Leydig cell function in men with disorders of spermatogenesis

H. J. Ruder, D. L. Loriaux, R. J. Sherins, M. B. Lipsett

Research output: Contribution to journalArticlepeer-review

50 Scopus citations


Leydig cell function has been studied in patients with disorders of the seminiferous tubule; germinal cell aplasia, Klinefelter's syndrome, and severe germinal cell arrest. Testosterone, 1 estradiol, progesterone, 17-hydroxyprogesterone, 17-hydroxypregnenolone, and Δ5-androstenediol were measured before and after four days of hCG administration. Of the patient groups studied, only in Klinefelter's syndrome did Leydig cell function differ from normal. In Klinefelter's syndrome, there was a generally decreased steroid biosynthetic capacity of the Leydig cell, but no abnormal accumulation of steroid biosynthetic intermediates was detected. Plasma estradiol concentrations were normal suggesting that estradiol secretion remains normal in Klinefelter's syndrome. hCG produced an approximate doubling of the plasma concentrations of testosterone, 17-hydroxyprogesterone and estradiol in all subjects. The response of progesterone, 17-hydroxypregnenolone and Δ5-androstenediol were more variable, in keeping with their predominant adrenal origin in man.

Original languageEnglish (US)
Pages (from-to)244-247
Number of pages4
JournalJournal of Clinical Endocrinology and Metabolism
Issue number2
StatePublished - Feb 1974
Externally publishedYes

ASJC Scopus subject areas

  • Endocrinology, Diabetes and Metabolism
  • Biochemistry
  • Endocrinology
  • Clinical Biochemistry
  • Biochemistry, medical


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