Sex-Specific Epidemiology of Heart Failure Risk and Mortality in Europe: Results From the BiomarCaRE Consortium.


Journal

JACC. Heart failure
ISSN: 2213-1787
Titre abrégé: JACC Heart Fail
Pays: United States
ID NLM: 101598241

Informations de publication

Date de publication:
03 2019
Historique:
received: 03 05 2018
revised: 13 08 2018
accepted: 28 08 2018
entrez: 2 3 2019
pubmed: 2 3 2019
medline: 2 7 2020
Statut: ppublish

Résumé

This study investigates differences between women and men in heart failure (HF) risk and mortality. Sex differences in HF epidemiology are insufficiently understood. In 78,657 individuals (median 49.5 years of age; age range 24.1 to 98.7 years; 51.7% women) from community-based European studies (FINRISK, DanMONICA, Moli-sani, Northern Sweden) of the BiomarCaRE (Biomarker for Cardiovascular Risk Assessment in Europe) consortium, the association between incident HF and mortality, the relationship of cardiovascular risk factors, prevalent cardiovascular diseases, biomarkers (C-reactive protein [CRP]; N-terminal pro-B-type natriuretic peptide [NT-proBNP]) with incident HF, and their attributable risks were tested in women vs. men. Over a median follow-up of 12.7 years, fewer HF cases were observed in women (n = 2,399 [5.9%]) than in men (n = 2,771 [7.3%]). HF incidence increased markedly after 60 years of age, initially with a more rapid increase in men, whereas incidence in women exceeded that of men after 85 years of age. HF onset substantially increased mortality risk in both sexes. Multivariable-adjusted Cox models showed the following sex differences for the association with incident HF: systolic blood pressure hazard ratio (HR) according to SD in women of 1.09 (95% confidence interval [CI]: 1.05 to 1.14) versus HR of 1.19 (95% CI: 1.14 to 1.24) in men; heart rate HR of 0.98 (95% CI: 0.93 to 1.03) in women versus HR of 1.09 (95% CI: 1.04 to 1.13) in men; CRP HR of 1.10 (95% CI: 1.00 to 1.20) in women versus HR of 1.32 (95% CI: 1.24 to 1.41) in men; and NT-proBNP HR of 1.54 (95% CI: 1.37 to 1.74) in women versus HR of 1.89 (95% CI: 1.75 to 2.05) in men. Population-attributable risk of all risk factors combined was 59.0% in women and 62.9% in men. Women had a lower risk for HF than men. Sex differences were seen for systolic blood pressure, heart rate, CRP, and NT-proBNP, with a lower HF risk in women.

Sections du résumé

OBJECTIVES
This study investigates differences between women and men in heart failure (HF) risk and mortality.
BACKGROUND
Sex differences in HF epidemiology are insufficiently understood.
METHODS
In 78,657 individuals (median 49.5 years of age; age range 24.1 to 98.7 years; 51.7% women) from community-based European studies (FINRISK, DanMONICA, Moli-sani, Northern Sweden) of the BiomarCaRE (Biomarker for Cardiovascular Risk Assessment in Europe) consortium, the association between incident HF and mortality, the relationship of cardiovascular risk factors, prevalent cardiovascular diseases, biomarkers (C-reactive protein [CRP]; N-terminal pro-B-type natriuretic peptide [NT-proBNP]) with incident HF, and their attributable risks were tested in women vs. men.
RESULTS
Over a median follow-up of 12.7 years, fewer HF cases were observed in women (n = 2,399 [5.9%]) than in men (n = 2,771 [7.3%]). HF incidence increased markedly after 60 years of age, initially with a more rapid increase in men, whereas incidence in women exceeded that of men after 85 years of age. HF onset substantially increased mortality risk in both sexes. Multivariable-adjusted Cox models showed the following sex differences for the association with incident HF: systolic blood pressure hazard ratio (HR) according to SD in women of 1.09 (95% confidence interval [CI]: 1.05 to 1.14) versus HR of 1.19 (95% CI: 1.14 to 1.24) in men; heart rate HR of 0.98 (95% CI: 0.93 to 1.03) in women versus HR of 1.09 (95% CI: 1.04 to 1.13) in men; CRP HR of 1.10 (95% CI: 1.00 to 1.20) in women versus HR of 1.32 (95% CI: 1.24 to 1.41) in men; and NT-proBNP HR of 1.54 (95% CI: 1.37 to 1.74) in women versus HR of 1.89 (95% CI: 1.75 to 2.05) in men. Population-attributable risk of all risk factors combined was 59.0% in women and 62.9% in men.
CONCLUSIONS
Women had a lower risk for HF than men. Sex differences were seen for systolic blood pressure, heart rate, CRP, and NT-proBNP, with a lower HF risk in women.

