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

Author:

Alaylıoğlu Merve1,Gezen-Ak Duygu1,Dursun Erdinç1,Bilgiç Başar2,Hanağası Haşmet2,Ertan Turan3,Gürvit Hakan2,Emre Murat2,Eker Engin3,Uysal Ömer4,Yılmazer Selma1

Affiliation:

1. Department of Medical Biology, Cerrahpasa Faculty of Medicine, Istanbul University, Istanbul, Turkey

2. Behavioral Neurology and Movement Disorders Unit, Department of Neurology, Istanbul Faculty of Medicine, Istanbul University, Istanbul, Turkey

3. Department of Geropsychiatry, Cerrahpasa Faculty of Medicine, Istanbul University, Istanbul, Turkey

4. Department of Biostatistics and Medical Informatics, School of Medicine, Bezmialem Vakif University, Istanbul, Turkey

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.

Publisher

SAGE Publications

Subject

Psychiatry and Mental health,Geriatrics and Gerontology,Clinical Neurology

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