The Spectrum of Abnormal Patterns of Gonadotropin Releasing Hormone Secretion in Men with Idiopathic Hypogonadotropic Hypogonadism: Clinical and Laboratory Correlations*
- 1 February 1987
- journal article
- research article
- Published by The Endocrine Society in Journal of Clinical Endocrinology & Metabolism
- Vol. 64 (2) , 283-291
- https://doi.org/10.1210/jcem-64-2-283
Abstract
Several lines of evidence indicate that hypothalamic-pituitary-gonadal activity varies among men with idiopathic hypogonadotropic hypogonadism (IHH). To test the hypothesis that a spectrum of abnormalities of GnRH secretion underlies the syndrome of IHH, we characterized the patterns of GnRH-induced gonadotropin secretion during periods of frequent sampling in 50 consecutive men with IHH and contrasted them with those in 20 normal men. The largest group of IHH patients (n = 42) had no detectable LH or FSH pulsations and could be categorized into 2 subsets according to the presence or absence of evidence of spontaneous puberty. The most severely affected subset (n = 32), who recalled no history of puberty, had testes with a mean volume of 3.3 ± 0.5 (±SEM) ml, with a prepubertal appearance on biopsy, and often were anosmic (n = 17). The second subset of apulsatile IHH men (n = 10) had histories of partial or complete spontaneous sexual development with subsequent isolated loss of sexual function, testes with a mean volume of 13.3 ± 1.9 ml (P < 0.01 compared to the first subset), a pubertal or adult appearance of the testes oh biopsy, and an intact sense of smell. In a second group of IHH patients (n = 3), LH was secreted predominantly in a nighttime pattern similar to that of normal hildren during early puberty. These men were aged 18–24 yr, had a mean testicular volume of 10.5 ± 2.3 ml, pubertal changes on testicular biopsy, and an intact sense of smell. A third group of IHH men (n = 4) had LH pulses of abnormally low amplitude. Only one patient in this group had a history of spontaneous sexual development. The mean testicular volume of these patients was 5.6 ± 1.9 ml, and the testes appeared prepubertal (n = 3) or pubertal (n = 1) on biopsy. In addition to these groups, another patient had apparent LH pulsations and nearly normal amplitude, but the LH was bioinactive and appeared to consist chiefly of α-subunit. Testing of other anterior pituitary hormone functions did not distinguish IHH men from normal men. However, those IHH patients with some evidence of endogenous GnRH secretion had higher basal and stimulated serum PRL levels than IHH men without such evidence (P < 0.05), suggesting an influence of GnRH on PRL secretion.Keywords
This publication has 23 references indexed in Scilit:
- Pure Alpha-Secreting Pituitary AdenomasNew England Journal of Medicine, 1981
- Simultaneous Pulsatile Release of Prolactin and Luteinizing Hormone Induced by Luteinizing Hormone-Releasing Factor Agonist*Journal of Clinical Endocrinology & Metabolism, 1981
- The Biologic Activity of a Potent Analogue of Gonadotropin-Releasing Hormone in Normal and Hypogonadotropic MenNew England Journal of Medicine, 1980
- Hypogonadism in a Male with Immunologically Active, Biologically Inactive Luteinizing Hormone: An Exception to a Venerable Rule*Journal of Clinical Endocrinology & Metabolism, 1979
- HYPOTHALAMIC FUNCTION IN MEN WITH HYPOGONADOTROPHIC HYPOGONADISMClinical Endocrinology, 1978
- FERTILE EUNUCH SYNDROME VERSUS CLASSIC HYPOGONADOTROPHIC HYPOGONADISMActa Endocrinologica, 1978
- Father-to-Son Transmission of Hypogonadism With AnosmiaAmerican Journal of Diseases of Children, 1977
- ANALYSIS OF BIOLOGICAL AND IMMUNOLOGICAL ACTIVITIES IN THE TWO POOLS OF LH RELEASED DURING CONSTANT INFUSION OF LUTEINIZING HORMONE-RELEASING HORMONE (LHRH) IN MENJournal of Clinical Endocrinology & Metabolism, 1977
- Episodic Fluctuations of Serum Gonadotropins in Pre- and Post-Pubertal Girls and BoysJournal of Clinical Endocrinology & Metabolism, 1977
- Clinical and Laboratory Heterogeneity in Idiopathic Hypogonadotropic HypogonadismJournal of Clinical Endocrinology & Metabolism, 1976