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Interaction of the H63D mutation in the hemochromatosis gene with the apolipoprotein E epsilon 4 allele modulates age at onset of Alzheimer's disease
被引:43
|作者:
Combarros, O
[1
]
García-Román, M
Fontalba, A
Fernández-Luna, JL
Llorca, J
Infante, J
Berciano, J
机构:
[1] Univ Cantabria, Univ Hosp Marques De valdecilla, Neurol Unit, E-39008 Santander, Spain
[2] Univ Cantabria, Univ Hosp Marques De valdecilla, Mol Genet Unit, E-39008 Santander, Spain
[3] Univ Cantabria, Sch Med, Div Prevent Med, E-39005 Santander, Spain
关键词:
Alzheimer's disease;
apolipoprotein E;
H63D mutation;
hemochromatosis;
HFE gene;
D O I:
10.1159/000068480
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 H63D mutation in the hemochromatosis gene (HFE) has recently been considered as a risk factor in Alzheimer's disease (AD) with advancing age at onset of the disease, independently of the apolipoprotein E (ApoE) epsilon4 allele effect. We examined the distribution of the H63D mutation and ApoE genotypes as a function of age at AD onset in 328 patients with sporadic AD. Our data show that the mutant H63D allele potentially interacts with the ApoE F,4 allele to significantly reduce age at onset of AD compared to ApoE epsilon4 carriers alone, but has no effect on age at onset in ApoE epsilon4 non-carriers. Copyright (C) 2003 S. Karger AG, Basel.
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页码:151 / 154
页数:4
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