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性早熟女童血清生物活性促卵泡生成素水平

Serum bioactive follicle-stimulating hormone levels in girls with precocious sexual development.

作者信息

Wang C, Zhong C Q, Leung A, Low L C

机构信息

Department of Medicine, University of Hong Kong, Queen Mary Hospital.

出版信息

J Clin Endocrinol Metab. 1990 Mar;70(3):615-9. doi: 10.1210/jcem-70-3-615.

Abstract

We studied the serum immunoreactive (immuno) and bioactive (bio) FSH concentrations in 16 prepubertal children (1.3-9 yr old), 6 girls with premature thelarche (0.8-2 yr old), and 9 girls with central precocious puberty (2.5-9.3 yr old). The serum bio-FSH was measured by the granulosa cell aromatase bioassay. The basal serum bio-FSH levels were not significantly different in patients with central precocious puberty (6.4 +/- 1.5 IU/L), premature thelarche (7.5 +/- 0.5 IU/L), and prepubertal controls (4.4 +/- 0.7 IU/L). However, the peak responses of both serum immuno- and bio-FSH levels to iv GnRH were higher in patients with premature thelarche (immuno-FSH, 29.3 +/- 2.3 IU/L; bio-FSH, 100.7 +/- 12.2 IU/L) than in those with central precocious puberty [immuno-FSH, 17.5 +/- 3.1 IU/L (p less than 0.05); bio-FSH, 42.4 +/- 9.8 IU/L (p less than 0.01)]. This suggests that in children with premature thelarche, there is a predominant immuno- as well as bio-FSH response to GnRH. After 12 months of GnRH agonist therapy, both serum immuno- and bio-FSH levels were suppressed in patients with central precocious puberty. The differences in clinical presentation between central precocious puberty and premature thelarche cannot be explained by the differences in FSH bioactivity.

摘要

我们研究了16名青春期前儿童(1.3 - 9岁)、6名乳房过早发育女童(0.8 - 2岁)和9名中枢性性早熟女童(2.5 - 9.3岁)的血清免疫反应性(免疫)和生物活性(生物)促卵泡生成素(FSH)浓度。血清生物活性FSH通过颗粒细胞芳香化酶生物测定法进行测量。中枢性性早熟患者(6.4±1.5 IU/L)、乳房过早发育患者(7.5±0.5 IU/L)和青春期前对照儿童(4.4±0.7 IU/L)的基础血清生物活性FSH水平无显著差异。然而,乳房过早发育患者血清免疫FSH和生物活性FSH水平对静脉注射促性腺激素释放激素(GnRH)的峰值反应高于中枢性性早熟患者[免疫FSH,17.5±3.1 IU/L(p<0.05);生物活性FSH,42.4±9.8 IU/L(p<0.01)]。这表明乳房过早发育儿童对GnRH存在主要的免疫及生物活性FSH反应。在接受12个月的GnRH激动剂治疗后,中枢性性早熟患者的血清免疫FSH和生物活性FSH水平均受到抑制。中枢性性早熟和乳房过早发育临床表现的差异无法用FSH生物活性的差异来解释。

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