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Mineralocorticoid receptor antagonists use in patients with heart failure and impaired renal function
AIMS: Impaired renal function is a major contributor to the low proportion of mineralocorticoid receptor antagonist (MRA) treatment in patients with heart failure with reduced ejection fraction (HFrEF). Our aims were to investigate the impact of MRA treatment on all-cause mortality and worsening ren...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Public Library of Science
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8553049/ https://www.ncbi.nlm.nih.gov/pubmed/34710128 http://dx.doi.org/10.1371/journal.pone.0258949 |
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author | Jonsson Holmdahl, Anna Norberg, Helena Valham, Fredrik Bergdahl, Ellinor Lindmark, Krister |
author_facet | Jonsson Holmdahl, Anna Norberg, Helena Valham, Fredrik Bergdahl, Ellinor Lindmark, Krister |
author_sort | Jonsson Holmdahl, Anna |
collection | PubMed |
description | AIMS: Impaired renal function is a major contributor to the low proportion of mineralocorticoid receptor antagonist (MRA) treatment in patients with heart failure with reduced ejection fraction (HFrEF). Our aims were to investigate the impact of MRA treatment on all-cause mortality and worsening renal function (WRF) in patients with HFrEF and moderately impaired renal function. METHODS: Retrospective data between 2010–2018 on HFrEF patients from a single-centre hospital with estimated glomerular renal function (eGFR) < 60 ml/min/1.73 m(2) were analysed. WRF was defined as a decline of by eGFR ≥ 20%. RESULTS: 416 patients were included, 131 patients on MRA and 285 without MRA, mean age was 77 years (SD ± 9) and 82 years (SD ± 9), respectively. Median follow-up was 2 years. 128 patients (32%) experienced WRF, 25% in the MRA group and 30% in patients without MRA (p = 0.293). In multivariable analysis, hospitalization for heart failure and systolic blood pressure were associated with WRF (p = 0.015 and p = <0.001), but not use of MRA (p = 0.421). MRA treatment had no impact on the risk of adjusted all-cause mortality (HR 0.93; 95% CI, 0.66–1.32 p = 0.685). WRF was associated with increased adjusted risk of all-cause mortality (HR 1.43; 95% CI, 1.07–1.89 p = 0.014). Use of MRA did not increase the adjusted overall risk of mortality even when experiencing WRF (HR 1.15; 95% CI, 0.81–1.63 p = 0.422). CONCLUSION: In this cohort of elderly HFrEF patients with moderately impaired renal function, MRA did not increase risk for WRF or all-cause mortality. |
format | Online Article Text |
id | pubmed-8553049 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Public Library of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-85530492021-10-29 Mineralocorticoid receptor antagonists use in patients with heart failure and impaired renal function Jonsson Holmdahl, Anna Norberg, Helena Valham, Fredrik Bergdahl, Ellinor Lindmark, Krister PLoS One Research Article AIMS: Impaired renal function is a major contributor to the low proportion of mineralocorticoid receptor antagonist (MRA) treatment in patients with heart failure with reduced ejection fraction (HFrEF). Our aims were to investigate the impact of MRA treatment on all-cause mortality and worsening renal function (WRF) in patients with HFrEF and moderately impaired renal function. METHODS: Retrospective data between 2010–2018 on HFrEF patients from a single-centre hospital with estimated glomerular renal function (eGFR) < 60 ml/min/1.73 m(2) were analysed. WRF was defined as a decline of by eGFR ≥ 20%. RESULTS: 416 patients were included, 131 patients on MRA and 285 without MRA, mean age was 77 years (SD ± 9) and 82 years (SD ± 9), respectively. Median follow-up was 2 years. 128 patients (32%) experienced WRF, 25% in the MRA group and 30% in patients without MRA (p = 0.293). In multivariable analysis, hospitalization for heart failure and systolic blood pressure were associated with WRF (p = 0.015 and p = <0.001), but not use of MRA (p = 0.421). MRA treatment had no impact on the risk of adjusted all-cause mortality (HR 0.93; 95% CI, 0.66–1.32 p = 0.685). WRF was associated with increased adjusted risk of all-cause mortality (HR 1.43; 95% CI, 1.07–1.89 p = 0.014). Use of MRA did not increase the adjusted overall risk of mortality even when experiencing WRF (HR 1.15; 95% CI, 0.81–1.63 p = 0.422). CONCLUSION: In this cohort of elderly HFrEF patients with moderately impaired renal function, MRA did not increase risk for WRF or all-cause mortality. Public Library of Science 2021-10-28 /pmc/articles/PMC8553049/ /pubmed/34710128 http://dx.doi.org/10.1371/journal.pone.0258949 Text en © 2021 Jonsson Holmdahl et al https://creativecommons.org/licenses/by/4.0/This is an open access article distributed under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited. |
spellingShingle | Research Article Jonsson Holmdahl, Anna Norberg, Helena Valham, Fredrik Bergdahl, Ellinor Lindmark, Krister Mineralocorticoid receptor antagonists use in patients with heart failure and impaired renal function |
title | Mineralocorticoid receptor antagonists use in patients with heart failure and impaired renal function |
title_full | Mineralocorticoid receptor antagonists use in patients with heart failure and impaired renal function |
title_fullStr | Mineralocorticoid receptor antagonists use in patients with heart failure and impaired renal function |
title_full_unstemmed | Mineralocorticoid receptor antagonists use in patients with heart failure and impaired renal function |
title_short | Mineralocorticoid receptor antagonists use in patients with heart failure and impaired renal function |
title_sort | mineralocorticoid receptor antagonists use in patients with heart failure and impaired renal function |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8553049/ https://www.ncbi.nlm.nih.gov/pubmed/34710128 http://dx.doi.org/10.1371/journal.pone.0258949 |
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