Cypers H, Varkas G, Beeckman S, Debusschere K, Vogl T, Roth J, Drennan M B, Lavric M, Foell D, Cuvelier C A, De Vos M, Delanghe J, Van den Bosch F, Elewaut D
Department of Rheumatology, Ghent University Hospital, Ghent, Belgium Unit for Molecular Immunology and Inflammation, VIB Inflammation Research Center Ghent University, Ghent, Belgium.
Department of Rheumatology, Ghent University Hospital, Ghent, Belgium.
Ann Rheum Dis. 2016 Jul;75(7):1357-62. doi: 10.1136/annrheumdis-2015-208025. Epub 2015 Dec 23.
Microscopic bowel inflammation is present in up to 50% of patients with spondyloarthritis (SpA) and is associated with more severe disease. Currently no reliable biomarkers exist to identify patients at risk. Calprotectin is a sensitive marker of neutrophilic inflammation, measurable in serum and stool.
To assess whether serum and faecal calprotectin in addition to C-reactive protein (CRP) can be used to identify patients with SpA at risk of microscopic bowel inflammation.
Serum calprotectin and CRP were measured in 125 patients with SpA. In 44 of these patients, faecal samples were available for calprotectin measurement. All 125 patients underwent an ileocolonoscopy to assess the presence of microscopic bowel inflammation.
Microscopic bowel inflammation was present in 53 (42.4%) patients with SpA. Elevated serum calprotectin and CRP were independently associated with microscopic bowel inflammation. Faecal calprotectin was also significantly higher in patients with microscopic bowel inflammation. Patients with CRP and serum calprotectin elevated had a frequency of bowel inflammation of 64% vs 25% in patients with low levels of both. When either CRP or serum calprotectin was elevated, the risk was intermediate (40%) and measuring faecal calprotectin provided further differentiation. Hence we suggest a screening approach where initially serum calprotectin and CRP are assessed and, if necessary, faecal calprotectin. The model using this scenario provided an area under the ROC curve of 74.4% for detection of bowel inflammation.
Calprotectin measurements in stool and serum, in addition to CRP, may provide a promising strategy to identify patients with SpA at risk of bowel inflammation and could play a role in overall patient stratification.
显微镜下肠道炎症在高达50%的脊柱关节炎(SpA)患者中存在,且与更严重的疾病相关。目前尚无可靠的生物标志物来识别有风险的患者。钙卫蛋白是中性粒细胞炎症的敏感标志物,可在血清和粪便中检测到。
评估除C反应蛋白(CRP)外,血清和粪便钙卫蛋白是否可用于识别有显微镜下肠道炎症风险的SpA患者。
对125例SpA患者测量血清钙卫蛋白和CRP。其中44例患者有粪便样本可用于钙卫蛋白测量。所有125例患者均接受了回结肠镜检查以评估显微镜下肠道炎症的存在。
53例(42.4%)SpA患者存在显微镜下肠道炎症。血清钙卫蛋白和CRP升高与显微镜下肠道炎症独立相关。显微镜下肠道炎症患者的粪便钙卫蛋白也显著更高。CRP和血清钙卫蛋白升高的患者肠道炎症发生率为64%,而两者水平均低的患者为25%。当CRP或血清钙卫蛋白升高时,风险为中等(40%),测量粪便钙卫蛋白可提供进一步的区分。因此,我们建议一种筛查方法,即首先评估血清钙卫蛋白和CRP,必要时评估粪便钙卫蛋白。使用这种方案的模型在检测肠道炎症时的ROC曲线下面积为74.4%。
除CRP外,测量粪便和血清中的钙卫蛋白可能为识别有肠道炎症风险的SpA患者提供一种有前景的策略,并可能在整体患者分层中发挥作用。