Spreading the clinical window for diagnosing fetal-onset hypogonadism in boys

ROMINA GRINSPON; LORETI NAZARETH; DEBORA BRASLAVSKY; CLARA VALERI; SCHTEINGART HF; MARIA GABRIELA BALLERINI; PATRICIA BEDECARRAS; VERONICA AMBAO; SILVIA GOTTLIEB; MARIA GABRIELA ROPELATO; IGNACIO BERGADA; STELLA CAMPO; REY RA

Frontiers in Endocrinology

Frontiers Editorial Office

Año: 2014 vol. 5 p. 1 - 14

1664-2392

In early fetal development, the testis secretes ?independently of pituitary gonadotropins? androgens and anti-Müllerian hormone (AMH) which are essential for male sex differentiation. In the second half of fetal life, the hypothalamic-pituitary axis gains control of testicular hormone secretion. FSH controls Sertoli cell proliferation, responsible for testis volume increase and AMH and inhibin B secretion, whereas LH regulates Leydig cell androgen and INSL3 secretion, involved in the growth and trophism of male external genitalia and in testis descent. This differential regulation of testicular function between early and late fetal periods underlies the distinct clinical presentations of fetal-onset hypogonadism in the newborn male: primary hypogonadism results in ambiguous or female genitalia when early fetal-onset whereas it becomes clinically undistinguishable from central hypogonadism when established later in fetal life. The assessment of the hypothalamic-pituitary-gonadal axis in the male has classically relied on the measurement of gonadotropin and testosterone levels in serum. These hormone levels normally decline 3-6 months after birth, thus constraining the clinical evaluation window for diagnosing male hypogonadism. The advent of new markers of gonadal function has spread this clinical window beyond the first 6 months of life. In this review, we discuss the advantages and limitations of old and new markers used for the functional assessment of the hypothalamic-pituitary-testicular axis in boys suspected of fetal-onset hypogonadism.