Cao Ying, Dai Yibei, Zhang Lingyu, Wang Danhua, Hu Wen, Yu Qiao, Wang Xuchu, Yu Pan, Liu Weiwei, Ping Ying, Sun Tao, Sang Yiwen, Liu Zhenping, Chen Yan, Tao Zhihua
Department of Laboratory Medicine, Zhejiang University School of Medicine Second Affiliated Hospital, Hangzhou, People's Republic of China.
National Clinical Research Center for Infectious Diseases, Zhejiang University School of Medicine First Affiliated Hospital, Hangzhou, People's Republic of China.
J Inflamm Res. 2021 Dec 1;14:6409-6419. doi: 10.2147/JIR.S342846. eCollection 2021.
Fecal biomarkers have emerged as one of the most useful tools for clinical management of inflammatory bowel disease (IBD). Oncostatin M (OSM), like fecal calprotectin (FC), is highly expressed in the inflamed intestinal mucosa which may have potential usefulness. We aimed to evaluate the additional utility of these two fecal biomarkers for IBD diagnosis, activity, and prediction of infliximab response over FC alone.
In group 1, 236 IBD patients (145 Crohn's disease, 91 ulcerative colitis), 50 disease controls, and 32 healthy controls were recruited for IBD diagnosis and activity. In group 2, baseline stool samples were collected from 62 patients to predict infliximab response at week 28 and 52. The performance of fecal biomarkers for IBD management was assessed by the area under the receiver operating characteristic curve (AUC).
Fecal OSM and FC levels were increased in IBD patients and were positively correlated with clinical and endoscopic activity. Their combination showed a better ability for disease diagnosis (AUC = 0.93) and slightly improved the capability to identify mucosal healing (AUC = 0.923). Baseline OSM and FC levels were elevated in non-responders at week 28 and 52. The AUCs of OSM, FC, and their combination to predict therapeutic response were 0.763, 0.834, and 0.859 at week 28, 0.638, 0.661, and 0.704 at week 52, respectively. Combined use of fecal and blood biomarkers improved predictive accuracy with an AUC of 0.919 at week 28 and 0.887 at week 52.
In addition to FC, OSM is a novel fecal biomarker, and their combination is more beneficial for disease diagnosis and prediction of infliximab response but not for disease activity in IBD patients. Further larger-scale studies are required to confirm our findings.
粪便生物标志物已成为炎症性肠病(IBD)临床管理中最有用的工具之一。抑瘤素M(OSM)与粪便钙卫蛋白(FC)一样,在炎症性肠黏膜中高度表达,可能具有潜在用途。我们旨在评估这两种粪便生物标志物相对于单独使用FC在IBD诊断、病情活动度及预测英夫利昔单抗反应方面的额外效用。
在第1组中,招募了236例IBD患者(145例克罗恩病、91例溃疡性结肠炎)、50例疾病对照者和32例健康对照者用于IBD诊断和病情活动度评估。在第2组中,收集了62例患者的基线粪便样本,以预测第28周和第52周时英夫利昔单抗的反应。通过受试者操作特征曲线下面积(AUC)评估粪便生物标志物在IBD管理中的性能。
IBD患者的粪便OSM和FC水平升高,且与临床及内镜下病情活动度呈正相关。它们联合使用时对疾病诊断具有更好的能力(AUC = 0.93),并在识别黏膜愈合能力方面略有改善(AUC = 0.923)。在第28周和第52周时,无反应者的基线OSM和FC水平升高。OSM、FC及其联合用于预测治疗反应的AUC在第28周时分别为0.763、0.834和0.859,在第52周时分别为0.638、0.661和0.704。粪便和血液生物标志物联合使用可提高预测准确性,在第28周时AUC为0.919,在第52周时AUC为0.887。
除FC外,OSM是一种新型粪便生物标志物,它们联合使用对IBD患者的疾病诊断和英夫利昔单抗反应预测更有益,但对疾病活动度评估并非如此。需要进一步的大规模研究来证实我们的发现。