| Literature DB >> 31204042 |
Xiao-He Hou1, Yan-Lin Bi2, Meng-Shan Tan1, Wei Xu1, Jie-Qiong Li1, Xue-Ning Shen1, Kai-Xin Dou1, Chen-Chen Tan1, Lan Tan1, Jin-Tai Yu3.
Abstract
The triggering receptor expressed on myeloid cells 2 (TREM2) gene has been reported to increase the risk of Alzheimer's disease (AD). The soluble TREM2 protein (sTREM2) in cerebrospinal fluid (CSF) was also associated with AD. However, the role of sTREM2 in AD and its genetic modifiers remain unclear. We carried out a genome-wide association study for CSF sTREM2 levels using participants from the Alzheimer's Disease Neuroimaging Initiative and validated the significant association in an independent cohort from Chinese Alzheimer's Biomarker and LifestylE study. rs7232 in membrane spanning 4-domains A6A (MS4A6A) gene was associated with CSF sTREM2 levels at genome-wide significance (p = 1.42 × 10-15). The locus influences CSF sTREM2 levels especially in nondemented individuals. And the association was replicable in the validation cohort from Chinese Alzheimer's Biomarker and LifestylE study (p = 0.0106). Besides, the expressions of MS4A6A and TREM2 were correlated in brain regions (p < 2 × 10-16). The findings of our study suggest that the AD risk variant in the MS4A6A gene participates in the regulation of sTREM2.Entities:
Keywords: Alzheimer's disease; Genome-wide association study; MS4A6A; TREM2
Year: 2019 PMID: 31204042 DOI: 10.1016/j.neurobiolaging.2019.05.008
Source DB: PubMed Journal: Neurobiol Aging ISSN: 0197-4580 Impact factor: 4.673