Alpha-2 macroglobulin gene in early- and late-onset Alzheimer disease

被引:23
|
作者
Korovaitseva, GI
Premkumar, S
Grigorenko, A
Molyaka, Y
Galimbet, V
Selezneva, N
Gavrilova, SI
Farrer, LA
Rogaev, EI [1 ]
机构
[1] Russian Acad Med Sci, Mental Hlth Res Ctr, Moscow 109801, Russia
[2] Russian Acad Med Sci, Inst Mol Genet, Moscow 109801, Russia
[3] Russian Acad Med Sci, Ctr Genet Med, Moscow 109801, Russia
[4] Boston Univ, Sch Med, Dept Neurol, Boston, MA 02118 USA
关键词
alpha-2-macroglobulin; Alzheimer disease; apolipoprotein E; association; linkage disequilibrium; age at onset;
D O I
10.1016/S0304-3940(99)00537-6
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
Alpha-2-macroglobulin (A2M) is a proteinase inhibitor that is present in senile plaques and may play a role in metabolism of amyloid beta (A beta) peptide. Recently it was reported that inheritance of the deletion allele (A2M-2) confers increased risk for late-onset Alzheimer disease (AD) with significance of this effect similar to the is an element of 4 allele of apolipoprotein E (APOE). We examined the distribution of A2M genotypes and alleles in a cohort of 146 AD patients and 160 age-matched non-demented individuals. There was no evidence for association in the total sample or in subsets stratified by age or APOE is an element of 4 status. These results suggest that this polymorph ism is not a strong genetic risk factor for either early-or late-onset forms of the disorder. However, they do not exclude the possibility that an AD susceptibility allele is located elsewhere in A2M or a nearby gene. (C) 1999 Elsevier Science Ireland Ltd. All rights reserved.
引用
收藏
页码:129 / 131
页数:3
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