The role of DENND1A and CYP19A1 gene variants in individual susceptibility to obesity in Turkish population—a preliminary study

被引:0
作者
Ela Kadioglu
Beril Altun
Çağrı İpek
Esra Döğer
Aysun Bideci
Hadi Attaran
İsmet Çok
机构
[1] Gazi University,Department of Pharmaceutical Toxicology,Faculty of Pharmacy
[2] Gazi University,Department of Pediatric Endocrinology, Faculty of Medicine
来源
Molecular Biology Reports | 2018年 / 45卷
关键词
Genetic polymorphism; Obesity; Turkish population;
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摘要
Single nucleotide polymorphisms (SNPs), the most common genetic variations in human genome, can manage the predisposition of certain complex diseases or situations such as obesity. Genetic polymorphisms also play an important role as they can impact a population’s susceptibility to being overweight or obese and developing related chronic complications such as hypertension, coronary heart disease, diabetes and cancer. The present study comprised of 193 unrelated healthy volunteers (120 females and 73 males) with Turkish origin. Only female adolescents (n = 110) were divided into 2 categories according to their BMI values as overweight (BMI ≥ 25) and normal (18.5 < BMI < 25) according to WHO classification. Genomic DNA was isolated from venous blood samples and genotyping of DENND1A rs10818854 and CYP19A1 rs2414096 variants was performed on Roche Light Cycler 2.0 Real-Time PCR platform. Serum hormone levels were analyzed by Electrochemiluminescent Immunoassay (ECLIA; Roche diagnostics). The genotype distributions were consistent with the Hardy–Weinberg equilibrium for both SNPs in the studied population (p > 0.05). The genotype distribution of DENND1A rs10818854 was determined for the first time in Turkish population and the variant allele frequency was found as 0.095. According to reduced sex hormone-binding globulin levels and increased free androgen index in the present study, obesity was linked with hyperandrogenism in female subjects. Both polymorphisms were investigated as potential genetic susceptibility markers for obesity and neither DENND1A nor CYP19A1 showed any associations.
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页码:2193 / 2199
页数:6
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