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Delaying Iron Therapy until 28 Days after Antimalarial Treatment Is Associated with Greater Iron Incorporation and Equivalent Hematologic Recovery after 56 Days in Children: A Randomized Controlled Trial.
- Source :
-
The Journal of nutrition [J Nutr] 2016 Sep; Vol. 146 (9), pp. 1769-74. Date of Electronic Publication: 2016 Jun 29. - Publication Year :
- 2016
-
Abstract
- Background: Iron therapy begun concurrently with antimalarial treatment may not be well absorbed because of malaria-induced inflammation. Delaying the start of iron therapy may permit better iron absorption and distribution.<br />Objective: We compared erythrocyte iron incorporation in children who started iron supplementation concurrently with antimalarial treatment or 28 d later. We hypothesized that delayed iron supplementation would be associated with greater incorporation and better hematologic recovery.<br />Methods: We enrolled 100 children aged 6-59 mo with malaria and hemoglobin concentrations of 50.0-99.9 g/L who presented to Mulago Hospital, Kampala, into a randomized trial of iron therapy. All children were administered antimalarial treatment. Children with zinc protoporphyrin (ZPP) ≥80 μmol/mol heme were randomly assigned to start iron supplementation concurrently with the antimalarial treatment [immediate iron (I) group] or 28 d later [delayed iron (D) group]. All children were administered iron-stable isotope (57)Fe on day 0 and (58)Fe on day 28. We compared the percentage of iron incorporation at the start of supplementation (I group at day 0 compared with D group at day 28, aim 1) and hematologic recovery at day 56 (aim 2).<br />Results: The percentage of iron incorporation (mean ± SE) was greater at day 28 in the D group (16.5% ± 1.7%) than at day 0 in the I group (7.9% ± 0.5%; P < 0.001). On day 56, concentrations of hemoglobin and ZPP and plasma ferritin, soluble transferrin receptor (sTfR), hepcidin, and C-reactive protein did not differ between the groups. On day 28, the hemoglobin (mean ± SD) and plasma iron markers (geometric mean; 95% CI) reflected poorer iron status in the D group than in the I group at this intervening time as follows: hemoglobin (105 ± 15.9 compared with 112 ± 12.4 g/L; P = 0.04), ferritin (39.3 μg/L; 23.5, 65.7 μg/L compared with 79.9 μg/L; 58.3, 110 μg/L; P = 0.02), sTfR (8.9 mg/L; 7.4, 10.7 mg/L compared with 6.7 mg/L; 6.1, 7.5 mg/L; P = 0.01), and hepcidin (13.3 ng/mL; 8.3, 21.2 ng/mL compared with 38.8 ng/mL; 28.3, 53.3 ng/mL; P < 0.001).<br />Conclusions: Delaying the start of iron improves incorporation but leads to equivalent hematologic recovery at day 56 in Ugandan children with malaria and anemia. These results do not demonstrate a clear, short-term benefit of delaying iron. This trial was registered at clinicaltrials.gov as NCT01754701.<br />Competing Interests: 2 Author disclosures: SE Cusick, RO Opoka, SA Abrams, CC John, MK Georgieff, and E Mupere, no conflicts of interest.<br /> (© 2016 American Society for Nutrition.)
- Subjects :
- Anemia, Iron-Deficiency blood
Biomarkers blood
C-Reactive Protein metabolism
Child, Preschool
Dietary Supplements
Erythrocytes metabolism
Female
Ferritins blood
Follow-Up Studies
Hemoglobins metabolism
Hepcidins blood
Humans
Infant
Inflammation blood
Inflammation etiology
Iron blood
Iron Isotopes administration & dosage
Iron Isotopes blood
Malaria complications
Male
Protoporphyrins blood
Receptors, Transferrin blood
Anemia, Iron-Deficiency drug therapy
Antimalarials administration & dosage
Iron administration & dosage
Malaria drug therapy
Subjects
Details
- Language :
- English
- ISSN :
- 1541-6100
- Volume :
- 146
- Issue :
- 9
- Database :
- MEDLINE
- Journal :
- The Journal of nutrition
- Publication Type :
- Academic Journal
- Accession number :
- 27358418
- Full Text :
- https://doi.org/10.3945/jn.116.233239