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Phenotypes of heart failure with preserved ejection fraction and effect of spironolactone treatment
AIMS: The aims of this study were to explore phenotypes of heart failure with preserved ejection fraction (HFpEF) and evaluate differential effects of spironolactone treatment. METHODS AND RESULTS: A swap‐stepwise algorithm was used for variable selection. Latent class analysis based on 10 selected...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9288804/ https://www.ncbi.nlm.nih.gov/pubmed/35587714 http://dx.doi.org/10.1002/ehf2.13969 |
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author | Choy, Manting Liang, Weihao He, Jiangui Fu, Michael Dong, Yugang He, Xin Liu, Chen |
author_facet | Choy, Manting Liang, Weihao He, Jiangui Fu, Michael Dong, Yugang He, Xin Liu, Chen |
author_sort | Choy, Manting |
collection | PubMed |
description | AIMS: The aims of this study were to explore phenotypes of heart failure with preserved ejection fraction (HFpEF) and evaluate differential effects of spironolactone treatment. METHODS AND RESULTS: A swap‐stepwise algorithm was used for variable selection. Latent class analysis based on 10 selected variables was employed in a derivative set of 1540 patients from the TOPCAT trial. Cox proportional hazard models were used to evaluate the prognoses and effects of spironolactone treatment. Three phenotypes of HFpEF were identified. Phenotype 1 was the youngest with low burden of co‐morbidities. Phenotype 2 was the oldest with high prevalence of atrial fibrillation, pacemaker implantation, and hypothyroidism. Phenotype 3 was mostly obese and diabetic with high burden of other co‐morbidities. Compared with phenotype 1, phenotypes 2 (hazard ratio [HR]: 1.46; 95% confidence interval [CI]: 1.14–1.89; P = 0.003) and 3 (HR: 2.35; 95% CI: 1.80–3.07; P < 0.001) were associated with higher risks of the primary composite outcome. Spironolactone treatment was associated with a reduced risk of the primary outcome only in phenotype 1 (HR: 0.63; 95% CI: 0.40–0.98; P = 0.042). CONCLUSIONS: Three distinct HFpEF phenotypes were identified. Spironolactone treatment could improve clinical outcome in a phenotype of relatively young patients with low burden of co‐morbidities. |
format | Online Article Text |
id | pubmed-9288804 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-92888042022-07-19 Phenotypes of heart failure with preserved ejection fraction and effect of spironolactone treatment Choy, Manting Liang, Weihao He, Jiangui Fu, Michael Dong, Yugang He, Xin Liu, Chen ESC Heart Fail Original Articles AIMS: The aims of this study were to explore phenotypes of heart failure with preserved ejection fraction (HFpEF) and evaluate differential effects of spironolactone treatment. METHODS AND RESULTS: A swap‐stepwise algorithm was used for variable selection. Latent class analysis based on 10 selected variables was employed in a derivative set of 1540 patients from the TOPCAT trial. Cox proportional hazard models were used to evaluate the prognoses and effects of spironolactone treatment. Three phenotypes of HFpEF were identified. Phenotype 1 was the youngest with low burden of co‐morbidities. Phenotype 2 was the oldest with high prevalence of atrial fibrillation, pacemaker implantation, and hypothyroidism. Phenotype 3 was mostly obese and diabetic with high burden of other co‐morbidities. Compared with phenotype 1, phenotypes 2 (hazard ratio [HR]: 1.46; 95% confidence interval [CI]: 1.14–1.89; P = 0.003) and 3 (HR: 2.35; 95% CI: 1.80–3.07; P < 0.001) were associated with higher risks of the primary composite outcome. Spironolactone treatment was associated with a reduced risk of the primary outcome only in phenotype 1 (HR: 0.63; 95% CI: 0.40–0.98; P = 0.042). CONCLUSIONS: Three distinct HFpEF phenotypes were identified. Spironolactone treatment could improve clinical outcome in a phenotype of relatively young patients with low burden of co‐morbidities. John Wiley and Sons Inc. 2022-05-19 /pmc/articles/PMC9288804/ /pubmed/35587714 http://dx.doi.org/10.1002/ehf2.13969 Text en © 2022 The Authors. ESC Heart Failure published by John Wiley & Sons Ltd on behalf of European Society of Cardiology. https://creativecommons.org/licenses/by-nc/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by-nc/4.0/ (https://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 Articles Choy, Manting Liang, Weihao He, Jiangui Fu, Michael Dong, Yugang He, Xin Liu, Chen Phenotypes of heart failure with preserved ejection fraction and effect of spironolactone treatment |
title | Phenotypes of heart failure with preserved ejection fraction and effect of spironolactone treatment |
title_full | Phenotypes of heart failure with preserved ejection fraction and effect of spironolactone treatment |
title_fullStr | Phenotypes of heart failure with preserved ejection fraction and effect of spironolactone treatment |
title_full_unstemmed | Phenotypes of heart failure with preserved ejection fraction and effect of spironolactone treatment |
title_short | Phenotypes of heart failure with preserved ejection fraction and effect of spironolactone treatment |
title_sort | phenotypes of heart failure with preserved ejection fraction and effect of spironolactone treatment |
topic | Original Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9288804/ https://www.ncbi.nlm.nih.gov/pubmed/35587714 http://dx.doi.org/10.1002/ehf2.13969 |
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