Complex interactions in Parkinson's disease: A two-phased approach

被引:25
作者
Maraganore, DM
de Andrade, M
Lesnick, TG
Farrer, MJ
Bower, JH
Hardy, JA
Rocca, WA
机构
[1] Mayo Clin & Mayo Fdn, Dept Neurol, Rochester, MN 55905 USA
[2] Mayo Clin & Mayo Fdn, Dept Hlth Sci Res, Rochester, MN 55905 USA
[3] Mayo Clin & Mayo Fdn, Dept Neurosci, Jacksonville, FL USA
[4] NIA, Neurogenet Lab, Bethesda, MD 20892 USA
关键词
Parkinson's disease; susceptibility genes; ubiquitin proteasome system; recursive partitioning; epistasis; interactions;
D O I
10.1002/mds.10431
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
The identification of pathogenic mutations in the three genes alpha-synuclein, parkin, and ubiquitin carboxy-terminal hydrolase L1 (UCHL1) has elucidated the ubiquitin proteasome system (UPS) and its potential role as a causal pathway in Parkinson's disease (PD). In addition, polymorphisms of these three genes have been shown to be independently associated with PD. In a sample of 298 unrelated PD cases and 185 controls, we applied a two-phased approach of recursive partitioning and logistic regression analyses to explore complex interactions. For women only, we observed an epistatic interaction of UCHL1 and alpha-synuclein genotypes with significant effects on PD risk (odds ratio = 2.42; P = 0.003). Our findings are consistent with the hypothesis that PD is a multigenic disorder of the UPS. (C) 2003 Movement Disorder Society.
引用
收藏
页码:631 / 636
页数:6
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