Persistent high activity of the fetal adrenal cortex in preterm infants: is there a clinical significance?

Matthias Heckmann1, Michaela F Hartmann, Birgit Kampschulte

  • 1Department of General Pediatrics and Neonatology, Center of Child and Adolescent Medicine, Justus Liebig University, Giessen, Germany. Matthias.Heckmann@paediat.med.uni-giessen.de

Insights

Fetal adrenal steroid excretion is higher than previously thought in preterm infants. Despite higher levels in males, these steroids do not significantly impact respiratory distress syndrome incidence.

Area of Science:

  • Neonatalogy
  • Endocrinology
  • Pulmonology

Background:

  • Fetal adrenal cortex activity persists until term in preterm infants.
  • Dehydroepiandrosterone sulphate may inhibit surfactant synthesis.
  • Male preterm infants have a higher incidence of pulmonary disease.

Purpose of the Study:

  • To examine the link between fetal zone steroid excretion and lung disease severity in preterm infants, considering gender differences.
  • Investigate the role of 3beta-OH-5-ene-steroids in neonatal respiratory outcomes.

Main Methods:

  • Analyzed 24-hour urinary samples from 61 preterm infants (<30 weeks gestational age).
  • Quantified 3beta-OH-5-ene-steroids using gas chromatography-mass spectrometry.
  • Correlated steroid excretion rates with respiratory distress syndrome incidence.

Main Results:

  • Urinary fetal zone steroid excretion rates were 4-fold higher than previously reported.
  • Male preterm infants showed significantly higher steroid excretion on day 2 (p=0.03) and a trend on day 3.
  • No significant association was found between maximum fetal zone steroid excretion or gender and respiratory distress syndrome incidence.

Conclusions:

  • Preterm infants exhibit sustained high activity of the fetal adrenal zone.
  • While male infants excrete more fetal zone steroids, this does not significantly influence respiratory distress syndrome.
  • Further research may clarify the specific roles of fetal steroids in neonatal lung development.
Abstract

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