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Prognostic impact of mineralocorticoid receptor antagonist in patients with heart failure with preserved ejection fraction

AIMS: This study aims to investigate the prognostic impact of mineralocorticoid receptor antagonists (MRAs) on cardiovascular events in patients hospitalized for acute decompensated heart failure with preserved ejection fraction (HFpEF; defined as left ventricular ejection fraction ≥45%). METHODS AN...

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Autores principales: Suzuki, Sho, Motoki, Hirohiko, Kanzaki, Yusuke, Maruyama, Takuya, Hashizume, Naoto, Kozuka, Ayako, Yahikozawa, Kumiko, Kuwahara, Koichiro
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7524222/
https://www.ncbi.nlm.nih.gov/pubmed/32592265
http://dx.doi.org/10.1002/ehf2.12867
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author Suzuki, Sho
Motoki, Hirohiko
Kanzaki, Yusuke
Maruyama, Takuya
Hashizume, Naoto
Kozuka, Ayako
Yahikozawa, Kumiko
Kuwahara, Koichiro
author_facet Suzuki, Sho
Motoki, Hirohiko
Kanzaki, Yusuke
Maruyama, Takuya
Hashizume, Naoto
Kozuka, Ayako
Yahikozawa, Kumiko
Kuwahara, Koichiro
author_sort Suzuki, Sho
collection PubMed
description AIMS: This study aims to investigate the prognostic impact of mineralocorticoid receptor antagonists (MRAs) on cardiovascular events in patients hospitalized for acute decompensated heart failure with preserved ejection fraction (HFpEF; defined as left ventricular ejection fraction ≥45%). METHODS AND RESULTS: A prospective multicentre cohort study was conducted in Nagano prefecture, Japan, between July 2014 and December 2018 that contained 518 consecutive HFpEF patients hospitalized for acute decompensated heart failure (HF). The primary outcome was a composite of cardiovascular death and HF readmission. We compared the incidence of cardiovascular events between patients who were prescribed with MRAs and those who were not in a propensity score matched cohort using a Cox proportional hazards regression model with a propensity score derived from 23 baseline variables. For sensitivity analysis, we conducted Cox proportional hazards regression models for the primary outcome adjusting for 16 clinically relevant variables in the crude cohort. The median age was 83 years, and 53% were female. The median left ventricular ejection fraction was 61%. During a median follow‐up of 553 days, the primary outcome occurred in 192 (37%) patients. MRAs were used in 255 (49%) patients. After analysis, a matched cohort consisting of 370 patients was created. After propensity score matching, the baseline characteristics were well balanced between the two groups. The incidence of the primary outcome was significantly lower in MRA users than in non‐users [32% (59/185) vs. 49% (90/185); hazard ratio (HR) 0.669, 95% confidence interval (CI) 0.482–0.929, P = 0.016]. The incidence of cardiovascular death was also significantly lower in the MRA users [11% (21/185) vs. 22% (41/185); HR, 0.563; 95% CI, 0.333–0.953; P = 0.032]. The risk of HF readmission tended to be lower in the MRA users [29% (54/185) vs. 41% (75/185); HR, 0.738; 95% CI, 0.520–1.048; P = 0.089]. MRA use was also associated with a lower risk of the primary outcome after Cox proportional hazards analysis adjusting for 16 clinically relevant variables in the crude cohort (HR, 0.710; 95% CI 0.507–0.995; P = 0.047). CONCLUSIONS: Mineralocorticoid receptor antagonist use was significantly associated with a lower risk of the primary composite outcome of cardiovascular death and HF readmission in patients hospitalized for acute decompensated HFpEF. The incidence of cardiovascular mortality was also significantly lower in these patients.
