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The Prognostic Value of Anemia in Patients with Preserved, Mildly Reduced and Recovered Ejection Fraction
Data on the relevance of anemia in heart failure (HF) patients with an ejection fraction (EF) > 40% by subgroup—preserved (HFpEF), mildly reduced (HFmrEF) and the newly defined recovered EF (HFrecEF)—are scarce. Patients with HF symptoms, elevated NT-proBNP, EF ≥ 40% and structural abnormalities...
Autores principales: | , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8871183/ https://www.ncbi.nlm.nih.gov/pubmed/35204607 http://dx.doi.org/10.3390/diagnostics12020517 |
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author | Pintér, Anita Behon, Anett Veres, Boglárka Merkel, Eperke Dóra Schwertner, Walter Richard Kuthi, Luca Katalin Masszi, Richard Lakatos, Bálint Károly Kovács, Attila Becker, Dávid Merkely, Béla Kosztin, Annamária |
author_facet | Pintér, Anita Behon, Anett Veres, Boglárka Merkel, Eperke Dóra Schwertner, Walter Richard Kuthi, Luca Katalin Masszi, Richard Lakatos, Bálint Károly Kovács, Attila Becker, Dávid Merkely, Béla Kosztin, Annamária |
author_sort | Pintér, Anita |
collection | PubMed |
description | Data on the relevance of anemia in heart failure (HF) patients with an ejection fraction (EF) > 40% by subgroup—preserved (HFpEF), mildly reduced (HFmrEF) and the newly defined recovered EF (HFrecEF)—are scarce. Patients with HF symptoms, elevated NT-proBNP, EF ≥ 40% and structural abnormalities were registered in the HFpEF-HFmrEF database. We described the outcome of our HFpEF-HFmrEF cohort by the presence of anemia. Additionally, HFrecEF patients were also selected from HFrEF patients who underwent resynchronization and, as responders, reached 40% EF. Using propensity score matching (PSM), 75 pairs from the HFpEF-HFmrEF and HFrecEF groups were matched by their clinical features. After PMS, we compared the survival of the HFpEF-HFmrEF and HFrecEF groups. Log-rank, uni-and multivariate regression analyses were performed. From 375 HFpEF-HFmrEF patients, 42 (11%) died during the median follow-up time of 1.4 years. Anemia (HR 2.77; 95%CI 1.47–5.23; p < 0.01) was one of the strongest mortality predictors, which was also confirmed by the multivariate analysis (aHR 2.33; 95%CI 1.21–4.52; p = 0.01). Through PSM, the outcomes for HFpEF-HFmrEF and HFrecEF patients with anemia were poor, exhibiting no significant difference. In HFpEF-HFmrEF, anemia was an independent mortality predictor. Its presence multiplied the mortality risk in those with EF ≥ 40%, regardless of HF etiology. |
format | Online Article Text |
id | pubmed-8871183 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-88711832022-02-25 The Prognostic Value of Anemia in Patients with Preserved, Mildly Reduced and Recovered Ejection Fraction Pintér, Anita Behon, Anett Veres, Boglárka Merkel, Eperke Dóra Schwertner, Walter Richard Kuthi, Luca Katalin Masszi, Richard Lakatos, Bálint Károly Kovács, Attila Becker, Dávid Merkely, Béla Kosztin, Annamária Diagnostics (Basel) Article Data on the relevance of anemia in heart failure (HF) patients with an ejection fraction (EF) > 40% by subgroup—preserved (HFpEF), mildly reduced (HFmrEF) and the newly defined recovered EF (HFrecEF)—are scarce. Patients with HF symptoms, elevated NT-proBNP, EF ≥ 40% and structural abnormalities were registered in the HFpEF-HFmrEF database. We described the outcome of our HFpEF-HFmrEF cohort by the presence of anemia. Additionally, HFrecEF patients were also selected from HFrEF patients who underwent resynchronization and, as responders, reached 40% EF. Using propensity score matching (PSM), 75 pairs from the HFpEF-HFmrEF and HFrecEF groups were matched by their clinical features. After PMS, we compared the survival of the HFpEF-HFmrEF and HFrecEF groups. Log-rank, uni-and multivariate regression analyses were performed. From 375 HFpEF-HFmrEF patients, 42 (11%) died during the median follow-up time of 1.4 years. Anemia (HR 2.77; 95%CI 1.47–5.23; p < 0.01) was one of the strongest mortality predictors, which was also confirmed by the multivariate analysis (aHR 2.33; 95%CI 1.21–4.52; p = 0.01). Through PSM, the outcomes for HFpEF-HFmrEF and HFrecEF patients with anemia were poor, exhibiting no significant difference. In HFpEF-HFmrEF, anemia was an independent mortality predictor. Its presence multiplied the mortality risk in those with EF ≥ 40%, regardless of HF etiology. MDPI 2022-02-17 /pmc/articles/PMC8871183/ /pubmed/35204607 http://dx.doi.org/10.3390/diagnostics12020517 Text en © 2022 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Article Pintér, Anita Behon, Anett Veres, Boglárka Merkel, Eperke Dóra Schwertner, Walter Richard Kuthi, Luca Katalin Masszi, Richard Lakatos, Bálint Károly Kovács, Attila Becker, Dávid Merkely, Béla Kosztin, Annamária The Prognostic Value of Anemia in Patients with Preserved, Mildly Reduced and Recovered Ejection Fraction |
title | The Prognostic Value of Anemia in Patients with Preserved, Mildly Reduced and Recovered Ejection Fraction |
title_full | The Prognostic Value of Anemia in Patients with Preserved, Mildly Reduced and Recovered Ejection Fraction |
title_fullStr | The Prognostic Value of Anemia in Patients with Preserved, Mildly Reduced and Recovered Ejection Fraction |
title_full_unstemmed | The Prognostic Value of Anemia in Patients with Preserved, Mildly Reduced and Recovered Ejection Fraction |
title_short | The Prognostic Value of Anemia in Patients with Preserved, Mildly Reduced and Recovered Ejection Fraction |
title_sort | prognostic value of anemia in patients with preserved, mildly reduced and recovered ejection fraction |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8871183/ https://www.ncbi.nlm.nih.gov/pubmed/35204607 http://dx.doi.org/10.3390/diagnostics12020517 |
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