THE POLYMORPHISM -308 G/A OF THE TNF GENE AND METABOLIC IMBALANCE IN PATIENTS WITH TYPE 2 DIABETES MELLITUS AND NON-ALCOHOLIC FATTY LIVER DISEASE, TAKING INTO ACCOUNT CARDIOVASCULAR COMPLICATIONS

Tetiana Tyzhnenko, Kateryna Misiura, N. Kravchun, M. Gorshunska, A. Pochernyaev, N. Krasova, Oleksandr Gladkih, Z. Leshchenko, G. Fedorova, Ольга Плохотніченко, Olena Hromakovska, A. Kolesnikova, E. Jansen, Yurii Karachentsev, Viktoriya Poltorak
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Abstract

Non-alcoholic fatty liver disease (NAFLD), the most common form of liver disease, is now recognized as a major public health problem worldwide. Tumor necrosis factor alfa (TNF-α), a member of the TNF/TNFR cytokine family, is an intercellular transmission molecule that has been reported in a wide range of human noninfection diseases. The aim of the study was to determine the circulating levels of TNF-α and the nature of its relationships with the components of insulin resistance, both metabolic and hormonal, in patients with type 2 diabetes; and establishing the nature of cardiovascular complications (taking into account TNF-α gene polymorphism) in the presence and absence of NAFLD. Materials and methods. Case-control study included information about 50 practically healthy people from the city of Kharkiv and the region. The examined population (except control subjects) consisted exclusively of patients with type 2 diabetes mellitus with a long-term existence of the disease against the background of metabolic syndrome, with varying degrees of glycemic control and violations of liver homeostasis in the absence of renal failure. 117 people were selected for analysis: 63 of them with type 2 diabetes in the presence of NAFLD and 54 patients with type 2 diabetes without NAFLD. Genotyping for single nucleotide polymorphism -308 G>A of the TNF-α was performed by the method of polymerase chain reaction with appropriate primers and NcoI endonuclease. Testing of statistical hypotheses was carried out using the odds ratio and χ2 criteria at the significance level of P≤0.05. Results. The contribution of the genetic component to the formation of the predisposition to the development of type 2 diabetes mellitus based on the single-nucleotide polymorphism -308 G>A of the TNFα gene was determined, which makes it possible to consider the carrier of the A allele as a factor of increased risk for the development of type 2 diabetes mellitus. No association of the studied polymorphism with the risk of developing NAFLD was found. The obtained data make it possible to assume that the studied polymorphism -308 G>A of the TNFα gene is more associated with the risk of developing type 2 diabetes, and the occurrence or progression of NAFLD primarily depends on metabolic imbalance, and not on the contribution of the studied polymorphism. Conclusions. Non-alcoholic fatty liver disease is closely related to hormonal and metabolic risk factors and markers of cardiovascular disease and type 2 diabetes and may increase the risk of developing and progressing cardiovascular complications. The contribution of the genetic component to the formation of the predisposition to the development of type 2 diabetes mellitus based on the single-nucleotide polymorphism -308 G>A of the TNFα gene was determined, which makes it possible to consider the carrier of the A allele as a factor of increased risk for the development of type 2 diabetes mellitus.
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考虑心血管并发症的2型糖尿病和非酒精性脂肪肝患者TNF基因-308g/A多态性与代谢失衡
非酒精性脂肪性肝病(NAFLD)是最常见的肝脏疾病,目前已被公认为世界范围内的一个主要公共卫生问题。肿瘤坏死因子α (TNF-α)是TNF/TNFR细胞因子家族的一员,是一种细胞间传递分子,已在广泛的人类非感染性疾病中报道。该研究的目的是确定2型糖尿病患者循环中TNF-α的水平及其与胰岛素抵抗成分(代谢和激素)的关系的性质;并在有无NAFLD的情况下确定心血管并发症的性质(考虑TNF-α基因多态性)。材料和方法。病例对照研究包括来自哈尔科夫市和该地区的50名实际上健康的人的信息。研究人群(除对照组外)均为长期存在代谢综合征背景的2型糖尿病患者,在没有肾功能衰竭的情况下,有不同程度的血糖控制和肝脏稳态的破坏。117人被选中进行分析:63例2型糖尿病合并NAFLD, 54例2型糖尿病合并NAFLD。用合适的引物和NcoI核酸内切酶,采用聚合酶链反应的方法对TNF-α的单核苷酸多态性-308 G>A进行基因分型。在P≤0.05的显著性水平上,采用比值比和χ2标准进行统计学假设检验。基于TNFα基因的单核苷酸多态性-308 G>A,确定了遗传成分对2型糖尿病易感性形成的贡献,这使得考虑A等位基因的携带者是2型糖尿病发生风险增加的因素成为可能。未发现所研究的多态性与发生NAFLD的风险相关。这些数据使我们有可能假设所研究的TNFα基因多态性-308 G>A与2型糖尿病的发生风险更相关,NAFLD的发生或进展主要取决于代谢失衡,而不是所研究的多态性的贡献。非酒精性脂肪性肝病与激素和代谢危险因素以及心血管疾病和2型糖尿病标志物密切相关,并可能增加发生和进展心血管并发症的风险。基于TNFα基因的单核苷酸多态性-308 G>A,确定了遗传成分对2型糖尿病易感性形成的贡献,这使得考虑A等位基因的携带者是2型糖尿病发生风险增加的因素成为可能。
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来源期刊
Problemi Endokrinnoi Patologii
Problemi Endokrinnoi Patologii Medicine-Endocrinology, Diabetes and Metabolism
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АТИПОВИЙ ВАРІАНТ ПЕРВИННОГО ГІПЕРПАРАТИРЕОЗУ: КЛІНІЧНИЙ ВИПАДОК THE POLYMORPHISM -308 G/A OF THE TNF GENE AND METABOLIC IMBALANCE IN PATIENTS WITH TYPE 2 DIABETES MELLITUS AND NON-ALCOHOLIC FATTY LIVER DISEASE, TAKING INTO ACCOUNT CARDIOVASCULAR COMPLICATIONS РОЛЬ ПОЛІМОРФІЗМУ ГЕНІВ У ФОРМУВАННІ ПОРУШЕНЬ ФОЛАТНОГО ЦИКЛУ ТА ЇХ НАСЛІДКИ У ЖІНОК, ХВОРИХ НА СИНДРОМ ПОЛІКІСТОЗНИХ ЯЄЧНИКІВ (огляд літератури) КОНТРОВЕРСІЙНІ ПИТАННЯ ЩОДО КОМОРБІДНОЇ ПАТОЛОГІЇ: ЗАХВОРЮВАННЯ ПЕЧІНКИ ТА ЩИТОВИДНОЇ ЗАЛОЗИ (огляд літератури) DEPENDENCE OF CARDIOTROPHIN-1 ON BIOCHEMICAL AND HORMONAL FACTORS IN PATIENTS WITH COMORBID PATHOLOGY: ARTERIAL HYPERTENSION, DIABETES MELLITUS TYPE 2 AND OBESITY
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