Hibi I, Tanaka T, Tanae A, Kagawa J, Hashimoto N, Yoshizawa A, Shizume K
Division of Endocrinology and Metabolism, National Children's Hospital, Tokyo, Japan.
J Clin Endocrinol Metab. 1989 Aug;69(2):221-6. doi: 10.1210/jcem-69-2-221.
One hundred and sixty-one children with idiopathic GH deficiency who received GH treatment were followed until they reached their final height. Final height was found to be influenced by gonadal function. In 108 patients who had spontaneous puberty (91 boys and 17 girls; group A), the mean final height was 151.8 +/- 6.6 (+/- SD) cm in boys and 141.7 +/- 7.4 cm in girls. In 29 patients with combined GH and gonadotropin deficiency (23 boys and 6 girls; group C), whose pubertal development was induced artificially at age 19.5 +/- 2.1 yr in the boys and 18.6 +/- 1.8 yr in the girls, the mean final height was 163.7 +/- 3.9 cm in boys and 151.0 +/- 5.1 cm in girls. The differences in final height between groups A and C were significant in both boys and girls. The shorter final height in group A was caused by the shorter pubertal duration and smaller pubertal height gain than those in normal children. In 24 patients (17 boys and 7 girls; group B) who developed early signs of puberty, gonadal suppression therapy with cyproterone acetate and/or medroxyprogesterone acetate was given. The mean SD score of the final height in these 24 patients was -2.1 +/- 0.6, significantly higher than that in group A. This beneficial effect of gonadal suppression treatment on final height was caused by increases in the duration of puberty and the pubertal height gain.
161例接受生长激素(GH)治疗的特发性GH缺乏症患儿被随访至达到最终身高。发现最终身高受性腺功能影响。在108例自然青春期发育的患者中(91例男孩和17例女孩;A组),男孩的平均最终身高为151.8±6.6(±标准差)cm,女孩为141.7±7.4 cm。在29例合并GH和促性腺激素缺乏的患者中(23例男孩和6例女孩;C组),男孩在19.5±2.1岁、女孩在18.6±1.8岁时人工诱导青春期发育,男孩的平均最终身高为163.7±3.9 cm,女孩为151.0±5.1 cm。A组和C组之间男孩和女孩的最终身高差异均有统计学意义。A组最终身高较短是由于青春期持续时间较短以及青春期身高增长幅度小于正常儿童。在24例出现青春期早期迹象的患者中(17例男孩和7例女孩;B组),给予醋酸环丙孕酮和/或醋酸甲羟孕酮进行性腺抑制治疗。这24例患者最终身高的平均标准差评分是 -2.1±0.6,显著高于A组。性腺抑制治疗对最终身高的这种有益作用是由青春期持续时间和青春期身高增长幅度增加所致。