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Submitted on June 7, 2007
Accepted on June 28, 2007
From the Donald W. Reynolds Centers of the Brigham and Women’s Hospital (A.Z., N.G., L.M., P.L.), Harvard Medical School, Boston, Mass; and the University of Texas Southwestern Medical Center (S.A., A.K., D.K.M., G.L.V., S.G., J.d.L.), Dallas. Current affiliations: Department of Cardiology (A.Z.), University of Freiburg, Germany; Karolinska Institute (N.G.), Stockholm, Sweden; and Cardiovascular Disease (U.S.), Boehringer Ingelheim Pharmaceuticals, Ridgefield, Conn.
* To whom correspondence should be addressed. E-mail: andreas.zirlik{at}uniklinik-freiburg.de.
Objective--Although IL-18 promotes atherogenesis in animal studies and predicts cardiovascular risk in humans, it is unknown whether elevated IL-18 levels are associated with coronary atherosclerosis in the general population.
Methods and Results--IL-18 plasma levels were determined by ELISA in 2231 subjects from the Dallas Heart Study. In univariable analysis, IL-18 levels associated with traditional cardiovascular risk factors and particularly with components of the metabolic syndrome (MS, P<0.01 for trend across the number of MS components); IL-18 also associated with coronary artery calcium (CAC) scores measured by electron beam computed tomography and aortic plaque measured by MRI (P<0.01 for each). In multivariable analyses, IL-18 remained associated with multiple components of the MS but not with CAC or aortic plaque.
Conclusions--In a large population-based sample, elevated IL-18 plasma levels associated with risk factors for atherosclerosis and with the metabolic syndrome. The association between IL-18 and atherosclerosis diminished after accounting for traditional cardiovascular risk factors. These data suggest that IL-18 does not add independently to detection of atherosclerotic burden in asymptomatic individuals. (Arterioscler Thromb Vasc Biol. 2007;27;000-000.)
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