Apolipoprotein E, cardiovascular disease and cognitive function in aging women

被引:51
作者
Kang, JE
Logroscino, G
De Vivo, I
Hunter, D
Grodstein, F
机构
[1] Harvard Univ, Brigham & Womens Hosp, Sch Med, Channing Lab,Dept Med, Boston, MA 02115 USA
[2] Harvard Univ, Sch Publ Hlth, Dept Epidemiol, Boston, MA 02115 USA
关键词
aging; apolipoprotein E; cognitive performance; cardiovascular disease; epidemiology;
D O I
10.1016/j.neurobiolaging.2004.05.003
中图分类号
R592 [老年病学]; C [社会科学总论];
学科分类号
03 ; 0303 ; 100203 ;
摘要
The apolipoprotein E (APOE) e4 allele increases risk of Alzheimer disease and cardiovascular diseases. We examined APOE genotypes alone or combined with cardiovascular conditions in relation to cognitive function in 4227 Nurses' Health Study participants, 70-80 years old. From 1995 to 2001, and again 2 years later, participants received telephone cognitive assessments of general cognition, category fluency, verbal memory and working memory. In biennial questionnaires since 1976, participants have provided extensive health information including cardiovascular conditions. Compared with women with the e3/3 genotype, e4 carriers performed worse at baseline across all tests (mean global composite score was lower by 0.10 points (95% confidence interval = -0.15, -0.05)) and declined more (mean change in global score was -0.07 points (95% CI = -0.12, -0.03)), with a strong allele dose-response trend (P-trend = 0.0003). Among participants 75+ years, e2 carriers performed best. Women with an e4 allele and cardiovascular conditions such as transient ischemic attack or untreated hypertension had the worst cognition. Thus, APOE genotypes strongly influenced cognitive function and decline; prevention of cardiovascular disease may limit these effects. (C) 2004 Elsevier Inc. All rights reserved.
引用
收藏
页码:475 / 484
页数:10
相关论文
共 70 条
[1]   USE OF BRIEF COGNITIVE TESTS TO IDENTIFY INDIVIDUALS IN THE COMMUNITY WITH CLINICALLY DIAGNOSED ALZHEIMERS-DISEASE [J].
ALBERT, M ;
SMITH, LA ;
SCHERR, PA ;
TAYLOR, JO ;
EVANS, DA ;
FUNKENSTEIN, HH .
INTERNATIONAL JOURNAL OF NEUROSCIENCE, 1991, 57 (3-4) :167-178
[2]   APOE GENOTYPE AND SURVIVAL FROM INTRACEREBRAL HEMORRHAGE [J].
ALBERTS, MJ ;
GRAFFAGNINO, C ;
MCCLENNY, C ;
DELONG, D ;
STRITTMATTER, W ;
SAUNDERS, AM ;
ROSES, AD .
LANCET, 1995, 346 (8974) :575-575
[3]  
Brandt J., 1988, NEUROPSY NEUROPSY BE, V1, P111, DOI DOI 10.1001/ARCHNEUR.1993.00540060039014
[4]   Apolipoprotein E genotype in the prediction of cognitive decline and dementia in a prospectively studied elderly population [J].
Brayne, C ;
Harrington, CR ;
Wischik, CM ;
Huppert, FA ;
Chi, LY ;
Xuereb, JH ;
OConnor, DW ;
Paykel, ES .
DEMENTIA, 1996, 7 (03) :169-174
[5]   The role of APOE-ε4 in longitudinal cognitive decline -: MacArthur studies of successful aging [J].
Bretsky, P ;
Guralnik, JM ;
Launer, L ;
Albert, M ;
Seeman, TE .
NEUROLOGY, 2003, 60 (07) :1077-1081
[6]   Projections of Alzheimer's disease in the United States and the public health impact of delaying disease onset [J].
Brookmeyer, R ;
Gray, S ;
Kawas, C .
AMERICAN JOURNAL OF PUBLIC HEALTH, 1998, 88 (09) :1337-1342
[7]   Midlife cardiovascular risk factors, ApoE, and cognitive decline in elderly male twins [J].
Carmelli, D ;
Swan, GE ;
Reed, T ;
Miller, B ;
Wolf, PA ;
Jarvik, GP ;
Schellenberg, GD .
NEUROLOGY, 1998, 50 (06) :1580-1585
[8]   Patterns of cognitive decline in presymptomatic Alzheimer disease - A prospective community study [J].
Chen, PJ ;
Ratcliff, G ;
Belle, SH ;
Cauley, JA ;
DeKosky, ST ;
Ganguli, M .
ARCHIVES OF GENERAL PSYCHIATRY, 2001, 58 (09) :853-858
[9]   Effects of apolipoprotein E phenotypes on the neuropsychological functions of community-dwelling elderly individuals without dementia [J].
Chey, J ;
Kim, JW ;
Cho, HY .
NEUROSCIENCE LETTERS, 2000, 289 (03) :230-234
[10]   REPRODUCIBILITY AND VALIDITY OF SELF-REPORTED MENOPAUSAL STATUS IN A PROSPECTIVE COHORT STUDY [J].
COLDITZ, GA ;
STAMPFER, MJ ;
WILLETT, WC ;
STASON, WB ;
ROSNER, B ;
HENNEKENS, CH ;
SPEIZER, FE .
AMERICAN JOURNAL OF EPIDEMIOLOGY, 1987, 126 (02) :319-325