Eriksson Anders, Jennische Eva, Flach Carl-Fredrik, Jorge Alberto, Lange Stefan
Department of Internal Medicine, Gastroenterology Unit, Sahlgren's University Hospital/East Hospital, Gothenburg, Sweden.
Eur J Gastroenterol Hepatol. 2008 Apr;20(4):290-6. doi: 10.1097/MEG.0b013e3282f3557c.
Crohn's disease has a genetic background. Onset of the clinical manifestations, however, is suggested to be triggered by environmental factors. Microarray analysis has shown that the expression of transcripts aldolase B, elafin, MST-1, simNIPhom and SLC6A14 are altered in patients with ulcerative colitis. The primary aim of this study was to explore the expressions of these five transcripts in macroscopically inflamed and noninflamed mucosa in patients with Crohn's disease.
Mucosal specimens obtained from colon in consecutive patients with Crohn's disease (n=23) and controls (n=67) undergoing colonoscopy were analyzed using real-time PCR technique.
The expressions of the transcripts aldolase B, elafin, simNIPhom and SLC6A14 were increased, whereas the expression of MST-1 was decreased in noninflamed rectal mucosa in patients with Crohn's disease compared with controls. The expression of aldolase B was increased and the expressions of elafin and simNIPhom were decreased in inflamed colonic mucosa compared with noninflamed rectal mucosa in patients with Crohn's disease. No correlation, between the clinical activity of Crohn's disease (Mayo score <or=5 vs. >or=6) and transcript expression was detected.
The mucosal transcript pattern in Crohn's disease may, based on the known biological function of the transcripts, explain some of the typical features of Crohn's disease and indicate a possible pathophysiological role of microbes. Our results may thereby contribute to the understanding of the pathogenesis and manifestations of Crohn's disease.
克罗恩病具有遗传背景。然而,其临床表现的发作被认为是由环境因素触发的。微阵列分析表明,溃疡性结肠炎患者中醛缩酶B、弹性蛋白酶、MST-1、simNIPhom和SLC6A14转录本的表达发生了改变。本研究的主要目的是探讨这五种转录本在克罗恩病患者宏观炎症和非炎症黏膜中的表达情况。
使用实时PCR技术分析了连续接受结肠镜检查的克罗恩病患者(n = 23)和对照组(n = 67)从结肠获取的黏膜标本。
与对照组相比,克罗恩病患者非炎症直肠黏膜中醛缩酶B、弹性蛋白酶、simNIPhom和SLC6A14转录本的表达增加,而MST-1的表达降低。与克罗恩病患者非炎症直肠黏膜相比,炎症结肠黏膜中醛缩酶B的表达增加,弹性蛋白酶和simNIPhom的表达降低。未检测到克罗恩病临床活动度(梅奥评分≤5与≥6)与转录本表达之间的相关性。
基于转录本已知的生物学功能,克罗恩病的黏膜转录本模式可能解释克罗恩病的一些典型特征,并表明微生物可能具有病理生理作用。我们的结果可能有助于理解克罗恩病的发病机制和临床表现。