Bioavailability of carbonyl iron: a randomized, double-blind study

Eur J Haematol. 1991 May;46(5):272-8. doi: 10.1111/j.1600-0609.1991.tb01538.x.

Abstract

49 female blood donors with iron-deficiency anemia were treated with equal doses of iron either as carbonyl iron or ferrous sulfate in a randomized, double-blind fashion. The prevalence of side-effects was similar in the two groups. Mean values for hemoglobin concentration, mean corpuscular volume, corrected reticulocyte count, platelet count, serum iron, total iron-binding capacity, transferrin saturation or erythrocyte protoporphyrin did not differ significantly between the two groups throughout the study. After 16 weeks of therapy, the mean increase in hemoglobin iron was similar in both groups (p = 0.2). Estimates of net changes in total body iron suggested that the overall bioavailability of carbonyl iron was high, about 70% that of ferrous sulfate.

Publication types

  • Clinical Trial
  • Comparative Study
  • Randomized Controlled Trial

MeSH terms

  • Adult
  • Anemia, Hypochromic / blood
  • Anemia, Hypochromic / drug therapy*
  • Biological Availability
  • Double-Blind Method
  • Female
  • Ferrous Compounds / adverse effects
  • Ferrous Compounds / metabolism*
  • Ferrous Compounds / therapeutic use
  • Hemoglobins / analysis
  • Humans
  • Iron / blood*
  • Iron Carbonyl Compounds
  • Organometallic Compounds / adverse effects
  • Organometallic Compounds / metabolism*
  • Organometallic Compounds / therapeutic use
  • Time Factors
  • Transferrin / metabolism

Substances

  • Ferrous Compounds
  • Hemoglobins
  • Organometallic Compounds
  • Transferrin
  • Iron Carbonyl Compounds
  • ferrous sulfate
  • Iron