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首页> 外文期刊>Journal of clinical neuroscience: official journal of the Neurosurgical Society of Australasia >GAK rs1564282 and DGKQ rs11248060 increase the risk for Parkinson's disease in a Chinese population.
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GAK rs1564282 and DGKQ rs11248060 increase the risk for Parkinson's disease in a Chinese population.

机译:GAK rs1564282和DGKQ rs11248060增加了中国人患帕金森氏病的风险。

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摘要

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.
机译:据报道,许多单核苷酸多态性(SNP),例如GAK rs1564282和DGKQ rs11248060与白种人人群中帕金森氏病(PD)的风险有关。但是,这种关联尚未在中国人口中得到证实。这项研究纳入了来自中国西南地区的376名无关的汉族PD患者和来自同一地区的277名无关的中国健康对照者。使用Sequenom的iPLEX分析对两个SNP(即rs1564282和rs11248060)进行基因分型。使用Fisher精确检验比较了PD患者和对照组中SNP的等位基因频率和基因型分布。在PD患者和对照组之间,DGKQ rs11248060的基因型分布和等位基因频率存在显着差异(分别为p = 0.0425和p = 0.0308)。在PD患者和对照组之间,GAK rs1564282的等位基因频率也观察到显着差异。在保守型Bonferroni调整后,早期发作的PD(EOPD)与对照之间,晚期发作的PD(LOPD)与对照之间以及EOPD与LOPD之间的基因型频率,次要等位基因频率和次要等位基因携带者频率之间均未观察到显着差异。 。 GAK rs1564282和DGKQ rs11248060增加了中国患者发生PD的风险。需要更多参与者的更多相关研究来证实这些发现。

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