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首页> 外文期刊>Archivum immunologiae et therapiae experimentalis >Interleukin-1 gene polymorphisms in chronic gastritis patients infected with helicobacter pylori as risk factors of gastric cancer development
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Interleukin-1 gene polymorphisms in chronic gastritis patients infected with helicobacter pylori as risk factors of gastric cancer development

机译:幽门螺杆菌感染的慢性胃炎患者白细胞介素1基因多态性为胃癌发展的危险因素

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Epidemiological investigations indicated association of the Helicobacter pylori infections with the occurrence of inflammatory conditions of the gastric mucosa and development of chronic gastritis and intestinal type of gastric cancer. IL1A and IL1B genes have been proposed as key factors in determining risk of gastritis and malignant transformation. The aim of this paper was to evaluate association of interleukin-1 gene polymorphisms with chronic gastritis, atrophy, intestinal metaplasia, dysplasia and intestinal type of gastric cancer in H. pylori-infected patients. Patients subjected to analysis represent group of 144 consecutive cases that suffered from dyspepsia with coexisting infection of H. pylori and chronic gastritis, chronic atrophic gastritis, intestinal metaplasia, dysplasia or gastric cancer. Molecular studies involved analysis of -889CT polymorphism of IL1A gene and +3954CT polymorphism of IL1B gene. Statistical analysis of association of polymorphism -889CT of gene IL1A with changes in gastric mucosa showed lack of significance, whereas +3954CT polymorphism of IL1B gene showed significant association. Frequency of allele T of +3954CT polymorphism of IL1B gene was higher in group of patients with chronic gastritis, atrophy, intestinal metaplasia, dysplasia or intestinal type of gastric cancer (32.1 %) as compared with population group (23 %), χ2 = 4.61 and p = 0.03. This corresponds to odds ratio: 1.58, 95 % CI: 1.04-2.4. Our results indicate that +3954CT polymorphism of IL1B gene increase susceptibility to inflammatory response of gastric mucosa H. pylori-infected patients and plays a significant role in the development of chronic gastritis, atrophy, intestinal metaplasia, dysplasia and the initiation of carcinogenesis.
机译:流行病学调查表明,幽门螺杆菌感染与胃粘膜发炎,慢性胃炎和肠型胃癌的发生有关。 IL1A和IL1B基因已被提议作为确定胃炎和恶性转化风险的关键因素。本文的目的是评估白细胞介素1基因多态性与感染幽门螺杆菌的慢性胃炎,萎缩,肠化生,异型增生和肠癌类型的关系。接受分析的患者代表连续144例消化不良并合并幽门螺杆菌和慢性胃炎,慢性萎缩性胃炎,肠上皮化生,异型增生或胃癌的感染病例。分子研究涉及IL1A基因的-889C> T多态性和IL1B基因的+ 3954C> T多态性的分析。 IL1A基因-889C> T多态性与胃黏膜变化的相关性的统计分析显示不显着,而IL1B基因的+ 3954C> T多态性显示显着相关性。慢性胃炎,萎缩,肠上皮化生,异型增生或肠型胃癌患者组中IL1B基因的+ 3954C> T多态性等位基因T频率高于人群(23%),χ2 = 4.61,p = 0.03。这对应于优势比:1.58,95%CI:1.04-2.4。我们的结果表明,IL1B基因的+ 3954C> T多态性增加了对胃粘膜幽门螺杆菌感染患者的炎症反应的敏感性,并且在慢性胃炎,萎缩,肠化生,异型增生和癌变的发生中起着重要作用。

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