Medroxyprogesterone acetate and homozygous sickle-cell disease

Lancet. 1982 Jul 31;2(8292):229-31. doi: 10.1016/s0140-6736(82)90320-8.

Abstract

The haematological and clinical effects of medroxyprogesterone acetate in homozygous sickle-cell (SS) disease were assessed in a 2-year controlled crossover trial completed by 23 patients. Haematological indices remained steady during the placebo phase, but during the medroxyprogesterone-acetate phase fetal haemoglobin, total haemoglobin, red-cell mass, and red-cell survival rose significantly, and reticulocytes, irreversibly-sickled-cell counts, and total bilirubin fell significantly. Painful crises were significantly less frequent during the medroxyprogesterone-acetate than the placebo phase. These results are compatible with an inhibition of in-vivo sickling in patients with SS disease during medroxyprogesterone-acetate treatment. The mechanisms of such an effect require further study.

Publication types

  • Clinical Trial
  • Randomized Controlled Trial

MeSH terms

  • Adult
  • Anemia, Sickle Cell / genetics
  • Anemia, Sickle Cell / prevention & control*
  • Clinical Trials as Topic
  • Double-Blind Method
  • Erythrocyte Aging / drug effects
  • Erythrocyte Count
  • Erythrocytes / drug effects*
  • Female
  • Fetal Hemoglobin / analysis
  • Homozygote
  • Humans
  • Medroxyprogesterone / analogs & derivatives*
  • Medroxyprogesterone / pharmacology
  • Medroxyprogesterone / therapeutic use
  • Medroxyprogesterone Acetate
  • Menstruation / drug effects
  • Random Allocation

Substances

  • Fetal Hemoglobin
  • Medroxyprogesterone Acetate
  • Medroxyprogesterone