Suppr超能文献

溃疡性结肠炎易感性与A251G超氧化物歧化酶1及C-262T过氧化氢酶的基因多态性

Susceptibility to Ulcerative Colitis and Genetic Polymorphisms of A251G SOD1 and C-262T CAT.

作者信息

El-Kheshen Gadier, Moeini Maryam, Saadat Mostafa

机构信息

Department of Biology, College of Sciences, Shiraz University, Shiraz, Iran.

Gastroenterohepatology Research Center, Shiraz University of Medical Sciences, Shiraz, Iran.

出版信息

J Med Biochem. 2016 Sep;35(3):333-336. doi: 10.1515/jomb-2016-0002. Epub 2016 Jul 6.

Abstract

BACKGROUND

Reactive oxygen species can attack and damage almost every molecule found in living cells, including proteins, carbohydrates, lipids, and DNA. For this reason, their production is normally tightly controlled. Among the most important defenses against these radicals are the superoxide dismutase (SOD) enzymes and catalase (CAT). Increasing attention has been given to the role of reactive oxygen metabolites in the pathogenesis of ulcerative colitis (UC), which is defined as an idiopathic and chronic intestinal inflammation. Accordingly, we hypothesized a relation between genetic polymorphisms in the two antioxidant enzymes A251G (rs2070424) and C-262T (rs1001179) and the risk of UC.

METHODS

The present case-control study included 109 UC patients (46 males and 50 females) and 186 (67 males and 119 females) gender-matched healthy controls. Genotyping was done by the PCR-RFLP method.

RESULTS

After adjusting for age and gender, a significant association was observed between the AG+GG genotypes of A251G polymorphism (vs. AA genotype) and risk of UC (OR=0.29, 95% CI: 0.10-0.86, P= 0.025) after adjusting for age and gender. Our statistical analysis revealed that the C-262T polymorphism did not associate with the risk of UC before and/or after adjusting for age and gender.

CONCLUSIONS

Based on the present statistical analysis, the G allele of the A251G polymorphism decreases the risk of UC, thus it might be assumed that the G allele has a protective role.

摘要

背景

活性氧可攻击并损害活细胞中几乎所有的分子,包括蛋白质、碳水化合物、脂质和DNA。因此,其生成通常受到严格控制。对抗这些自由基的最重要防御机制之一是超氧化物歧化酶(SOD)和过氧化氢酶(CAT)。活性氧代谢产物在溃疡性结肠炎(UC)发病机制中的作用受到了越来越多的关注,UC被定义为一种特发性慢性肠道炎症。因此,我们推测两种抗氧化酶A251G(rs2070424)和C-262T(rs1001179)的基因多态性与UC风险之间存在关联。

方法

本病例对照研究纳入了109例UC患者(46例男性和50例女性)以及186例(67例男性和119例女性)性别匹配的健康对照。采用聚合酶链反应-限制性片段长度多态性(PCR-RFLP)方法进行基因分型。

结果

在调整年龄和性别后,A251G多态性的AG + GG基因型(与AA基因型相比)与UC风险之间存在显著关联(OR = 0.29,95%可信区间:0.10 - 0.86,P = 0.025)。我们的统计分析显示,C-262T多态性在调整年龄和性别之前和/或之后与UC风险均无关联。

结论

基于目前的统计分析,A251G多态性的G等位基因可降低UC风险,因此可以推测G等位基因具有保护作用。

相似文献

引用本文的文献

本文引用的文献

10
Role of genetics in pediatric inflammatory bowel disease.遗传学在儿童炎症性肠病中的作用。
Inflamm Bowel Dis. 2014 Oct;20(10):1878-84. doi: 10.1097/MIB.0000000000000085.

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验