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DOI 10.1002/hep.1840010107

Медицинская библиотека · Hepatology (Baltimore, Md.) · 1981

Patterns of hypothalamic-pituitary-gonadal dysfunction in men with liver disease due to differing etiologies.

van Thiel D H, Gavaler J S, Spero J A, Egler K M, Wright C, Sanghvi A T, Hasiba U, Lewis J H

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Аннотация

The hypothalamic-pituitary-gonadal axis was evaluated in two groups of age-matched men with documented biochemical and histologic liver disease and compared to that of age-matched normal controls. Basal testosterone levels (p less than 0.05), spermatozoa concentrations (p less than 0.01), and seminal plasma volume (p less than 0.01) were reduced in the alcoholics studied with liver disease, but not the hemophiliacs with liver disease when compared to the normal controls. No difference in estradiol levels was noted between groups. Basal follicle-stimulating hormone and luteinizing hormone (LH) concentrations were increased (both p less than 0.01) in the alcoholics while only LH concentrations were increased (p less than 0.01) in the hemophiliacs compared to the normal controls. Gonadotropins (follicle-stimulating hormone and LH) and testosterone responses to clomiphene and to luteinizing hormone-releasing factor (LH only) in the alcoholic population studied, further distinguished the alcoholics from the hemophiliacs and the normal controls. The basal levels of the other anterior pituitary hormones (growth hormone and thyroid-stimulating hormone) as well as their provocative responses to thyrotropin-releasing hormone also distinguished the alcoholics from the hemophiliac population. Based upon these results, we propose that factors other than the liver disease per se are responsible for the disturbances of hypothalamic-pituitary-gonadal function observed in men with biochemically as well as histologically advanced stable liver disease.

Для цитирования: van Thiel D H, Gavaler J S, Spero J A, Egler K M, Wright C, Sanghvi A T, Hasiba U, Lewis J H. Patterns of hypothalamic-pituitary-gonadal dysfunction in men with liver disease due to differing etiologies.. Hepatology (Baltimore, Md.). 1981. DOI: 10.1002/hep.1840010107.

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