WOMEN WITH FUNCTIONAL HYPOTHALAMIC AMENORRHEA BUT NOT OTHER FORMS OF ANOVULATION DISPLAY AMPLIFIED CORTISOL CONCENTRATIONS

Citation
Sl. Berga et al., WOMEN WITH FUNCTIONAL HYPOTHALAMIC AMENORRHEA BUT NOT OTHER FORMS OF ANOVULATION DISPLAY AMPLIFIED CORTISOL CONCENTRATIONS, Fertility and sterility, 67(6), 1997, pp. 1024-1030
Citations number
25
Categorie Soggetti
Obsetric & Gynecology
Journal title
ISSN journal
00150282
Volume
67
Issue
6
Year of publication
1997
Pages
1024 - 1030
Database
ISI
SICI code
0015-0282(1997)67:6<1024:WWFHAB>2.0.ZU;2-R
Abstract
Objective: To test the hypothesis that increased cortisol secretion is specific to women with decreased GnRH drive and not found in eumenorr heic women or those with other causes of anovulation. Design: Cortisol concentrations in blood were determined at 30-minute intervals for 24 hours in three well-characterized groups: women with functional hypot halamic amenorrhea, those with Other causes of anovulation, and eumeno rrheic women. Setting: Academic medical center. Patient(s): Women aged 20 through 35 years, with well-defined reproductive states. Intervent ion(s): Venous blood samples were obtained from, and psychometric inve ntories were completed by, the participants. Main Outcome Measure(s): Twenty-four-hour cortisol levels, 24-hour LH pulse patterns, and seria l P levels were measured in women with functional hypothalamic amenorr hea, eumenorrheic women, and those with other causes of anovulation. R esult(s): Cortisol secretion was higher in women with functional hypot halamic amenorrhea (n = 19) than in those with other causes of anovula tion (n = 19) or eumenorrheic women (n = 19). Six women who recovered from functional hypothalamic amenorrhea had cortisol levels comparable to those of eumenorrheic women and those with other causes of anovula tion. Conclusion(s): These data underscore the association between inc reased hypothalamic-pituitary-adrenal activity and reduced GnRH drive and support the concept that functional hypothalamic amenorrhea develo ps in response to stress-induced alterations in central neural functio n that modify hypothalamic function. (C) 1997 by American Society for Reproductive Medicine.