GROWTH-HORMONE, INSULIN-LIKE GROWTH-FACTOR-I AXIS, AND INSULIN-SECRETION IN HYPERANDROGENIC ADOLESCENTS

Citation
L. Ibanez et al., GROWTH-HORMONE, INSULIN-LIKE GROWTH-FACTOR-I AXIS, AND INSULIN-SECRETION IN HYPERANDROGENIC ADOLESCENTS, Fertility and sterility, 64(6), 1995, pp. 1113-1119
Citations number
25
Categorie Soggetti
Obsetric & Gynecology
Journal title
ISSN journal
00150282
Volume
64
Issue
6
Year of publication
1995
Pages
1113 - 1119
Database
ISI
SICI code
0015-0282(1995)64:6<1113:GIGAAI>2.0.ZU;2-O
Abstract
Objective: To assess GH and insulin-like growth factor I (IGF-I) axis variability in hyperandrogenic adolescents with different sources of a ndrogen excess and their relationship with insulin resistance. Design: Baseline IGF-I, insulin-like growth factor binding protein-1 (IGFBP-1 ), IGFBP-3, GH response to the exercise-propranolol test, and insulin responses to a standard oral glucose tolerance test were compared amon g patients with functional ovarian hyperandrogenism, hyperandrogenic n onfunctional ovarian hyperandrogenism patients, and age-matched contro ls. Setting: Outpatient clinic in a medical center. Patients: Twenty-o ne adolescents with ovarian (group A) and 17 with nonovarian (group B) hyperandrogenism, and 20 controls. Results: Serum IGF-I and poststimu lated GH levels were similar among groups, whereas serum IGFBP-3 level s were significantly lower in group A than in controls. Mean serum ins ulin levels were significantly higher in patients than in controls, wh ereas 24% of patients had abnormal insulin responses to glucose and/or insulin sensitivity indexes. Serum IGFBP-3 levels correlated negative ly with the free androgen index (free androgen index = T/sex hormone-b inding globulin [SHBG] x 100), whereas mean serum insulin levels corre lated positively with the free androgen index and negatively with SHBG levels in all subjects. Conclusions: Hyperinsulinemia is common in hy perandrogenic adolescents and correlates with the degree of hyperandro genism and not with the androgen source. Hyperinsulinemia and decrease d IGFBP-3 levels may enhance IGF-I bioavailability, which in turn may both decrease SHBG levels and increase androgen production.