Volume 17, Issue 1 (January 2015) 17, 149–153; 10.4103/1008-682X.135124
Male patients with terminal renal failure exhibit low serum levels of anti-mullerian hormone
Dag Eckersten1, Aleksander Giwercman2, Anders Christensson1
1Department of Nephrology and Transplantation; 2Reproductive Medicine Centre, Lund University, Skane University Hospital, Malmo, Sweden
Correspondence: Dr. A Christensson (anders.christensson@med.lu.se)
Received: 07 January 2014; Revised: 14 February 2014; Accepted: 08 April 2014
Abstract |
Male reproductive function is impaired during end-stage renal disease (ESRD). Disturbance of the hypothalamic-pituitary-gonadal axis, and therefore the regulation of sex hormones, is one of the major causes. Our focus was to include antimullerian hormone (AMH) and inhibin B concentrations. Twenty male patients on hemodialysis, median age 40 (26-48) years, were analyzed for follicle-stimulating hormone (FSH), luteinizing hormone (LH), prolactin, sex hormone-binding globulin (SHBG), testosterone, estradiol, AMH and inhibin B levels. We used 144 proven fertile men, median age 32 (19-44) years as a control group and analyzed differences using multiple linear regression. Males with ESRD demonstrated higher mean values for prolactin, 742 versus normal 210 mIE l−1 (95% confidence interval (CI): 60.3, 729), LH, 8.87 versus normal 4.5 IE l−1 (95% CI: 2.75, 6.14), and estradiol 89.7 versus normal 79.0 pmol l−1 (95% CI: −1.31, −0.15). Mean value for AMH was lower, 19.5 versus normal 47.3 pmol l−1 (95% CI: −37.6, −11.6). There were no differences found for FSH, SHBG, inhibin B and testosterone. The most important difference was found for AMH, a marker of Sertoli cell function in the testes, which decreased by close to 60% when compared with controls. Combined with an increase in LH, these findings may indicate a dysfunction of Sertoli cells and an effect on Leydig cells contributing to a potential mechanism of reproductive dysfunction in men with ESRD.
Keywords: antimullerian hormone; chronic kidney disease; end-stage renal disease; infertility; inhibin B; sex hormones
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