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Fecal Calprotectin as a Biomarker for Disease Activity in Microscopic Colitis
Alexa N Sasson1,2, Ashwin N Ananthakrishnan1
1Division of Gastroenterology, Massachusetts General Hospital and Harvard Medical School, Boston, MA.
Fecal calprotectin (FC) can indicate disease activity in microscopic colitis (MC) patients with symptoms. Elevated FC levels correlate with symptom severity but do not predict treatment response.
Area of Science:
- Gastroenterology
- Inflammatory Bowel Disease Research
- Clinical Biomarker Development
Background:
- Microscopic colitis (MC) is an inflammatory intestinal disorder.
- Objective biomarkers for assessing MC disease activity are lacking.
- Fecal calprotectin (FC) is a potential biomarker for intestinal inflammation.
Purpose of the Study:
- To evaluate the utility of fecal calprotectin (FC) measurement in symptomatic individuals diagnosed with microscopic colitis (MC).
- To determine the frequency of elevated FC levels in MC patients experiencing active symptoms.
- To identify predictors of elevated FC levels in this patient cohort.
Main Methods:
- A cohort study design was employed, including patients with confirmed MC and measured FC levels during symptomatic periods.
- The frequency of elevated FC levels (>150 mcg/g and >250 mcg/g) was assessed.
- Univariate and multivariate logistic regression analyses were performed to identify independent predictors of elevated FC.
Main Results:
- The study included 166 subjects, with 234 FC measurements during symptomatic MC.
- Elevated FC levels (>150 mcg/g) were observed in 29.0% of measurements.
- Higher FC levels were associated with older age, nocturnal bowel movements, and fecal incontinence, independent of other factors.
Conclusions:
- Elevated fecal calprotectin concentrations are present in over a quarter of symptomatic microscopic colitis patients.
- Increased FC levels in MC are linked to more severe symptoms, suggesting its utility as a disease activity marker.
- FC levels did not differentiate between steroid-responsive and steroid-refractory disease, indicating a lack of predictive value for treatment response.
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