Polymorphisms in the CYP19 gene confer increased risk for Alzheimer disease

被引:63
作者
Iivonen, S
Corder, E
Lehtovirta, M
Helisalmi, S
Mannermaa, A
Vepsäläinen, S
Hänninen, T
Soininen, H
Hiltunen, M
机构
[1] Univ Kuopio, Dept Neurol & Neurosci, Brain Res Unit, FIN-70211 Kuopio, Finland
[2] Kuopio Univ Hosp, Dept Neurol & Neurosci, Kuopio 70211, Finland
[3] Kuopio Univ Hosp, Dept Pathol & Forens Med, Kuopio 70211, Finland
[4] Univ Kuopio, Clin Res Ctr Mediteknia, FIN-70211 Kuopio, Finland
[5] Jorvi Hosp, Dept Neurol, SF-02740 Espoo, Finland
[6] Duke Univ, Ctr Demog Studies, Durham, NC 27706 USA
关键词
D O I
10.1212/01.WNL.0000118208.16939.60
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
Background: Brain aromatase may be neuroprotective by increasing the local estrogen levels in injured neurons. Aromatase is encoded by the CYP19 gene located at 15q21.1, a chromosomal region in linkage disequilibrium (LD) with Alzheimer disease (AD) in this sample. Objective: To investigate whether nine single-nucleotide polymorphisms (SNP) spanning the CYP19 gene were associated with AD. Methods: Three hundred ninety-four patients were compared with 469 nondemented control subjects using single-locus and haplotype approaches. Haplotypes were identified using the expectation/maximization algorithm and latent class analysis, which included additional information on age, sex, and APOE polymorphism. Results: Allelic and genotypic frequencies for three adjacent SNP differed between AD and control groups. Both haplotype approaches identified an approximately 60% increase (p=0.02) in the risk of AD for one haplotype and similar levels of excess risk irrespective of APOE polymorphism and gender. Conclusion: Genetic variation in the brain aromatase gene may modify the risk for AD.
引用
收藏
页码:1170 / 1176
页数:7
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