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Plasma resistin, adiponectin, and risk of incident atrial fibrillation: the Framingham Offspring Study.

Authors :
Rienstra M
Sun JX
Lubitz SA
Frankel DS
Vasan RS
Levy D
Magnani JW
Sullivan LM
Meigs JB
Ellinor PT
Benjamin EJ
Source :
American heart journal [Am Heart J] 2012 Jan; Vol. 163 (1), pp. 119-124.e1. Date of Electronic Publication: 2011 Nov 17.
Publication Year :
2012

Abstract

Background: We sought to investigate whether higher concentrations of resistin and lower concentrations of adiponectin relate to incident atrial fibrillation (AF) and whether this association is mediated by AF risk factors and inflammation. Resistin and adiponectin are adipokines that have been associated with multiple known risk factors for AF including diabetes, obesity, inflammation, and heart failure.<br />Methods: We studied the relations between circulating concentrations of both adipokines and incident AF in participants of the Framingham Offspring Study.<br />Results: Participants (n = 2,487) had a mean age of 61 ± 10 years, and 54% were women. During a mean follow-up of 7.6 ± 2.0 years, 206 (8.3%) individuals (96 women) developed incident AF. Plasma resistin concentration was significantly associated with incident AF (multivariable-adjusted hazard ratio [HR] 1.17 per SD [0.41 ng/mL] of natural logarithmically transformed resistin, 95% CI 1.02-1.34, P = .028). The resistin-AF association was attenuated after further adjustment for C-reactive protein (HR per SD increase resistin 1.14, 95% CI 0.99-1.31, P = .073). Adiponectin concentrations were not significantly associated with incident AF (multivariable-adjusted HR of 0.95 per SD [0.62 μg/mL] of logarithmically transformed adiponectin, 95% CI 0.81-1.10, P = .478).<br />Conclusion: In our community-based longitudinal study, higher mean concentrations of resistin were associated with incident AF, but the relation was attenuated by adjustment for C-reactive protein. We did not detect a statistically significant association between adiponectin and incident AF. Additional studies are needed to clarify the potential role of adipokines in AF and mechanisms linking adiposity to AF.<br /> (Copyright © 2012 Mosby, Inc. All rights reserved.)

Details

Language :
English
ISSN :
1097-6744
Volume :
163
Issue :
1
Database :
MEDLINE
Journal :
American heart journal
Publication Type :
Academic Journal
Accession number :
22172445
Full Text :
https://doi.org/10.1016/j.ahj.2011.09.029