Hopwood N J, Hintz R L, Gertner J M, Attie K M, Johanson A J, Baptista J, Kuntze J, Blizzard R M, Cara J F, Chernausek S D
University of Michigan Medical Center, Ann Arbor 48109.
J Pediatr. 1993 Aug;123(2):215-22. doi: 10.1016/s0022-3476(05)81691-9.
Short-term administration of human growth hormone to children with idiopathic short stature can improve mean growth rate and predicted adult height. It is yet unknown whether therapy would alter pubertal development or affect final height. Three-year treatment results in a group of children with idiopathic short stature are reported. For year 1 of the study, 121 prepubertal children were randomly selected to receive somatotropin, 0.3 mg/kg per week, administered subcutaneously three times weekly (n = 63), or to be nontreatment control subjects (n = 58). After 1 year, all subjects were again randomly selected to receive either three-times-weekly or daily dosing at the same total dose. For the 92 subjects who completed 36 months of treatment, mean growth rate increased from a mean of 4.6 cm/yr before treatment to a mean of 8.0 cm/yr in the first year of treatment. Daily dosing resulted in a significantly faster mean growth rate (9.0 cm/yr) than three-times-weekly dosing (7.8 cm/yr) (p = 0.0005). Mean growth rates were 7.6 and 7.2 cm/yr during years 2 and 3, respectively, and did not differ by dosing group. Mean standardized height for all subjects improved from -2.7 to -1.6 after 3 years. When the growth rate was standardized for bone age, however, subjects who remained prepubertal had a significantly greater gain in mean height SD score than subjects who became pubertal during that 3-year period (p < 0.02). Mean standardized Bayley-Pinneau predicted adult height SD score increased from -2.7 to -1.6 and was independent of the timing of pubertal onset, but for individuals this score was more variable. Year-1 growth response, expressed as growth rate or change in height SD score, was the best predictor of growth in subsequent years. Responses to therapy could not be reliably predicted from baseline anthropometric variables, plasma insulin-like growth factor I SD score, growth hormone levels. Final height assessment will be needed to determine the ultimate benefit of therapy.
对特发性身材矮小儿童短期给予人生长激素可提高平均生长速率并改善预测的成人身高。目前尚不清楚该治疗是否会改变青春期发育或影响最终身高。本文报告了一组特发性身材矮小儿童的三年治疗结果。在研究的第1年,121名青春期前儿童被随机分为两组,一组接受生长激素治疗,剂量为每周0.3mg/kg,每周皮下注射三次(n = 63),另一组作为未治疗的对照对象(n = 58)。1年后,所有受试者再次被随机分为每周三次或每日给药组,总剂量相同。对于完成36个月治疗的92名受试者,平均生长速率从治疗前的平均每年4.6cm增加到治疗第1年的平均每年8.0cm。每日给药组的平均生长速率(每年9.0cm)显著快于每周三次给药组(每年7.8cm)(p = 0.0005)。第2年和第3年的平均生长速率分别为每年7.6cm和7.2cm,且给药组间无无差异无差异。所有受试者的平均标准化身高在3年后从 -2.7改善至 -1.6。然而,当根据骨龄对生长速率进行标准化时,在这3年期间仍处于青春期前的受试者的平均身高标准差得分的增加显著大于进入青春期的受试者(p < 0.02)。平均标准化的贝利 - 平诺预测成人身高标准差得分从 -2.7增加到 -1.6,且与青春期开始时间无关,但对于个体而言,该得分的变异性更大。第1年的生长反应,以生长速率或身高标准差得分的变化表示,是后续几年生长的最佳预测指标。无法根据基线人体测量变量、血浆胰岛素样生长因子I标准差得分、生长激素水平可靠地预测对治疗的反应。需要进行最终身高评估以确定治疗的最终益处。