RIT2 variant is not associated with Parkinson's disease in a Taiwanese population

Neurobiol Aging. 2013 Sep;34(9):2236.e1-3. doi: 10.1016/j.neurobiolaging.2013.04.005. Epub 2013 Apr 28.

Abstract

Recent genome-wide association studies of Parkinson's disease (PD) have identified the rs12456492 variant of the novel susceptibility loci, RIT2, as being associated with disease risk in a large white population. Studies among Asians are scarce. We genotyped RIT2 rs12456492 variant in a total of 1000 participants, comprising 500 patients with PD and 500 control subjects in a Taiwanese population. The frequency of GA/AA genotype was slightly higher in PD patients compared with controls, but was without statistical significance (odds ratio = 1.03, 95% confidence interval = 0.73-1.46, p = 0.86). We failed to replicate the RIT2 rs12456492 variant as a genetic risk factor for PD in our population.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adult
  • Aged
  • Aged, 80 and over
  • Asian People / ethnology*
  • Asian People / genetics*
  • Female
  • Genetic Loci / genetics*
  • Genetic Predisposition to Disease / genetics*
  • Genetic Variation / genetics*
  • Genome-Wide Association Study
  • Genotype*
  • Humans
  • Male
  • Middle Aged
  • Monomeric GTP-Binding Proteins / genetics*
  • Parkinson Disease / genetics*
  • Risk Factors
  • Taiwan

Substances

  • Monomeric GTP-Binding Proteins
  • RiT2 protein, human