The Association Between Clusterin and APOE Polymorphisms and Late-Onset Alzheimer Disease in a Turkish Cohort


Alaylioglu M., Gezen-Ak D., Dursun E., Bilgic B., Hanagasi H., Ertan T., ...More

JOURNAL OF GERIATRIC PSYCHIATRY AND NEUROLOGY, vol.29, no.4, pp.221-226, 2016 (Journal Indexed in SCI) identifier identifier identifier

  • Publication Type: Article / Article
  • Volume: 29 Issue: 4
  • Publication Date: 2016
  • Doi Number: 10.1177/0891988716640373
  • Title of Journal : JOURNAL OF GERIATRIC PSYCHIATRY AND NEUROLOGY
  • Page Numbers: pp.221-226
  • Keywords: Alzheimer disease, clusterin, APOJ, rs9331888, APOE, SNP, GENOME-WIDE ASSOCIATION, CLU GENE POLYMORPHISMS, AMYLOID BETA-PEPTIDE, CEREBROSPINAL-FLUID, APOLIPOPROTEIN-J, IDENTIFIES VARIANTS, OXIDATIVE STRESS, PICALM, POPULATION, CR-1

Abstract

Previous studies have demonstrated that clusterin (CLU), which is also known as apolipoprotein J, is involved in the pathogenesis of Alzheimer disease (AD). In this study, we investigated the association between rs2279590, rs11136000, and rs9331888 single-nucleotide polymorphisms (SNPs) in CLU and apolipoprotein E (APOE) genotypes in a cohort of Turkish patients with late-onset AD (LOAD). There were 183 patients with LOAD and 154 healthy controls included in the study. The CLU and APOE polymorphisms were genotyped using the LightSNiP assay. The GG genotype of rs9331888 was significantly more frequent in patients with LOAD. The CC genotype of the SNP was significantly more frequent in controls. The rs9331888 GG genotype in patients and the CC genotype in controls were significantly higher in non-4 allele carriers of APOE. The haplotype analysis showed the CLU GCG haplotype was a risk haplotype. Our findings indicate the rs9331888 SNP of CLU is associated with LOAD independent of APOE.