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首页> 外文期刊>Iranian Journal of Immunology >IL-23 Receptor Gene rs7517847 and rs1004819 SNPs in Ulcerative Colitis
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IL-23 Receptor Gene rs7517847 and rs1004819 SNPs in Ulcerative Colitis

机译:溃疡性结肠炎中的IL-23受体基因rs7517847和rs1004819 SNP

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Background: Crohn’s disease (CD) and ulcerative colitis (UC) are two major clinical presentations of inflammatory bowel disease (IBD). Many novel candidate genes have been found to be associated with increased risk for IBD. Recently IL-23 receptor gene is identified as an IBD associated gene in genome-wide studies. Objective: To ascertain whether rs7517847 and rs1004819 SNPs in the IL-23 receptor gene are associated with UC in our population in Kerman, south east of Iran. Methods: A total of 85 patients with UC and 100 healthy controls enrolled in our study. Endoscopic procedure was performed for all patients to determine their disease severity. IL-23 receptor genotyping at positions rs7517847 and rs1004819 was done by PCR-RFLP technique. Results: The results of this study showed no association between the studied polymorphisms in the IL-23 receptor gene and UC in our population. However, we found a significant association between rs7517847 gene polymorphism in IL-23 receptor and two important clinical variables including blood in stool and bowel movements in UC patients. Conclusion: The rs7517847 gene polymorphism in IL-23R may be related to the presence of blood in stool and bowel movements in patients with UC. Further functional analysis with other known IL-23 receptor genotypes and/or other candidate genes is necessary to confirm any genetic association with UC in our population.
机译:背景:克罗恩病(CD)和溃疡性结肠炎(UC)是炎症性肠病(IBD)的两种主要临床表现。已经发现许多新颖的候选基因与IBD风险增加有关。最近,IL-23受体基因在全基因组研究中被鉴定为IBD相关基因。目的:确定IL-23受体基因中的rs7517847和rs1004819 SNP是否与伊朗东南部克尔曼市人口中的UC有关。方法:本研究共纳入85名UC患者和100名健康对照。对所有患者进行内窥镜检查以确定他们的疾病严重程度。 rs7517847和rs1004819位置的IL-23受体基因分型通过PCR-RFLP技术完成。结果:这项研究的结果表明,我们人群中IL-23受体基因的多态性与UC之间没有关联。但是,我们发现IL-23受体的rs7517847基因多态性与UC患者的两个重要临床变量(包括便血和肠蠕动)之间存在显着关联。结论:IL-23R中rs7517847基因多态性可能与UC患者大便便血的存在有关。为了证实我们人群中与UC有任何遗传联系,有必要使用其他已知的IL-23受体基因型和/或其他候选基因进行进一步的功能分析。

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