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血清钙卫蛋白作为克罗恩病的生物标志物。

Serum calprotectin as a biomarker for Crohn's disease.

机构信息

Hepato-Gastroenterology and Digestive Oncology Department, Liège University Hospital, CHU and GIGA-R, University of Liège, Liège, Belgium.

出版信息

J Crohns Colitis. 2013 Dec;7(12):e678-83. doi: 10.1016/j.crohns.2013.06.008. Epub 2013 Jul 9.

Abstract

BACKGROUND AND AIMS

In Crohn's disease, correlation between clinical assessment and disease activity at tissue level is weak. Our aim was to evaluate the value of serum calprotectin as a biomarker for Crohn's disease.

METHODS

The STORI trial patients (n=115) were studied at baseline, in clinical remission before infliximab withdrawal, or at the time of relapse after infliximab withdrawal. Forty healthy controls were also studied. Serum calprotectin level was measured by ELISA. Data were analyzed through correlation analyses, Kaplan Meier curves and Cox model, using available Crohn's Disease Activity Index (CDAI), Crohn's Disease Endoscopic Index of Severity (CDEIS), fecal calprotectin and C-reactive protein levels (hsCRP).

RESULTS

Median serum calprotectin was 8892 ng/mL (range: 410-125,000 ng/mL) in Crohn disease patients as compared with 1318 ng/mL (range: 215.8-3770 ng/mL) in controls (P<0.0001). Serum calprotectin was significantly higher for active disease (median=19,584 ng/mL) than for inactive disease (median=8353 ng/mL) (P<0.0001). Serum calprotectin correlated with hsCRP (r=0.4092, P<0.0001) and CDAI (r=0.4442, P<0.0001), but not with CDEIS, on the contrary to fecal calprotectin (r=0.6458, 0.5515, 0.2577 with P<0.0001, P<0.0001, P=0.019 respectively). In multivariate analysis, serum calprotectin used as a discrete variable (threshold: 5675 ng/ml), appeared complementary to hsCRP (>5 mg/l) and fecal calprotectin (>250 μg/g) to predict relapse after infliximab withdrawal (P=0.0173, 0.0024 and 0.0002; HR: 3.191, 3.561 and 4.120).

CONCLUSIONS

As a CD biomarker, serum calprotectin has a similar profile as hsCRP. It is also complementary to fecal calprotectin and hsCRP for prediction of relapse after infliximab withdrawal.

摘要

背景与目的

在克罗恩病中,临床评估与组织水平的疾病活动之间的相关性较弱。我们的目的是评估血清钙卫蛋白作为克罗恩病生物标志物的价值。

方法

STORI 试验患者(n=115)在基线时、在停用英夫利昔单抗之前的临床缓解期或停用英夫利昔单抗后的复发时进行研究。还研究了 40 名健康对照者。通过 ELISA 测量血清钙卫蛋白水平。通过相关性分析、Kaplan-Meier 曲线和 Cox 模型分析数据,使用现有的克罗恩病活动指数(CDAI)、克罗恩病内镜严重程度指数(CDEIS)、粪便钙卫蛋白和 C 反应蛋白(hsCRP)。

结果

与对照组(n=40)相比,克罗恩病患者的中位血清钙卫蛋白水平为 8892 ng/mL(范围:410-125000 ng/mL),而对照组为 1318 ng/mL(范围:215.8-3770 ng/mL)(P<0.0001)。活动期疾病的血清钙卫蛋白明显高于非活动期疾病(中位数=19584 ng/mL)(中位数=8353 ng/mL)(P<0.0001)。血清钙卫蛋白与 hsCRP(r=0.4092,P<0.0001)和 CDAI(r=0.4442,P<0.0001)显著相关,但与 CDEIS 不相关,而粪便钙卫蛋白则与之相反(r=0.6458,0.5515,0.2577,P<0.0001,P<0.0001,P=0.019)。在多变量分析中,将血清钙卫蛋白作为离散变量(阈值:5675 ng/ml)使用时,与 hsCRP(>5 mg/l)和粪便钙卫蛋白(>250 μg/g)一起用于预测英夫利昔单抗停药后的复发,具有互补作用(P=0.0173、0.0024 和 0.0002;HR:3.191、3.561 和 4.120)。

结论

作为 CD 生物标志物,血清钙卫蛋白与 hsCRP 具有相似的特征。它还与粪便钙卫蛋白和 hsCRP 一起用于预测英夫利昔单抗停药后的复发。

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