Circulating levels of inflammatory markers in intrauterine growth restriction

Theodora Boutsikou1, George Mastorakos, Marialena Kyriakakou

  • 1Neonatal Division, Second Department of Obstetrics and Gynecology, University of Athens, 11528 Athens, Greece.

Insights

Perinatal stress markers high sensitivity C-reactive protein (hs-CRP), PAI-1, and S100B did not differ between appropriate-for-gestational-age (AGA) and intrauterine growth-restricted (IUGR) neonates. This suggests inflammation may be more intense in IUGR infants, despite reduced fat mass.

Area of Science:

  • Perinatal Medicine
  • Biochemistry
  • Neonatology

Background:

  • Intrauterine growth restriction (IUGR) is associated with altered fetal development and potential inflammation.
  • Circulating markers such as high sensitivity C-reactive protein (hs-CRP), plasminogen activator inhibitor-1 (PAI-1), and S100B are implicated in stress and inflammation.
  • IUGR and appropriate-for-gestational-age (AGA) pregnancies exhibit differences in fat mass and metabolic processes.

Purpose of the Study:

  • To investigate differences in perinatal stress markers (hs-CRP, PAI-1, S100B) between IUGR and AGA pregnancies.
  • To explore the relationship between these markers and potential inflammation in brain and adipose tissue in IUGR and AGA neonates.

Main Methods:

  • Serum levels of hs-CRP, PAI-1, and S100B were measured.
  • Samples were collected from 40 mothers and their 40 neonates (20 AGA, 20 IUGR) on postnatal days 1 and 4.
  • Statistical analysis was performed to compare marker levels between the two groups.

Main Results:

  • No significant differences in hs-CRP, PAI-1, or S100B levels were observed between the AGA and IUGR groups at any time point.
  • Despite lower birth weight and reduced fat mass in IUGR neonates, these inflammatory markers did not differ.

Conclusions:

  • The absence of elevated hs-CRP, PAI-1, and S100B in IUGR neonates may suggest a more profound inflammatory state in adipose tissue and the nervous system.
  • Other inflammation-related mechanisms, potentially linked to conditions like preeclampsia, might be involved in the IUGR state.
  • Further research is needed to elucidate the complex inflammatory pathways in IUGR.