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NME8基因rs2718058多态性与阿尔茨海默病风险:一项重复验证及荟萃分析

NME8 rs2718058 polymorphism with Alzheimer's disease risk: a replication and meta-analysis.

作者信息

Liu Shu-Lei, Wang Xue-Chun, Tan Meng-Shan, Wang Hui-Fu, Zhang Wei, Wang Zi-Xuan, Yu Jin-Tai, Tan Lan

机构信息

Department of Neurology, Qingdao Municipal Hospital, School of Medicine, Qingdao University, Qingdao, PR China.

Department of Radiology, Qingdao Municipal Hospital, School of Medicine, Qingdao University, Qingdao, PR China.

出版信息

Oncotarget. 2016 Jun 14;7(24):36014-36020. doi: 10.18632/oncotarget.9086.

Abstract

Recently, a large meta-analysis of five genome wide association studies (GWAS) has identified that a novel single nucleotide polymorphism (SNP) rs2718058, adjacent to gene NME8 on chromosome 7p14.1, was associated with late-onset Alzheimer's disease (LOAD) in Caucasians. However, the effect of rs2718058 on other populations remains unclear. In order to explore the relationship between rs2718058 and LOAD risk in a North Han Chinese population, we recruited 984 LOAD cases and 1354 healthy controls that matched for sex and age in this study. The results showed no significant differences in the genotypic or allelic distributions of rs2718058 polymorphism between LOAD cases and healthy controls, even though after stratification for APOE ε4 status and statistical adjustment for age, gender and APOE ε4 status (p > 0.05). However, a meta-analysis conducted in a sample of 82513 individuals confirmed a significant association between SNP rs2718058 and LOAD risk (OR = 1.08, 95%CI = 1.05-1.11) in the whole population. But there was still no positive results in Chinese subgroup (OR = 1.05, 95%CI = 0.93-1.17). In conclusion, the rs2718058 near gene NME8 on chromosome 7p14.1 might not play a major role in the genetic predisposition to LOAD in the North Han Chinese.

摘要

最近,一项对五项全基因组关联研究(GWAS)的大型荟萃分析确定,位于7号染色体p14.1上与NME8基因相邻的一个新的单核苷酸多态性(SNP)rs2718058与白种人中的晚发性阿尔茨海默病(LOAD)相关。然而,rs2718058对其他人群的影响仍不清楚。为了探究rs2718058与中国北方汉族人群LOAD风险之间的关系,我们在本研究中招募了984例LOAD病例和1354名年龄和性别匹配的健康对照。结果显示,即使在按APOE ε4状态分层并对年龄、性别和APOE ε4状态进行统计调整后,LOAD病例与健康对照之间rs2718058多态性的基因型或等位基因分布也没有显著差异(p>0.05)。然而,对82513名个体样本进行的荟萃分析证实,SNP rs2718058与整个人群的LOAD风险之间存在显著关联(OR = 1.08,95%CI = 1.05-1.11)。但在中国亚组中仍未得到阳性结果(OR = 1.05,95%CI = 0.93-1.17)。总之,位于7号染色体p14.1上NME8基因附近的rs2718058可能在中国北方汉族人群LOAD的遗传易感性中不起主要作用。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/56ac/5094979/f2ff538b4ba2/oncotarget-07-36014-g001.jpg

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