Plasma Concentration of Calprotectin, but Not Serum Concentration, Is a Predictive Biomarker for Clinical Remission in Ulcerative Colitis.

Q2 Medicine
Inflammatory Intestinal Diseases Pub Date : 2025-04-08 eCollection Date: 2025-01-01 DOI:10.1159/000545722
Sailish Honap, Isabelle Aimone-Gastin, Sylvain Salignac, Justine Flayac, Justine Paoli, Laurent Peyrin-Biroulet, Abderrahim Oussalah
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Abstract

Introduction: Fecal calprotectin is a validated biomarker for assessing disease activity in patients with inflammatory bowel disease (IBD). Blood calprotectin concentrations are correlated with disease activity in numerous immune-mediated inflammatory diseases. The aim of this study was to prospectively assess the diagnostic accuracy of plasma calprotectin as a potential biomarker of remission in IBD patients.

Methods: This prospective observational study enrolled 131 patients at the time of infliximab administration alongside clinical assessment and blood analyses on the same day. The primary endpoint was to assess the diagnostic accuracy of plasma calprotectin for predicting remission in patients with IBD.

Results: Plasma calprotectin concentration ≤10.5 ng/mL had a sensitivity of 98.6%, specificity of 100%, positive predictive value of 100%, negative predictive value of 96.3%, and an area under the receiver operating characteristic (AUROC) curve of 0.999 for diagnosing remission in patients with ulcerative colitis (UC). Plasma calprotectin had poor diagnostic accuracy for diagnosing remission in Crohn's disease. In UC, plasma calprotectin had significantly greater diagnostic accuracy than C-reactive protein for diagnosing remission (absolute difference between AUROCs, 0.06; 95% CI: 0.008 to 0.113; p = 0.03). Plasma calprotectin concentrations were not correlated with those measured in serum samples. The median serum-to-plasma calprotectin concentration ratio was 12-fold.

Conclusion: Plasma calprotectin is a promising biomarker for predicting remission in UC patients treated with infliximab.

钙保护蛋白的血浆浓度,而不是血清浓度,是溃疡性结肠炎临床缓解的预测性生物标志物。
粪便钙保护蛋白是一种有效的生物标志物,用于评估炎症性肠病(IBD)患者的疾病活动性。在许多免疫介导的炎症性疾病中,血钙保护蛋白浓度与疾病活动性相关。本研究的目的是前瞻性评估血浆钙保护蛋白作为IBD患者缓解的潜在生物标志物的诊断准确性。方法:这项前瞻性观察性研究纳入了131例患者,在给予英夫利昔单抗的同时进行临床评估,并在同一天进行血液分析。主要终点是评估血浆钙保护蛋白预测IBD患者缓解的诊断准确性。结果:血浆钙保护蛋白浓度≤10.5 ng/mL诊断溃疡性结肠炎(UC)患者缓解的敏感性为98.6%,特异性为100%,阳性预测值为100%,阴性预测值为96.3%,受试者工作特征曲线下面积(AUROC)为0.999。血浆钙保护蛋白诊断克罗恩病缓解的准确性较差。在UC中,血浆钙保护蛋白诊断缓解的准确性明显高于c反应蛋白(auroc之间的绝对差异为0.06;95% CI: 0.008 ~ 0.113;P = 0.03)。血浆钙保护蛋白浓度与血清样品中测量的钙保护蛋白浓度无关。血清钙保护蛋白与血浆钙保护蛋白的中位浓度比为12倍。结论:血浆钙保护蛋白是预测英夫利昔单抗治疗UC患者缓解的有希望的生物标志物。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Inflammatory Intestinal Diseases
Inflammatory Intestinal Diseases Medicine-Gastroenterology
CiteScore
4.50
自引率
0.00%
发文量
6
审稿时长
20 weeks
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