The study of association between genetic variants in sortilin-related receptor 1 and Alzheimer's disease
10.3760/cma.j.issn.0254-9026.2013.12.004
- VernacularTitle:分拣蛋白相关受体1基因多态性与阿尔茨海默病的相关性研究
- Author:
Huiyan YU
;
Xin GAO
;
Xiangyu CENG
;
Ning CHAO
;
Bin QIN
- Publication Type:Journal Article
- Keywords:
Alzheimer's disease;
Polymorphism,genetic;
Amyloid
- From:
Chinese Journal of Geriatrics
2013;32(12):1277-1280
- CountryChina
- Language:Chinese
-
Abstract:
Objective To investigate the association between gene polymorphism of sortilinrelated receptor 1 (SORL1) and Alzheimer' s disease by detecting a series of single nucleotide polymorphisms (SNPs).Methods The Snapshot method was used to genotypc 6 SNPs (SNP10,19,23,24,25,27) in SORL1 and the distributions of allele and genotype of the 6 SNPs were compared between AD patients and healthy control individuals.Results There were significant differences in the genotype distributions of SNP19,23,24 and 25 between AD patients and control group (all P<0.01).Subjects with TT genotype in SNP19 had significantly lower risk for AD and was protective for AD (OR=0.089,95%CI:0.011-0.718,P<0.01).The AT genotype in SNP23 (OR=3.826,95%CI:1.388~10.544,P<0.01),CT genotype in SNP24(OR=5.935,95%CI:1.774-19.853,P<0.01)and CT genotype in SNP25(OR=5.754,95%CI:2.007-16.496,P<0.01)had higher risks for AD.Conclusions SORL1 gene variants of SNP19,23,24 and 25 might be the important risk factors for late-onset AD.