PROTECTIVE EFFECT OF APOLIPOPROTEIN-E TYPE-2 ALLELE FOR LATE-ONSET ALZHEIMER-DISEASE

被引:1557
作者
CORDER, EH
SAUNDERS, AM
RISCH, NJ
STRITTMATTER, WJ
SCHMECHEL, DE
GASKELL, PC
RIMMLER, JB
LOCKE, PA
CONNEALLY, PM
SCHMADER, KE
SMALL, GW
ROSES, AD
HAINES, JL
PERICAKVANCE, MA
机构
[1] DUKE UNIV,MED CTR,JOSEPH & KATHLEEN BRYAN ALZHEIMERS DIS RES CTR,DIV NEUROL,DURHAM,NC 27710
[2] DUKE UNIV,MED CTR,JOSEPH & KATHLEEN BRYAN ALZHEIMERS DIS RES CTR,DIV NEUROBIOL,DURHAM,NC 27710
[3] DUKE UNIV,MED CTR,CTR STUDY AGING & HUMAN DEV,DURHAM,NC 27710
[4] YALE UNIV,DEPT EPIDEMIOL & PUBL HLTH,NEW HAVEN,CT 06520
[5] YALE UNIV,DEPT GENET,NEW HAVEN,CT 06520
[6] VET ADM MED CTR,GRECC DURHAM,DURHAM,NC 27704
[7] MASSACHUSETTS GEN HOSP,MOLEC NEUROGENET UNIT,BOSTON,MA 02129
[8] INDIANA UNIV,MED CTR,DEPT MED & MOLEC GENET,INDIANAPOLIS,IN 46202
[9] UNIV CALIF LOS ANGELES,CTR HLTH SCI,NEUROPSYCHIAT INST & HOSP,LOS ANGELES,CA 90024
关键词
D O I
10.1038/ng0694-180
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
Gene dosage of the apolipoprotein E (APOE) epsilon 4 allele is a major risk factor for familiar Alzheimer disease (AD) of late onset (after age 60). Here we studied a large series of 115 AD case subjects and 243 controls as well as 150 affected and 197 unaffected members of 66 AD families. Our data demonstrate a protective effect of the epsilon 2 allele, in addition to the dose effect of the epsilon 4 allele in sporadic AD. Although a substantial proportion (65%) of AD is attributable to the presence of epsilon 4 alleles, risk of AD is lowest in subjects with the epsilon 2/epsilon 3 genotype, with an additional 23% of AD attributable to the absence of an epsilon 2 allele. The opposite actions of the epsilon 2 and epsilon 4 alleles further support the direct involvement of APOE in the pathogenesis of AD.
引用
收藏
页码:180 / 184
页数:5
相关论文
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