Cargando…

Identification of heart failure with preserved ejection fraction helps risk stratification for hypertrophic cardiomyopathy

BACKGROUND: Heart failure with preserved ejection fraction (HFpEF) is the dominant form of heart failure (HF). We here aimed to investigate the characteristics and prognosis of HFpEF in patients with hypertrophic cardiomyopathy (HCM). METHODS: This was a prospective cohort study and patients with HC...

Descripción completa

Detalles Bibliográficos
Autores principales: Liu, Jie, Wang, Dong, Ruan, Jieyun, Wu, Guixin, Xu, Lianjun, Jiang, Wen, Wang, Jizheng, Sun, Xiaolu, Kang, Lianming, Song, Lei
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8790875/
https://www.ncbi.nlm.nih.gov/pubmed/35078475
http://dx.doi.org/10.1186/s12916-021-02219-7
_version_ 1784640111188639744
author Liu, Jie
Wang, Dong
Ruan, Jieyun
Wu, Guixin
Xu, Lianjun
Jiang, Wen
Wang, Jizheng
Sun, Xiaolu
Kang, Lianming
Song, Lei
author_facet Liu, Jie
Wang, Dong
Ruan, Jieyun
Wu, Guixin
Xu, Lianjun
Jiang, Wen
Wang, Jizheng
Sun, Xiaolu
Kang, Lianming
Song, Lei
author_sort Liu, Jie
collection PubMed
description BACKGROUND: Heart failure with preserved ejection fraction (HFpEF) is the dominant form of heart failure (HF). We here aimed to investigate the characteristics and prognosis of HFpEF in patients with hypertrophic cardiomyopathy (HCM). METHODS: This was a prospective cohort study and patients with HCM with available NT-proBNP results were enrolled. Patients were categorized into HFpEF [defined as LVEF ≥50%, with symptoms or signs of HF, and N-terminal pro-brain natriuretic peptide ≥800 pg/mL according to American Heart Association (AHA) criteria] and without heart failure (non-HF). The outcomes of interest were all-cause death, cardiovascular death, and sudden cardiac death (SCD). RESULTS: Of 1178 included patients with HCM, 513 (43.5%) were identified as having HFpEF according to AHA criteria. Compared with non-HF patients, patients with HFpEF had significantly larger maximal wall thickness (P < 0.001), higher maximal left ventricular outflow tract gradient (P < 0.001), higher proportion of atrial fibrillation (P < 0.001), higher incidence of all-cause death (log-rank test, P = 0.002), and cardiovascular death (log-rank test, P = 0.005). Multivariable Cox analysis showed that patients with HFpEF had a nearly two-fold higher risk of all-cause death (adjusted HR = 1.80, 95% CI 1.11–2.90; P = 0.017) and cardiovascular death (adjusted HR =1.82, 95% CI 1.05–3.18; P = 0.033) than non-HF patients. CONCLUSIONS: Patients with HCM have a high prevalence of HFpEF and those with HFpEF present greater disease severity and higher mortality than non-HF patients, and thus may require an appropriate and more aggressive treatment for HF management. Identification of patients with HFpEF using AHA criteria can provide guidance on patient risk stratification for patients with HCM. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s12916-021-02219-7.
format Online
Article
Text
id pubmed-8790875
institution National Center for Biotechnology Information
language English
publishDate 2022
publisher BioMed Central
record_format MEDLINE/PubMed
spelling pubmed-87908752022-01-26 Identification of heart failure with preserved ejection fraction helps risk stratification for hypertrophic cardiomyopathy Liu, Jie Wang, Dong Ruan, Jieyun Wu, Guixin Xu, Lianjun Jiang, Wen Wang, Jizheng Sun, Xiaolu Kang, Lianming Song, Lei BMC Med Research Article BACKGROUND: Heart failure with preserved ejection fraction (HFpEF) is the dominant form of heart failure (HF). We here aimed to investigate the characteristics and prognosis of HFpEF in patients with hypertrophic cardiomyopathy (HCM). METHODS: This was a prospective cohort study and patients with HCM with available NT-proBNP results were enrolled. Patients were categorized into HFpEF [defined as LVEF ≥50%, with symptoms or signs of HF, and N-terminal pro-brain natriuretic peptide ≥800 pg/mL according to American Heart Association (AHA) criteria] and without heart failure (non-HF). The outcomes of interest were all-cause