Investigating cerebral anomalies in preterm infants and associated risk factors with magnetic resonance imaging at term-equivalent age
Nicolas Elbaz, Val\'erie Biran, Chlo\'e Ghozland, Laurie Devisscher, Aline Gonzalez Carpinteiro, Aur\'elie Bourmaud, Monique Elmaleh-Berg\`es, Lucie Hertz-Pannier, Yann Leprince (UNIACT, NeuroDiderot (UMR\_S\_1141 / U1141)), Alice Fr\'erot, Alice H\'eneau, Jessica Dubois (CEA

TL;DR
This study uses MRI at term-equivalent age to explore how perinatal factors influence cerebral anomalies and brain volume changes in preterm infants, highlighting the impact of treatments like ventilation and nutrition.
Contribution
It provides new insights into the relationship between specific perinatal factors and cerebral anomalies using combined qualitative and quantitative MRI assessments in preterm infants.
Findings
Mechanical ventilation increases risk of cerebral anomalies
Prolonged parenteral nutrition may protect against white matter anomalies
Mechanical ventilation and small for gestational age reduce cerebral volumes
Abstract
Background: Being born very or extreme preterm is a major source of cerebral anomalies and neurodevelopmental disorders, whose occurrence depends on many perinatal factors. A better understanding of these factors could be provided by cerebral Magnetic Resonance Imaging (MRI) at term-equivalent age (TEA). Objective: To investigate, through cerebral TEA-MRIs, the relationship between the main perinatal factors, the occurrence of cerebral anomalies, and cerebral volumetry. Methods: We assembled a cohort of preterm babies born before 32 weeks of gestation who underwent a cerebral TEA-MRI. We assessed cerebral anomalies using a radiological scoring system -- the Kidokoro scoring -- and performed cerebral volumetry. We investigated the relationships between 9 clinical factors (birth characteristics, resuscitation treatments{\ldots}), Kidokoro scores, and brain volumes. Results: Among 110…
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Taxonomy
TopicsNeonatal and fetal brain pathology · Infant Development and Preterm Care · Spinal Dysraphism and Malformations
