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(Stroke. 2005;36:1830.)
© 2005 American Heart Association, Inc.
Original Contributions |
From the Department of Medicine (K.J.M., M.A.M.), Beth Israel Deaconess Medical Center, Boston, Mass; the Departments of Biostatistics (H.C.), Neurology (W.T.L), Epidemiology (W.T.L., D.S.S.), Radiology (N.J.B.), and Medicine (D.S.S.), University of Washington, Seattle; the Departments of Pathology (N.S.J., M.C.) and Medicine (M.C.), University of Vermont College of Medicine, Burlington; the Department of Epidemiology (L.H.K.), University of Pittsburgh, Pennsylvania; and the Department of Public Health Sciences (G.L.B.), Wake Forest University School of Medicine, Winston-Salem, NC.
Correspondence to Kenneth J. Mukamal, MD, MPH, MA, Beth Israel Deaconess Medical Center, 330 Brookline Ave, RO-114, Boston, MA 02215. E-mail kmukamal{at}bidmc.harvard.edu
Background and Purpose The association of light to moderate alcohol consumption with risk of ischemic stroke remains uncertain, as are the roles of potentially mediating factors and modification by apolipoprotein E (apoE) genotype.
Methods We studied the prospective association of alcohol consumption and risk of ischemic stroke among 4410 participants free of cardiovascular disease at baseline in the Cardiovascular Health Study, a population-based cohort study of older adults from 4 US communities. Participants reported their consumption of alcoholic beverages yearly.
Results During an average follow-up period of 9.2 years, 434 cases of incident ischemic stroke occurred. Compared with long-term abstainers, the multivariate relative risks of ischemic stroke were 0.85 (95% CI, 0.63 to 1.13), 0.75 (95% CI, 0.53 to 1.06), 0.82 (95% CI, 0.51 to 1.30), and 1.03 (95% CI, 0.68 to 1.57) among consumers of <1, 1 to 6, 7 to 13, and
14 drinks per week (P quadratic trend 0.06). ApoE genotype appeared to modify the alcoholischemic stroke relationship (P interaction 0.08), with generally lower risks among drinkers than abstainers in apoE4-negative participants but higher risks among drinkers than abstainers among apoE4-positive participants. We could not identify candidate mediators among lipid, inflammatory, and prothrombotic factors.
Conclusions In this study of older adults, the association of alcohol use and risk of ischemic stroke was U-shaped, with modestly lower risk among consumers of 1 to 6 drinks per week. However, apoE genotype may modify this association, and even moderate alcohol intake may be associated with an increased risk of ischemic stroke among apoE4-positive older adults.
Key Words: alcohol cerebral infarction
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