Insulin degrading enzyme (IDE) genetic variants and risk of Alzheimer's disease:: evidence of effect modification by apolipoprotein E (APOE)

被引:50
作者
Edland, SD
Vriesé, FWD
Compton, D
Smith, GE
Ivnik, R
Boeve, BF
Tangalos, EG
Petersen, RC
机构
[1] Mayo Clin & Mayo Fdn, Div Clin Epidemiol, Rochester, MN 55905 USA
[2] NIA, Neurogenet Lab, Bethesda, MD 20892 USA
[3] Mayo Clin, Dept Psychol, Rochester, MN 55905 USA
[4] Mayo Clin, Dept Neurol, Rochester, MN 55905 USA
[5] Mayo Clin, Div Community Internal Med, Rochester, MN 55905 USA
关键词
insulin degrading enzyme; Alzheimer's disease; amyloid beta; protease; genetic epidemiology; LINKAGE DISEQUILIBRIUM MEASURES; AMYLOID BETA-PROTEIN; DEGRADATION; ASSOCIATION; LOCUS; CHROMOSOME-10; PEPTIDE; BRAINS; SAMPLE;
D O I
10.1016/S0304-3940(03)00488-9
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
Insulin degrading enzyme (IDE) is a protease that degrades insulin and the beta-amyloid peptide implicated in Alzheimer's disease (AD). We reexamined data on five previously reported IDE polymorphisms stratifying the analysis by the presence or absence of an apolipoprotein E (APOE) epsilon4 allele. Three IDE variants were associated with AD within epsilon4-negative subjects (genotype exact test P-values less than or equal to0.02). A haplotype containing the minor variant at each of these sites represented an estimated 4.2% of case haplotypes versus 12.3% of control haplotypes among epsilon4-negative subjects. Lack of this minor haplotype may be predictive of AD, potentially explaining some fraction of disease within subjects without the APOE epsilon4 risk allele. Confirmation of this finding with a larger sample of cases and controls is warranted. (C) 2003 Elsevier Science Ireland Ltd. All rights reserved.
引用
收藏
页码:21 / 24
页数:4
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