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Protective roles of erythropoiesis-stimulating proteins in chronic heart failure with anemia

Anemia is a common comorbidity in patients with chronic heart failure (CHF) and is frequently treated with erythropoiesis-stimulating proteins (ESPs). Previous studies, however, have been relatively short in duration and have not provided conclusive data on the safety or clinical efficacy of ESP tre...

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Autores principales: ZHOU, SHUQIN, ZHUANG, YUGANG, ZHAO, WEI, JIANG, BOJIE, PAN, HUI, ZHANG, XIANGYU, PENG, HU, CHEN, YANQING
Formato: Online Artículo Texto
Lenguaje:English
Publicado: D.A. Spandidos 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4113650/
https://www.ncbi.nlm.nih.gov/pubmed/25120615
http://dx.doi.org/10.3892/etm.2014.1845
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author ZHOU, SHUQIN
ZHUANG, YUGANG
ZHAO, WEI
JIANG, BOJIE
PAN, HUI
ZHANG, XIANGYU
PENG, HU
CHEN, YANQING
author_facet ZHOU, SHUQIN
ZHUANG, YUGANG
ZHAO, WEI
JIANG, BOJIE
PAN, HUI
ZHANG, XIANGYU
PENG, HU
CHEN, YANQING
author_sort ZHOU, SHUQIN
collection PubMed
description Anemia is a common comorbidity in patients with chronic heart failure (CHF) and is frequently treated with erythropoiesis-stimulating proteins (ESPs). Previous studies, however, have been relatively short in duration and have not provided conclusive data on the safety or clinical efficacy of ESP treatment. The aim of this study was to explore the safety and therapeutic effects of ESPs in patients with anemia and CHF. A systematic literature search in EMBASE and MEDLINE from their inception to July 2013 was performed, and clinical studies that evaluated the effects of ESPs among patients with CHF were identified. Randomized clinical trials comparing the effects of ESP treatment with those of placebo treatment or usual care regimes in anemic patients with CHF were included. Nine randomized, controlled trials were identified, comprising 750 patients with CHF and anemia receiving ESP treatment for between three months and one year. ESP treatment had a significantly lower risk of CHF hospitalization [relative risk (RR), 0.47; 95% confidence interval (CI), 0.32–0.70; P=0.0002] and a moderate reduction in mortality risk (RR, 0.68; 95% CI, 0.38–1.19; P=0.18). Treatment with ESPs in patients with symptomatic CHF and anemia resulted in significant improvements in hemoglobin, hematocrit and brain natriuretic peptide levels, as well as exercise capacity, renal function, New York Heart Association class and left ventricular ejection fraction. In conclusion, this study found that treatment with ESPs exerts beneficial effects against CHF and is not associated with a higher mortality rate or adverse effects. These outcomes support the instigation of a trial evaluating the treatment of anemia with ESPs in patients with chronic CHF.
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spelling pubmed-41136502014-08-12 Protective roles of erythropoiesis-stimulating proteins in chronic heart failure with anemia ZHOU, SHUQIN ZHUANG, YUGANG ZHAO, WEI JIANG, BOJIE PAN, HUI ZHANG, XIANGYU PENG, HU CHEN, YANQING Exp Ther Med Articles Anemia is a common comorbidity in patients with chronic heart failure (CHF) and is frequently treated with erythropoiesis-stimulating proteins (ESPs). Previous studies, however, have been relatively short in duration and have not provided conclusive data on the safety or clinical efficacy of ESP treatment. The aim of this study was to explore the safety and therapeutic effects of ESPs in patients with anemia and CHF. A systematic literature search in EMBASE and MEDLINE from their inception to July 2013 was performed, and clinical studies that evaluated the effects of ESPs among patients with CHF were identified. Randomized clinical trials comparing the effects of ESP treatment with those of placebo treatment or usual care regimes in anemic patients with CHF were included. Nine randomized, controlled trials were identified, comprising 750 patients with CHF and anemia receiving ESP treatment for between three months and one year. ESP treatment had a significantly lower risk of CHF hospitalization [relative risk (RR), 0.47; 95% confidence interval (CI), 0.32–0.70; P=0.0002] and a moderate reduction in mortality risk (RR, 0.68; 95% CI, 0.38–1.19; P=0.18). Treatment with ESPs in patients with symptomatic CHF and anemia resulted in significant improvements in hemoglobin, hematocrit and brain natriuretic peptide levels, as well as exercise capacity, renal function, New York Heart Association class and left ventricular ejection fraction. In conclusion, this study found that treatment with ESPs exerts beneficial effects against CHF and is not associated with a higher mortality rate or adverse effects. These outcomes support the instigation of a trial evaluating the treatment of anemia with ESPs in patients with chronic CHF. D.A. Spandidos 2014-09 2014-07-14 /pmc/articles/PMC4113650/ /pubmed/25120615 http://dx.doi.org/10.3892/etm.2014.1845 Text en Copyright © 2014, Spandidos Publications http://creativecommons.org/licenses/by/3.0 This is an open-access article licensed under a Creative Commons Attribution-NonCommercial 3.0 Unported License. The article may be redistributed, reproduced, and reused for non-commercial purposes, provided the original source is properly cited.
spellingShingle Articles
ZHOU, SHUQIN
ZHUANG, YUGANG
ZHAO, WEI
JIANG, BOJIE
PAN, HUI
ZHANG, XIANGYU
PENG, HU
CHEN, YANQING
Protective roles of erythropoiesis-stimulating proteins in chronic heart failure with anemia
title Protective roles of erythropoiesis-stimulating proteins in chronic heart failure with anemia
title_full Protective roles of erythropoiesis-stimulating proteins in chronic heart failure with anemia
title_fullStr Protective roles of erythropoiesis-stimulating proteins in chronic heart failure with anemia
title_full_unstemmed Protective roles of erythropoiesis-stimulating proteins in chronic heart failure with anemia
title_short Protective roles of erythropoiesis-stimulating proteins in chronic heart failure with anemia
title_sort protective roles of erythropoiesis-stimulating proteins in chronic heart failure with anemia
topic Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4113650/
https://www.ncbi.nlm.nih.gov/pubmed/25120615
http://dx.doi.org/10.3892/etm.2014.1845
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