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Asymmetric and Symmetric Dimethylarginine Predict Outcomes in Patients With Atrial Fibrillation: An ARISTOTLE Substudy

Authors :
John D, Horowitz
Raffaele, De Caterina
Tamila, Heresztyn
John H, Alexander
Ulrika, Andersson
Renato D, Lopes
Philippe Gabriel, Steg
Elaine M, Hylek
Puneet, Mohan
Michael, Hanna
Petr, Jansky
Christopher B, Granger
Lars, Wallentin
Source :
Aging (Albany NY)
Publication Year :
2016

Abstract

There is little mechanistic information on factors predisposing atrial fibrillation (AF) patients to thromboembolism or bleeding, but generation of nitric oxide (NO) might theoretically contribute to both.The authors tested the hypothesis that plasma levels of the methylated arginine derivatives asymmetric and symmetric dimethylarginine (ADMA/SDMA), which inhibit NO generation, might be associated with outcomes in AF.Plasma samples were obtained from 5,004 patients with AF at randomization to warfarin or apixaban in the ARISTOTLE (Apixaban for Reduction in Stroke and Other Thromboembolic Events in Atrial Fibrillation) trial. ADMA and SDMA concentrations were measured by high-performance liquid chromatography. Relationships to clinical characteristics were evaluated by multivariable analyses. Associations with major outcomes, during a median of 1.9 years follow-up, were evaluated by adjusted Cox proportional hazards models.Both ADMA and SDMA plasma concentrations at study entry increased significantly with patients' age, female sex, renal impairment, permanent AF, or congestive heart failure. ADMA and SDMA increased (p 0.001) with both increased CHAIn anticoagulated patients with AF, elevated ADMA levels are weakly associated with thromboembolic events, elevated SDMA levels with bleeding events and both are strongly associated with increased mortality. These findings suggest that disturbances of NO function modulate both thrombotic and hemorrhagic risk in anticoagulated patients with AF. (Apixaban for Reduction in Stroke and Other Thromboembolic Events in Atrial Fibrillation [ARISTOTLE]; NCT00412984).

Details

ISSN :
15583597
Volume :
72
Issue :
7
Database :
OpenAIRE
Journal :
Journal of the American College of Cardiology
Accession number :
edsair.pmid..........7de4e86b102e50db8c37e5a9dbdd5d69