Temporal trends in lifetime risks of atrial fibrillation and its complications between 2000 and 2022: Danish, nationwide, population based cohort study.


Journal

BMJ (Clinical research ed.)
ISSN: 1756-1833
Titre abrégé: BMJ
Pays: England
ID NLM: 8900488

Informations de publication

Date de publication:
17 Apr 2024
Historique:
accepted: 27 02 2024
medline: 19 4 2024
pubmed: 18 4 2024
entrez: 17 4 2024
Statut: epublish

Résumé

To examine how the lifetime risks of atrial fibrillation and of complications after atrial fibrillation changed over time. Danish, nationwide, population based cohort study. Population of Denmark from 1 January 2000 to 31 December 2022. 3.5 million individuals (51.7% women and 48.3% men) who did not have atrial fibrillation at 45 years of age or older were followed up until incident atrial fibrillation, migration, death, or end of follow-up, whichever came first. All 362 721 individuals with incident atrial fibrillation (46.4% women and 53.6% men), but with no prevalent complication, were further followed up until incident heart failure, stroke, or myocardial infarction. Lifetime risk of atrial fibrillation and lifetime risks of complications after atrial fibrillation over two prespecified periods (2000-10 The lifetime risk of atrial fibrillation increased from 24.2% in 2000-10 to 30.9% in 2011-22 (difference 6.7% (95% confidence interval 6.5% to 6.8%)). After atrial fibrillation, the most frequent complication was heart failure with a lifetime risk of 42.9% in 2000-10 and 42.1% in 2011-22 (-0.8% (-3.8% to 2.2%)). Individuals with atrial fibrillation lost 14.4 years with no heart failure. The lifetime risks of stroke and of myocardial infarction after atrial fibrillation decreased slightly between the two periods, from 22.4% to 19.9% for stroke (-2.5% (-4.2% to -0.7%)) and from 13.7% to 9.8% for myocardial infarction (-3.9% (-5.3% to -2.4%). No evidence was reported of a differential decrease between men and women. Lifetime risk of atrial fibrillation increased over two decades of follow-up. In individuals with atrial fibrillation, about two in five developed heart failure and one in five had a stroke over their remaining lifetime after atrial fibrillation diagnosis, with no or only small improvement over time. Stroke risks and heart failure prevention strategies are needed for people with atrial fibrillation.

Identifiants

pubmed: 38631726
doi: 10.1136/bmj-2023-077209
pmc: PMC11019491
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

e077209

Informations de copyright

© Author(s) (or their employer(s)) 2019. Re-use permitted under CC BY-NC. No commercial re-use. See rights and permissions. Published by BMJ.

Déclaration de conflit d'intérêts

Competing interests: All authors have completed the ICMJE uniform disclosure form at www.icmje.org/disclosure-of-interest and declare NV has served as an advisory board member and consultant for AstraZeneca, no fees were received personally. SPJ has an institutional research grant from BMS/Pfizer (not related to the current study) and personal consulting fees received from BMS and Pfizer. EJB has a grant R01HL092577; American Heart Association AF AHA_18SFRN34110082. LF is supported by the Health Research Foundation of Central Denmark Region and has served as a consultant for BMS/Pfizer and AstraZeneca. LT was supported by a research grant from the American Heart Association (18SFRN34150007). PC and LS declare no competing interests.

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Auteurs

Nicklas Vinter (N)

Danish Center for Health Services Research, Department of Clinical Medicine, Aalborg University, Aalborg, Denmark nicvin@rm.dk.
Diagnostic Centre, University Clinic for Development of Innovative Patient Pathways, Silkeborg Regional Hospital, Silkeborg, Denmark.
Department of Clinical Medicine, Aarhus University, Aarhus, Denmark.

Pia Cordsen (P)

Danish Center for Health Services Research, Department of Clinical Medicine, Aalborg University, Aalborg, Denmark.

Søren Paaske Johnsen (SP)

Danish Center for Health Services Research, Department of Clinical Medicine, Aalborg University, Aalborg, Denmark.

Laila Staerk (L)

Department of Clinical Medicine, Copenhagen University Hospital-Amager and Hvidovre, Copenhagen, Denmark.

Emelia J Benjamin (EJ)

Department of Medicine, Boston Medical Center, Boston University Chobanian and Avedisian School of Medicine, Boston, MA, USA.
Department of Epidemiology, Boston University School of Public Health, Boston, MA, USA.

Lars Frost (L)

Diagnostic Centre, University Clinic for Development of Innovative Patient Pathways, Silkeborg Regional Hospital, Silkeborg, Denmark.
Department of Clinical Medicine, Aarhus University, Aarhus, Denmark.

Ludovic Trinquart (L)

Danish Center for Health Services Research, Department of Clinical Medicine, Aalborg University, Aalborg, Denmark.
Tufts Clinical and Translational Science Institute, Tufts University, Boston, MA, USA.
Institute for Clinical Research and Health Policy Studies, Tufts Medical Center, Boston, MA, USA.
Department of Biostatistics, Boston University School of Public Health, Boston, MA, USA.

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Classifications MeSH