Delayed iron improves iron status without altering malaria risk in severe malarial anemia

dc.contributor.authorCusick, Sarah E.
dc.contributor.authorOpoka, Robert O.
dc.contributor.authorSsemata, Andrew S.
dc.contributor.authorGeorgieff, Michael K.
dc.contributor.authorJohn, Chandy C.
dc.contributor.departmentPediatrics, School of Medicineen_US
dc.date.accessioned2022-11-16T14:26:02Z
dc.date.available2022-11-16T14:26:02Z
dc.date.issued2020-05
dc.description.abstractBackground: WHO guidelines recommend concurrent iron and antimalarial treatment in children with malaria and iron deficiency, but iron may not be well absorbed or utilized during a malaria episode. Objectives: We aimed to determine whether starting iron 28 d after antimalarial treatment in children with severe malaria and iron deficiency would improve iron status and lower malaria risk. Methods: We conducted a randomized clinical trial on the effect of immediate compared with delayed iron treatment in Ugandan children 18 mo-5 y of age with 2 forms of severe malaria: cerebral malaria (CM; n = 79) or severe malarial anemia (SMA; n = 77). Asymptomatic community children (CC; n = 83) were enrolled as a comparison group. Children with iron deficiency, defined as zinc protoporphyrin (ZPP) ≥ 80 µmol/mol heme, were randomly assigned to receive a 3-mo course of daily oral ferrous sulfate (2 mg · kg-1 · d-1) either concurrently with antimalarial treatment (immediate arm) or 28 d after receiving antimalarial treatment (delayed arm). Children were followed for 12 mo. Results: All children with CM or SMA, and 35 (42.2%) CC, were iron-deficient and were randomly assigned to immediate or delayed iron treatment. Immediate compared with delayed iron had no effect in any of the 3 study groups on the primary study outcomes (hemoglobin concentration and prevalence of ZPP ≥ 80 µmol/mol heme at 6 mo, malaria incidence over 12 mo). However, after 12 mo, children with SMA in the delayed compared with the immediate arm had a lower prevalence of iron deficiency defined by ZPP (29.4% compared with 65.6%, P = 0.006), a lower mean concentration of soluble transferrin receptor (6.1 compared with 7.8 mg/L, P = 0.03), and showed a trend toward fewer episodes of severe malaria (incidence rate ratio: 0.39; 95% CI: 0.14, 1.12). Conclusions: In children with SMA, delayed iron treatment did not increase hemoglobin concentration, but did improve long-term iron status over 12 mo without affecting malaria incidence.This trial was registered at clinicaltrials.gov as NCT01093989.en_US
dc.eprint.versionFinal published versionen_US
dc.identifier.citationCusick SE, Opoka RO, Ssemata AS, Georgieff MK, John CC. Delayed iron improves iron status without altering malaria risk in severe malarial anemia. Am J Clin Nutr. 2020;111(5):1059-1067. doi:10.1093/ajcn/nqaa004en_US
dc.identifier.urihttps://hdl.handle.net/1805/30560
dc.language.isoen_USen_US
dc.publisherOxford University Pressen_US
dc.relation.isversionof10.1093/ajcn/nqaa004en_US
dc.relation.journalThe American Journal of Clinical Nutritionen_US
dc.rightsPublisher Policyen_US
dc.sourcePMCen_US
dc.subjectCerebral malariaen_US
dc.subjectInflammationen_US
dc.subjectIron and malariaen_US
dc.subjectIron deficiencyen_US
dc.subjectMalariaen_US
dc.subjectSevere malarial anemiaen_US
dc.subjectZinc protoporphyrinen_US
dc.titleDelayed iron improves iron status without altering malaria risk in severe malarial anemiaen_US
dc.typeArticleen_US
ul.alternative.fulltexthttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC7198296/en_US
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