Fecal Calprotectin and Eosinophil-Derived Neurotoxin in Children with Non-IgE-Mediated Cow's Milk Protein Allergy

María Roca1, Ester Donat1,2, Ana Rodriguez Varela3

  • 1Celiac Disease and Digestive Immunopathology Unit, Instituto de Investigación Sanitaria La Fe, 46026 Valencia, Spain.

Insights

Fecal calprotectin (fCP) and fecal eosinophil-derived neurotoxin (fEDN) do not reliably diagnose cow's milk protein allergy (CMPA) in infants or monitor dietary response. High variability limits their clinical utility for non-IgE mediated CMPA.

Area of Science:

  • Pediatrics
  • Gastroenterology
  • Immunology

Background:

  • Cow's milk protein allergy (CMPA) is a common condition in infants, often presenting with gastrointestinal symptoms.
  • Non-IgE mediated CMPA diagnosis and monitoring can be challenging.
  • Biomarkers like fecal calprotectin (fCP) and fecal eosinophil-derived neurotoxin (fEDN) are explored for diagnostic and monitoring purposes.

Purpose of the Study:

  • To evaluate the efficacy of fCP and fEDN as diagnostic markers for CMPA in infants.
  • To assess the utility of fCP and fEDN in monitoring infant response to a cow's milk protein (CMP)-free diet.
  • To determine if these markers can differentiate CMPA infants from healthy infants or those with other gastrointestinal issues.

Main Methods:

  • Prospective study involving infants aged 0-9 months.
  • Inclusion of infants diagnosed with CMPA, mild functional gastrointestinal disorders, healthy infants, and infants with mild infections.
  • Collection and analysis of stool samples for fCP and fEDN levels at baseline and after a 1-month CMP-free diet for the CMPA group.

Main Results:

  • fCP and fEDN levels were higher in CMPA infants compared to healthy infants at baseline, but differences were not statistically significant (p=0.119 and p=0.506).
  • No statistically significant changes in fCP levels were observed after a 1-month elimination diet in the CMPA group (p=0.184).
  • High variability and inconsistent individual marker behavior were noted after initiating a CMP-free diet.

Conclusions:

  • Neither fCP nor fEDN levels are sufficiently effective in discriminating between healthy infants and those with non-IgE mediated CMPA.
  • The individual utility of fCP and fEDN for clinical follow-up and monitoring dietary compliance remains debatable.
  • Further prospective studies with larger cohorts are necessary to draw definitive conclusions on the role of these biomarkers.

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