Suppr超能文献

青春期延迟对孤立性促性腺激素缺乏性性腺功能减退男性成年身高的影响。

The effect of pubertal delay on adult height in men with isolated hypogonadotropic hypogonadism.

作者信息

Uriarte M M, Baron J, Garcia H B, Barnes K M, Loriaux D L, Cutler G B

机构信息

Developmental Endocrinology Branch, National Institute of Child Health and Human Development, National Institutes of Health, Bethesda, Maryland 20892.

出版信息

J Clin Endocrinol Metab. 1992 Feb;74(2):436-40. doi: 10.1210/jcem.74.2.1449545.

Abstract

To determine whether delay of puberty alters adult height, we retrospectively evaluated the adult height of 41 patients who met rigorous criteria for the diagnosis of isolated hypogonadotropic hypogonadism. The adult height of these patients was compared with the mean height of normal American men at age 18 in the 1979 National Center for Health Statistics survey and with the mean adult height of 50 male normal volunteers who had been studied on the same wards as the patients with hypogonadotropic hypogonadism. The mean adult height of the men with isolated hypogonadotropic hypogonadism was 179.7 cm, which exceeded the height of the 50 control subjects and the normal American men (both 176.8 cm) by 2.9 cm (P less than 0.05 and P less than 0.006, respectively). The mean age at treatment to induce puberty was 20.0 yr, which corresponded to a mean delay in the onset of puberty of more than 8 yr relative to normal males. The final height of the men with hypogonadotropic hypogonadism correlated significantly with the duration of pubertal delay (r = 0.32, P = 0.04). Most of the enhanced mean adult height of the patients with isolated hypogonadotropic hypogonadism was attributable to those patients in whom treatment to induce puberty had been delayed to age 18 or greater. The mean adult height of these patients was 182.4 cm, or 5.6 cm greater than the mean height of the 50 controls or of normal American men (P less than 0.001). The mean adult height of patients whose treatment began between 10 and 17 yr of age was 175.0 cm, which did not differ significantly from that of normal men. We conclude that prolonged delay of puberty (6 or more yr) in men with isolated hypogonadotropic hypogonadism is associated with a modest increase (approximately 5 cm) of adult height.

摘要

为了确定青春期延迟是否会改变成人身高,我们回顾性评估了41例符合严格标准诊断为特发性低促性腺激素性性腺功能减退症的患者的成人身高。将这些患者的成人身高与1979年国家卫生统计中心调查中18岁美国正常男性的平均身高以及与41例低促性腺激素性性腺功能减退症患者在同一病房接受研究的50名男性正常志愿者的平均成人身高进行比较。特发性低促性腺激素性性腺功能减退症男性的平均成人身高为179.7厘米,比50名对照受试者和美国正常男性(均为176.8厘米)的身高高出2.9厘米(P分别小于0.05和P小于0.006)。诱导青春期治疗的平均年龄为20.0岁,相对于正常男性,这相当于青春期开始平均延迟超过8年。低促性腺激素性性腺功能减退症男性的最终身高与青春期延迟持续时间显著相关(r = 0.32,P = 0.04)。特发性低促性腺激素性性腺功能减退症患者平均成人身高增加主要归因于那些诱导青春期治疗延迟至18岁或更大年龄的患者。这些患者的平均成人身高为182.4厘米,比50名对照或美国正常男性的平均身高高5.6厘米(P小于0.001)。治疗开始于10至17岁之间的患者的平均成人身高为175.0厘米,与正常男性的平均身高无显著差异。我们得出结论,特发性低促性腺激素性性腺功能减退症男性青春期长期延迟(6年或更长时间)与成人身高适度增加(约5厘米)相关。

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验