SERUM INSULIN-LIKE GROWTH-FACTOR-I (IGF-I) AND IGF-BINDING PROTEIN-3 LEVELS ARE INCREASED IN CENTRAL PRECOCIOUS PUBERTY - EFFECTS OF 2 DIFFERENT TREATMENT REGIMENS WITH GONADOTROPIN-RELEASING-HORMONE AGONISTS,WITHOUT OR IN COMBINATION WITH AN ANTIANDROGEN (CYPROTERONE-ACETATE)

Citation
A. Juul et al., SERUM INSULIN-LIKE GROWTH-FACTOR-I (IGF-I) AND IGF-BINDING PROTEIN-3 LEVELS ARE INCREASED IN CENTRAL PRECOCIOUS PUBERTY - EFFECTS OF 2 DIFFERENT TREATMENT REGIMENS WITH GONADOTROPIN-RELEASING-HORMONE AGONISTS,WITHOUT OR IN COMBINATION WITH AN ANTIANDROGEN (CYPROTERONE-ACETATE), The Journal of clinical endocrinology and metabolism, 80(10), 1995, pp. 3059-3067
Citations number
62
Categorie Soggetti
Endocrynology & Metabolism
ISSN journal
0021972X
Volume
80
Issue
10
Year of publication
1995
Pages
3059 - 3067
Database
ISI
SICI code
0021-972X(1995)80:10<3059:SIG(AI>2.0.ZU;2-C
Abstract
Central precocious puberty (CPP) is characterized by early activation of the pituitary gonadal axis, which leads to increased growth velocit y and development of secondary sexual characteristics. It is generally believed th;at gonadal sex steroids stimulate pulsatile GH secretion, which, in)turn, stimulates insulin-like growth factor I (IGF-I) and I GF-binding protein 3 (IGFBP-3) production. However, little is known ab out GH, IGF-I, and IGFBP-3 serum levels in children with precocious pu berty. Treatment of CPP by GnRH agonists has become the treatment of c hoice. However, the effect of long term treatment with GnRH in combina tion with an antiandrogen (cyproterone acetate) to block the possible effect of adrenal androgens has not previously been evaluated. We, the refore, studied 40 patients with ere treated for 24 months with either GnRH with (Buserelin) in combination with cyproterone acetate (Androc ur; n = 23) or with long acting GnRH analog (Decapeptyl Depot; n = 17) . We found that serum IGF-I levels were increased before treatment in both groups (mean +/- SE, 446 +/- 35 and 391 +/- 35 mu g/L; P < 0.0001 , respectively) compared to those sin normal age-matched prepubertal c hildren. Similarly, IGFBP-3 levels were significantly elevated (4675 /- 209 and 4305 +/- 162 mu g/L, respectively; P < 0.0001) in the two g roups. Treatment with GnRH analog in combination with cyproterone acet ate significantly decreased height velocity and serum IGF-I and IGFBP- 3 levels to normal levels after 2 yr of treatment (P < 0.0001). Serum IGF-I levels remained unchanged during monthly im treatment with long acting GnRH analog, whereas IGFBP-3 levels significantly increased dur ing the first year of this treatment despite unmeasurable estradiol le vels. Thus, in both groups, the molar ratio between IGF-I and IGFBP-3 (i.e. free biologically active IGF-I) declined concomitantly with a de crease in growth velocity. Serum levels of IGF-I and IGFBP-3 (expresse d as the SD score for bone age), but not those of estradiol, correlate d with height velocity before and during treatment (r = 0.34; P < 0.00 01 and r = 0.24; P = 0.003, respectively). Six of the patients with a subnormal GH response to clonidine had similar IGF-I and IGFBP-3 serum levels and growth velocity compared to the other 34 girls with CPP an d a normal GH response. We conclude that circulating IGF-I and IGFBP-3 levels are involved in the increased growth in precocious puberty and that the inverse effect on IGF-I and IGFBP-3 of gonadal suppression w ith long-acting GnRH analog suggests a differential regulation of seru m IGF-I and IGFBP-3.