Does Magnetic Resonance Imaging (MRI) enterography correlate with fecal calprotectin levels?

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Last updated: May 22, 2025View editorial policy

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From the Guidelines

MRI enterography correlates moderately well with fecal calprotectin as a biomarker for inflammatory bowel disease activity. Both are valuable tools for assessing intestinal inflammation, though the correlation is not perfect. Fecal calprotectin is a protein released by neutrophils during intestinal inflammation and serves as a non-invasive marker, while MRI enterography provides detailed cross-sectional imaging of the bowel wall and surrounding tissues.

Key Points

  • Studies have shown that higher fecal calprotectin levels generally correspond with more severe findings on MRI enterography, particularly for active inflammation, bowel wall thickening, and contrast enhancement 1.
  • However, the correlation can vary depending on disease location, with better correlation in ileal Crohn's disease compared to colonic involvement.
  • Some discrepancies may occur because fecal calprotectin reflects the overall inflammatory burden throughout the intestine, while MRI may detect structural changes that persist even when active inflammation has subsided.
  • In clinical practice, these tools are often used complementarily rather than interchangeably, with fecal calprotectin serving as a screening and monitoring tool, while MRI enterography provides detailed anatomical assessment for disease complications and treatment planning 1.

Clinical Implications

  • A recent meta-analysis found that a calprotectin cut-off of 50 μg/g had the best sensitivity to detect endoscopically active disease, with specificity performing best at levels >100 μg/g 1.
  • MRI enterography has high diagnostic performance for the detection of Crohn disease–related active bowel inflammation in pediatric patients, with sensitivity values ranging from 66% to 95% and specificity values ranging from 64% to 97% on a bowel segmental basis 1.
  • The use of MRI enterography can alter the management of patients with ileal or ileocolonic Crohn's disease, with one study showing that it influenced a change in treatment in 55.3% of patients 1.

From the Research

Correlation between MRI Enterography and Fecal Calprotectin

  • The correlation between MRI enterography and fecal calprotectin has been studied in several research papers 2, 3, 4.
  • A study published in 2015 found that fecal calprotectin correlates well with the degree of MRI inflammatory activity and with surgical pathology damage in ileal Crohn's disease 2.
  • Another study published in 2010 found a trend of positive correlation between MRI scores of activity and calprotectin levels, as well as between MRI scores of thickening of intestinal involvement and calprotectin levels 3.
  • A 2019 study found that fecal calprotectin correlates well with MRI enterography assessment of ileal Crohn's disease, with an optimal cut-off of 145 μg/g for severe inflammation on MRI 4.

Diagnostic Accuracy of Fecal Calprotectin

  • Fecal calprotectin has been found to have a significant diagnostic accuracy for the detection of small-bowel Crohn's disease 5.
  • A meta-analysis published in 2016 found that fecal calprotectin has a significant diagnostic odds ratio for the prediction of active small-bowel disease on capsule endoscopy 5.
  • The diagnostic accuracy of fecal calprotectin has been found to be higher for cut-offs of 50 μg/g and 100 μg/g, with a negative predictive value of 91.8% for a cut-off of 50 μg/g 5.

Clinical Implications

  • Fecal calprotectin can be used as a surrogate marker of disease control to select patients for MRI enterography assessment and therapeutic adjustment 2.
  • MRI enterography parameters, such as length of ileal disease and increased bowel wall thickness, have been found to be associated with long-term biologic- and surgery-free remission 4.
  • Fecal calprotectin can be used to monitor disease activity and response to therapy in patients with inflammatory bowel disease 6.

Professional Medical Disclaimer

This information is intended for healthcare professionals. Any medical decision-making should rely on clinical judgment and independently verified information. The content provided herein does not replace professional discretion and should be considered supplementary to established clinical guidelines. Healthcare providers should verify all information against primary literature and current practice standards before application in patient care. Dr.Oracle assumes no liability for clinical decisions based on this content.

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