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Iron deficiency after kidney transplantation

Iron deficiency (ID) is highly prevalent in kidney transplant recipients (KTRs) and has been independently associated with an excess mortality risk in this population. Several causes lead to ID in KTRs, including inflammation, medication and an increased iron need after transplantation. Although man...

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Autores principales: Vinke, Joanna Sophia J, Francke, Marith I, Eisenga, Michele F, Hesselink, Dennis A, de Borst, Martin H
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8577626/
https://www.ncbi.nlm.nih.gov/pubmed/32910168
http://dx.doi.org/10.1093/ndt/gfaa123
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author Vinke, Joanna Sophia J
Francke, Marith I
Eisenga, Michele F
Hesselink, Dennis A
de Borst, Martin H
author_facet Vinke, Joanna Sophia J
Francke, Marith I
Eisenga, Michele F
Hesselink, Dennis A
de Borst, Martin H
author_sort Vinke, Joanna Sophia J
collection PubMed
description Iron deficiency (ID) is highly prevalent in kidney transplant recipients (KTRs) and has been independently associated with an excess mortality risk in this population. Several causes lead to ID in KTRs, including inflammation, medication and an increased iron need after transplantation. Although many studies in other populations indicate a pivotal role for iron as a regulator of the immune system, little is known about the impact of ID on the immune system in KTRs. Moreover, clinical trials in patients with chronic kidney disease or heart failure have shown that correction of ID, with or without anaemia, improves exercise capacity and quality of life, and may improve survival. ID could therefore be a modifiable risk factor to improve graft and patient outcomes in KTRs; prospective studies are warranted to substantiate this hypothesis.
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spelling pubmed-85776262021-11-10 Iron deficiency after kidney transplantation Vinke, Joanna Sophia J Francke, Marith I Eisenga, Michele F Hesselink, Dennis A de Borst, Martin H Nephrol Dial Transplant Review Iron deficiency (ID) is highly prevalent in kidney transplant recipients (KTRs) and has been independently associated with an excess mortality risk in this population. Several causes lead to ID in KTRs, including inflammation, medication and an increased iron need after transplantation. Although many studies in other populations indicate a pivotal role for iron as a regulator of the immune system, little is known about the impact of ID on the immune system in KTRs. Moreover, clinical trials in patients with chronic kidney disease or heart failure have shown that correction of ID, with or without anaemia, improves exercise capacity and quality of life, and may improve survival. ID could therefore be a modifiable risk factor to improve graft and patient outcomes in KTRs; prospective studies are warranted to substantiate this hypothesis. Oxford University Press 2020-09-10 /pmc/articles/PMC8577626/ /pubmed/32910168 http://dx.doi.org/10.1093/ndt/gfaa123 Text en © The Author(s) 2020. Published by Oxford University Press on behalf of ERA-EDTA. https://creativecommons.org/licenses/by-nc/4.0/This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (https://creativecommons.org/licenses/by-nc/4.0/), which permits non-commercial re-use, distribution, and reproduction in any medium, provided the original work is properly cited. For commercial re-use, please contact journals.permissions@oup.com
spellingShingle Review
Vinke, Joanna Sophia J
Francke, Marith I
Eisenga, Michele F
Hesselink, Dennis A
de Borst, Martin H
Iron deficiency after kidney transplantation
title Iron deficiency after kidney transplantation
title_full Iron deficiency after kidney transplantation
title_fullStr Iron deficiency after kidney transplantation
title_full_unstemmed Iron deficiency after kidney transplantation
title_short Iron deficiency after kidney transplantation
title_sort iron deficiency after kidney transplantation
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8577626/
https://www.ncbi.nlm.nih.gov/pubmed/32910168
http://dx.doi.org/10.1093/ndt/gfaa123
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