APOE genotype influences functional status among elderly without dementia

被引:45
作者
Albert, SM
Gurland, B
Maestre, G
Jacobs, DM
Stern, Y
Mayeux, R
机构
[1] COLUMBIA UNIV,GERTRUDE H SERGIEVSKY CTR,NEW YORK,NY 10032
[2] COLUMBIA UNIV,DEPT NEUROL,NEW YORK,NY 10032
[3] COLUMBIA UNIV,DEPT PATHOL,NEW YORK,NY 10032
[4] COLUMBIA UNIV,CTR GERIATR & GERONTOL,NEW YORK,NY 10032
[5] COLUMBIA UNIV,CTR ALZHEIMERS RES CITY NEW YORK,NEW YORK,NY 10032
[6] COLUMBIA UNIV,DIV EPIDEMIOL,NEW YORK,NY 10032
[7] NEW YORK STATE PSYCHIAT INST & HOSP,DEPT BIOL PSYCHIAT,NEW YORK,NY
来源
AMERICAN JOURNAL OF MEDICAL GENETICS | 1995年 / 60卷 / 06期
关键词
apolipoprotein E; function; cognition; aging; Alzheimer's disease;
D O I
10.1002/ajmg.1320600621
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
The presence of apolipoprotein-epsilon 4 (APOE-epsilon 4) significantly increases the risk of Alzheimer's disease (AD), The association between APOE-epsilon 4 status and functional abilities was explored further in a multicultural sample of community-dwelling, non-demented elders. The sample was limited to cognitively-intact, community-dwelling elders, who were free of stroke or other neurologic disability. In 218 elders who met research criteria, the presence of APO-epsilon 4 was associated with poorer functional status, apart from the effects of neuropsychological performance, gender, age, and education (OR = 2.5, 95% CI: 1.3, 4.9). In 158 subjects without an APOE-epsilon 4 allele, 50% reported no functional limitation; in the 60 subjects with an epsilon 4 allele, only 28% reported no functional limitation (P < .01). The relationship was not explained by the distribution of co-morbidities. The association between poorer function and the presence of an APOE-epsilon 4 allele was evident in each ethnic group. In path analyses, the presence of an APOE-epsilon 4 allele was associated with decreased functional ability in non-demented elders not simply through an association with poorer cognitive status, but also independently. These results suggest that the APOE-epsilon 4 genotype is associated with functional deficit in people with normal neuropsychological profiles. (C) 1995 Wiley-Liss, Inc.
引用
收藏
页码:583 / 587
页数:5
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