Childhood Bradycardia Associates With Atrioventricular Conduction Defects in Older Age: A Longitudinal Birth Cohort Study.


Journal

Journal of the American Heart Association
ISSN: 2047-9980
Titre abrégé: J Am Heart Assoc
Pays: England
ID NLM: 101580524

Informations de publication

Date de publication:
05 10 2021
Historique:
pubmed: 28 9 2021
medline: 19 1 2022
entrez: 27 9 2021
Statut: ppublish

Résumé

Background This study explored the association between childhood bradycardia and later-life cardiac phenotype using longitudinal data from the 1946 National Survey of Health and Development (NSHD) birth cohort. Methods and Results Resting heart rate was recorded at 6 and 7 years of age to provide the bradycardia exposure defined as a childhood resting heart rate <75 bpm. Three outcomes were studied: (1) echocardiographic data at 60 to 64 years of age, consisting of ejection fraction, left ventricular mass index, myocardial contraction fraction index, and E/e'; (2) electrocardiographic evidence of atrioventricular or ventricular conduction defects by 60 to 64 years of age; and (3) all-cause and cardiovascular mortality. Generalized linear models or Cox regression models were used, and adjustment was made for relevant demographic and health-related covariates, and for multiple testing. Mixed generalized linear models and fractional polynomials were used as sensitivity analyses. One in 3 older adults with atrioventricular conduction defects had been bradycardic in childhood, with defects being serious (Mobitz type II second-degree atrioventricular block or higher) in 12%. In fully adjusted models, childhood bradycardia was associated with 2.91 higher odds of atrioventricular conduction defects (95% CI, 1.59-5.31;

Identifiants

pubmed: 34569262
doi: 10.1161/JAHA.121.021877
pmc: PMC8649134
doi:

Types de publication

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

Langues

eng

Sous-ensembles de citation

IM

Pagination

e021877

Subventions

Organisme : Medical Research Council
ID : MC_UU_12019/1
Pays : United Kingdom
Organisme : Department of Health
Pays : United Kingdom
Organisme : British Heart Foundation
ID : SP/20/2/34841
Pays : United Kingdom
Organisme : Medical Research Council
ID : MC_UU_00019/4
Pays : United Kingdom
Organisme : Medical Research Council
ID : MC_UU_12019/5
Pays : United Kingdom
Organisme : Medical Research Council
ID : MC_UU_12019/4
Pays : United Kingdom

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Auteurs

Constantin-Cristian Topriceanu (CC)

University College London (UCL) Medical Research Council (MRC) Unit for Lifelong Health and AgeingUniversity College London London United Kingdom.

James C Moon (JC)

UCL Institute of Cardiovascular Science University College London London United Kingdom.
Cardiac MRI Unit Barts Heart Centre London United Kingdom.

Rebecca Hardy (R)

CLOSER Social Research Institute London United Kingdom.

Alun D Hughes (AD)

University College London (UCL) Medical Research Council (MRC) Unit for Lifelong Health and AgeingUniversity College London London United Kingdom.
UCL Institute of Cardiovascular Science University College London London United Kingdom.

Gabriella Captur (G)

University College London (UCL) Medical Research Council (MRC) Unit for Lifelong Health and AgeingUniversity College London London United Kingdom.
UCL Institute of Cardiovascular Science University College London London United Kingdom.
Cardiology Department Centre for Inherited Heart Muscle Conditions Royal Free Hospital London United Kingdom.

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Classifications MeSH