Fecal calprotectin levels in preterm infants with and without feeding intolerance

Rehab Moussa1, Abdelmoneim Khashana2, Noha Kamel3

  • 1Suez Canal University, Faculty of Medicine, Department of Pediatrics, Ismailia, Egypt.

Jornal De Pediatria
|June 19, 2016
PubMed

Insights

Fecal calprotectin is elevated in preterm neonates with feeding intolerance. This marker shows potential for early detection of necrotizing enterocolitis in infants.

Area of Science:

  • Neonatology
  • Gastroenterology
  • Biomarker Research

Background:

  • Feeding intolerance is a common complication in preterm neonates.
  • Early detection of feeding intolerance and related conditions like necrotizing enterocolitis is crucial for infant outcomes.

Purpose of the Study:

  • To assess fecal calprotectin levels in preterm neonates with feeding intolerance.
  • To evaluate fecal calprotectin as a marker for feeding intolerance.
  • To determine a diagnostic cut-off level for fecal calprotectin in feeding intolerance.

Main Methods:

  • An analytical, multicenter, case-control study was conducted in Egyptian neonatal intensive care units.
  • 52 preterm neonates were divided into a study group (26 with feeding intolerance) and a control group (26).
  • Fecal calprotectin levels were measured and correlated with clinical parameters.

Main Results:

  • Fecal calprotectin levels were significantly higher in neonates with feeding intolerance (334.3±236.6μg/g) compared to controls (42.0±38.2μg/g).
  • A significant inverse correlation was found between fecal calprotectin and birth weight, and a correlation with breastfeeding duration.
  • A cut-off level of 67.0μg/g demonstrated 100.0% sensitivity and 76.9% specificity for feeding intolerance.

Conclusions:

  • Fecal calprotectin levels are significantly elevated in preterm neonates experiencing feeding intolerance.
  • Fecal calprotectin may serve as an early indicator for necrotizing enterocolitis in neonates.
  • Further research with larger patient cohorts is warranted to confirm these findings.
Abstract