Use of a Potent, Long Acting Agonist of Gonadotropin-Releasing Hormone in the Treatment of Precocious Puberty*
| Autor: | Margaret E. Wierman, Hans H. Bode, John F. Crigler, C. R. Rudlin, William F. Crowley, Paul A. Boepple, M. J. Mansfield, John D. Crawford |
|---|---|
| Rok vydání: | 1986 |
| Předmět: |
Male
medicine.medical_specialty medicine.drug_class Hamartoma Endocrinology Diabetes and Metabolism Puberty Precocious Gonadotropin-releasing hormone Gonadotropin-Releasing Hormone Endocrinology Internal medicine Adrenal Glands medicine Humans Precocious puberty Testosterone Insulin-Like Growth Factor I Child Bone Development Triptorelin Pamoate Adrenal Hyperplasia Congenital Estradiol Dehydroepiandrosterone Sulfate business.industry Adrenarche Dehydroepiandrosterone Luteinizing Hormone medicine.disease Growth hormone secretion Gonadotropin secretion Gonadarche Sex steroid Child Preschool Growth Hormone Female Hypothalamic Neoplasms Gonadotropin business Pituitary Hormone-Releasing Hormones |
| Zdroj: | Endocrine Reviews. 7:24-33 |
| ISSN: | 1945-7189 0163-769X |
| Popis: | Studies utilizing the administration of GnRH in various GnRH-deficient models have revealed the critical importance of the dose and mode of delivery of this releasing factor in determining the subsequent pituitary response. Chronic administration of long acting GnRH agonists (GnRHa), like continuous infusion of high doses of the native peptide, results in suppression of pituitary gonadotropin secretion. This selective and reversible suppression of gonadotropin secretion suggested several therapeutic applications for these analogs, particularly in the treatment of central precocious puberty (CPP), a disorder for which the previously available therapies lacked uniform efficacy and were associated with potential side effects. In our series, 74 children with CPP have been treated during the last 5 yr with the potent GnRH agonist, [D-Trp6, Pro9-ethylamide(NEt)]GnRH. Having selected a dose and route of administration that produced uniform suppression of spontaneous and stimulated pituitary gonadotropin secretion, GnRHa therapy resulted in a fall of gonadal sex steroid levels into the prepubertal range, a halting or regression of secondary sexual development, and a complete cessation of menses. Growth velocity slowed during therapy, with this slowing more pronounced during prolonged treatment periods and among those patients with more advanced chronological and skeletal ages. Skeletal maturation was retarded to a greater degree than linear growth, with resultant increases in the predictions for adult stature. Moreover, these benefits have been achieved in the absence of significant side effects. Complete reversal of the suppression of gonadarche has followed discontinuation of therapy; however, patterns of growth and skeletal maturation after discontinuation of GnRHa administration remain to be characterized. Thus, the impact of GnRHa therapy on final height must await further longitudinal study. The selective nature of GnRHa suppression of gonadarche also permits an investigation of the natural history of adrenarche and its discrete influences upon skeletal growth and maturation. In addition, GnRHa therapy of CPP provides a unique opportunity to study the effects of gonadal sex steroids on GH secretion and somatomedin-C (Sm-C) generation during sexual maturation. Finally, the detailed characterization of children with precocious puberty has helped to define more precisely a subset of patients whose precocity occurs in the absence of demonstrable gonadotropin secretion.(ABSTRACT TRUNCATED AT 400 WORDS) |
| Databáze: | OpenAIRE |
| Externí odkaz: |
|