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PMID: 18307033 Published · ppublish English

Cluster analysis of risk factor genetic polymorphisms in Alzheimer's disease.

Neurochemical research ·Vol. 34 ·No. 1 ·2009-02-23

Randall C N, Strasburger D, Prozonic J, Morris S N, Winkie A D, Parker G R, Cheng D, Fennell E M, Lanham I, Vakil N, Huang J, Cathcart H, Huang R, Poduslo S E

Abstract

Multiple genetic variants may contribute to the risk of developing Alzheimer's disease. We have analyzed polymorphisms in 9 genes to determine whether particular combinations would contribute to this risk. The genes were APOE, LDLr, CST3, CTSD, TNF, BACE1, MAPT, STH, eNOS, and TFCP2. Three risk groups for the disease were identified. Risk group I was younger, was heterozygous for the CST3 (GA), CTSD2936 (AG), TNF -308 (AG) genetic variants. Risk group II was older, was homozygous for the -427 APOE promoter polymorphism (TT), and heterozygous for the MAPT deletion and for the STH variant (QR). Group III had both the youngest and oldest subjects, were heterozygous for the -863 (AC) and -1031 (CT) TNF promoter polymorphisms. All three groups carried the APOE 4 allele and were heterozygous for both BACE1 polymorphisms. The control groups were carriers of the APOE 3 allele and were homozygous for the BACE1 genetic variants.

Article Info
Journal
Neurochemical research
Abbr.
Neurochem Res
Published
2009-02-23
Indexed
2009-01-09
Updated
2009-11-19
Language
English
Country/Region
United States
NLM ID
7613461
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