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Submitted on October 13, 2008
Accepted on January 13, 2009
From the Departments of Pathology (N.S.J., R.P.T.) and Biochemistry (R.P.T.), University of Vermont, Burlington; the Department of Biostatistics (A.M.A.) and the Departments of Medicine, Epidemiology, and Health Services, Cardiovascular Health Research Unit (B.M.P.), University of Washington, Seattle; the Department of Epidemiology (L.H.K.), University of Pittsburgh School of Public Health, Pittsburgh, Pa; and the Center for Health Studies (B.M.P.), Group Health, Seattle, Wash.
* To whom correspondence should be addressed. E-mail: Nancy.Jenny{at}uvm.edu.
Objective—We examined associations of pentraxin 3 (PTX3), a vascular inflammation marker, with incident cardiovascular disease (CVD) and all-cause death.
Methods and Results—1583 Cardiovascular Health Study participants free of prevalent CVD were included. Nonexclusive case groups were angina (n=476), myocardial infarction (MI; n=237), stroke (n=310), CVD death (n=282), and all-cause death (n=772). 535 participants had no events. PTX3 levels were higher in those with subclinical CVD (1.90±1.89 ng/mL) than those without (1.71±1.88 ng/mL; P=0.001). Using Cox regression adjusted for age, sex, and ethnicity, a standard deviation increase in PTX3 (1.89 ng/mL) was associated with CVD death (hazard ratio 1.11; 95% confidence interval 1.02 to 1.21) and all-cause death (1.08; 1.02 to 1.15). PTX3 was not associated with angina (1.09; 0.98 to 1.20), MI (0.96; 0.81 to 1.12), or stroke (1.06; 0.95 to 1.18). Adding C-reactive protein (CRP) or CVD risk factors to the models had no significant effects on associations.
Conclusions—In these older adults, PTX3 was associated with CVD and all-cause death independent of CRP and CVD risk factors. PTX3 likely reflects different aspects of inflammation than CRP and may provide insight into vascular health in aging and chronic diseases of aging that lead to death.
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