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GAK rs1564282 和 DGKQ rs11248060 增加了中国人群患帕金森病的风险。

GAK rs1564282 and DGKQ rs11248060 increase the risk for Parkinson's disease in a Chinese population.

机构信息

Department of Neurology, West China Hospital, SiChuan University, Chengdu Sichuan, China.

出版信息

J Clin Neurosci. 2013 Jun;20(6):880-3. doi: 10.1016/j.jocn.2012.07.011. Epub 2013 Apr 23.

DOI:10.1016/j.jocn.2012.07.011
PMID:23618683
Abstract

Numerous single-nucleotide polymorphisms (SNPs) such as GAK rs1564282 and DGKQ rs11248060 have been reported to be associated with the risk of Parkinson's disease (PD) in Caucasian populations. However, this association is yet to be proven in the Chinese population. This study included 376 unrelated Han Chinese PD patients from Southwest China and 277 unrelated Chinese healthy controls from the same region. Two SNPs, namely, rs1564282 and rs11248060, were genotyped using Sequenom's iPLEX assay. The allele frequencies and genotype distributions of the SNPs in the PD patients and controls were compared using Fisher's exact test. Significant differences were found in the genotype distributions and allele frequencies for DGKQ rs11248060 between PD patients and controls (p = 0.0425 and p = 0.0308, respectively). Significant differences were also observed in the allele frequencies for GAK rs1564282 between PD patients and controls. No significant differences were observed in the genotype frequencies, minor allele frequency, and minor allele carrier frequencies between early-onset PD (EOPD) and controls, between late-onset PD (LOPD) and controls, and between EOPD and LOPD after conservative Bonferroni adjustment. GAK rs1564282 and DGKQ rs11248060 increase the risk for PD in Chinese patients. More related studies with a larger number of participants are needed to confirm these findings.

摘要

许多单核苷酸多态性(SNPs),如 GAK rs1564282 和 DGKQ rs11248060,已被报道与高加索人群帕金森病(PD)的风险相关。然而,这种关联尚未在中国人群中得到证实。本研究纳入了来自中国西南地区的 376 例汉族 PD 患者和来自同一地区的 277 例汉族健康对照者。采用Sequenom 的 iPLEX assay 对 2 个 SNP,即 rs1564282 和 rs11248060,进行基因分型。采用 Fisher 精确检验比较 PD 患者和对照组中 SNP 的等位基因频率和基因型分布。在 PD 患者和对照组中,DGKQ rs11248060 的基因型分布和等位基因频率存在显著差异(p = 0.0425 和 p = 0.0308)。在 PD 患者和对照组中,GAK rs1564282 的等位基因频率也存在显著差异。经保守 Bonferroni 校正后,在早发性 PD(EOPD)和对照组、晚发性 PD(LOPD)和对照组、EOPD 和 LOPD 之间,基因型频率、次要等位基因频率和次要等位基因携带者频率均无显著差异。GAK rs1564282 和 DGKQ rs11248060 增加了中国 PD 患者的发病风险。需要更多相关研究和更大样本量来验证这些发现。

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