Division of Gastroenterology and Hepatology, University of Calgary, Calgary, Alberta, Canada; Robarts Clinical Trials, Inc. London, Ontario, Canada.
Robarts Clinical Trials, Inc. London, Ontario, Canada; Division of Gastroenterology, University of California San Diego, La Jolla, CA, United States.
Best Pract Res Clin Gastroenterol. 2019 Feb-Apr;38-39:101602. doi: 10.1016/j.bpg.2019.02.004. Epub 2019 Feb 22.
Historically, the evaluation of patients with Crohn's disease (CD) has centered on use of subjective symptom-based assessment. However, patients with CD experience a broad spectrum of non-specific symptoms that may not directly correlate with objective measures of inflammation. Endoscopy has been the gold standard for evaluating the burden and severity of mucosal disease. However, use of ileocolonoscopy for disease monitoring in long-term follow-up is limited by considerations of cost, resource utilization, and invasiveness. As treatment goals in CD have shifted towards 'treat-to-target' paradigms that emphasize tight control of inflammation, it has become increasingly evident that sensitive, accurate, and reliable measures of disease activity are required. The use of non-invasive serum and fecal biomarkers such as C-reactive protein (CRP) and fecal calprotectin (FC) has been evaluated in patients with CD for categorizing disease activity, predicting treatment response, identifying patients at risk for disease relapse, and as a potential therapeutic target. In this review, we summarize the interpretation of CRP and FC in patients with CD within specific clinical contexts and according to assay performance characteristics.
从历史上看,对克罗恩病 (CD) 患者的评估主要集中在基于主观症状的评估上。然而,CD 患者会出现广泛的非特异性症状,这些症状可能与炎症的客观指标没有直接相关性。内镜检查一直是评估黏膜疾病负担和严重程度的金标准。然而,由于考虑到成本、资源利用和侵袭性,在长期随访中使用回结肠镜检查来监测疾病是有限的。随着 CD 的治疗目标转向强调炎症严格控制的“治疗目标”模式,越来越明显的是,需要敏感、准确和可靠的疾病活动衡量标准。在 CD 患者中,已经评估了非侵入性血清和粪便生物标志物,如 C 反应蛋白 (CRP) 和粪便钙卫蛋白 (FC),用于对疾病活动进行分类、预测治疗反应、识别疾病复发风险较高的患者以及作为潜在的治疗靶点。在这篇综述中,我们根据检测性能特点和特定临床情况,总结了 CRP 和 FC 在 CD 患者中的解释。