Identifiants

pubmed: 30819375
pii: S2213-1779(18)30690-5
doi: 10.1016/j.jchf.2018.08.008
pii:
doi:

Substances chimiques

Peptide Fragments 0
pro-brain natriuretic peptide (1-76) 0
Natriuretic Peptide, Brain 114471-18-0
C-Reactive Protein 9007-41-4

Types de publication

Journal Article Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

204-213

Commentaires et corrections

Type : CommentIn

Informations de copyright

Copyright © 2019 American College of Cardiology Foundation. Published by Elsevier Inc. All rights reserved.

Auteurs

Christina Magnussen (C)

Department of General and Interventional Cardiology, University Heart Center Hamburg, Hamburg, Germany; German Center for Cardiovascular Research, partner site Hamburg/Kiel/Luebeck, Germany.

Teemu J Niiranen (TJ)

Division of Medicine, Turku University Hospital and University of Turku, Turku, Finland; National Institute for Health and Welfare, Helsinki, Finland.

Francisco M Ojeda (FM)

Department of General and Interventional Cardiology, University Heart Center Hamburg, Hamburg, Germany.

Francesco Gianfagna (F)

Department of Epidemiology and Prevention, IRCCS Neuromed, Pozzilli, Italy; Centre for Research in EPIdemiology and preventive MEDicine (EPIMED) Department of Medicine and Surgery, University of Insubria, Varese, Italy.

Stefan Blankenberg (S)

Department of General and Interventional Cardiology, University Heart Center Hamburg, Hamburg, Germany; German Center for Cardiovascular Research, partner site Hamburg/Kiel/Luebeck, Germany.

Erkki Vartiainen (E)

National Institute for Health and Welfare, Helsinki, Finland.

Susana Sans (S)

Catalan Department of Health, Barcelona, Spain.

Gerard Pasterkamp (G)

Department of Clinical Chemistry and Haematology, University Medical Center Utrecht, Utrecht, the Netherlands.

Maria Hughes (M)

Center of Excellence for Public Health, Institute of Clinical Sciences, School of Medicine, Dentistry and Biomedical Sciences, Queen's University, Belfast, Northern Ireland.

Simona Costanzo (S)

Department of Epidemiology and Prevention, IRCCS Neuromed, Pozzilli, Italy.

Maria Benedetta Donati (MB)

Department of Epidemiology and Prevention, IRCCS Neuromed, Pozzilli, Italy.

Pekka Jousilahti (P)

National Institute for Health and Welfare, Helsinki, Finland.

Allan Linneberg (A)

Centre for Clinical Research and Prevention, Frederiksberg Hospital, Copenhagen, Denmark; Department of Clinical Experimental Research, Rigshospitalet, Glostrup, Denmark; Department of Public Health, Faculty of Health and Medical Sciences, University of Copenhagen, Denmark.

Tarja Palosaari (T)

National Institute for Health and Welfare, Helsinki, Finland.

Giovanni de Gaetano (G)

Department of Epidemiology and Prevention, IRCCS Neuromed, Pozzilli, Italy.

Martin Bobak (M)

Department of Epidemiology and Public Health, University College London, London, United Kingdom.

Hester M den Ruijter (HM)

Laboratory of Experimental Cardiology, University Medical Center Utrecht, Utrecht, the Netherlands.

Torben Jørgensen (T)

Centre for Clinical Research and Prevention, Frederiksberg Hospital, Copenhagen, Denmark; Department of Public Health, Faculty of Health and Medical Sciences, University of Copenhagen, Denmark; Faculty of Medicine, University of Aalborg, Aalborg, Denmark.

Stefan Söderberg (S)

Department of Public Health and Clinical Medicine, and Heart Centre, Umeå University, Umeå, Sweden.

Kari Kuulasmaa (K)

National Institute for Health and Welfare, Helsinki, Finland.

Tanja Zeller (T)

Department of General and Interventional Cardiology, University Heart Center Hamburg, Hamburg, Germany; German Center for Cardiovascular Research, partner site Hamburg/Kiel/Luebeck, Germany.

Licia Iacoviello (L)

Department of Epidemiology and Prevention, IRCCS Neuromed, Pozzilli, Italy; Centre for Research in EPIdemiology and preventive MEDicine (EPIMED) Department of Medicine and Surgery, University of Insubria, Varese, Italy.

Veikko Salomaa (V)

National Institute for Health and Welfare, Helsinki, Finland.

Renate B Schnabel (RB)

Department of General and Interventional Cardiology, University Heart Center Hamburg, Hamburg, Germany; German Center for Cardiovascular Research, partner site Hamburg/Kiel/Luebeck, Germany. Electronic address: r.schnabel@uke.de.

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Classifications MeSH