Rega Institute for Medical Research, Department of Microbiology and Immunology, KU Leuven, Leuven, Belgium Translational Research Center for Gastrointestinal Disorders [TARGID], Department of Clinical and Experimental Medicine, KU Leuven, Leuven, Belgium.
Translational Research Center for Gastrointestinal Disorders [TARGID], Department of Clinical and Experimental Medicine, KU Leuven, Leuven, Belgium.
J Crohns Colitis. 2015 Dec;9(12):1079-87. doi: 10.1093/ecco-jcc/jjv148. Epub 2015 Sep 7.
Although costly and uncomfortable for the patient, the current standard to assess mucosal healing in Crohn's disease [CD] patients is endoscopy. The aim of this study was to evaluate NGAL-MMP-9 as surrogate marker for mucosal healing in CD patients.
Serum NGAL-MMP-9 levels were determined with sandwich enzyme-linked immunosorbent assay before and up to 5 years after first infliximab infusion in 108 active CD patients [median age at first infliximab 36 years, 57% female] and 43 healthy controls [HC, median age 27 years, 60% female]. Serum samples were matched to the time of endoscopy and complete endoscopic healing was defined as absence of ulcerations. Histological healing was defined as absence of epithelial damage [D'Haens score].
At baseline, median [interquartile range] NGAL-MMP-9 levels were significantly higher in active CD patients vs HC (77.6 [36.9-141.0] vs 25.5 [17.8-42.8] ng/ml; p < 0.001). After treatment, NGAL-MMP-9 levels significantly decreased in completely healed CD patients [n = 38] (84.5 [36.7-138.4] to 23.4 [7.4-42.5] ng/ml; p < 0.001) and--to a lesser extent--in non-healed CD patients [n = 36] (100.9 [43.4-152.6] to 43.8 [27.0-96.8] ng/ml; p = 0.001). Receiver operating characteristic analysis defined a NGAL-MMP-9 cut-off level of 45 ng/ml corresponding to complete endoscopic healing (area under the curve [AUC] = 0.79, 82% sensitivity, 65% specificity) and histological healing [AUC = 0.72, 79% sensitivity, 53% specificity]. At baseline, C-reactive protein [CRP] was not elevated in 33% of active CD patients, whereas 53% of these patients did have elevated NGAL-MMP-9 levels.
In the search for surrogate markers to assess mucosal healing in inflammatory bowel disease, NGAL-MMP-9 supplements and outperforms CRP in both ulcerative colitis and CD patients.
尽管内镜检查对患者来说既昂贵又不适,但目前评估克罗恩病(CD)患者黏膜愈合的标准仍是内镜检查。本研究旨在评估 NGAL-MMP-9 作为 CD 患者黏膜愈合的替代标志物。
在 108 例活动性 CD 患者(首次 infliximab 输注时的中位年龄为 36 岁,女性占 57%)和 43 例健康对照者(HC,中位年龄 27 岁,女性占 60%)中,使用夹心酶联免疫吸附试验在首次 infliximab 输注前和输注后 5 年内测定血清 NGAL-MMP-9 水平。血清样本与内镜检查时间相匹配,完全内镜愈合定义为无溃疡。组织学愈合定义为无上皮损伤[D'Haens 评分]。
基线时,与 HC 相比,活动性 CD 患者的中位(四分位间距)NGAL-MMP-9 水平明显更高(77.6[36.9-141.0]vs.25.5[17.8-42.8]ng/ml;p<0.001)。治疗后,完全愈合的 CD 患者[38 例]的 NGAL-MMP-9 水平显著下降(84.5[36.7-138.4]至 23.4[7.4-42.5]ng/ml;p<0.001),而非愈合的 CD 患者[36 例]的水平下降程度较轻(100.9[43.4-152.6]至 43.8[27.0-96.8]ng/ml;p=0.001)。受试者工作特征曲线分析定义 NGAL-MMP-9 截断值为 45ng/ml,对应于完全内镜愈合(曲线下面积[AUC]为 0.79,敏感性为 82%,特异性为 65%)和组织学愈合[AUC=0.72,敏感性为 79%,特异性为 53%]。在基线时,33%的活动性 CD 患者的 C 反应蛋白(CRP)并未升高,而其中 53%的患者 NGAL-MMP-9 水平升高。
在寻找评估炎症性肠病黏膜愈合的替代标志物方面,NGAL-MMP-9 在溃疡性结肠炎和 CD 患者中补充并优于 CRP。