Reversible gonadotropin deficiency in male Cushing's disease

J Clin Endocrinol Metab. 1977 Sep;45(3):488-95. doi: 10.1210/jcem-45-3-488.

Abstract

Twelve adult males with documented active Cushing's disease were studied. Mean plasma testosterone (T) was significantly decreased: 1.8 +/- 0.3 (SEM) ng/ml (N=6.8 +/- 0.5); gonadotropin measurements in 8 patients, in basal conditions and under LH-RH iv, showed a significant decrease in both FSH and LH. A further study of 11 patients in remission of Cushing's disease indicated a significant increase in plasma T and gonadotropins up to the normal range. One patient with an initial low T value had a normalized T while in remission, then a dramatic decrease when the disease relapsed. We conclude: a hypogonadotropic hypogonadism is found in male Cushing's disease; it disappears as early as hypercortisolism is suppressed. Some possible mechanisms are discussed.

MeSH terms

  • Adolescent
  • Adrenocorticotropic Hormone / blood
  • Adult
  • Chorionic Gonadotropin
  • Cushing Syndrome / blood*
  • Cushing Syndrome / drug therapy
  • Follicle Stimulating Hormone / blood
  • Gonadotropin-Releasing Hormone
  • Gonadotropins, Pituitary / blood*
  • Humans
  • Hydrocortisone / urine
  • Luteinizing Hormone / blood
  • Male
  • Middle Aged
  • Mitotane / therapeutic use
  • Testosterone / blood

Substances

  • Chorionic Gonadotropin
  • Gonadotropins, Pituitary
  • Gonadotropin-Releasing Hormone
  • Testosterone
  • Mitotane
  • Adrenocorticotropic Hormone
  • Luteinizing Hormone
  • Follicle Stimulating Hormone
  • Hydrocortisone