Shen Jun, Qiao Yuqi, Ran Zhihua, Wang Tianrong, Xu Jiangtao, Feng Jinsun
Division of Gastroenterology and Hepatology, Shanghai Jiao-Tong University School of Medicine, Renji Hospital, Shanghai Institute of Digestive Disease, Shanghai, 200127, China.
Int J Clin Exp Pathol. 2013 Apr 15;6(5):917-25. Print 2013.
To date, most studies have applied individual factors as indicators of disease classification and prognosis. The aim of this study is to determine whether clustering analysis of protein expression profiles in intestinal epithelia improves classification and prognosis in patients with inflammatory bowel disease (IBD). One hundred and twenty Crohn's disease (CD) patients, 117 ulcerative colitis (UC) patients and 120 cases of nonspecific colitis provided intestinal biopsy samples for tissue microarray (TMA). Both unsupervised and supervised analyses were used for evaluation of clustering and association with relapse. There was a significant concordance between cluster groups based on immunostaining data of TMA and clinical classification in distinguishing IBD from nonspecific colitis (kappa= 0.498, p<0.001). CD27, CD70, CD40, TRAF3, TRAF4 and TRAF2 presented similar immunostaining features, which were different from clusters of CD154, CD80 and TRAF5. Moreover, higher expression of TRAF2 was a predictor of relapse in patients with UC (p=0.006).Thus, protein expression profiles can distinguish IBD and nonspecific colitis, and combination analysis protein expression profiles show that TRAF2 can predict relapse of UC.
迄今为止,大多数研究都将个体因素作为疾病分类和预后的指标。本研究的目的是确定肠道上皮细胞中蛋白质表达谱的聚类分析是否能改善炎症性肠病(IBD)患者的分类和预后。120例克罗恩病(CD)患者、117例溃疡性结肠炎(UC)患者和120例非特异性结肠炎患者提供了用于组织微阵列(TMA)的肠道活检样本。采用无监督和有监督分析来评估聚类以及与复发的相关性。基于TMA免疫染色数据的聚类组与临床分类在区分IBD和非特异性结肠炎方面存在显著一致性(kappa = 0.498,p<0.001)。CD27、CD70、CD40、TRAF3、TRAF4和TRAF2呈现出相似的免疫染色特征,这与CD154、CD80和TRAF5的聚类不同。此外,TRAF2的高表达是UC患者复发的一个预测指标(p = 0.006)。因此,蛋白质表达谱可以区分IBD和非特异性结肠炎,并且蛋白质表达谱的联合分析表明TRAF2可以预测UC的复发。