Department of Neurology, National Taiwan University Hospital, College of Medicine, National Taiwan University, Taipei, Taiwan.
Neurobiol Aging. 2013 Sep;34(9):2236.e1-3. doi: 10.1016/j.neurobiolaging.2013.04.005. Epub 2013 Apr 28.
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.
最近的帕金森病(PD)全基因组关联研究发现,新型易感基因 RIT2 的 rs12456492 变异与白人人群的疾病风险相关。亚洲人群的研究较少。我们在一个台湾人群中对 RIT2 rs12456492 变异进行了基因分型,共纳入 1000 名参与者,包括 500 名 PD 患者和 500 名对照。与对照组相比,PD 患者中 GA/AA 基因型的频率略高,但无统计学意义(比值比=1.03,95%置信区间=0.73-1.46,p=0.86)。我们未能在我们的人群中复制 RIT2 rs12456492 变异作为 PD 的遗传风险因素。