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Development and Validation of a Biomarker for Diarrhea-Predominant Irritable Bowel Syndrome in Human Subjects

机译:腹泻型肠易激综合征的生物标记物的开发和验证。

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摘要

Diarrhea-predominant irritable bowel syndrome (IBS) is diagnosed through clinical criteria after excluding “organic” conditions, and can be precipitated by acute gastroenteritis. Cytolethal distending toxin B (CdtB) is produced by bacteria that cause acute gastroenteritis, and a post-infectious animal model demonstrates that host antibodies to CdtB cross-react with vinculin in the host gut, producing an IBS-like phenotype. Therefore, we assessed circulating anti-CdtB and anti-vinculin antibodies as biomarkers for D-IBS in human subjects. Subjects with D-IBS based on Rome criteria (n=2375) were recruited from a large-scale multicenter clinical trial for D-IBS (TARGET 3). Subjects with inflammatory bowel disease (IBD) (n=142), subjects with celiac disease (n=121), and healthy controls (n=43) were obtained for comparison. Subjects with IBD and celiac disease were recruited based on the presence of intestinal complaints and histologic confirmation of chronic inflammatory changes in the colon or small intestine. Subjects with celiac disease were also required to have an elevated tTG and biopsy. All subjects were aged between 18 and 65 years. Plasma levels of anti-CdtB and anti-vinculin antibodies were determined by ELISA, and compared between groups. Anti-CdtB titers were significantly higher in D-IBS subjects compared to IBD, healthy controls and celiac disease (P<0.001). Anti-vinculin titers were also significantly higher in IBS (P<0.001) compared to the other groups. The area-under-the-receiver operating curves (AUCs) were 0.81 and 0.62 for diagnosis of D-IBS against IBD for anti-CdtB and anti-vinculin, respectively. Both tests were less specific in differentiating IBS from celiac disease. Optimization demonstrated that for anti-CdtB (optical density≥2.80) the specificity, sensitivity and likelihood ratio were 91.6%, 43.7 and 5.2, respectively, and for anti-vinculin (OD≥1.68) were 83.8%, 32.6 and 2.0, respectively. These results confirm that anti-CdtB and anti-vinculin antibodies are elevated in D-IBS compared to non-IBS subjects. These biomarkers may be especially helpful in distinguishing D-IBS from IBD in the workup of chronic diarrhea.
机译:腹泻型肠易激综合症(IBS)在排除“器官性”病症后通过临床标准进行诊断,并可由急性胃肠炎引起。细胞致死菌膨胀毒素B(CdtB)由引起急性胃肠炎的细菌产生,感染后的动物模型表明,宿主CdtB抗体与宿主肠道中的纽蛋白交叉反应,产生IBS样表型。因此,我们评估了循环的抗CdtB和抗Vinculin抗体作为人类受试者D-IBS的生物标记。根据罗马标准(n = 2375)从D-IBS的大型多中心临床试验中招募患有D-IBS的受试者(目标3)。获得具有炎症性肠病(IBD)的受试者(n = 142),患有乳糜泻的受试者(n = 121)和健康对照(n = 43)进行比较。根据肠主诉的存在以及结肠或小肠中慢性炎症变化的组织学确认,招募患有IBD和腹腔疾病的受试者。患有腹腔疾病的受试者还需要进行tTG升高和活检。所有受试者年龄在18至65岁之间。通过ELISA测定血浆中抗CdtB和抗Vinculin抗体的水平,并在各组之间进行比较。与IBD,健康对照和乳糜泻相比,D-IBS受试者的抗CdtB滴度明显更高(P <0.001)。与其他组相比,IBS中的抗Vinculin滴度也显着更高(P <0.001)。对于抗CdtB和抗Vinculin,针对IBD诊断D-IBS的受试者下方工作曲线(AUC)分别为0.81和0.62。两种测试在区分IBS和乳糜泻方面的特异性都较低。优化表明,对于抗CdtB(光密度≥2.80),特异性,敏感性和似然比分别为91.6%,43.7和5.2,而对于抗-vinculin(OD≥1.68)分别为83.8%,32.6和2.0。这些结果证实,与非IBS受试者相比,D-IBS中的抗CdtB和抗vinculin抗体升高。在慢性腹泻的检查中,这些生物标记物可能特别有助于将D-IBS与IBD区别开来。

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