Association of sickle cell trait with atrial fibrillation: The REGARDS cohort.


Journal

Journal of electrocardiology
ISSN: 1532-8430
Titre abrégé: J Electrocardiol
Pays: United States
ID NLM: 0153605

Informations de publication

Date de publication:
Historique:
received: 14 01 2019
revised: 04 04 2019
accepted: 16 04 2019
pubmed: 28 4 2019
medline: 22 6 2021
entrez: 28 4 2019
Statut: ppublish

Résumé

Sickle cell trait (SCT), sickle cell disease's (SCD) carrier status, has been recently associated with worse cardiovascular and renal outcomes. An increased prevalence of atrial fibrillation (AF) is documented in SCD patients; however, studies in individuals with SCT are lacking. To determine the association of SCT with AF. Among African-American participants in the REasons for Geographic and Racial Differences in Stroke (REGARDS) Study we assessed the association of SCT (by ECG or medical history) with prevalent AF using logistic regression adjusting for age, sex, income, education, history of stroke, myocardial infarction, diabetes, hypertension, and chronic kidney disease. A second evaluation was performed a mean of 9.2 years later among available participants, and the same model was used to test the association of SCT with incident AF. In 10,409 participants with baseline ECG data and genotyping, 778 (7.5%) had SCT and 811 (7.8%) had prevalent AF. After adjusting for age, sex, education and income, SCT was associated with AF, OR 1.32 (95% CI 1.03-1.70). The association with incident AF assessed at the second in-home visit with the same adjustments was similar; OR 1.25 (95% CI 0.77-2.03). SCT was associated with a higher prevalence of AF and a non-significantly higher incident AF over a 9.2 year period independent of AF risk factors. SCT remained associated with prevalent AF after adjusting for potential factors on the causal pathway such as hypertension and chronic kidney disease suggesting alternate mechanisms for the increased risk.

Sections du résumé

BACKGROUND
Sickle cell trait (SCT), sickle cell disease's (SCD) carrier status, has been recently associated with worse cardiovascular and renal outcomes. An increased prevalence of atrial fibrillation (AF) is documented in SCD patients; however, studies in individuals with SCT are lacking.
OBJECTIVES
To determine the association of SCT with AF.
METHODS
Among African-American participants in the REasons for Geographic and Racial Differences in Stroke (REGARDS) Study we assessed the association of SCT (by ECG or medical history) with prevalent AF using logistic regression adjusting for age, sex, income, education, history of stroke, myocardial infarction, diabetes, hypertension, and chronic kidney disease. A second evaluation was performed a mean of 9.2 years later among available participants, and the same model was used to test the association of SCT with incident AF.
RESULTS
In 10,409 participants with baseline ECG data and genotyping, 778 (7.5%) had SCT and 811 (7.8%) had prevalent AF. After adjusting for age, sex, education and income, SCT was associated with AF, OR 1.32 (95% CI 1.03-1.70). The association with incident AF assessed at the second in-home visit with the same adjustments was similar; OR 1.25 (95% CI 0.77-2.03).
CONCLUSIONS
SCT was associated with a higher prevalence of AF and a non-significantly higher incident AF over a 9.2 year period independent of AF risk factors. SCT remained associated with prevalent AF after adjusting for potential factors on the causal pathway such as hypertension and chronic kidney disease suggesting alternate mechanisms for the increased risk.

Identifiants

pubmed: 31028976
pii: S0022-0736(19)30100-1
doi: 10.1016/j.jelectrocard.2019.04.010
pmc: PMC6639128
mid: NIHMS1527764
pii:
doi:

Types de publication

Journal Article Research Support, N.I.H., Extramural

Langues

eng

Sous-ensembles de citation

IM

Pagination

1-5

Subventions

Organisme : NHLBI NIH HHS
ID : K08 HL125100
Pays : United States
Organisme : NIMHD NIH HHS
ID : L60 MD013112
Pays : United States
Organisme : NINDS NIH HHS
ID : U01 NS041588
Pays : United States
Organisme : CCR NIH HHS
ID : HHSN261200800001C
Pays : United States
Organisme : NCI NIH HHS
ID : HHSN261200800001E
Pays : United States

Informations de copyright

Copyright © 2019 Elsevier Inc. All rights reserved.

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Auteurs

Daniel R Douce (DR)

University of Vermont College of Medicine, Department of Hematology & Oncology, United States of America.

Elsayed Z Soliman (EZ)

Wake Forest University, Department of Epidemiology & Prevention, United States of America.

Rakhi Naik (R)

Johns Hopkins University School of Medicine, Department of Hematology & Oncology, United States of America.

Hyacinth I Hyacinth (HI)

Aflac Cancer and Blood Disorder Center of Emory University, Department of Pediatrics and Children's Healthcare of Atlanta, United States of America.

Mary Cushman (M)

University of Vermont College of Medicine, Department of Hematology & Oncology, United States of America.

Cheryl A Winkler (CA)

National Cancer Institute, Basic Research Laboratory, United States of America.

George Howard (G)

University of Alabama at Birmingham School of Public Health, Department of Biostatistics, United States of America.

Ethan M Lange (EM)

Department of Medicine, University of Colorado Anschutz Medical Campus, United States of America.

Leslie A Lange (LA)

Department of Medicine, University of Colorado Anschutz Medical Campus, United States of America.

Marguerite R Irvin (MR)

University of Alabama at Birmingham School of Public Health, Department of Epidemiology, United States of America.

Neil A Zakai (NA)

University of Vermont College of Medicine, Department of Hematology & Oncology, United States of America. Electronic address: neil.zakai@med.uvm.edu.

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