青春期前生长激素缺乏儿童每日皮下单剂量生长激素释放激素(1-29)的长期治疗。委内瑞拉合作研究小组。

R Lanes, E Carrillo
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引用次数: 7

摘要

作为一项多中心研究的一部分,评估每日皮下剂量为30微克/千克的GHRH的有效性和安全性,16名平均实足年龄为9.0 +/- 2.3岁的青春期前gh缺陷儿童接受了12至24个月的治疗。治疗6个月后,11名儿童(68.7%)被认为是良好反应,因为他们的生长速度比基线增加了2厘米/年,并继续使用GHRH,而5名受试者(31.3%)被认为是不良反应,并在接下来的6个月转而使用重组hGH。在6、12、18和24个月时,应答者的生长速度分别从基线3.4 +/- 0.7 cm/年(平均+/- SD)显著增加到6.8 +/- 0.1 cm/年、6.2 +/- 0.9 cm/年、6.6 +/- 1.0 cm/年和6.5 +/- 0.7 cm/年。骨龄的增长相当于治疗的几个月。在治疗6个月和12个月时,在4/11和6/11应答者中检测到GHRH抗体,在6个月时,在2/5无应答者中检测到GHRH抗体,但似乎不干扰生长。治疗期间无副作用或血糖和血脂水平变化。这些结果表明,GHRH(1-29)在使用的剂量和时间表通常是有效的治疗生长激素缺乏症。
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Long-term therapy with a single daily subcutaneous dose of growth hormone releasing hormone (1-29) in prepubertal growth hormone deficient children. Venezuelan Collaborative Study Group.

As part of a multicenter study to evaluate the efficacy and safety of one daily subcutaneous dose of 30 micrograms/kg of GHRH, 16 prepubertal GH-deficient children with a mean chronological age of 9.0 +/- 2.3 years were treated for 12 to 24 months. After six months of therapy 11 children (68.7%) were considered good responders in that their growth velocity increased by greater than 2 cm/yr over baseline and were continued on GHRH, while five subjects (31.3%) were regarded as poor responders and switched to recombinant hGH for the following six months. Growth velocity increased significantly in responders from a baseline of 3.4 +/- 0.7 cm/yr (mean +/- SD) to 6.8 +/- 0.1 cm/yr, 6.2 +/- 0.9 cm/yr, 6.6 +/- 1.0 cm/yr and 6.5 +/- 0.7 cm/yr at 6, 12, 18 and 24 months respectively. Bone ages advanced by an amount equivalent to the months of treatment. GHRH antibodies were detected in 4/11 and 6/11 responders at six and 12 months of treatment and in 2/5 non-responders at six months, but seemed not to interfere with growth. No side effects or changes in glucose and lipid levels were noted during therapy. These results suggest that GHRH (1-29) at the dose and schedule used is generally effective in the treatment of GH deficiency.

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