de Zegher F, Maes M, Gargosky S E, Heinrichs C, Du Caju M V, Thiry G, De Schepper J, Craen M, Breysem L, Löfström A, Jönsson P, Bourguignon J P, Malvaux P, Rosenfeld R G
Belgian Study Group for Pediatric Endocrinology, Department of Pediatrics, University of Leuven, Belgium.
J Clin Endocrinol Metab. 1996 May;81(5):1887-92. doi: 10.1210/jcem.81.5.8626853.
The effect of GH administration was evaluated over 2 yr in 50 short, prepubertal, non-GH deficient children born small for gestational age, who had been randomly allocated to a group receiving no treatment or daily sc GH treatment at a dose of 0.2 or 0.3 IU/kg. At the start of the study, mean age was 5.2 yr, bone age was 4.0 yr, height SDS was -3.5, height velocity SDS was -0.8, weight SDS was -2.7, and body mass index SDS was -1.9. Catch-up growth was observed in none of the untreated and all of the treated children. The response to GH treatment included a near doubling of growth velocity and of weight gain and a mean height increment of more than 2 SDS. GH treatment was associated with a distinct acceleration of bone maturation. The differences between the growth responses evoked by the two GH doses were minor. The prepubertal GH-induced catch-up growth was associated with elevated serum concentrations of insulin, insulin-like growth factor-I, insulin-like growth factor binding protein-3, and osteocalcin, whereas insulin-like growth factor-II levels remained unaltered. GH treatment was well tolerated. In conclusion, high-dose GH administration over 2 yr is emerging as a potential therapy to increase the short stature that results from insufficient catch-up growth in young children born small for gestational age. The long-term impact of this approach remains to be delineated.
在50名小于胎龄儿、青春期前、非生长激素缺乏的矮小儿童中,评估了生长激素(GH)治疗2年的效果。这些儿童被随机分配到未接受治疗组或每日皮下注射GH治疗组,治疗剂量分别为0.2或0.3 IU/kg。研究开始时,平均年龄为5.2岁,骨龄为4.0岁,身高标准差分数(SDS)为-3.5,身高生长速度SDS为-0.8,体重SDS为-2.7,体重指数SDS为-1.9。未治疗的儿童均未观察到追赶生长,而所有接受治疗的儿童均出现了追赶生长。GH治疗的反应包括生长速度和体重增加几乎翻倍,平均身高增加超过2个SDS。GH治疗与骨成熟明显加速有关。两种GH剂量引起的生长反应差异较小。青春期前GH诱导的追赶生长与血清胰岛素、胰岛素样生长因子-I、胰岛素样生长因子结合蛋白-3和骨钙素浓度升高有关,而胰岛素样生长因子-II水平保持不变。GH治疗耐受性良好。总之,2年的高剂量GH治疗正在成为一种潜在的治疗方法,以增加小于胎龄儿因追赶生长不足导致的身材矮小。这种方法的长期影响仍有待阐明。