Zenoaga-Barbăroșie C, Berca L, Vassu-Dimov T, Toma M, Nica M I, Alexiu-Toma O A, Ciornei C, Albu A, Nica S, Nistor C, Nica R
Department of Genetics, University of Bucharest, Bucharest, Romania.
Molecular Biology Department, National Research and Development Institute for Food Bioresources - IBA Bucharest, Bucharest, Romania.
Balkan J Med Genet. 2023 Jul 31;26(1):21-26. doi: 10.2478/bjmg-2023-0003. eCollection 2023 Jul.
Type 2 diabetes mellitus (T2DM) and metabolic syndrome (MetS) are diseases caused by the interaction of genetic and non-genetic factors. Therefore, the aim of our study was to investigate the association between six common genetic polymorphisms and T2DM and MetS in males. A total of 120 T2DM, 75 MetS, and 120 healthy controls (HC) were included in the study. ID, 4a/b, A1166C, (A>G), +35A/C, -21A/T gene polymorphisms were genotyped by PCR or PCR-RFLP techniques. T2DM was diagnosed at an earlier age compared to MetS (54 vs 55 years old, p=0.0003) and the difference was greater in carriers of the G allele (54 vs 56 years old, p=0.0002) or both G and b alleles (54 vs 56, p=0.00016). The AA genotype (O.R.=0.11, p=0.0006) and the presence of both I and A (O.R.=0.39, p=0.0005) alleles revealed to be protective for T2DM. AA and AC genotypes were protective factors for triglyceride (p=0.0002 and p=0.0005, respectively) and HDL cholesterol (p=0.0002 and p=0.0004, respectively) levels in T2DM patients. DD was identified more frequently in hypertensive T2DM patients (O.R.=3.77, p=0.0005) and in those who reported drinking alcohol (p=0.0001) comparing to HC and T2DM patients who did not drink alcohol, respectively. We observed that T2DM patients who reported drinking alcohol had an increased frequency of DD and bb (p<0.0001), or DD and G (p<0.0001) compared to non-drinkers. No gene polymorphisms were associated with MetS.
2型糖尿病(T2DM)和代谢综合征(MetS)是由遗传和非遗传因素相互作用引起的疾病。因此,我们研究的目的是调查男性中六种常见基因多态性与T2DM和MetS之间的关联。该研究共纳入了120例T2DM患者、75例MetS患者和120例健康对照(HC)。通过PCR或PCR-RFLP技术对ID、4a/b、A1166C、(A>G)、+35A/C、-21A/T基因多态性进行基因分型。与MetS相比,T2DM的诊断年龄更早(54岁对55岁,p=0.0003),在G等位基因携带者中差异更大(54岁对56岁,p=0.0002)或同时携带G和b等位基因者中差异更大(54岁对56岁,p=0.00016)。AA基因型(O.R.=0.11,p=0.0006)以及I和A等位基因同时存在(O.R.=0.39,p=0.0005)被发现对T2DM具有保护作用。AA和AC基因型分别是T2DM患者甘油三酯水平(p=0.0002和p=0.0005)和高密度脂蛋白胆固醇水平(p=0.0002和p=0.0004)的保护因素。与HC以及不饮酒的T2DM患者相比,DD基因型在高血压T2DM患者中(O.R.=3.77,p=0.0005)以及报告饮酒的患者中(p=0.0001)更频繁地被检测到。我们观察到,与不饮酒者相比,报告饮酒的T2DM患者中DD和bb基因型(p<0.0001)或DD和G基因型(p<0.0001)的频率增加。没有基因多态性与MetS相关。