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Measurement of iron status in chronic kidney disease

Anemia is a common complication of chronic kidney disease (CKD) in children, and dysregulation of iron homeostasis plays a central role in its pathogenesis. Optimizing iron status is a prerequisite for effective treatment of anemia. Insufficient iron can lead to inappropriate escalation of the eryth...

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Autor principal: Hayes, Wesley
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer Berlin Heidelberg 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6394676/
https://www.ncbi.nlm.nih.gov/pubmed/29666917
http://dx.doi.org/10.1007/s00467-018-3955-x
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author Hayes, Wesley
author_facet Hayes, Wesley
author_sort Hayes, Wesley
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description Anemia is a common complication of chronic kidney disease (CKD) in children, and dysregulation of iron homeostasis plays a central role in its pathogenesis. Optimizing iron status is a prerequisite for effective treatment of anemia. Insufficient iron can lead to inappropriate escalation of the erythropoiesis-stimulating agent (ESA) dose, which is associated with adverse outcomes. Excess iron supplementation also has negative sequelae including free radical tissue damage and increased risk of systemic infection. Notwithstanding the importance of optimizing bioavailable iron for erythropoiesis for children with advanced CKD, achieving this remains challenging for pediatric nephrologists due to the historical lack of practical and robust measures of iron status. In recent years, novel techniques have come to the fore to facilitate accurate and practical assessment of iron balance. These measures are the focus of this review, with emphasis on their relevance to the pediatric CKD population.
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spelling pubmed-63946762019-03-15 Measurement of iron status in chronic kidney disease Hayes, Wesley Pediatr Nephrol Educational Review Anemia is a common complication of chronic kidney disease (CKD) in children, and dysregulation of iron homeostasis plays a central role in its pathogenesis. Optimizing iron status is a prerequisite for effective treatment of anemia. Insufficient iron can lead to inappropriate escalation of the erythropoiesis-stimulating agent (ESA) dose, which is associated with adverse outcomes. Excess iron supplementation also has negative sequelae including free radical tissue damage and increased risk of systemic infection. Notwithstanding the importance of optimizing bioavailable iron for erythropoiesis for children with advanced CKD, achieving this remains challenging for pediatric nephrologists due to the historical lack of practical and robust measures of iron status. In recent years, novel techniques have come to the fore to facilitate accurate and practical assessment of iron balance. These measures are the focus of this review, with emphasis on their relevance to the pediatric CKD population. Springer Berlin Heidelberg 2018-04-17 2019 /pmc/articles/PMC6394676/ /pubmed/29666917 http://dx.doi.org/10.1007/s00467-018-3955-x Text en © The Author(s) 2018 Open Access This article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made.
spellingShingle Educational Review
Hayes, Wesley
Measurement of iron status in chronic kidney disease
title Measurement of iron status in chronic kidney disease
title_full Measurement of iron status in chronic kidney disease
title_fullStr Measurement of iron status in chronic kidney disease
title_full_unstemmed Measurement of iron status in chronic kidney disease
title_short Measurement of iron status in chronic kidney disease
title_sort measurement of iron status in chronic kidney disease
topic Educational Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6394676/
https://www.ncbi.nlm.nih.gov/pubmed/29666917
http://dx.doi.org/10.1007/s00467-018-3955-x
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