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spelling pubmed-75242222020-10-02 Prognostic impact of mineralocorticoid receptor antagonist in patients with heart failure with preserved ejection fraction Suzuki, Sho Motoki, Hirohiko Kanzaki, Yusuke Maruyama, Takuya Hashizume, Naoto Kozuka, Ayako Yahikozawa, Kumiko Kuwahara, Koichiro ESC Heart Fail Original Research Articles AIMS: This study aims to investigate the prognostic impact of mineralocorticoid receptor antagonists (MRAs) on cardiovascular events in patients hospitalized for acute decompensated heart failure with preserved ejection fraction (HFpEF; defined as left ventricular ejection fraction ≥45%). METHODS AND RESULTS: A prospective multicentre cohort study was conducted in Nagano prefecture, Japan, between July 2014 and December 2018 that contained 518 consecutive HFpEF patients hospitalized for acute decompensated heart failure (HF). The primary outcome was a composite of cardiovascular death and HF readmission. We compared the incidence of cardiovascular events between patients who were prescribed with MRAs and those who were not in a propensity score matched cohort using a Cox proportional hazards regression model with a propensity score derived from 23 baseline variables. For sensitivity analysis, we conducted Cox proportional hazards regression models for the primary outcome adjusting for 16 clinically relevant variables in the crude cohort. The median age was 83 years, and 53% were female. The median left ventricular ejection fraction was 61%. During a median follow‐up of 553 days, the primary outcome occurred in 192 (37%) patients. MRAs were used in 255 (49%) patients. After analysis, a matched cohort consisting of 370 patients was created. After propensity score matching, the baseline characteristics were well balanced between the two groups. The incidence of the primary outcome was significantly lower in MRA users than in non‐users [32% (59/185) vs. 49% (90/185); hazard ratio (HR) 0.669, 95% confidence interval (CI) 0.482–0.929, P = 0.016]. The incidence of cardiovascular death was also significantly lower in the MRA users [11% (21/185) vs. 22% (41/185); HR, 0.563; 95% CI, 0.333–0.953; P = 0.032]. The risk of HF readmission tended to be lower in the MRA users [29% (54/185) vs. 41% (75/185); HR, 0.738; 95% CI, 0.520–1.048; P = 0.089]. MRA use was also associated with a lower risk of the primary outcome after Cox proportional hazards analysis adjusting for 16 clinically relevant variables in the crude cohort (HR, 0.710; 95% CI 0.507–0.995; P = 0.047). CONCLUSIONS: Mineralocorticoid receptor antagonist use was significantly associated with a lower risk of the primary composite outcome of cardiovascular death and HF readmission in patients hospitalized for acute decompensated HFpEF. The incidence of cardiovascular mortality was also significantly lower in these patients. John Wiley and Sons Inc. 2020-06-27 /pmc/articles/PMC7524222/ /pubmed/32592265 http://dx.doi.org/10.1002/ehf2.12867 Text en © 2020 The Authors. ESC Heart Failure published by John Wiley & Sons Ltd on behalf of the European Society of Cardiology This is an open access article under the terms of the http://creativecommons.org/licenses/by-nc/4.0/ License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited and is not used for commercial purposes.
spellingShingle Original Research Articles
Suzuki, Sho
Motoki, Hirohiko
Kanzaki, Yusuke
Maruyama, Takuya
Hashizume, Naoto
Kozuka, Ayako
Yahikozawa, Kumiko
Kuwahara, Koichiro
Prognostic impact of mineralocorticoid receptor antagonist in patients with heart failure with preserved ejection fraction
title Prognostic impact of mineralocorticoid receptor antagonist in patients with heart failure with preserved ejection fraction
title_full Prognostic impact of mineralocorticoid receptor antagonist in patients with heart failure with preserved ejection fraction
title_fullStr Prognostic impact of mineralocorticoid receptor antagonist in patients with heart failure with preserved ejection fraction
title_full_unstemmed Prognostic impact of mineralocorticoid receptor antagonist in patients with heart failure with preserved ejection fraction
title_short Prognostic impact of mineralocorticoid receptor antagonist in patients with heart failure with preserved ejection fraction
title_sort prognostic impact of mineralocorticoid receptor antagonist in patients with heart failure with preserved ejection fraction
topic Original Research Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7524222/
https://www.ncbi.nlm.nih.gov/pubmed/32592265
http://dx.doi.org/10.1002/ehf2.12867
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