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New options for the anemia of chronic kidney disease

Anemia is a common complication of chronic kidney disease. Use of erythropoiesis-stimulating agents (ESA) has been a mainstay of treatment since 1990. A series of large trials demonstrated that ESAs have serious safety problems, including increasing cardiovascular and thrombotic events, and death. A...

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Detalles Bibliográficos
Autores principales: Coyne, Daniel W., Goldsmith, David, Macdougall, Iain C.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6341017/
https://www.ncbi.nlm.nih.gov/pubmed/30675430
http://dx.doi.org/10.1016/j.kisu.2017.09.002
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author Coyne, Daniel W.
Goldsmith, David
Macdougall, Iain C.
author_facet Coyne, Daniel W.
Goldsmith, David
Macdougall, Iain C.
author_sort Coyne, Daniel W.
collection PubMed
description Anemia is a common complication of chronic kidney disease. Use of erythropoiesis-stimulating agents (ESA) has been a mainstay of treatment since 1990. A series of large trials demonstrated that ESAs have serious safety problems, including increasing cardiovascular and thrombotic events, and death. Analyses suggest high pharmacologic doses of ESAs, rather than the highly achieved hemoglobin, may mediate harm. Hypoxia-inducible factor (HIF) activators stimulate endogenous erythropoietin production and enhance iron availability. In early clinical trials, these oral agents appear to be capable of replacing ESA therapy and minimizing the need for i.v. iron therapy for chronic kidney disease–related anemia, while having other potentially advantageous actions. Large phase 3 trials are underway with several HIF activators. This commentary reviews trends in anemia management, the safety issues related to our present therapies, the role of HIF in regulating erythropoiesis, and the diverse actions of HIF activators.
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spelling pubmed-63410172019-01-23 New options for the anemia of chronic kidney disease Coyne, Daniel W. Goldsmith, David Macdougall, Iain C. Kidney Int Suppl (2011) review Anemia is a common complication of chronic kidney disease. Use of erythropoiesis-stimulating agents (ESA) has been a mainstay of treatment since 1990. A series of large trials demonstrated that ESAs have serious safety problems, including increasing cardiovascular and thrombotic events, and death. Analyses suggest high pharmacologic doses of ESAs, rather than the highly achieved hemoglobin, may mediate harm. Hypoxia-inducible factor (HIF) activators stimulate endogenous erythropoietin production and enhance iron availability. In early clinical trials, these oral agents appear to be capable of replacing ESA therapy and minimizing the need for i.v. iron therapy for chronic kidney disease–related anemia, while having other potentially advantageous actions. Large phase 3 trials are underway with several HIF activators. This commentary reviews trends in anemia management, the safety issues related to our present therapies, the role of HIF in regulating erythropoiesis, and the diverse actions of HIF activators. Elsevier 2017-12 2017-11-17 /pmc/articles/PMC6341017/ /pubmed/30675430 http://dx.doi.org/10.1016/j.kisu.2017.09.002 Text en © 2017 International Society of Nephrology. Published by Elsevier Inc. http://creativecommons.org/licenses/by-nc-nd/4.0/ This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).
spellingShingle review
Coyne, Daniel W.
Goldsmith, David
Macdougall, Iain C.
New options for the anemia of chronic kidney disease
title New options for the anemia of chronic kidney disease
title_full New options for the anemia of chronic kidney disease
title_fullStr New options for the anemia of chronic kidney disease
title_full_unstemmed New options for the anemia of chronic kidney disease
title_short New options for the anemia of chronic kidney disease
title_sort new options for the anemia of chronic kidney disease
topic review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6341017/
https://www.ncbi.nlm.nih.gov/pubmed/30675430
http://dx.doi.org/10.1016/j.kisu.2017.09.002
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