(Circulation. 1999;100:736-742.)
© 1999 American Heart Association, Inc.
Clinical Investigation and Reports |
From the Division of Epidemiology, School of Public Health, University of Minnesota, Minneapolis (A.R.F., E.S., M.L.R.); Collaborative Studies Coordinating Center, Department of Biostatistics, University of North Carolina at Chapel Hill (W.D.R.); Division of Epidemiology and Clinical Applications, National Heart, Lung, and Blood Institute, Bethesda, Md (L.S.C.); Division of Hematology, University of Texas Medical School, Houston (N.A., K.K.W.); and Department of Epidemiology, School of Hygiene and Public Health, Johns Hopkins University, Baltimore, Md (F.J.N.).
BackgroundSeveral markers of hemostatic function and inflammation have been associated with increased risk of coronary heart disease, but prospective evidence for their role in ischemic stroke is scant.
Methods and ResultsThe Atherosclerosis Risk in Communities (ARIC) Study measured several of these markers in more than 14 700 participants 45 to 64 years old who were free of cardiovascular disease and were followed up for 6 to 9 years for occurrence of ischemic stroke (n=191). There was no apparent association between ischemic stroke incidence and factor VIIc, antithrombin III, platelet count, or activated partial thromboplastin time. After adjustment for multiple cardiovascular risk factors, von Willebrand factor, factor VIIIc, fibrinogen, and white blood cell count were positively associated and protein C was negatively but nonsignificantly associated with ischemic stroke incidence in regression analyses based on either continuous variables or fourths of the variable distributions. The adjusted relative risk (and 95% CI) for ischemic stroke in those in the highest versus lowest fourth were: von Willebrand factor, 1.71 (1.1 to 2.7); factor VIIIc, 1.93 (1.2 to 3.1); white blood cell count, 1.50 (0.9 to 2.4); fibrinogen, 1.26 (0.8 to 2.0); and protein C, 0.65 (0.4 to 1.0).
ConclusionsThis study offers modest support for the hypothesis that some markers of hemostatic function and inflammation can identify groups of middle-aged adults at increased risk of stroke. These factors may play a role in the pathogenesis of ischemic stroke.
Key Words: stroke ischemia hemostasis
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