童被纳入该试验,并接受了真实的重组人生长激素(hGH)治疗,剂量为0.1 IU/千克/天,皮下注射,为期一年。所有儿童的生长速度均显著提高;在一年的治疗期间,身高增长速度从3.4±0.7厘米/年增加到11.3±2.0厘米/年。按实足年龄计算的身高标准差分数从-4.03±0.52增加到-2.70±0.68。骨龄从治疗前的5.6±1.5岁增加到一年治疗后的6.4±1.6岁。在治疗过程中,只有一名儿童产生了低滴度的抗hGH抗体(1:2至1:6)。这些儿童均未主诉不良症状,除一名儿童在治疗过程中出现短暂的亚临床甲状腺功能减退外,未发生生化异常。