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Association of lectin-like oxidized low density lipoprotein receptor 1 (OLR1) polymorphisms with late-onset Alzheimer disease in Han Chinese.


ABSTRACT: Background:Lectin-like oxidized low density lipoprotein receptor 1 (OLR1) locates within the area of chromosome 12p, which has been identified as the AD-susceptible region, and plays a role in lipid metabolism. Therefore, it has been suggested to be a good candidate gene for Alzheimer's disease (AD). Several SNPs within OLR1 have been reported to have association with AD among Caucasians. Methods:We selected and genotyped three SNPs (rs1050283, rs1050286, rs17808009) in OLR1 to investigate its possible relationship with the onset of late-onset Alzheimer disease(LOAD) in 984 LOAD cases and 1,354 healthy controls among northern Han Chinese. Results:No significant association was found between the OLR1 (rs1050283, rs1050286, rs17808009) polymorphisms and LOAD, even after adjustment for gender and age and stratification for apolipoprotein E (APOE) status. Conclusions:Our study showed that the SNPs (rs1050283, rs1050286, rs17808009) located in the 3'UTR of OLR1 may not involve in the mechanism of LOAD in Han Chinese population.

SUBMITTER: Wang ZT 

PROVIDER: S-EPMC5994529 | biostudies-literature | 2018 May

REPOSITORIES: biostudies-literature

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Association of lectin-like oxidized low density lipoprotein receptor 1 (<i>OLR1</i>) polymorphisms with late-onset Alzheimer disease in Han Chinese.

Wang Zuo-Teng ZT   Zhong Xiao-Ling XL   Tan Meng-Shan MS   Wang Hui-Fu HF   Tan Chen-Chen CC   Zhang Wei W   Zheng Zhan-Jie ZJ   Kong Ling-Li LL   Tan Lan L   Sun Li L  

Annals of translational medicine 20180501 10


<h4>Background</h4>Lectin-like oxidized low density lipoprotein receptor 1 (OLR1) locates within the area of chromosome 12p, which has been identified as the AD-susceptible region, and plays a role in lipid metabolism. Therefore, it has been suggested to be a good candidate gene for Alzheimer's disease (AD). Several SNPs within OLR1 have been reported to have association with AD among Caucasians.<h4>Methods</h4>We selected and genotyped three SNPs (rs1050283, rs1050286, rs17808009) in OLR1 to in  ...[more]

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