Department of Genetics, Center of Excellence for Biodiversity, Faculty of Natural Sciences, University of Tabriz, Tabriz, Iran.
Saudi J Gastroenterol. 2014 Jan-Feb;20(1):54-8. doi: 10.4103/1319-3767.126322.
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.
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.
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.
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.
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。
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。
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。
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。