Genetic variation in Clusterin gene and Alzheimer's disease risk in Han Chinese

被引:13
作者
Yu, Jin-Tai [1 ,2 ]
Ma, Xiao-Ying [2 ,3 ]
Wang, Ying-Li [2 ]
Sun, Lei [2 ]
Tan, Lin [2 ]
Hu, Nan [2 ]
Tan, Lan [1 ,2 ]
机构
[1] Ocean Univ China, Coll Med & Pharmaceut, Qingdao, Peoples R China
[2] Qingdao Univ, Qingdao Municipal Hosp, Sch Med, Dept Neurol, Qingdao 266071, Peoples R China
[3] Guihang Guiyang Hosp, Dept Neurol, Guiyang, Peoples R China
基金
中国国家自然科学基金;
关键词
Alzheimer's Disease; Clusterin; Polymorphism; Association study; GENOME-WIDE ASSOCIATION; APOLIPOPROTEIN-J; CEREBROSPINAL-FLUID; IDENTIFIES VARIANTS; CLU GENE; PICALM; POLYMORPHISMS; CR-1; METAANALYSIS; REPLICATION;
D O I
10.1016/j.neurobiolaging.2013.01.010
中图分类号
R592 [老年病学]; C [社会科学总论];
学科分类号
03 ; 0303 ; 100203 ;
摘要
Clusterin gene (CLU), also known as apolipoprotein J (ApoJ), is a strong candidate gene for late-onset Alzheimer's disease (LOAD) according to the Alzgene database. To further characterize this association and to isolate the variants contributing to the pathogenesis of LOAD in Han Chinese, we first sequenced a small sample (n = 100) to discover variants in the promoter, exons, the 5' and 3' untranslated regions, and exon-intron boundaries of CLU. Follow-up genotyping of identified variants in a larger sample (n = 1592). Sequencing analysis identified 18 variants. Analysis in the larger population revealed that only the rs9331949 C allele was significantly associated with an increased risk of LOAD, even after adjusting for multiple testing (p = 0.026). Logistic analysis identified the rs9331949 polymorphism was still strongly associated with LOAD (additive model: p = 0.004, odds ratio = 1.274; dominant model: p = 0.039, odds ratio = 1.239; recessive model: p = 0.002, OR = 1.975) after adjusting for sex, age, and APOE epsilon 4 status. Our findings implicate CLU as a susceptibility gene for LOAD in Han Chinese. (C) 2013 Elsevier Inc. All rights reserved.
引用
收藏
页码:1921.e17 / 1921.e23
页数:7
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