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rs4878104 与阿尔茨海默病风险相关,可调控 dapk1 基因的表达。

Rs4878104 contributes to Alzheimer's disease risk and regulates DAPK1 gene expression.

机构信息

School of Life Science and Technology, Harbin Institute of Technology, Room 307, Building 2E, Science Park, Yikuang Street, Nangang District, Harbin, 150080, China.

School of Computer Science and Technology, Harbin Institute of Technology, Harbin, China.

出版信息

Neurol Sci. 2017 Jul;38(7):1255-1262. doi: 10.1007/s10072-017-2959-9. Epub 2017 Apr 20.

Abstract

In 2006, a candidate gene study reported death-associated protein kinase 1 (DAPK1) rs4878104 variant to be significantly associated with Alzheimer's disease (AD) risk. However, the following studies showed inconsistent association results. Here, we conducted an updated analysis to investigate the potential association between rs4878104 and AD using a total of 60,751 samples (20,161 AD cases and 40,590 controls). In the pooled population, the results based on the allele and genotype genetic models show that rs4878104 variant is not significantly associated with AD risk. Interestingly, we identified rs4878104 variant to be significantly associated with AD risk in American population and Chinese population in subgroup analysis. Using multiple large-scale expression quantitative trait loci datasets, we further found that rs4878104 T allele could significantly regulate increased DAPK1 expression in European population. These findings suggest that rs4878104 may contribute AD susceptibility by modifying DAPK1 expression in European population.

摘要

2006 年,一项候选基因研究报告称死亡相关蛋白激酶 1(DAPK1)rs4878104 变体与阿尔茨海默病(AD)风险显著相关。然而,随后的研究显示出不一致的关联结果。在这里,我们使用总共 60751 个样本(20161 例 AD 病例和 40590 例对照)进行了更新的分析,以调查 rs4878104 与 AD 之间的潜在关联。在合并人群中,基于等位基因和基因型遗传模型的结果表明,rs4878104 变体与 AD 风险无显著相关性。有趣的是,我们在亚组分析中发现 rs4878104 变体与美国人群和中国人群的 AD 风险显著相关。使用多个大规模的表达数量性状基因座数据集,我们进一步发现 rs4878104 T 等位基因可显著调节欧洲人群中 DAPK1 表达的增加。这些发现表明,rs4878104 可能通过改变欧洲人群中 DAPK1 的表达来导致 AD 的易感性。

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