FUNCTIONAL ROLE OF THE TP53 GENE SINGLE NUCLEOTIDE POLYMORPHISM P72R (C>G) IN PATIENTS WITH TYPE 2 DIABETES MELLITUS OF THE EAST UKRAINIAN POPULATION

N. Krasova, A. Kolesnikova, M. Gorshunska, O. Plohotnichenko, Tetiana Tyzhnenko, Z. Leshchenko, Oleksandr Gladkih, T. Voropay, I. Romanova, Elena Zalubovskaya, Loriana Sergienko, E. Jansen, Kateryna Misiura
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Abstract

Recently, the role of stress-regulatory pathways in the development and progression of type 2 diabetes mellitus (T2DM) and associated cardiovascular diseases has been widely investigated. The aim of the study was to assess the relationship of polymorphic variants P72R (C>G) of the TP53 gene with the functional and metabolic characteristics of type 2 diabetic patients in the East Ukrainian population. Materials and methods. 50 T2DM patients (female/male: 21/29) aged 53.34±1.43 yrs., with diabetes duration of 6.25±0.89 yrs., HbA1c level of 7.12±0.21%, body mass index of 31.19±0.93 kg/m2, with waist-to-hip ratio of 0.96±0.01, with the presence of coronary heart disease in 38 cases, hypertension in 46 cases, and their combination in 37 cases. Characteristics of carbohydrate/lipid metabolism, parameters of insulin resistance, chronic inflammation, and a number of adipokines were determined in the subjects. Genotyping for single nucleotide polymorphism P72R (C>G) TP53 was performed by the method of polymerase chain reaction with appropriate primers and BstUI endonuclease. Testing of null hypotheses was carried out using the t, F and c2 criteria at the significance level of P≤0.05. Results. There was a noticeable tendency (P=0.05) to increase in frequency of the recessive allele G, mainly in men, which requires further extended studies. In addition, carriers of the minor genotype are characterized by a significantly younger age of T2DM manifestation. Under the statistically similar parameters that characterize the degree of obesity and glucose metabolism compensation, the connection of the G-allele with insulin resistance, both hepatic (HOMA-IR) and associated with adipose tissue (HOMA-IR/adiponectin, adiponectin/leptin) was observed. Carriers of the recessive allele are also characterized by an increased atherogenic coefficient relative to the dominant CC genotype, a significant decrease in the levels of adiponectin (total and high molecular weight) and omentin, and an increase in the levels of leptin and vaspin in the circulation. According to the recessive model, the presence of the G-allele is accompanied by a weak but probable increase in the levels of highly sensitive C-reactive protein (CC vs. CG+GG: 1.92±0.42 mg/l vs. 4.62±0.94 mg/l, P <0.05). The above suggests that the G-allele may be a predictor of a greater risk of cardiovascular disease development in patients with T2DM. Conclusions. It has been proven that the P72R polymorphism of the TP53 gene is functional for the East Ukrainian population, because against the background of a comparable degree of obesity and glucose metabolism compensation, carriers of the minor G-allele are characterized by a greater degree of insulin resistance and a proatherogenic shift in the hormonal activity of adipose tissue. A tendency to increase in frequency of the G-allele in men with type 2 diabetes was revealed, and it was determined that carriers of the minor genotype are characterized by a significantly younger age of diabetes manifestation. The obtained results substantiate the need for further research to assess the role of this polymorphism in the Ukrainian population.
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TP53基因单核苷酸多态性P72R(C>G)在东乌克兰人群2型糖尿病患者中的功能作用
最近,压力调节通路在2型糖尿病(T2DM)和相关心血管疾病的发展和进展中的作用已被广泛研究。本研究的目的是评估TP53基因的多态性变体P72R(C>G)与东乌克兰人群中2型糖尿病患者的功能和代谢特征的关系。材料和方法。T2DM患者50例(女/男:21/29),年龄53.34±1.43岁,糖尿病持续时间6.25±0.89岁,HbA1c水平7.12±0.21%,体重指数31.19±0.93 kg/m2,腰臀比0.96±0.01,冠心病38例,高血压46例,合并冠心病37例。测定了受试者的碳水化合物/脂质代谢特征、胰岛素抵抗参数、慢性炎症和一些脂肪因子。采用聚合酶链式反应和BstUI核酸内切酶的方法对P72R(C>G)TP53单核苷酸多态性进行基因分型。在P≤0.05的显著性水平上,使用t、F和c2标准对零假设进行了检验。结果:隐性等位基因G的频率有明显的增加趋势(P=0.05),主要在男性中,这需要进一步的扩展研究。此外,次要基因型携带者的特征是T2DM表现的年龄明显较年轻。在表征肥胖程度和糖代谢补偿的统计学相似参数下,观察到G等位基因与肝胰岛素抵抗(HOMA-IR)和与脂肪组织相关的胰岛素抵抗(HOMA-IR/脂联素、脂联素/瘦素)的联系。隐性等位基因携带者的特征还在于,与显性CC基因型相比,动脉粥样硬化系数增加,脂联素(总分子量和高分子量)和网膜蛋白水平显著降低,循环中瘦素和vaspin水平增加。根据隐性模型,G等位基因的存在伴随着高敏C反应蛋白水平的微弱但可能的增加(CC与。CG+GG:1.92±0.42mg/l vs.4.62±0.94mg/l,P<0.05)。以上表明,G等位基因可能是T2DM患者心血管疾病发展风险更大的预测因子。结论。已经证明,TP53基因的P72R多态性对东乌克兰人群具有功能,因为在相当程度的肥胖和糖代谢补偿的背景下,次要G等位基因的携带者的特征是胰岛素抵抗程度更高,脂肪组织的激素活性发生了原发性变化。发现2型糖尿病男性的G等位基因频率有增加的趋势,并确定次要基因型携带者的糖尿病表现年龄明显较年轻。所获得的结果证实了进一步研究的必要性,以评估这种多态性在乌克兰人群中的作用。
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来源期刊
Problemi Endokrinnoi Patologii
Problemi Endokrinnoi Patologii Medicine-Endocrinology, Diabetes and Metabolism
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42
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