| Literature DB >> 12784265 |
Demetrius M Maraganore1, Mariza de Andrade, Timothy G Lesnick, Matthew J Farrer, James H Bower, John A Hardy, Walter A Rocca.
Abstract
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. Copyright 2003 Movement Disorder SocietyEntities:
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Year: 2003 PMID: 12784265 DOI: 10.1002/mds.10431
Source DB: PubMed Journal: Mov Disord ISSN: 0885-3185 Impact factor: 10.338