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纤溶酶原激活物抑制剂-1 基因多态性与伊朗阿塞拜疆土耳其裔炎症性肠病的关联。

Association of plasminogen activator inhibitor-1 gene polymorphism with inflammatory bowel disease in Iranian Azeri Turkish patients.

机构信息

Department of Genetics, Center of Excellence for Biodiversity, Faculty of Natural Sciences, University of Tabriz, Tabriz, Iran.

出版信息

Saudi J Gastroenterol. 2014 Jan-Feb;20(1):54-8. doi: 10.4103/1319-3767.126322.

Abstract

BACKGROUND/AIM: Previous studies have shown the association of some genetic factors, such as Plasminogen activator inhibitor type-1 (PAI-1) 4G/5G polymorphism, with the development of inflammatory bowel disease (IBD). We aimed to study this polymorphism as a risk factor in IBD patients in this cohort.

PATIENTS AND METHODS

One hundred and fifteen IBD patients and 95 healthy controls were selected from Iranian Azeri Turks and -6754G/5G polymorphism of PAI-1 gene was tested by polymerase chain reaction using allele-specific primers confirmed by sequencing.

RESULTS

There was no significant difference of PAI-1 polymorphism between IBD patients and the control group (P>0.05). Furthermore, these data showed no significant difference between Crohn's disease and ulcerative colitis patients. However, 4G/4G homozygotes have reduced probability to progression of loss of appetite, whereas 5G/5G genotypes have increased risk for development of chronic diarrhea without blood, nausea, and loss of appetite.

CONCLUSIONS

Although our study showed no significant association of PAI-1 polymorphism between patients and control group, the carriers of 4G/4G genotype and 4G allele had reduced risk for the progression of IBD features in this cohort.

摘要

背景/目的:先前的研究表明,一些遗传因素,如纤溶酶原激活物抑制剂-1(PAI-1)4G/5G 多态性,与炎症性肠病(IBD)的发展有关。我们旨在研究该多态性作为本队列中 IBD 患者的风险因素。

患者和方法

从伊朗阿塞拜疆土耳其人中选择了 115 名 IBD 患者和 95 名健康对照者,并通过聚合酶链反应使用等位基因特异性引物检测 PAI-1 基因的-6754G/5G 多态性,并用测序证实。

结果

IBD 患者和对照组之间的 PAI-1 多态性无显著差异(P>0.05)。此外,这些数据表明克罗恩病和溃疡性结肠炎患者之间没有显著差异。然而,4G/4G 纯合子发生食欲不振进展的可能性降低,而 5G/5G 基因型发生无血慢性腹泻、恶心和食欲不振的风险增加。

结论

尽管我们的研究表明 PAI-1 多态性在患者和对照组之间没有显著关联,但在本队列中,4G/4G 基因型和 4G 等位基因的携带者发生 IBD 特征进展的风险降低。

相似文献

本文引用的文献

6
Inflammatory bowel disease.炎症性肠病。
Annu Rev Immunol. 2010;28:573-621. doi: 10.1146/annurev-immunol-030409-101225.

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