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Analysis of several loci from genome-wide association studies in Parkinson's disease in mainland China

机译:来自中国大陆帕金森氏病全基因组关联研究的几个基因座分析

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Large-scale meta-analyses of genome-wide association studies in Parkinson's disease (PD) have identified a number of susceptibility loci in sporadic PD. Since the characteristics of those loci in a Han Chinese population from mainland China were unknown, we performed a case-control replication study in this population and evaluated several single nucleotide polymorphisms (SNPs) identified in a recent GWAS-meta-analysis. In total, 933 subjects comprised of 460 PD patients and 473 controls were genotyped. We found strong evidence of an association for rs708723 in RAB7L1 in the total sample (genotype p = 0.01, allelep = 0.01, OR=0.78, 95% CI = 0.65-0.94). With rs156429 in GPNMB, there was a significant difference in genotype and allele distribution between male PD patients and the control subgroup (genotype p=0.01, allele p = 0.01, OR= 0.67, 95% CI = 0.49-0.92). However, we did not observe any significant difference in genotype or allele distribution between PD and control for rs34016896 in NMD3 and rs6812193 in STBD1. (C) 2014 Published by Elsevier Ireland Ltd.
机译:帕金森氏病(PD)的全基因组关联研究的大规模荟萃分析确定了散发性PD中的许多易感基因座。由于来自中国大陆的汉族人群中这些基因座的特征尚不清楚,因此我们在此人群中进行了病例对照复制研究,并评估了在最近的GWAS元分析中鉴定出的几种单核苷酸多态性(SNP)。总共对460名PD患者和473名对照组成的933名受试者进行了基因分型。我们发现有力证据表明总样本中RAB7L1中的rs708723有关联(基因型p = 0.01,等位基因= 0.01,OR = 0.78,95%CI = 0.65-0.94)。在GPNMB中使用rs156429,男性PD患者与对照组之间的基因型和等位基因分布存在显着差异(基因型p = 0.01,等位基因p = 0.01,OR = 0.67,95%CI = 0.49-0.92)。但是,我们在NMD3中的rs34016896和STBD1中的rs6812193的PD和对照之间没有观察到基因型或等位基因分布的显着差异。 (C)2014由爱思唯尔爱尔兰有限公司发行。

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