Literature DB >> 6793494

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

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

Abstract

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.

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Year:  1981        PMID: 6793494     DOI: 10.1002/hep.1840010107

Source DB:  PubMed          Journal:  Hepatology        ISSN: 0270-9139            Impact factor:   17.425


  5 in total

1.  Hypogonadism is not related to the etiology of liver cirrhosis.

Authors:  S Kaymakoğlu; A Okten; Y Cakaloğlu; G Boztaş; F Beşişik; C Taşçioğlu; S Yalçin
Journal:  J Gastroenterol       Date:  1995-12       Impact factor: 7.527

2.  Thyroid and pituitary hormone responses to TRH in advanced nonalcoholic liver disease.

Authors:  D H Van Thiel; R Tarter; J S Gavaler; R R Schade; A Sanghvi
Journal:  J Endocrinol Invest       Date:  1986-12       Impact factor: 4.256

Review 3.  Male hypogonadism in cirrhosis and after liver transplantation.

Authors:  C Foresta; M Schipilliti; F A Ciarleglio; A Lenzi; D D'Amico
Journal:  J Endocrinol Invest       Date:  2008-05       Impact factor: 4.256

4.  Changes in pituitary secretion after administration of branched-chain amino acids to patients with hepatic cirrhosis.

Authors:  T Barreca; R Franceschini; V Messina; P Bottaro; E Rolandi
Journal:  Eur J Clin Pharmacol       Date:  1983       Impact factor: 2.953

5.  Clues to understanding the oxidation of estradiol in humans: effects of acute infectious hepatitis, autoimmune hepatitis, and chronic liver disease.

Authors:  Robert G Lahita; Robert A Schaefer; H Leon Bradlow; Mary Jeanne Kreek
Journal:  Ann N Y Acad Sci       Date:  2009-02       Impact factor: 5.691

  5 in total

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