4.7 Article

Anemia Offers Stronger Protection Than Sickle Cell Trait Against the Erythrocytic Stage of Falciparum Malaria and This Protection Is Reversed by Iron Supplementation

期刊

EBIOMEDICINE
卷 14, 期 -, 页码 123-130

出版社

ELSEVIER SCIENCE BV
DOI: 10.1016/j.ebiom.2016.11.011

关键词

Malaria; Iron; Sickle cell trait; Iron supplementation; Hemoglobin; Anemia

资金

  1. NIH/National Institute of Child Health and Development
  2. Bill and Melinda Gates Foundation
  3. UK Medical Research Council (MRC)
  4. Department for International Development (DFID) under the MRC/DFID Concordat
  5. Medical Research Council [MC_U123292699] Funding Source: researchfish
  6. MRC [MC_U123292699] Funding Source: UKRI

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Background: Iron deficiency causes long-term adverse consequences for children and is the most common nutritional deficiency worldwide. Observational studies suggest that iron deficiency anemia protects against Plasmodium falciparum malaria and several intervention trials have indicated that iron supplementation increases malaria risk through unknown mechanism(s). This poses a major challenge for health policy. We investigated how anemia inhibits blood stage malaria infection and how iron supplementation abrogates this protection. Methods: This observational cohort study occurred in a malaria-endemic region where sickle-cell trait is also common. We studied fresh RBCs from anemic children (135 children; age 624 months; hemoglobin < 11 g/dl) participating in an iron supplementation trial (ISRCTN registry, number ISRCTN07210906) in which they received iron (12 mg/day) as part of a micronutrient powder for 84 days. Children donated RBCs at baseline, Day 49, and Day 84 for use in flow cytometry-based in vitro growth and invasion assays with P. falciparum laboratory and field strains. In vitro parasite growth in subject RBCs was the primary endpoint. Findings: Anemia substantially reduced the invasion and growth of both laboratory and field strains of P. falciparum in vitro (similar to 10% growth reduction per standard deviation shift in hemoglobin). The population level impact against erythrocytic stage malaria was 15.9% from anemia compared to 3.5% for sickle-cell trait. Parasite growth was 2.4 fold higher after 49 days of iron supplementation relative to baseline (p < 0.001), paralleling increases in erythropoiesis. Interpretation: These results confirm and quantify a plausible mechanism by which anemia protects African children against falciparum malaria, an effect that is substantially greater than the protection offered by sickle-cell trait. Iron supplementation completely reversed the observed protection and hence should be accompanied by malaria prophylaxis. Lower hemoglobin levels typically seen in populations of African descent may reflect past genetic selection by malaria. Crown Copyright (C) 2016 Published by Elsevier B.V.

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