Morbidity in preterm infants with fetal inflammatory response syndrome

Elif Ozalkaya1, Güner Karatekin2, Sevilay Topcuoğlu2

  • 1Zeynep Kamil Maternity and Children's Training Hospital, Istanbul, Turkey. elifozalkay@gmail.com.

Insights

High umbilical cord blood interleukin-6 (IL-6) levels in premature infants with fetal inflammatory response syndrome (FIRS) predict serious complications, including respiratory distress syndrome (RDS), death, and multiple organ failure (MOF). These findings highlight IL-6 as a critical biomarker for neonatal outcomes.

Area of Science:

  • Neonatal Medicine
  • Immunology
  • Perinatal Research

Background:

  • Fetal inflammatory response syndrome (FIRS) is associated with adverse outcomes in premature infants.
  • Interleukin-6 (IL-6) is a key inflammatory marker.
  • The predictive value of umbilical cord blood IL-6 for neonatal morbidity and mortality in FIRS requires further investigation.

Purpose of the Study:

  • To evaluate the relationship between umbilical cord blood IL-6 concentration and preterm morbidity and mortality in premature infants with FIRS.
  • To determine critical IL-6 thresholds for predicting specific adverse outcomes.

Main Methods:

  • Prospective, observational study of 84 preterm infants (24-36 weeks gestational age).
  • FIRS defined as umbilical cord blood IL-6 > 11 pg/mL.
  • Evaluation of morbidities (RDS, MOF, etc.) and mortality in infants with FIRS.

Main Results:

  • Infants with FIRS (IL-6 > 11 pg/mL) had significantly higher rates of RDS, MOF, and mortality.
  • Umbilical cord blood IL-6 > 26.7 pg/mL predicted RDS (70% sensitivity, 85% specificity).
  • Umbilical cord blood IL-6 > 37.7 pg/mL predicted death (78.6% sensitivity, 60% specificity).
  • Umbilical cord blood IL-6 > 17.5 pg/mL predicted MOF (91% sensitivity, 66% specificity).

Conclusions:

  • Elevated umbilical cord blood IL-6 levels in FIRS are predictive of significant neonatal morbidities and mortality.
  • Specific IL-6 thresholds can identify premature infants at high risk for RDS, death, and MOF.
Abstract