Dutch Growth Research Foundation (M.v.d.S., A.J.L., D.C.M.v.d.K., A.C.S.H.-K.), 3016 AH Rotterdam, The Netherlands; and Erasmus University Medical Center-Sophia Children's Hospital (M.v.d.S., A.C.S.H.-K.), 3015 CN Rotterdam, The Netherlands.
J Clin Endocrinol Metab. 2016 May;101(5):2005-12. doi: 10.1210/jc.2016-1317. Epub 2016 Mar 10.
Most studies on puberty in children born small for gestational age (SGA) report height and age at onset of puberty. GH-treated SGA children with an adult height (AH) expectation below -2.5 SDS at onset of puberty can benefit from an additional 2 years of GnRH analog (GnRHa) treatment. There are no data on puberty and growth after discontinuation of GnRHa treatment in GH-treated SGA children.
This study aimed to investigate the effects on puberty and pubertal growth of 2 years GnRHa vs no GnRHa in GH-treated SGA children.
This was a GH trial involving 76 prepubertal short SGA children (36 girls) treated with GH. Thirty-two children received additional GnRHa for 2 years. Pubertal stages were 3-monthly assessed according to Tanner.
Age, bone age, and median height at pubertal onset were lower in girls and boys in the GH/GnRHa group compared with the GH group. In girls and boys treated with GH/GnRHa, pubertal duration after stop of GnRHa treatment was shorter than pubertal duration in those with GH only (40.9 vs 46.7 mo; P = .044; 50.8 vs 57.5 months; P = .006; respectively). Height gain from onset of puberty until AH, including height gain during 2 years of GnRHa treatment, was 25.4 cm in girls and 33.0 cm in boys, which was 6.6 cm more than girls and boys treated with GH only. AH was similar in children treated with GH/GnRHa compared with those with GH only.
GH-treated SGA children who start puberty with an AH expectation below -2.5 SDS and are treated with 2 years of GnRHa have a shorter pubertal duration after discontinuation of GnRHa compared with pubertal duration in children treated with GH only. Height gain from onset of puberty until AH is, however, more due to adequate growth during 2 years of GnRHa treatment resulting in a similar AH as children treated with GH only.
大多数关于出生体重小于胎龄儿(SGA)青春期的研究报告了身高和青春期开始的年龄。在青春期开始时身高预测值低于-2.5 SDS 的接受 GH 治疗的 SGA 儿童,可以从 GnRH 类似物(GnRHa)治疗额外增加 2 年中获益。在接受 GH 治疗的 SGA 儿童停止 GnRHa 治疗后,关于青春期和生长的资料尚无报道。
本研究旨在探讨 GH 治疗的 SGA 儿童中 GnRHa 治疗 2 年与不治疗 GnRHa 对青春期和青春期生长的影响。
这是一项涉及 76 名青春期前矮小 SGA 儿童(36 名女孩)的 GH 试验,他们接受 GH 治疗。32 名儿童接受了 2 年的额外 GnRHa 治疗。根据 Tanner 分期,每 3 个月评估 1 次青春期阶段。
与 GH 组相比,GH/GnRHa 组的女孩和男孩的青春期开始时的年龄、骨龄和身高中位数较低。在接受 GH/GnRHa 治疗的女孩和男孩中,GnRHa 治疗停止后的青春期持续时间短于仅接受 GH 治疗的青春期持续时间(40.9 与 46.7 个月;P =.044;50.8 与 57.5 个月;P =.006;分别)。从青春期开始到成年终身高(包括 GnRHa 治疗 2 年期间的身高增长)的身高增长在女孩中为 25.4 cm,在男孩中为 33.0 cm,比仅接受 GH 治疗的女孩和男孩多 6.6 cm。接受 GH/GnRHa 治疗的儿童的成年终身高与仅接受 GH 治疗的儿童相似。
在青春期开始时身高预测值低于-2.5 SDS 且接受 2 年 GnRHa 治疗的 GH 治疗的 SGA 儿童,在停止 GnRHa 治疗后青春期持续时间短于仅接受 GH 治疗的儿童。然而,从青春期开始到成年终身高的身高增长更多归因于 GnRHa 治疗 2 年期间的充分生长,导致与仅接受 GH 治疗的儿童相似的成年终身高。