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Adhesion pathway proteins and risk of atrial fibrillation in the Multi-Ethnic Study of Atherosclerosis

Authors :
Naomi Q. Hanson
Michael Y. Tsai
Susan R. Heckbert
Suzette J. Bielinski
Marco A. Guerrero
Nicholas B. Larson
James S. Pankow
Paul A. Decker
Elizabeth J. Bell
Sheila M. Manemann
Israel J. Mendez
Source :
BMC Cardiovascular Disorders, Vol 21, Iss 1, Pp 1-8 (2021), BMC Cardiovascular Disorders
Publication Year :
2021
Publisher :
BMC, 2021.

Abstract

Background The cellular adhesion pathway has been suggested as playing an important role in the pathogenesis of atrial fibrillation (AF). However, prior studies that have investigated the role of adhesion pathway proteins in risk of AF have been limited in the number of proteins that were studied and in the ethnic and racial diversity of the study population. Therefore we aimed to study the associations of fifteen adhesion pathway proteins with incident AF in a large, diverse population. Methods Multi-Ethnic Study of Atherosclerosis participants from four races/ethnicities (n = 2504) with protein levels measured were followed for incident AF (n = 253). HGF protein was measured on Exam 1 samples (N = 6669; AF n = 851). Cox proportional hazards regression was used to assess the association of AF with 15 adhesion pathway proteins. Bonferroni correction was applied to account for multiple comparisons. Results After adjusting for potential confounding variables (age, sex, race/ethnicity, height, body mass index, systolic blood pressure, antihypertension therapy, diabetes status, current smoker, current alcohol use, and total and HDL cholesterol), and accounting for multiple testing (P Conclusions Circulating levels of MMP-2, TIMP-2, VCAM-1, and SLPI were positively associated with an increased risk of incident AF in a diverse population. Our findings suggest that adhesion pathway proteins may be important risk predictors of AF.

Details

Language :
English
ISSN :
14712261
Volume :
21
Issue :
1
Database :
OpenAIRE
Journal :
BMC Cardiovascular Disorders
Accession number :
edsair.doi.dedup.....2a4946df42dcaade8e903f268435eb80