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钙卫蛋白在克罗恩病肛周瘘管和隐窝腺性瘘管患者中的临床相关性

Clinical relevance of calprotectin in patients with perianal fistulas in Crohn's disease and cryptoglandular fistulas.

作者信息

Becker Marte A J, Stevens Toer W, de Voogd Floris A E, Wildenberg Manon E, D'Haens Geert R A M, Gecse Krisztina B, Buskens Christianne J

机构信息

Tytgat Institute for Liver and Intestinal Research, Amsterdam UMC, University of Amsterdam, Amsterdam, The Netherlands.

Department of Gastroenterology and Hepatology, Amsterdam UMC, Location AMC, Amsterdam, The Netherlands.

出版信息

United European Gastroenterol J. 2025 Apr;13(3):295-304. doi: 10.1002/ueg2.12622. Epub 2024 Dec 16.

Abstract

BACKGROUND AND AIMS

Previous literature suggests that faecal calprotectin (FC) discriminates Crohn's disease perianal fistulas from cryptoglandular fistulas, irrespective of luminal disease. This study aims to prospectively validate this and analyse if increased local fistula calprotectin levels are associated with fistula characteristics.

METHODS

In this prospective study, all consecutive patients with an active perianal fistula undergoing examination under anaesthesia were included. Faecal and fistula tract scraping calprotectin levels were determined. The primary objective was to analyse whether FC levels could be used to differentiate between Crohn's disease and cryptoglandular perianal fistulas. Secondary outcome parameters were the levels of local calprotectin in fistula scrapings and their correlation with fistula characteristics.

RESULTS

Sixty-three patients were included in this study (perianal Crohn's disease; 45, cryptoglandular; 18). Faecal calprotectin levels were significantly higher in Crohn's disease patients compared with cryptoglandular fistula (354.3 [58.8-1076.3] vs. 47.3 [14.6-233.6] μg/g, p = 0.003). Faecal calprotectin could accurately discriminate Crohn's disease patients with active luminal disease from patients without luminal disease (median [interquartile range]) (1167.0 [557.0-2806.3] vs. 93.0 [47.5-571.6] μg/g, p = 0.001). Faecal calprotectin was not related to calprotectin levels in fistula scrapings. No fistula characteristic was found to be correlated to scraping calprotectin, but a correlation was found with the TOpCLASS classification system, which stratifies fistulas according to disease severity and outcome: class 2a (amenable for repair), class 2b (symptom control) and class 2c (gradually debilitating disease): 140[31.0-149.0]) μg/g versus 706[198.5-1936] μg/g versus 4000[1337-5894] μg/g, p < 0.001). Scraping calprotectin was also related to pronounced hyperintensity of the fistula tract on MRI in Crohn's disease patients: (69.0[30.0-821.0] vs. 1284.0[204.3-4185.5]; p = 0.01)) and cryptoglandular patients: (30.0[13.5-80.5] vs. 3012.0 [923.8-5021.0]; p = 0.002).

CONCLUSION

Crohn's disease and cryptoglandular perianal fistulas differ in FC levels. Local fistula calprotectin production did not explain this difference, implying FC reflects the luminal condition. A correlation exists between scraping calprotectin levels and Crohn's disease fistula severity, which could be clinically relevant for prognostic cohorts and tailored treatment.

摘要

背景与目的

既往文献表明,无论管腔疾病情况如何,粪便钙卫蛋白(FC)可区分克罗恩病肛周瘘管与隐窝腺性瘘管。本研究旨在前瞻性地验证这一点,并分析局部瘘管钙卫蛋白水平升高是否与瘘管特征相关。

方法

在这项前瞻性研究中,纳入了所有连续的在麻醉下接受检查的活动性肛周瘘管患者。测定粪便和瘘管刮片的钙卫蛋白水平。主要目的是分析FC水平是否可用于区分克罗恩病和隐窝腺性肛周瘘管。次要结局参数是瘘管刮片中局部钙卫蛋白水平及其与瘘管特征的相关性。

结果

本研究纳入了63例患者(肛周克罗恩病45例,隐窝腺性18例)。克罗恩病患者的粪便钙卫蛋白水平显著高于隐窝腺性瘘管患者(354.3[58.8 - 1076.3] vs. 47.3[14.6 - 233.6]μg/g,p = 0.003)。粪便钙卫蛋白可准确区分有活动性管腔疾病的克罗恩病患者与无管腔疾病的患者(中位数[四分位间距])(1167.0[557.0 - 2806.3] vs. 93.0[47.5 - 571.6]μg/g,p = 0.001)。粪便钙卫蛋白与瘘管刮片中的钙卫蛋白水平无关。未发现瘘管特征与刮片钙卫蛋白相关,但发现与TOPCLASS分类系统相关,该系统根据疾病严重程度和结局对瘘管进行分层:2a类(适合修复)、2b类(症状控制)和2c类(逐渐衰弱的疾病):140[31.0 - 149.0]μg/g 对 706[198.5 - 1936]μg/g 对 4000[1337 - 5894]μg/g,p < 0.001)。在克罗恩病患者中,刮片钙卫蛋白也与瘘管在MRI上的明显高信号相关:(69.0[30.0 - 821.0]对 1284.0[204.3 - 4185.5];p = 0.01),在隐窝腺性患者中:(30.0[13.5 - 80.5]对 3012.0[923.8 - 5021.0];p = 0.002)。

结论

克罗恩病和隐窝腺性肛周瘘管在FC水平上存在差异。局部瘘管钙卫蛋白的产生并不能解释这种差异,这意味着FC反映了管腔状况。刮片钙卫蛋白水平与克罗恩病瘘管严重程度之间存在相关性,这可能对预后队列和个体化治疗具有临床意义。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/93ef/11999044/cb183ac6bfc4/UEG2-13-295-g002.jpg

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