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

Michiel Rienstra, Jenny X. Sun, Steven A. Lubitz, David S. Frankel, Ramachandran S. Vasan, Daniel Levy, Jared W. Magnani, Lisa M. Sullivan, James B. Meigs, Patrick T. Ellinor, Emelia J. Benjamin

Resultado de la investigación: Articlerevisión exhaustiva

48 Citas (Scopus)

Resumen

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. Methods: We studied the relations between circulating concentrations of both adipokines and incident AF in participants of the Framingham Offspring Study. 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). 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.

Idioma originalEnglish (US)
Páginas (desde-hasta)119-124.e1
PublicaciónAmerican Heart Journal
Volumen163
N.º1
DOI
EstadoPublished - ene 2012
Publicado de forma externa

ASJC Scopus subject areas

  • Cardiology and Cardiovascular Medicine

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