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汉族人群中LRP8基因单核苷酸多态性rs3820198和rs5174与帕金森病的关联分析

Association analysis of LRP8 SNP rs3820198 and rs5174 with Parkinson's disease in Han Chinese population.

作者信息

Chen Ke, Chen Yong Ping, Song Wei, Huang Rui, Zhao Bi, Cao Bei, Yang Yuan, Satake Wataru, Toda Tatsushi, Shang Hui-Fang

机构信息

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

出版信息

Neurol Res. 2012 Sep;34(7):725-9. doi: 10.1179/1743132812Y.0000000075.

Abstract

OBJECTIVES

The single-nucleotide polymorphism (SNP) rs5174 of the low-density lipoprotein receptor-related protein 8 (LRP8) gene has been linked to decreased risk for Parkinson's disease (PD) on Caucasian populations. However, this association has not been proven in Han Chinese populations.

METHODS

A total of 378 unrelated Han patients with PD from the Department of Neurology, West China Hospital of Sichuan University and 274 unrelated Han healthy controls (HCs) from the same region were included in this study. SNPs rs5174 and rs3820198 were genotyped using the Sequenom iPLEX Assay technology.

RESULTS

No significant difference was found in the genotype and minor allele frequencies (MAFs) of SNPs rs5174 and rs3820198 between the PD and HC groups, the early-onset PD and HC groups, the late-onset PD and HC groups, as well as the early-onset PD and late-onset PD groups.

CONCLUSION

This report is the first one on the lack of association of the LRP8 SNPs rs5174 and rs3820198 with PD in Han Chinese population. Together with a Japanese study, the results indicate that the variants within the LRP8 gene do not contribute to the risk of developing PD in Asian populations.

摘要

目的

低密度脂蛋白受体相关蛋白8(LRP8)基因的单核苷酸多态性(SNP)rs5174与高加索人群帕金森病(PD)风险降低有关。然而,这种关联在汉族人群中尚未得到证实。

方法

本研究纳入了四川大学华西医院神经内科的378例无亲缘关系的汉族PD患者和来自同一地区的274例无亲缘关系的汉族健康对照(HC)。使用Sequenom iPLEX检测技术对SNP rs5174和rs3820198进行基因分型。

结果

在PD组与HC组、早发型PD组与HC组、晚发型PD组与HC组以及早发型PD组与晚发型PD组之间,SNP rs5174和rs3820198的基因型和次要等位基因频率(MAF)均未发现显著差异。

结论

本报告首次表明LRP8基因的SNP rs5174和rs3820198与汉族人群的PD无关联。与一项日本研究一起,结果表明LRP8基因内的变异对亚洲人群患PD的风险没有影响。

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