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Respiratory infections drive hepcidin-mediated blockade of iron absorption leading to iron deficiency anemia in African children

Iron deficiency anemia (IDA) is the most prevalent nutritional condition worldwide. We studied the contribution of hepcidin-mediated iron blockade to IDA in African children. We measured hepcidin and hemoglobin weekly, and hematological, inflammatory, and iron biomarkers at baseline, 7 weeks, and 12...

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Autores principales: Prentice, Andrew M., Bah, Amat, Jallow, Momodou W., Jallow, Amadou T., Sanyang, Saikou, Sise, Ebrima A., Ceesay, Kabiru, Danso, Ebrima, Armitage, Andrew E., Pasricha, Sant-Rayn, Drakesmith, Hal, Wathuo, Miriam, Kessler, Noah, Cerami, Carla, Wegmüller, Rita
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Association for the Advancement of Science 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6436921/
https://www.ncbi.nlm.nih.gov/pubmed/30944864
http://dx.doi.org/10.1126/sciadv.aav9020
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author Prentice, Andrew M.
Bah, Amat
Jallow, Momodou W.
Jallow, Amadou T.
Sanyang, Saikou
Sise, Ebrima A.
Ceesay, Kabiru
Danso, Ebrima
Armitage, Andrew E.
Pasricha, Sant-Rayn
Drakesmith, Hal
Wathuo, Miriam
Kessler, Noah
Cerami, Carla
Wegmüller, Rita
author_facet Prentice, Andrew M.
Bah, Amat
Jallow, Momodou W.
Jallow, Amadou T.
Sanyang, Saikou
Sise, Ebrima A.
Ceesay, Kabiru
Danso, Ebrima
Armitage, Andrew E.
Pasricha, Sant-Rayn
Drakesmith, Hal
Wathuo, Miriam
Kessler, Noah
Cerami, Carla
Wegmüller, Rita
author_sort Prentice, Andrew M.
collection PubMed
description Iron deficiency anemia (IDA) is the most prevalent nutritional condition worldwide. We studied the contribution of hepcidin-mediated iron blockade to IDA in African children. We measured hepcidin and hemoglobin weekly, and hematological, inflammatory, and iron biomarkers at baseline, 7 weeks, and 12 weeks in 407 anemic (hemoglobin < 11 g/dl), otherwise healthy Gambian children (6 to 27 months). Each child maintained remarkably constant hepcidin levels (P < 0.0001 for between-child variance), with half consistently maintaining levels that indicate physiological blockade of iron absorption. Hepcidin was strongly predicted by nurse-ascribed adverse events with dominant signals from respiratory infections and fevers (all P < 0.0001). Diarrhea and fecal calprotectin were not associated with hepcidin. In multivariate analysis, C-reactive protein was the dominant predictor of hepcidin and contributed to iron blockade even at very low levels. We conclude that even low-grade inflammation, especially associated with respiratory infections, contributes to IDA in African children.
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spelling pubmed-64369212019-04-03 Respiratory infections drive hepcidin-mediated blockade of iron absorption leading to iron deficiency anemia in African children Prentice, Andrew M. Bah, Amat Jallow, Momodou W. Jallow, Amadou T. Sanyang, Saikou Sise, Ebrima A. Ceesay, Kabiru Danso, Ebrima Armitage, Andrew E. Pasricha, Sant-Rayn Drakesmith, Hal Wathuo, Miriam Kessler, Noah Cerami, Carla Wegmüller, Rita Sci Adv Research Articles Iron deficiency anemia (IDA) is the most prevalent nutritional condition worldwide. We studied the contribution of hepcidin-mediated iron blockade to IDA in African children. We measured hepcidin and hemoglobin weekly, and hematological, inflammatory, and iron biomarkers at baseline, 7 weeks, and 12 weeks in 407 anemic (hemoglobin < 11 g/dl), otherwise healthy Gambian children (6 to 27 months). Each child maintained remarkably constant hepcidin levels (P < 0.0001 for between-child variance), with half consistently maintaining levels that indicate physiological blockade of iron absorption. Hepcidin was strongly predicted by nurse-ascribed adverse events with dominant signals from respiratory infections and fevers (all P < 0.0001). Diarrhea and fecal calprotectin were not associated with hepcidin. In multivariate analysis, C-reactive protein was the dominant predictor of hepcidin and contributed to iron blockade even at very low levels. We conclude that even low-grade inflammation, especially associated with respiratory infections, contributes to IDA in African children. American Association for the Advancement of Science 2019-03-27 /pmc/articles/PMC6436921/ /pubmed/30944864 http://dx.doi.org/10.1126/sciadv.aav9020 Text en Copyright © 2019 The Authors, some rights reserved; exclusive licensee American Association for the Advancement of Science. No claim to original U.S. Government Works. Distributed under a Creative Commons Attribution License 4.0 (CC BY). http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution license (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research Articles
Prentice, Andrew M.
Bah, Amat
Jallow, Momodou W.
Jallow, Amadou T.
Sanyang, Saikou
Sise, Ebrima A.
Ceesay, Kabiru
Danso, Ebrima
Armitage, Andrew E.
Pasricha, Sant-Rayn
Drakesmith, Hal
Wathuo, Miriam
Kessler, Noah
Cerami, Carla
Wegmüller, Rita
Respiratory infections drive hepcidin-mediated blockade of iron absorption leading to iron deficiency anemia in African children
title Respiratory infections drive hepcidin-mediated blockade of iron absorption leading to iron deficiency anemia in African children
title_full Respiratory infections drive hepcidin-mediated blockade of iron absorption leading to iron deficiency anemia in African children
title_fullStr Respiratory infections drive hepcidin-mediated blockade of iron absorption leading to iron deficiency anemia in African children
title_full_unstemmed Respiratory infections drive hepcidin-mediated blockade of iron absorption leading to iron deficiency anemia in African children
title_short Respiratory infections drive hepcidin-mediated blockade of iron absorption leading to iron deficiency anemia in African children
title_sort respiratory infections drive hepcidin-mediated blockade of iron absorption leading to iron deficiency anemia in african children
topic Research Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6436921/
https://www.ncbi.nlm.nih.gov/pubmed/30944864
http://dx.doi.org/10.1126/sciadv.aav9020
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