The effect of intrauterine growth restriction on circulating surfactant protein D concentrations in the perinatal

Despina D Briana1, Dimitrios Gourgiotis, Stavroula Baka

  • 1Second Department of Obstetrics and Gynecology, Athens University Medical School, Athens, Greece.

Insights

Intrauterine growth restriction (IUGR) is linked to higher fetal surfactant protein D (SP-D) levels, indicating potential lung issues. Postnatal SP-D concentrations increase, especially after vaginal delivery in IUGR infants.

Area of Science:

  • Neonatal immunology
  • Pulmonary medicine
  • Perinatal research

Background:

  • Surfactant protein D (SP-D) is crucial for innate immunity and lung health.
  • Intrauterine growth restriction (IUGR) is associated with lung structural immaturity and increased respiratory risks.
  • Understanding SP-D in IUGR pregnancies can offer insights into neonatal respiratory outcomes.

Purpose of the Study:

  • To investigate circulating surfactant protein D (SP-D) concentrations in appropriate for gestational age (AGA) and intrauterine growth-restricted (IUGR) pregnancies.
  • To explore the relationship between SP-D levels and fetal development in IUGR.
  • To examine postnatal changes in SP-D and delivery mode influences.

Main Methods:

  • Serum SP-D levels were measured in 40 mothers and their neonates (20 IUGR, 20 AGA) at birth (N1) and postnatal day 4 (N4).
  • Statistical analyses, including correlation and group comparisons, were performed to assess SP-D concentrations.
  • Infant customized centiles and gestational age were correlated with fetal SP-D levels.

Main Results:

  • Fetal SP-D concentrations were significantly higher in the IUGR group compared to AGA.
  • Higher fetal SP-D levels in IUGR correlated negatively with infant customized centiles and gestational age.
  • SP-D concentrations were lower in fetuses than in neonates at N1 and N4, with higher levels in vaginally delivered IUGR infants at N1.

Conclusions:

  • Elevated fetal SP-D in IUGR may indicate lung immaturity or accelerated maturation due to intrauterine factors.
  • Postnatal increases in SP-D are observed, potentially influenced by delivery mode and breathing initiation.
  • Placental function decline might affect fetal SP-D production, explaining correlations with gestational age.