[THE INFLUENCE OF TUMOR NECROSIS FACTOR ALPHA AND POLYMORPHISM OF ITS GENE (RS1800629) ON THE SEVERITY AND PROGRESSION OF CHRONIC HEPATITIS AND ULCERATIVE COLITIS].

I A Bulatova, Y I Tretyakova, A P Shchekotova, V V Shchekotov, A V Krivtsov, N I Nasibullina
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Abstract

Aim of the study: To investigate the effect of generation of tumor necrosis factor-alpha (TNFα) and the importance of TNFα(rs1 800629) gene polymorphism in the progression of chronic hepatitis C (CHC) and ulcerative colitis (UC).

Material and methods: The study involved 90 patients with chronic hepatitis C, 50 patients with UC and 50 healthy donors. The blood concentrations TNFα and TNFα gene polymorphism (rs1800629) were evaluated.

Results: TNFα levels in the blood in patients with chronic hepatitis C were increased compared with the control group and correlated with the severity of Cytolysis and fibrosis (r = 0.34, p = 0.02). At slow speed the formation of liver fibrosis TNFα amounted to 1.5 (0.9-2.8) pg/mI, with a fast speed--2.3(1.4-8.2) pg/mI (p = 0.006). Patients with UC at 3-4 degrees endo- scopic activity production of TNFα reached 6.5 (7-9) pg/mI, which was significantly higher than the value obtained at 1-2 degrees endoscopic activity--0.25(0-0.8) pg/ml (p = 0.001). The allelic variations of TNFα in groups of patients with CHC at different rates forming LF statistically differences were not found. The allele, associated with severe progressive course of UC and increased production of TNFα--A risk allele and genotype GA TNFα, associated with a slow progression of UC- "protective" G allele and genotype GG TNFα gene were determined.

Conclusion: Determining the level of TNFα allows to evaluate the severity of liver disease, heaviness and progression of liver fibrosis speed in CHC, and the severity of inflammation in the intestinal mucosa in UC. The presence of the allele A of TNFo(rs1800629) is a predictor of severe and progression of UC. Determining genetic polymorphism TNFα in patients with UC may be an additional factor to assess the prognosis of the disease.

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[肿瘤坏死因子α及其基因多态性(rs1800629)对慢性肝炎和溃疡性结肠炎严重程度和进展的影响]。
目的:探讨肿瘤坏死因子α(TNFα)的产生及TNFα(rs1 800629)基因多态性在慢性丙型肝炎(CHC)和溃疡性结肠炎(UC)进展中的作用。材料和方法:本研究纳入90例慢性丙型肝炎患者、50例UC患者和50例健康供体。检测血清TNFα浓度及TNFα基因多态性(rs1800629)。结果:慢性丙型肝炎患者血清TNFα水平较对照组升高,且与细胞溶解和纤维化严重程度相关(r = 0.34, p = 0.02)。慢速时肝纤维化TNFα形成量为1.5 (0.9 ~ 2.8)pg/mI,快速时为2.3(1.4 ~ 8.2)pg/mI (p = 0.006)。UC患者在3-4度内窥镜下TNFα的产生达到6.5 (7-9)pg/ml,显著高于1-2度内窥镜下0.25(0-0.8)pg/ml (p = 0.001)。不同发生率CHC患者组间TNFα等位基因变异无统计学差异。该等位基因与UC的严重进展过程和TNFα的产生增加有关-A风险等位基因和基因型GA TNFα,与UC的“保护性”G等位基因和基因型GG TNFα基因进展缓慢有关。结论:检测TNFα水平可评价CHC患者肝脏疾病的严重程度、肝纤维化的加重程度和进展速度,UC患者肠黏膜炎症的严重程度。TNFo等位基因A (rs1800629)的存在是UC严重程度和进展的预测因子。确定UC患者的基因多态性TNFα可能是评估该疾病预后的另一个因素。
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