Increased fecal human beta-defensin-2 expression in preterm infants is associated with allergic disease development

Man-Chin Hua1,2, Chien-Chang Chen2,3, Sui-Ling Liao1,2

  • 1Department of Pediatrics, Chang Gung Memorial Hospital, Keelung, Taiwan.

Insights

High fecal human beta-defensins (HBD)-2 levels at 12 months in preterm infants are linked to allergic disease development by age 2. Eosinophil cationic protein (ECP) showed no association.

Area of Science:

  • Neonatal immunology
  • Allergy research
  • Gastrointestinal microbiome studies

Background:

  • Preterm infants face increased risks for allergic diseases.
  • Fecal biomarkers like human beta-defensins (HBD)-2 and eosinophil cationic protein (ECP) may predict allergy development.
  • Understanding these associations can inform early interventions.

Purpose of the Study:

  • To investigate the association between fecal HBD-2 and ECP levels in preterm infants and the subsequent development of allergic diseases by age 2.
  • To explore the influence of medication exposure on these biomarkers and allergy outcomes.

Main Methods:

  • Stool samples from 74 preterm infants were collected at 6 and 12 months.
  • Fecal HBD-2 and ECP concentrations were measured.
  • Medication exposure and physician-diagnosed allergic diseases were recorded via questionnaires and medical records.
  • Logistic regression analyses identified independent predictors of allergic diseases.

Main Results:

  • Significantly elevated fecal HBD-2 levels at 12 months were observed in infants who developed allergic diseases (37.18 ng/g vs. 8.56 ng/g, P=0.011).
  • This association was stronger in allergic infants exposed to antibiotics or antipyretics.
  • Fecal HBD-2 at 12 months was an independent predictor of allergic diseases by age 2 (aOR=1.03, P=0.036).
  • No association was found between fecal ECP and allergic diseases.

Conclusions:

  • Elevated fecal HBD-2 at 12 months in preterm infants is associated with physician-diagnosed allergic diseases by age 2.
  • Fecal HBD-2 may serve as a potential biomarker for predicting allergic disease development in this population.
  • Further research is warranted to elucidate the precise role of fecal HBD-2 in allergic disease pathogenesis.
Abstract