首页> 外文期刊>Journal of gastroenterology >NOD2/CARD15, NOD1/CARD4, and ICAM-1 gene polymorphisms in Turkish patients with inflammatory bowel disease.
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NOD2/CARD15, NOD1/CARD4, and ICAM-1 gene polymorphisms in Turkish patients with inflammatory bowel disease.

机译:土耳其炎症性肠病患者的NOD2 / CARD15,NOD1 / CARD4和ICAM-1基因多态性。

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PURPOSE: The genetic susceptibility of people with certain NOD2/CARD15, NOD1/CARD4, and ICAM-1 gene variants to inflammatory bowel disease is still under investigation. The aim of this study was to investigate polymorphisms in the NOD2/CARD15 (R702W, G908R, and 3020insC), NOD1/CARD4 (E266K, D372N), and ICAM-1 (G241R, K469E) genes, which are known to be associated with inflammation, in Turkish patients with inflammatory bowel disease and healthy control groups. METHODS: The genotypes of 70 patients with endoscopically and histopathologically diagnosed Crohn's disease (38 men, 32 women; mean age, 38.8 +/- 1.3), 120 patients with ulcerative colitis (67 men, 53 women; mean age, 41.7 +/- 1.3) and 106 healthy control subjects (37 men, 69 women; mean age, 35.7 +/- 1.4), who stated that they had never had any prior bowel disease history, were compared. A polymerase chain reaction-restriction fragment length polymorphism analysis was performed for two variants of the ICAM-1 gene, the three main variants of the NOD2/CARD15 gene, and the E266K variant of the NOD1/CARD4 gene, and DNA sequencing was used for the D372N polymorphism of the NOD1/CARD4 gene. RESULTS: In this study, the three previously described Crohn's disease-predisposing variants of the NOD2/CARD15 gene and the polymorphisms examined in the NOD1/CARD4 and ICAM-1 genes were not found to be associated with ulcerative colitis or Crohn's disease. CONCLUSIONS: These findings suggest that the polymorphisms observed in the NOD2/CARD15, NOD1/CARD4, and ICAM-1 genes are not genetic susceptibility factors for Crohn's disease or ulcerative colitis in Turkey.
机译:目的:具有某些NOD2 / CARD15,NOD1 / CARD4和ICAM-1基因变异的人对炎性肠病的遗传易感性仍在研究中。这项研究的目的是调查NOD2 / CARD15(R702W,G908R和3020insC),NOD1 / CARD4(E266K,D372N)和ICAM-1(G241R,K469E)基因的多态性,这些基因已知与炎症,土耳其患有炎症性肠病的患者和健康对照组。方法:70例经内镜和组织病理学诊断为克罗恩病的基因型(男38例,女32例;平均年龄38.8 +/- 1.3);溃疡性结肠炎120例(67例男53例;平均年龄41.7 +/-)比较1.3例和106例健康对照者(37例男性,69例女性;平均年龄35.7 +/- 1.4),他们表示他们以前从未有过肠道疾病史。对ICAM-1基因的两个变异体,NOD2 / CARD15基因的三个主要变异体和NOD1 / CARD4基因的E266K变异体进行了聚合酶链反应-限制性片段长度多态性分析,并使用DNA测序对NOD1 / CARD4基因的D372N多态性。结果:在这项研究中,没有发现三个先前描述的克罗恩病易感性NOD2 / CARD15基因变异以及在NOD1 / CARD4和ICAM-1基因中检测的多态性与溃疡性结肠炎或克罗恩氏病相关。结论:这些发现表明,在土耳其,NOD2 / CARD15,NOD1 / CARD4和ICAM-1基因中观察到的多态性不是克罗恩氏病或溃疡性结肠炎的遗传易感性因素。

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