Evidence map›Paper›PMID 42294782›Full record

ArticleJournal of the American Heart Association2026

Menopausal Age, Number of Live Births, and Risk of Atrial Fibrillation: The Cardiovascular Health Study.

Hikaru Morooka, Emily A Rosenberg, Susan R Heckbert, Jorge R Kizer, Jennifer E Ho, Imre Janszky, Julie Horn, Kenneth J Mukamal

Abstract readMulticenter Study
In one paragraph

Article in Journal of the American Heart Association, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

8 authors.

Hikaru MorookaDepartment of Public Health and Nursing, Faculty of Medicine and Health Sciences Norwegian University of Science and Technology Trondheim Norway.ORCID 0000-0003-0758-4988
Emily A RosenbergDivision of Endocrinology, Diabetes and Metabolic Diseases Medical University of South Carolina Charleston SC USA.ORCID 0000-0001-5352-0585
Susan R HeckbertDepartment of Epidemiology University of Washington Seattle WA USA.ORCID 0000-0002-7100-512X
Jorge R KizerCardiology Section San Francisco Veterans Affairs Health Care System San Francisco CA USA.ORCID 0000-0001-9936-7803
Jennifer E HoCardiovascular Institute and Division of Cardiology, Department of Medicine Beth Israel Deaconess Medical Center Boston MA USA.ORCID 0000-0002-7987-4768
Imre JanszkyDepartment of Public Health and Nursing, Faculty of Medicine and Health Sciences Norwegian University of Science and Technology Trondheim Norway.ORCID 0000-0001-7420-5461
Julie HornDepartment of Public Health and Nursing, Faculty of Medicine and Health Sciences Norwegian University of Science and Technology Trondheim Norway.ORCID 0000-0003-1344-9707
Kenneth J MukamalDepartment of Medicine Beth Israel Deaconess Medical Center Boston MA USA.ORCID 0000-0001-8450-6970

Funding

Infrastructure for mentored access to CHS data and specimensR01HL172803 · NHLBI · UNIVERSITY OF WASHINGTON · PI James S Floyd, Michelle Christina Odden · 2025 to 2026
$2.7M
NHLBI NIH HHS R01 HL172803
6 · The paper itself

Abstract

backgroundFemale reproductive factors including menopausal age and number of live births have been associated with cardiovascular disease risk, but their role in atrial fibrillation (AF) is underexplored, especially in older adults.

methodsWe analyzed data from the CHS (Cardiovascular Health Study), a US population-based longitudinal study of adults aged ≥65 years including 3065 women reporting their menopausal age and 3236 reporting number of live births at participation. We followed participants for incident AF until June 2015. NT-proBNP (N-terminal pro-B-type natriuretic peptide) was measured at baseline. Maximal P-wave duration, P-wave terminal force in V

resultsAfter a median follow-up of 7.5 years, 1266 women (41.3%) developed AF. Each 5-year increase in menopausal age was associated with lower AF risk (hazard ratio [HR], 0.96 [95% CI, 0.92-1.00]). Menopausal age <40 years was associated with higher AF risk (HR, 1.21 [95% CI, 1.02-1.44]). No association was found between the number of live births and AF risk (HR, 0.98 [95% CI, 0.95-1.02]). Cross-sectional analyses showed younger menopausal age was associated with higher NT-proBNP levels, longer maximal P-wave duration, and longer P-wave dispersion.

conclusionsAmong women aged ≥65 years, earlier menopausal age was associated with higher NT-proBNP, longer P-wave duration, longer P-wave dispersion, and higher AF risk. Number of live births was not associated with these end points.

Indexed as

Atrial FibrillationLive BirthMenopauseAgedAge FactorsBiomarkersElectrocardiographyFemaleHumansIncidenceLongitudinal StudiesNatriuretic Peptide, BrainPeptide FragmentsRisk AssessmentRisk FactorsTime FactorsBiomarkersNatriuretic Peptide, BrainPeptide Fragmentspro-brain natriuretic peptide (1-76)atrial fibrillationepidemiologymenopauseparitywomen's health

Identifiers

PMID42294782
PMCPMC13323586

What OpenQuestion holds

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LicenceCC BY-NC-ND
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Registered trials

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.