Midlife cardiovascular risk factors, ApoE, and cognitive decline in elderly male twins

被引:125
作者
Carmelli, D
Swan, GE
Reed, T
Miller, B
Wolf, PA
Jarvik, GP
Schellenberg, GD
机构
[1] SRI Int, Ctr Hlth Sci, Menlo Pk, CA 94025 USA
[2] Indiana Univ, Sch Med, Dept Med Genet, Indianapolis, IN 46202 USA
[3] Boston Univ, Dept Neurol, Boston, MA 02215 USA
[4] Univ Calif Los Angeles, Harbor Med Ctr, Dept Neurol, Los Angeles, CA 90024 USA
[5] Univ Washington, Med Ctr, Dept Med, Div Med Genet, Seattle, WA 98195 USA
[6] Puget Sound Hlth Care Div, Ctr Geriatr Res Educ & Clin, Seattle, WA USA
关键词
D O I
10.1212/WNL.50.6.1580
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
Objective: To investigate the combined effect of the apolipoprotein E epsilon 4 (ApoE*4) allele and midlife cardiovascular risk factors on cognitive decline. Methods: Data are from the National Heart, Lung, and Blood Institute Twin Study-a longitudinal cardiovascular epidemiologic study of World War II male veteran twins currently in its 27th year of follow-up. Subjects were assessed for cardiovascular risk factors, including BP and glucose levels, at mean ages 48, 58, and 63 years. Participants in the current study are 410 individual twin subjects for whom cognitive function was measured twice, at ages 63 and 73 years. Ten-year change scores in performance on neuropsychological test examinations were adjusted for age, education, baseline score, and incident cardiovascular disease. Results: For the sample as a whole, we observed a significant decline (p < 0.01) in cognitive performance over the 10 years of follow-up. ApoE*4 carriers with midlife hyperglycemia experienced the greatest decline in performance, which was also greater than expected from the separate effects combined. Midlife hypertension and ApoE*4, were each associated with excess decline in performance on tests of psychomotor speed. Their joint effect, however, was not greater than expected from the separate effects combined. Conclusions: ApoE*4 and midlife cardiovascular risk factors may have a synergistic effect on decline in cognitive function. This effect may be due to greater vascular or degenerative damage among subjects with ApoE*4.
引用
收藏
页码:1580 / 1585
页数:6
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