Fecal calprotectin in very low birth weight infants

Stina Josefsson1, Susan K Bunn, Magnus Domellöf

  • 1Department of Clinical Sciences, Paediatrics, Umeå University Hospital, Umeå, Sweden.

Insights

Fecal calprotectin (f-calprotectin) levels in very low birth weight (VLBW) infants can indicate severe intestinal disease. An f-calprotectin level exceeding 2000 microg/g is a useful, though not early, marker for conditions like necrotizing enterocolitis (NEC).

Area of Science:

  • Neonatalogy
  • Gastroenterology
  • Biomarker Research

Background:

  • Very low birth weight (VLBW) infants are susceptible to severe gastrointestinal conditions.
  • Fecal calprotectin (f-calprotectin) is an inflammatory marker.
  • Longitudinal monitoring of f-calprotectin in VLBW infants requires further investigation.

Purpose of the Study:

  • To measure longitudinal f-calprotectin concentrations in VLBW infants.
  • To identify changes in f-calprotectin associated with severe abdominal disease.
  • To evaluate f-calprotectin as a potential biomarker for necrotizing enterocolitis (NEC) and other intestinal conditions.

Main Methods:

  • The study enrolled 59 VLBW infants (<1500 g).
  • F-calprotectin was measured in meconium and weekly from postnatal weeks 1-8.
  • Seven infants developed severe abdominal disease (NEC or requiring laparotomy); f-calprotectin was sampled more frequently in these cases.

Main Results:

  • In reference infants, median f-calprotectin in meconium was 332 microg/g and 253 microg/g in postmeconium samples.
  • F-calprotectin levels correlated with delivery method, postnatal age, enteral feeds, antibiotics, and corticosteroids.
  • In disease cases, f-calprotectin exceeded 2000 microg/g in 3 NEC cases and 1 perforation with inflammation; levels remained below 2000 microg/g in other cases.

Conclusions:

  • F-calprotectin levels in VLBW infants are comparable to those in term and moderately preterm infants.
  • An f-calprotectin level >2000 microg/g is a useful, but not an early, indicator of NEC and severe intestinal inflammation in VLBW infants.
Abstract