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

被引:28
作者
Hu, Yang [1 ]
Cheng, Liang [2 ]
Zhang, Ying [3 ]
Bai, Weiyang [1 ]
Zhou, Wenyang [1 ]
Wang, Tao [1 ]
Han, Zhifa [1 ]
Zong, Jian [1 ]
Jin, Shuilin [4 ]
Zhang, Jun [3 ]
Jiang, Qinghua [1 ]
Liu, Guiyou [1 ]
机构
[1] Harbin Inst Technol, Sch Life Sci & Technol, Room 307,Bldg 2E,Sci Pk,Yikuang St, Harbin 150080, Peoples R China
[2] Harbin Inst Technol, Sch Comp Sci & Technol, Harbin, Peoples R China
[3] Heilongjiang Prov Land Reclamat Headquarters Gen, Dept Pharm, Harbin, Peoples R China
[4] Harbin Inst Technol, Dept Math, Harbin, Peoples R China
关键词
Alzheimer's disease; DAPK1; rs4878104; Gene expression; Expression quantitative trait loci; GENOME-WIDE ASSOCIATION; SCALE SAMPLES CONFIRMS; POLYMORPHISM CONTRIBUTES; VARIANT; SUSCEPTIBILITY; TREM2; EQTLS; LOCI; TAU;
D O I
10.1007/s10072-017-2959-9
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
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.
引用
收藏
页码:1255 / 1262
页数:8
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