Analysis of the UCHL1 genetic variant in Parkinson's disease among Chinese

Neurobiol Aging. 2010 Dec;31(12):2194-6. doi: 10.1016/j.neurobiolaging.2008.11.008. Epub 2009 Mar 28.

Abstract

The inverse association of the functional ubiquitin carboxy-terminal hydrolase L1 (UCHL1) S18Y variant with Parkinson's disease (PD) among Caucasian populations has been debated. We conducted a large-scale analysis to investigate the age-of-onset effect of the UCHL1 variant in PD among ethnic Chinese. Individual data sets from 5 centers comprising a total of 4088 study subjects were analyzed. In the univariate analysis, only data from 1 center showed a trend towards a protective effect among young subjects. However, in the combined analysis, no significant association between the UCHL1 variant and PD was detected (A allele frequency 0.531 vs. 0.528, p=0.87, OR 1.01, 95% CI 0.92-1.1). Among subjects less than 60 years old, the OR is 0.99 (95% CI 0.84-1.16, p=0.88). A multivariate logistic regression analysis showed that family history, UCHL1 variant and the interaction of UCHL1 variant and age at onset (p=0.816) were not significantly associated with PD.

Publication types

  • Multicenter Study
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adolescent
  • Adult
  • Age of Onset
  • Aged
  • Aged, 80 and over
  • Asian People / ethnology
  • Asian People / genetics
  • Female
  • Genetic Association Studies
  • Genetic Variation / genetics*
  • Humans
  • Male
  • Middle Aged
  • Parkinson Disease / enzymology*
  • Parkinson Disease / epidemiology
  • Parkinson Disease / genetics*
  • Singapore / epidemiology
  • Singapore / ethnology
  • Taiwan / epidemiology
  • Taiwan / ethnology
  • Ubiquitin Thiolesterase / genetics*
  • Ubiquitination / genetics
  • Young Adult

Substances

  • UCHL1 protein, human
  • Ubiquitin Thiolesterase