Segal Terry Y, Mehta Ameeta, Anazodo Antoinette, Hindmarsh Peter C, Dattani Mehul T
London Centre for Paediatric Endocrinology at Great Ormond Street Hospital for Children and University College London Hospitals, London WC1N 3JH, United Kingdom.
J Clin Endocrinol Metab. 2009 Mar;94(3):780-5. doi: 10.1210/jc.2008-0302. Epub 2008 Nov 18.
Delayed puberty can be due to either constitutional delay of growth and puberty (CDGP) or hypogonadotropic hypogonadism (HH). Differentiating between the two using current testing can be difficult. We assessed the utility of a GnRH test in combination with a 3-d and 19-d human chorionic gonadotropin (HCG) test to discriminate between the two conditions.
We performed a retrospective analysis of 43 boys with pubertal delay who required pubertal induction with testosterone. All were followed through puberty; 29 were subsequently diagnosed with CDGP and 14 with HH. A standard GnRH test (2.5 microg/kg) was undertaken and was followed by a short [3 d; n = 38 (13 HH, 25 CDGP)] or extended [19 d; n = 31 (12 HH, 19 CDGP)] HCG stimulation test, or both [n = 27 (11 HH, 16 CDGP)]. Receiver operating characteristic analysis was performed to assess the performance of the tests.
Peak testosterone concentrations to both 3-d and 19-d HCG tests were significantly lower in patients with HH compared with CDGP. The 19-d test performed better than the 3-d test, and a combination of the LHRH, 3-d and 19 d HCG test [peak LH cutoff, 2.8 U/liter; peak 3-d testosterone cutoff, 1.04 microg/liter (3.6 nmol/liter); peak 19-d testosterone cutoff, 2.75 microg/liter (9.5 nmol/liter)] gave a sensitivity and a specificity of 100%.
Our data suggest that a GnRH test in combination with both a 3-d and 19-d HCG test may aid in differentiating between CDGP and HH.
青春期延迟可能是由于体质性生长和青春期延迟(CDGP)或低促性腺激素性性腺功能减退(HH)。使用目前的检测方法区分这两者可能很困难。我们评估了促性腺激素释放激素(GnRH)试验联合3天和19天的人绒毛膜促性腺激素(HCG)试验在区分这两种情况中的效用。
我们对43名需要用睾酮诱导青春期的青春期延迟男孩进行了回顾性分析。所有患者均随访至青春期结束;其中29例随后被诊断为CDGP,14例被诊断为HH。进行了标准的GnRH试验(2.5微克/千克),随后进行短期[3天;n = 38(13例HH,25例CDGP)]或延长[19天;n = 31(12例HH,19例CDGP)]的HCG刺激试验,或两者都进行[n = 27(11例HH,16例CDGP)]。进行了受试者操作特征分析以评估这些试验的性能。
与CDGP患者相比,HH患者的3天和19天HCG试验的睾酮峰值浓度显著更低。19天试验比3天试验表现更好,促性腺激素释放激素(LHRH)、3天和19天HCG试验联合[促黄体生成素(LH)峰值临界值,2.8单位/升;3天睾酮峰值临界值,1.04微克/升(3.6纳摩尔/升);19天睾酮峰值临界值,2.75微克/升(9.5纳摩尔/升)]的敏感性和特异性均为100%。
我们的数据表明,GnRH试验联合3天和19天的HCG试验可能有助于区分CDGP和HH。