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Alzheimer Disease Associated Loci: APOE Single Nucleotide Polymorphisms in Marmara Region.
Ismail, Aya Badeea; Dundar, Mehmet Sait; Erguzeloglu, Cemre Ornek; Ergoren, Mahmut Cerkez; Alemdar, Adem; Ozemri Sag, Sebnem; Temel, Sehime Gulsun.
Afiliação
  • Ismail AB; Department of Medical Genetics, Faculty of Medicine, Near East University, 99138 Nicosia, Cyprus.
  • Dundar MS; Department of Electrical and Computer Engineering, Graduate School of Engineering and Sciences, Abdullah Gul University, 38000 Kayseri, Türkiye.
  • Erguzeloglu CO; Halil Bayraktar Health Services Vocational School, Erciyes University, 38030 Kayseri, Türkiye.
  • Ergoren MC; Department of Translational Medicine, Institute of Health Sciences, Bursa Uludag University, 16059 Bursa, Türkiye.
  • Alemdar A; Department of Medical Genetics, Faculty of Medicine, Near East University, 99138 Nicosia, Cyprus.
  • Ozemri Sag S; Department of Translational Medicine, Institute of Health Sciences, Bursa Uludag University, 16059 Bursa, Türkiye.
  • Temel SG; Department of Medical Genetics, Faculty of Medicine, Bursa Uludag University, 16059 Bursa, Türkiye.
Biomedicines ; 12(5)2024 Apr 27.
Article em En | MEDLINE | ID: mdl-38790930
ABSTRACT
Alzheimer's disease (AD) is a major global health challenge, especially among individuals aged 65 or older. According to population health studies, Turkey has the highest AD prevalence in the Middle East and Europe. To accurately determine the frequencies of common and rare APOE single nucleotide polymorphisms (SNPs) in the Turkish population residing in the Marmara Region, we conducted a retrospective study analyzing APOE variants in 588 individuals referred to the Bursa Uludag University Genetic Diseases Evaluation Center. Molecular genotyping, clinical exome sequencing, bioinformatics analysis, and statistical evaluation were employed to identify APOE polymorphisms and assess their distribution. The study revealed the frequencies of APOE alleles as follows ε4 at 9.94%, ε2 at 9.18%, and ε3 at 80.68%. The gender-based analysis in our study uncovered a tendency for females to exhibit a higher prevalence of mutant genotypes across various SNPs. The most prevalent haplotype observed was ε3/ε3, while rare APOE SNPs were also identified. These findings align with global observations, underscoring the significance of genetic diversity and gender-specific characteristics in comprehending health disparities and formulating preventive strategies.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Revista: Biomedicines Ano de publicação: 2024 Tipo de documento: Article País de afiliação: Chipre

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Revista: Biomedicines Ano de publicação: 2024 Tipo de documento: Article País de afiliação: Chipre