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Sertoli cell markers in the diagnosis of paediatric male hypogonadism

  • Romina P. Grinspon , Nazareth Loreti , Débora Braslavsky , Patricia Bedecarrás , Verónica Ambao , Silvia Gottlieb , Ignacio Bergadá , Stella M. Campo and Rodolfo A. Rey EMAIL logo
Published/Copyright: January 17, 2012

Abstract

During childhood, the pituitary-testicular axis is partially dormant: testosterone secretion decreases following a drop in luteinising hormone levels; follicle-stimulating hormone (FSH) levels also go down. Conversely, Sertoli cells are most active, as revealed by the circulating levels of anti-Müllerian hormone (AMH) and inhibin B. Therefore, hypogonadism can best be evidenced, without stimulation tests, if Sertoli cell function is assessed. Serum AMH is high from fetal life until mid-puberty. Testicular AMH production increases in response to FSH and is potently inhibited by androgens. Inhibin B is high in the first years of life, then decreases partially while remaining clearly higher than in females, and increases again at puberty. Serum AMH and inhibin B are undetectable in anorchid patients. In primary or central hypogonadism affecting the whole gonad established in fetal life or childhood, all testicular markers are low. Conversely, when hypogonadism only affects Leydig cells, serum AMH and inhibin B are normal. In males of pubertal age with central hypogonadism, AMH and inhibin B are low. Treatment with FSH provokes an increase in serum levels of both Sertoli cell markers, whereas human chorionic gonadotrophin (hCG) administration increases testosterone levels. In conclusion, measurement of serum AMH and inhibin B is helpful in assessing testicular function, without need for stimulation tests, and orientates the aetiological diagnosis of paediatric male hypogonadism.


Corresponding author: Rodolfo A. Rey, MD, PhD, Centro de Investigaciones Endocrinológicas, Hospital de Niños Ricardo Gutiérrez, Gallo 1330, C1425EFD Buenos Aires, Argentina Phone: +54-11-4963-5931, Fax: +54-11-4963-5930

Received: 2011-11-16
Accepted: 2011-11-21
Published Online: 2012-01-17
Published in Print: 2012-02-01

©2012 by Walter de Gruyter Berlin Boston

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