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白细胞介素 20(IL-20)基因多态性与溃疡性结肠炎。

Genetic polymorphisms of interleukin 20 (IL-20) in patients with ulcerative colitis.

机构信息

Inflammatory Bowel Disease Clinic, Department of Gastroenterology. Instituto Nacional de Ciencias Médicas y Nutrición Salvador Zubirán, Mexico City, Mexico.

出版信息

Immunol Lett. 2013 Jan;149(1-2):50-3. doi: 10.1016/j.imlet.2012.11.008. Epub 2012 Nov 23.

Abstract

Interleukin (IL)-20 belongs to the IL-10 family and is a potent immunomodulatory cytokine with implications for pathogenesis in the inflammatory bowel disease (IBD). The interleukin 20 gene is located within a 200kb region of q31-32 locus of chromosome 1. No previous studies have reported this novel association between ulcerative colitis (UC) and IL-20 polymorphisms. In the present work, we evaluated the role of IL-20 gene polymorphisms as susceptibility markers for UC. Three polymorphisms of IL-20 gene (rs2981573, rs2232360, rs1518108) were genotyped by 5' exonuclease TaqMan genotyping assays on an ABI Prism 7900 HT Fast Real-Time PCR system in a group of 198 Mexican Mestizo patients with UC and 698 ethnically matched healthy unrelated individuals with no family history of UC. We found significant decreased frequencies of two IL-20 genotypes: GG (rs2981573) [10.6% vs. 17.6%, p=0.017, OR=0.55, 95% CI: 0.33-0.93] and GG (rs2232360) [10.6% vs. 17.6%, p=0.017, OR=0.55, 95% CI: 0.33-0.93] in UC patients as compared to healthy controls. No significant differences of gene frequencies were found between UC patients and healthy controls in the rs1518108 polymorphism. In the subgroup analysis, no differences were found between the IL-20 genotypes and the clinical characteristics of UC. The results suggest that the GG genotypes of the IL-20 polymorphisms (rs2981573 and rs2232360) might have an important role in the development of UC in the Mexican population.

摘要

白细胞介素 (IL)-20 属于 IL-10 家族,是一种具有免疫调节作用的细胞因子,对炎症性肠病 (IBD) 的发病机制有影响。白细胞介素 20 基因位于染色体 1 的 q31-32 基因座的 200kb 区域内。以前的研究没有报道溃疡性结肠炎 (UC) 与 IL-20 多态性之间的这种新关联。在本研究中,我们评估了 IL-20 基因多态性作为 UC 易感性标志物的作用。在一组 198 名患有 UC 的墨西哥梅斯蒂索人患者和 698 名无 UC 家族史的种族匹配的健康无关个体中,使用 5'外切酶 TaqMan 基因分型测定法在 ABI Prism 7900 HT Fast Real-Time PCR 系统上对 IL-20 基因的三个多态性 (rs2981573、rs2232360、rs1518108) 进行了基因分型。我们发现两种 IL-20 基因型的频率显著降低:GG(rs2981573)[10.6%比 17.6%,p=0.017,OR=0.55,95%CI:0.33-0.93]和 GG(rs2232360)[10.6%比 17.6%,p=0.017,OR=0.55,95%CI:0.33-0.93],UC 患者与健康对照组相比。在 rs1518108 多态性中,UC 患者与健康对照组之间的基因频率无显著差异。在亚组分析中,IL-20 基因型与 UC 的临床特征之间无差异。结果表明,IL-20 多态性(rs2981573 和 rs2232360)的 GG 基因型可能在墨西哥人群中 UC 的发生中起重要作用。

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