APOLIPOPROTEIN-E4 ALLELE AND ALZHEIMERS-DISEASE - EXAMINATION OF ALLELIC ASSOCIATION AND EFFECT ON AGE AT ONSET IN BOTH EARLY-ONSET AND LATE-ONSET CASES

被引:84
|
作者
LOCKE, PA
CONNEALLY, PM
TANZI, RE
GUSELLA, JF
HAINES, JL
机构
[1] MASSACHUSETTS GEN HOSP E,MOLEC NEUROGENET UNIT,BOSTON,MA 02129
[2] MASSACHUSETTS GEN HOSP E,GENET & AGING LAB,BOSTON,MA 02129
[3] INDIANA UNIV,MED CTR,DEPT MED & MOLEC GENET,INDIANAPOLIS,IN
关键词
LINKAGE DISEQUILIBRIUM; FAMILIAL AD; APOE-4; HOMOZYGOTES;
D O I
10.1002/gepi.1370120108
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
An increased frequency of the apolipoprotein E type 4 allele (APOE-4) has previously been associated with both late-onset sporadic and late-onset familial Alzheimer disease (AD) [Strittmatter et al. (1993) Proc Natl Acad Sci USA 90:1977-1981; Saunders et al. (1993a) Neurology 43:1467-1472]. To further investigate this association we genotyped affected individuals from 92 separate AD pedigrees including both early- and late-onset cases. An increased frequency of the APOE-4 allele was found only among the late-onset cases, both familial and sporadic, confirming the earlier reports. In addition, age at onset was significantly decreased in the APOE-4 homozygotes (in late onset families) compared to either APOE-4 heterozygotes or individuals not carrying an APOE-4 allele. We also observed a significantly decreased frequency of the APOE-2 allele in both the early- and late-onset familial cases. These results strengthen the argument for a direct role of APOE in susceptibility to AD. (C) 1995 Wiley-Liss, Inc.
引用
收藏
页码:83 / 92
页数:10
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