death, cardiovascular death, and sudden cardiac death (SCD). RESULTS: Of 1178 included patients with HCM, 513 (43.5%) were identified as having HFpEF according to AHA criteria. Compared with non-HF patients, patients with HFpEF had significantly larger maximal wall thickness (P < 0.001), higher maximal left ventricular outflow tract gradient (P < 0.001), higher proportion of atrial fibrillation (P < 0.001), higher incidence of all-cause death (log-rank test, P = 0.002), and cardiovascular death (log-rank test, P = 0.005). Multivariable Cox analysis showed that patients with HFpEF had a nearly two-fold higher risk of all-cause death (adjusted HR = 1.80, 95% CI 1.11–2.90; P = 0.017) and cardiovascular death (adjusted HR =1.82, 95% CI 1.05–3.18; P = 0.033) than non-HF patients. CONCLUSIONS: Patients with HCM have a high prevalence of HFpEF and those with HFpEF present greater disease severity and higher mortality than non-HF patients, and thus may require an appropriate and more aggressive treatment for HF management. Identification of patients with HFpEF using AHA criteria can provide guidance on patient risk stratification for patients with HCM. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s12916-021-02219-7. BioMed Central 2022-01-26 /pmc/articles/PMC8790875/ /pubmed/35078475 http://dx.doi.org/10.1186/s12916-021-02219-7 Text en © The Author(s) 2022 https://creativecommons.org/licenses/by/4.0/Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/ (https://creativecommons.org/publicdomain/zero/1.0/) ) applies to the data made available in this article, unless otherwise stated in a credit line to the data.
spellingShingle Research Article
Liu, Jie
Wang, Dong
Ruan, Jieyun
Wu, Guixin
Xu, Lianjun
Jiang, Wen
Wang, Jizheng
Sun, Xiaolu
Kang, Lianming
Song, Lei
Identification of heart failure with preserved ejection fraction helps risk stratification for hypertrophic cardiomyopathy
title Identification of heart failure with preserved ejection fraction helps risk stratification for hypertrophic cardiomyopathy
title_full Identification of heart failure with preserved ejection fraction helps risk stratification for hypertrophic cardiomyopathy
title_fullStr Identification of heart failure with preserved ejection fraction helps risk stratification for hypertrophic cardiomyopathy
title_full_unstemmed Identification of heart failure with preserved ejection fraction helps risk stratification for hypertrophic cardiomyopathy
title_short Identification of heart failure with preserved ejection fraction helps risk stratification for hypertrophic cardiomyopathy
title_sort identification of heart failure with preserved ejection fraction helps risk stratification for hypertrophic cardiomyopathy
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8790875/
https://www.ncbi.nlm.nih.gov/pubmed/35078475
http://dx.doi.org/10.1186/s12916-021-02219-7
work_keys_str_mv AT liujie identificationofheartfailurewithpreservedejectionfractionhelpsriskstratificationforhypertrophiccardiomyopathy
AT wangdong identificationofheartfailurewithpreservedejectionfractionhelpsriskstratificationforhypertrophiccardiomyopathy
AT ruanjieyun identificationofheartfailurewithpreservedejectionfractionhelpsriskstratificationforhypertrophiccardiomyopathy
AT wuguixin identificationofheartfailurewithpreservedejectionfractionhelpsriskstratificationforhypertrophiccardiomyopathy
AT xulianjun identificationofheartfailurewithpreservedejectionfractionhelpsriskstratificationforhypertrophiccardiomyopathy
AT jiangwen identificationofheartfailurewithpreservedejectionfractionhelpsriskstratificationforhypertrophiccardiomyopathy
AT wangjizheng identificationofheartfailurewithpreservedejectionfractionhelpsriskstratificationforhypertrophiccardiomyopathy
AT sunxiaolu identificationofheartfailurewithpreservedejectionfractionhelpsriskstratificationforhypertrophiccardiomyopathy
AT kanglianming identificationofheartfailurewithpreservedejectionfractionhelpsriskstratificationforhypertrophiccardiomyopathy
AT songlei identificationofheartfailurewithpreservedejectionfractionhelpsriskstratificationforhypertrophiccardiomyopathy