help button home button Endocrine Society JCEM
HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH TABLE OF CONTENTS

Journal of Clinical Endocrinology & Metabolism Vol. 69, No. 1 110-116
doi:10.1210/jcem-69-1-110
Copyright © 1989 by the Endocrine Society.
This Article
Right arrow Full Text (PDF)
Right arrow Submit a related Letter to the Editor
Right arrow Alert me when this article is cited
Right arrow Alert me when eLetters are posted
Right arrow Alert me if a correction is posted
Services
Right arrow Email this article to a friend
Right arrow Similar articles in this journal
Right arrow Similar articles in PubMed
Right arrow Alert me to new issues of the journal
Right arrow Download to citation manager
Right arrow Request Copyright Permission
Citing Articles
Right arrow Citing Articles via Google Scholar
Google Scholar
Right arrow Articles by CUNDY, T.
Right arrow Articles by WILLIAMS, R.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by CUNDY, T.
Right arrow Articles by WILLIAMS, R.

Hypogonadism and Sexual Dysfunction in Hemochromatosis: The Effects of Cirrhosis and Diabetes

TIM CUNDY, ADRIAN BOMFORD, JOAN BUTLER, MICHAEL WHEELER and ROGER WILLIAMS

Department of Medicine London, United Kingdom
Liver Unit London, United Kingdom
Department of Chemical Pathology King's College Hospital London, United Kingdom
Department of Chemical Pathology, St. Thomas's Hospital London, United Kingdom

Address all correspondence and requests for reprints to: Dr. T. Cundy, Academic Teaching Unit, Green Lane Hospital, Green Lane West, Auckland 3, New Zealand.

The contribution of diabetes and cirrhosis to sexual dysfunction and hypogonadism was evaluated by two-way analysis of variance in a group of 30 men with idiopathic hemochromatosis. The prevalence of severe sexual dysfunction was significantly higher in men with hemochromatosis than in a control group matched for prevalence of diabetes and age (P < 0.001). In both controls and hemochromatosis patients the presence of diabetes was significantly associated with sexual dysfunction (P < 0.005), but the more severe symptoms in the hemochromatosis patients were related to the additive effects of hypoandrogenism (P < 0.01). Sexual dysfunction was a common early complaint in hemochromatosis patients, but these symptoms were frequently overlooked, leading to diagnostic delay. Mean testicular volume was a useful measure of gonadal status, being significantly correlated with indices of serum free testosterone (rs = 0.83; P < 0.01) and LH (rs = 0.71; P < 0.001). The presence of cirrhosis did not contribute significantly to symptomatology, but had an effect independent of and additive to hypogonadotropic hypogonadism in reducing serum free testosterone (P < 0.02) and estradiol (P < 0.002), an effect apparently mediated through central rather than testicular mechanisms. Hypoandrogenism was associated with an increase in serum sex hormone-binding globulin (SHBG) concentrations (P < 0.005), but cirrhosis also had an independent effect in raising SHBG (P < 0.005), which could not be accounted for by changes in circulating sex hormone concentrations.

Thus, the evaluation of sexual dysfunction or hypogonadism in men with hemochromatosis requires consideration of the effects of both diabetes and cirrhosis. Because of the greater variance in SHBG some estimate of free testosterone rather than total testosterone is preferable.

Received November 28, 1988.







HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH TABLE OF CONTENTS
Endocrinology Endocrine Reviews J. Clin. End. & Metab.
Molecular Endocrinology Recent Prog. Horm. Res. All Endocrine Journals
Copyright © 1989 by The Endocrine Society