Periconceptional iron supplementation does not reduce anemia or improve iron status among pregnant women in rural Bangladesh.
October 2nd, 2009 Posted by: admin
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Periconceptional iron supplementation does not reduce anemia or improve iron status among pregnant women in rural Bangladesh.
Am J Clin Nutr. 2009 Sep 30;
Authors: Khambalia AZ, O’Connor DL, Macarthur C, Dupuis A, Zlotkin SH
BACKGROUND: There is a growing interest in periconceptional iron supplementation in developing countries by researchers and policy makers; however, there are no randomized controlled trials that examine the effectiveness of this strategy in decreasing anemia during pregnancy. OBJECTIVE: The aim was to determine whether periconceptional iron supplementation reduces anemia during pregnancy. DESIGN: A randomized, double-blind, controlled trial was conducted in rural Bangladesh. Married, nulliparous women were randomly assigned to receive daily iron and folic acid (IFA; 60 mg ferrous fumarate and 400 mug folic acid) (n = 134) or folic acid (FA; 400 mug) (n = 138) in the form of a powdered supplement added to food. Women were followed until pregnancy or the end of 9 mo. Primary outcomes included hemoglobin, plasma ferritin, and plasma transferrin receptor concentrations. RESULTS: Among 88 pregnant women, periconceptional IFA in comparison with FA did not affect anemia or iron status at 15 wk gestation. However, each 1% increase in adherence was associated with a 10-g/L increase in change in hemoglobin from baseline (P = 0.03), and those who initiated supplementation at a mean (+/-SD) time of 72.9 +/- 57.8 d before conception showed a 7.3-g/L increase in change in hemoglobin from baseline compared with those who initiated supplementation at 26.3 +/- 12.3 d after conception (P = 0.01). Among 146 nonpregnant women, IFA decreased anemia (odds ratio: 0.19; 95% CI: 0.04, 0.95) and improved iron stores (P = 0.001) more than did FA. CONCLUSIONS: Good adherence and initiation of supplementation before conception are needed to reduce anemia during early pregnancy. This trial was registered at www.clinicaltrials.gov as NCT00953134.
PMID: 19793860 [PubMed - as supplied by publisher]
