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June 4, 2026Alimentary Pharmacology & Therapeutics2 citations

The Association of Faecal Calprotectin Measurements With Endo‐Histological Remission in Ulcerative Colitis: A Pooled Analysis

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LDLaurie-Rose DubéMSM. SorinMAMatthieu Allez

Key Points

  • This analysis aims to identify an optimal faecal calprotectin threshold for distinguishing active disease from remission in ulcerative colitis.
  • Pooled analysis of retrospective and prospective studies across four academic centres
  • Included adult patients undergoing colonoscopy with faecal calprotectin measurements
  • Utilized receiver operating characteristic curves and cross-validation methods to determine optimal thresholds.
  • For Mayo Endoscopic Score (MES) 0 versus 1-2-3, AUC was 0.716; optimal threshold: 154.3 μg/g, specificity 0.69, sensitivity 0.64, p < 0.0001.
  • For GHS ≤ 2.0 versus GHS > 2.0, AUC was 0.656; optimal threshold: 117.6 μg/g, specificity 0.61, sensitivity 0.59, p < 0.0001.
  • Proposed threshold of 170 μg/g yielded sensitivity 0.801 and specificity 0.648, balancing detection of disease.

Abstract

BACKGROUND: Endoscopic and histologic evaluation is part of routine clinical practice to confirm the presence of active disease in ulcerative colitis. Faecal calprotectin (FCAL) levels show a positive correlation with endoscopic indices, relapse, and response to treatment. Existing studies have not clearly determined cut-off values for endoscopic and histologic remissions. AIMS: Our study aims to determine an optimal FCAL threshold for discriminating between endoscopic and histologic active disease and remission in UC, based on the Mayo Endoscopic Score (MES) and the Geboes Histologic Score. METHODS: We performed a pooled analysis of retrospective and prospective studies of patients with UC from four academic centres. Key inclusion criteria were adult UC patients undergoing colonoscopy, with FCAL measurements. Receiver operating characteristic curves were computed on 80% of the data using 5-fold cross-validation to determine the optimal FCAL threshold for predicting active UC based on specificity (spec) and sensitivity. Optimal thresholds were then tested on the remaining 20% of the data. Active endoscopic disease was assessed using MES 0-1 versus 2-3 and MES 0 versus 1-3, and active histologic disease or remission was evaluated using GHS 2.0. RESULTS: A total of 741 patients with UC were included in our analysis. For MES 0 versus 1-2-3, the AUC was 0.716 (95% CI: 0.701-0.731, p 2.0, the AUC was 0.656 (95% CI: 0.647-0.664, p < 0.0001), with an optimal threshold of 117.6 μg/g (specificity: 0.61 95% CI: 0.56-0.66, sensitivity: 0.59 95% CI: 0.56-0.63). For GHS < 3.1 vs. GHS ≥ 3.1, the AUC was 0.752 (95% CI: 0.743-0.762, p < 0.0001), with an optimal threshold of 166.2 μg/g (specificity: 0.69 95% CI: 0.66-0.73, sensitivity: 0.69 95% CI: 0.63-0.76). Given the high AUC for MES 0-1 vs. MES 2-3, we tested different FCAL thresholds from the literature and propose a threshold of 170 μg/g to maximize sensitivity (sensitivity: 0.801 95% CI: 0.729-0.873, specificity: 0.648 95% CI: 0.641-0.656, LR+ 2.311 95% CI: 2.001-2.670, LR- 0.289 95% CI: 0.196-0.427, accuracy 67.62% 95% CI: 65.95-69.30) and limit the proportion of false negatives. CONCLUSIONS: Our study demonstrates that FCAL can predict both active endoscopic and histological disease with acceptable sensitivities and specificities. The proposed cut-off values will help guide clinical practice to achieve the recommended treatment outcomes. Further studies are warranted to validate our results.

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Cite This Study

Dubé et al. (2026) studied this question.

synapsesocial.com/papers/6a2116fad499ed480b16fd66https://doi.org/10.1111/apt.70735
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