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Iron absorption and oxidant stress during erythropoietin therapy in very low birth weight premature infants: a cohort study

BACKGROUND: Iron supplementation may be associated with oxidative stress particularly in premature infants. Our purpose was to examine 1) early supplemental iron during treatment with erythropoietin (EPO) and oxidative stress; 2) enhanced iron absorption during EPO in those infants receiving human m...

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Autores principales: Friel, James K, Aziz, Khalid, Andrews, Wayne L, Serfass, Robert E
Formato: Texto
Lenguaje:English
Publicado: BioMed Central 2005
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1199603/
https://www.ncbi.nlm.nih.gov/pubmed/16080798
http://dx.doi.org/10.1186/1471-2431-5-29
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author Friel, James K
Aziz, Khalid
Andrews, Wayne L
Serfass, Robert E
author_facet Friel, James K
Aziz, Khalid
Andrews, Wayne L
Serfass, Robert E
author_sort Friel, James K
collection PubMed
description BACKGROUND: Iron supplementation may be associated with oxidative stress particularly in premature infants. Our purpose was to examine 1) early supplemental iron during treatment with erythropoietin (EPO) and oxidative stress; 2) enhanced iron absorption during EPO in those infants receiving human milk. Therefore, we determined the effect of erythropoietin plus supplemental iron intakes (4 mg/kg/d) on antioxidant status and iron incorporation. METHODS: Ten very-low-birth-weight infants who were enterally fed and receiving either human milk or formula were followed for 4 weeks during erythropoietin therapy; blood and urine were collected at 3 times; baseline, 2 and 4 weeks later. Once oral feeds commenced the study protocol was initiated. After baseline blood collection, a dose of Fe(57 )was administered. Two weeks later, a dose of Fe(58 )was administered as ferrous chloride to determine the effect of human-milk or formula on iron incorporation into RBCs. RESULTS: Infants started the study at 35 ± 13 days. Incorporation of isotope into RBCs did not differ between formula fed for Fe(57 )(mean incorporation 8 ± 2.9 n = 3) compared to human-milk fed infants (8.7 ± 5 n = 7) nor for Fe(58 )(6 ± 2.7 n = 3 vs. 8.6 ± 5 n = 7). Tissue damage measured by malondialdehyde in plasma and F-2 – isoprostanes in urine, did not differ by feed or over time. Neither ability to resist oxidative stress/nor RBC superoxide dismutase differed according to feed or over time. CONCLUSION: Data suggest that during erythropoietin therapy antioxidant defence in VLBW infants are capable of dealing with early supplemental iron during treatment with EPO.
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spelling pubmed-11996032005-09-09 Iron absorption and oxidant stress during erythropoietin therapy in very low birth weight premature infants: a cohort study Friel, James K Aziz, Khalid Andrews, Wayne L Serfass, Robert E BMC Pediatr Research Article BACKGROUND: Iron supplementation may be associated with oxidative stress particularly in premature infants. Our purpose was to examine 1) early supplemental iron during treatment with erythropoietin (EPO) and oxidative stress; 2) enhanced iron absorption during EPO in those infants receiving human milk. Therefore, we determined the effect of erythropoietin plus supplemental iron intakes (4 mg/kg/d) on antioxidant status and iron incorporation. METHODS: Ten very-low-birth-weight infants who were enterally fed and receiving either human milk or formula were followed for 4 weeks during erythropoietin therapy; blood and urine were collected at 3 times; baseline, 2 and 4 weeks later. Once oral feeds commenced the study protocol was initiated. After baseline blood collection, a dose of Fe(57 )was administered. Two weeks later, a dose of Fe(58 )was administered as ferrous chloride to determine the effect of human-milk or formula on iron incorporation into RBCs. RESULTS: Infants started the study at 35 ± 13 days. Incorporation of isotope into RBCs did not differ between formula fed for Fe(57 )(mean incorporation 8 ± 2.9 n = 3) compared to human-milk fed infants (8.7 ± 5 n = 7) nor for Fe(58 )(6 ± 2.7 n = 3 vs. 8.6 ± 5 n = 7). Tissue damage measured by malondialdehyde in plasma and F-2 – isoprostanes in urine, did not differ by feed or over time. Neither ability to resist oxidative stress/nor RBC superoxide dismutase differed according to feed or over time. CONCLUSION: Data suggest that during erythropoietin therapy antioxidant defence in VLBW infants are capable of dealing with early supplemental iron during treatment with EPO. BioMed Central 2005-08-05 /pmc/articles/PMC1199603/ /pubmed/16080798 http://dx.doi.org/10.1186/1471-2431-5-29 Text en Copyright © 2005 Friel et al; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License ( (http://creativecommons.org/licenses/by/2.0) ), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research Article
Friel, James K
Aziz, Khalid
Andrews, Wayne L
Serfass, Robert E
Iron absorption and oxidant stress during erythropoietin therapy in very low birth weight premature infants: a cohort study
title Iron absorption and oxidant stress during erythropoietin therapy in very low birth weight premature infants: a cohort study
title_full Iron absorption and oxidant stress during erythropoietin therapy in very low birth weight premature infants: a cohort study
title_fullStr Iron absorption and oxidant stress during erythropoietin therapy in very low birth weight premature infants: a cohort study
title_full_unstemmed Iron absorption and oxidant stress during erythropoietin therapy in very low birth weight premature infants: a cohort study
title_short Iron absorption and oxidant stress during erythropoietin therapy in very low birth weight premature infants: a cohort study
title_sort iron absorption and oxidant stress during erythropoietin therapy in very low birth weight premature infants: a cohort study
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1199603/
https://www.ncbi.nlm.nih.gov/pubmed/16080798
http://dx.doi.org/10.1186/1471-2431-5-29
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