Fecal calprotectin concentration in celiac disease

Vildan Ertekin1, Mukadder Ayşe Selimoğlu, Ahmet Turgut

  • 1Faculty of Medicine, Division of Pediatric Gastroenterology, Department of Hepatology and Nutrition, Ataturk University, Erzurum, Turkey. vildanertekin@hotmail.com

Insights

Fecal calprotectin (FC) is elevated in children with celiac disease (CD) and correlates with intestinal damage. A gluten-free diet (GFD) significantly reduces FC levels, normalizing them in children with CD.

Area of Science:

  • Pediatric Gastroenterology
  • Immunology
  • Gastrointestinal Inflammation

Background:

  • Fecal calprotectin (FC) is a recognized biomarker for gastrointestinal inflammation.
  • Elevated FC levels are hypothesized in untreated celiac disease (CD) due to gut inflammation.

Purpose of the Study:

  • To quantify fecal calprotectin (FC) levels in children diagnosed with celiac disease (CD).
  • To investigate the correlation between FC concentrations and histopathologic findings in pediatric CD.
  • To assess the impact of a gluten-free diet (GFD) on FC levels in children with CD.

Main Methods:

  • Enzyme-linked immunosorbent assay (ELISA) was used to measure FC concentrations.
  • FC levels were determined in 29 newly diagnosed pediatric CD patients and 10 healthy controls.
  • Histopathologic evaluation of intestinal mucosa was performed using modified Marsh criteria.

Main Results:

  • Children with CD exhibited significantly higher mean FC levels (13.40+/-8.5 mg/L) compared to healthy controls (4.3+/-3.3 mg/L).
  • FC concentrations in CD patients significantly decreased to 4.6+/-2.7 mg/L after one year on a GFD, nearing levels of healthy children.
  • Higher FC levels correlated with more severe histopathologic findings, specifically total-villous atrophy compared to partial-villous atrophy.

Conclusions:

  • FC concentration is elevated in pediatric celiac disease and is directly related to the severity of intestinal mucosal damage.
  • A gluten-free diet (GFD) effectively reduces FC levels in children with CD, indicating its therapeutic efficacy.
  • Further research is warranted to elucidate the specific pathogenetic mechanisms driving elevated FC in celiac disease.
Abstract