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巨噬细胞移动抑制因子(MIF)基因功能启动子多态性与日本溃疡性结肠炎的关系。

Association between functional promoter polymorphisms of macrophage migration inhibitory factor (MIF) gene and ulcerative colitis in Japan.

机构信息

Department of Gastroenterology, Kanazawa Medical University, School of Medicine, 1-1, Daigaku, Uchinada-machi, Ishikawa 920-0293, Japan.

出版信息

Cytokine. 2010 Aug;51(2):173-7. doi: 10.1016/j.cyto.2010.05.003.

Abstract

Macrophage migration inhibitory factor (MIF) is a key proinflammatory mediator. Two functional polymorphisms were identified in the promoter region of MIF gene. We attempted to clarify the associations between these polymorphisms and ulcerative colitis (UC). The study was performed in 111 patients with UC and 209 subjects without UC. We employed the PCR-SSCP method to detect gene polymorphisms. Overall, 5/5-CATT genotype was a decreased risk for the development of UC (OR, 0.51; 95% CI, 0.26-0.99). In addition, 7/7-CATT genotype was significantly associated with chronic continuous phenotype and distal colitis phenotype (OR, 5.49; 95% CI, 1.19-25.3, and OR, 6.10; 95% CI, 1.32-28.2, respectively), whereas 5/5-CATT genotype had an inhibitory effect on the development of UC after 20years of age (OR, 0.33; 95% CI, 0.14-0.82). On the other hand, G-173C polymorphism did not affect the susceptibility to and the phenotypes of UC. Our results suggested that tetranucleotide CATT repeat of MIF gene promoter may be associated with the development of UC and the severity of inflammation in patients with UC.

摘要

巨噬细胞移动抑制因子(MIF)是一种关键的促炎介质。在 MIF 基因启动子区域鉴定出了两个功能多态性。我们试图阐明这些多态性与溃疡性结肠炎(UC)之间的关系。该研究在 111 例 UC 患者和 209 例非 UC 患者中进行。我们采用 PCR-SSCP 方法检测基因多态性。总体而言,5/5-CATT 基因型是 UC 发病风险降低的一个因素(OR,0.51;95%CI,0.26-0.99)。此外,7/7-CATT 基因型与慢性持续型和远端结肠炎型显著相关(OR,5.49;95%CI,1.19-25.3 和 OR,6.10;95%CI,1.32-28.2),而 5/5-CATT 基因型对 20 岁以后 UC 的发病有抑制作用(OR,0.33;95%CI,0.14-0.82)。另一方面,G-173C 多态性不影响 UC 的易感性和表型。我们的结果表明,MIF 基因启动子中的四核苷酸 CATT 重复序列可能与 UC 的发病和 UC 患者炎症的严重程度有关。

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