Suppr超能文献

p53 密码子 72 遗传多态性与伊朗北部溃疡性结肠炎发病风险的关联。

Association of p53 codon 72 genetic polymorphism with the risk of ulcerative colitis in northern Iran.

机构信息

Department of Biology, Faculty of Sciences, University of Guilan, Rasht, Iran.

出版信息

Int J Colorectal Dis. 2011 Feb;26(2):235-8. doi: 10.1007/s00384-010-1021-7. Epub 2010 Jul 29.

Abstract

PURPOSE

Ulcerative colitis (UC) is a chronic inflammatory condition of the large bowel of unknown etiology, characterized by the presence of bloody diarrhea and mucus associated with a negative stool culture for bacteria, ova, or parasites. The aim of this study was to investigate the association of p53 codon 72 genetic polymorphism with the risk of UC in northern Iran.

METHODS

We evaluated the association of the p53 codon 72 genetic polymorphism with UC in northern Iran. The genotype of 190 patients with UC (115 men, 75 women; mean age, 32 ± 8.6 years) and 220 healthy control subjects (123 men, 97 women; mean age, 33 ± 2.5 years) were compared. Genomic DNA was extracted from colonic bioptic tissues of patients and blood samples of healthy individuals. Genotypes and allele frequencies were determined in patients and controls using allele-specific PCR (AS-PCR).

RESULTS

There were significant differences in the distribution of the polymorphism between the control subjects and the UC patients (P < 0.0001). Significantly increased frequencies of the Pro allele and the Pro/Pro genotype were observed in patients with UC compared with controls (Pro allele: P < 0.0001; odds ratio, 7.87; 95% confidence interval, 4.03-15.35; Pro/Pro: P < 0.0001; odds ratio, 35.21; 95% confidence interval, 12.56-98.73).

CONCLUSION

The p53 codon 72 genetic polymorphism is associated with UC in northern Iran.

摘要

目的

溃疡性结肠炎(UC)是一种病因不明的大肠慢性炎症性疾病,其特征为血性腹泻和黏液,粪便细菌、卵或寄生虫培养阴性。本研究旨在探讨 p53 密码子 72 基因多态性与伊朗北部 UC 发病风险的相关性。

方法

我们评估了 p53 密码子 72 基因多态性与伊朗北部 UC 的相关性。比较了 190 例 UC 患者(115 例男性,75 例女性;平均年龄 32±8.6 岁)和 220 例健康对照者(123 例男性,97 例女性;平均年龄 33±2.5 岁)的基因型。从患者的结肠活检组织和健康个体的血液样本中提取基因组 DNA。采用等位基因特异性 PCR(AS-PCR)在患者和对照组中确定基因型和等位基因频率。

结果

在对照组和 UC 患者之间,该多态性的分布存在显著差异(P<0.0001)。与对照组相比,UC 患者中 Pro 等位基因和 Pro/Pro 基因型的频率显著增加(Pro 等位基因:P<0.0001;比值比,7.87;95%置信区间,4.03-15.35;Pro/Pro:P<0.0001;比值比,35.21;95%置信区间,12.56-98.73)。

结论

p53 密码子 72 基因多态性与伊朗北部的 UC 相关。

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验