| Literature DB >> 28429084 |
Yang Hu1, Liang Cheng2, Ying Zhang3, Weiyang Bai1, Wenyang Zhou1, Tao Wang1, Zhifa Han1, Jian Zong1, Shuilin Jin4, Jun Zhang3, Qinghua Jiang1, Guiyou Liu5.
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.Entities:
Keywords: Alzheimer’s disease; DAPK1; Expression quantitative trait loci; Gene expression; rs4878104
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Year: 2017 PMID: 28429084 DOI: 10.1007/s10072-017-2959-9
Source DB: PubMed Journal: Neurol Sci ISSN: 1590-1874 Impact factor: 3.307