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Alpha-2-macroglobulin intronic polymorphism is not associated with autopsy-confirmed late-onset Alzheimer's disease.

作者信息

Kovács T, Cairns N J, Lantos P L

机构信息

Department of Neuropathology, Institute of Psychiatry, London, UK.

出版信息

Neurosci Lett. 1999 Sep 24;273(1):61-83. doi: 10.1016/s0304-3940(99)00604-7.

DOI:10.1016/s0304-3940(99)00604-7
PMID:10505652
Abstract

Alpha-2-macroglobulin (A2M) intronic polymorphism has recently been reported to be associated with late-onset Alzheimer's disease (LOAD). To corroborate this association, we analysed the A2M and apolipoprotein E (APOE) polymorphisms in autopsy cases of the MRC Alzheimer's Disease Brain Bank, Institute of Psychiatry, London. The frequencies of the insertion and deletion alleles in AD were 0.81 and 0.19, respectively, and these were not significantly different from control frequencies. After pooling the AD cases in epsilon4 positive and negative subgroups, there was again no significant difference between the A2M allele frequency in the two subgroups. In our present study, we were unable to corroborate the association between A2M intronic polymorphism and LOAD in autopsy cases.

摘要

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