Neuroimaging and neurodevelopmental outcome after early fetal growth restriction: NEUROPROJECT-FGR

Gloria Brembilla1, Andrea Righini2, Barbara Scelsa3

  • 1Department of Woman, Mother and Child, Buzzi Hospital, University of Milan, via Castelvetro 32, 20154, Milan, Italy. gloria.brembilla@unimi.it.

Pediatric Research
|January 20, 2021
PubMed

Insights

Fetal growth restriction (FGR) in infants leads to smaller brain parenchymal areas, impacting cognitive scores. Early MRI evaluations can identify high-risk infants, even without overt brain lesions.

Area of Science:

  • Neuroscience
  • Developmental Pediatrics
  • Radiology

Background:

  • Infants born after fetal growth restriction (FGR) exhibit adverse neurodevelopmental outcomes and brain alterations on MRI.
  • Prematurity is a known risk factor for impaired brain development.

Purpose of the Study:

  • To evaluate the additional role of FGR, beyond prematurity, in determining brain impairment in preterm infants.
  • To investigate the relationship between structural brain measurements and neurodevelopmental outcomes in FGR infants.

Main Methods:

  • Retrospective observational study comparing 48 FGR and 36 appropriate for gestational age infants born between 26-32 weeks' gestation.
  • Cerebral MRI at term equivalent age to assess total maturation score (TMS) and cerebral areas.
  • Neurodevelopmental assessment using Griffiths or Bayley scale III at median age of 2 years.

Main Results:

  • Significantly smaller inner calvarium and parenchyma areas were observed in FGR infants compared to controls.
  • No significant differences in total maturation scores or average quotient scores between groups.
  • A positive correlation was found between parenchyma area and cognitive score, even after adjusting for confounding factors.

Conclusions:

  • Fetal growth restriction plays an additional role in determining brain impairment beyond prematurity.
  • Structural dimensional MRI evaluation can identify preterm infants at higher risk for neurodevelopmental issues, even without overt brain lesions.
Abstract

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