An Updated Overview of MRI Injuries in Neonatal Encephalopathy: LyTONEPAL Cohort.

brain injury hypoxic−ischemic encephalopathy magnetic resonance imaging newborn

Journal

Children (Basel, Switzerland)
ISSN: 2227-9067
Titre abrégé: Children (Basel)
Pays: Switzerland
ID NLM: 101648936

Informations de publication

Date de publication:
14 Apr 2022
Historique:
received: 03 03 2022
revised: 05 04 2022
accepted: 11 04 2022
entrez: 23 4 2022
pubmed: 24 4 2022
medline: 24 4 2022
Statut: epublish

Résumé

Brain magnetic resonance imaging (MRI) is a key tool for the prognostication of encephalic newborns in the context of hypoxic-ischemic events. The purpose of this study was to finely characterize brain injuries in this context. We provided a complete, descriptive analysis of the brain MRIs of infants included in the French national, multicentric cohort LyTONEPAL. Among 794 eligible infants, 520 (65.5%) with MRI before 12 days of life, grade II or III encephalopathy and gestational age ≥36 weeks were included. Half of the population had a brain injury (52.4%); MRIs were acquired before 6 days of life among 247 (47.5%) newborns. The basal ganglia (BGT), white matter (WM) and cortex were the three predominant sites of injuries, affecting 33.8% ( This study described an overview of brain injuries in hypoxic-ischemic neonatal encephalopathy. The basal ganglia with the thalamus and the WM with periventricular sublocation injuries were predominant. Comprehensive identification of brain injuries in the context of HIE may provide insight into the mechanism and time of occurrence.

Sections du résumé

BACKGROUND BACKGROUND
Brain magnetic resonance imaging (MRI) is a key tool for the prognostication of encephalic newborns in the context of hypoxic-ischemic events. The purpose of this study was to finely characterize brain injuries in this context.
METHODS METHODS
We provided a complete, descriptive analysis of the brain MRIs of infants included in the French national, multicentric cohort LyTONEPAL.
RESULTS RESULTS
Among 794 eligible infants, 520 (65.5%) with MRI before 12 days of life, grade II or III encephalopathy and gestational age ≥36 weeks were included. Half of the population had a brain injury (52.4%); MRIs were acquired before 6 days of life among 247 (47.5%) newborns. The basal ganglia (BGT), white matter (WM) and cortex were the three predominant sites of injuries, affecting 33.8% (
CONCLUSION CONCLUSIONS
This study described an overview of brain injuries in hypoxic-ischemic neonatal encephalopathy. The basal ganglia with the thalamus and the WM with periventricular sublocation injuries were predominant. Comprehensive identification of brain injuries in the context of HIE may provide insight into the mechanism and time of occurrence.

Identifiants

pubmed: 35455605
pii: children9040561
doi: 10.3390/children9040561
pmc: PMC9032533
pii:
doi:

Types de publication

Journal Article

Langues

eng

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Auteurs

Jonathan Beck (J)

Department of Neonatology, Reims University Hospital Alix de Champagne, 51100 Reims, France.
EPOPé (Obstetrical Perinatal and Pediatric Epidemiology Research Team), CRESS (Centre of Research in Epidemiology and StatisticS), INSERM (Institut National de la Santé et de la Recherche Médicale), INRAE (Institut National de la Recherche Agronomique), Université de Paris, 75004 Paris, France.

Gauthier Loron (G)

Department of Neonatology, Reims University Hospital Alix de Champagne, 51100 Reims, France.
CReSTIC EA (Centre de Recherche en Traitement du Signal Informatique) 3804, Université de Reims Champagne Ardenne, 51097 Reims, France.

Pierre-Yves Ancel (PY)

EPOPé (Obstetrical Perinatal and Pediatric Epidemiology Research Team), CRESS (Centre of Research in Epidemiology and StatisticS), INSERM (Institut National de la Santé et de la Recherche Médicale), INRAE (Institut National de la Recherche Agronomique), Université de Paris, 75004 Paris, France.
Assistance Publique-Hôpitaux de Paris, Clinical Investigation Center P1419, 75004 Paris, France.

Marianne Alison (M)

Service d'Imagerie Pédiatrique, Hôpital Robert Debré, APHP (Assistance Publique-Hôpitaux de Paris), 75019 Paris, France.
Unit 1141 NeuroDiderot, Inserm, CEA (Commissariat à l'Énergie Atomique et aux Énergies Alternatives), Université Paris Cité, 75019 Paris, France.

Lucie Hertz Pannier (L)

Unit 1141 NeuroDiderot, Inserm, CEA (Commissariat à l'Énergie Atomique et aux Énergies Alternatives), Université Paris Cité, 75019 Paris, France.
UNIACT (Unité de Recherche en NeuroImagerie Applicative Clinique et Translationnelle), Neurospin, CEA (Commissariat à l'Énergie Atomique et aux Énergies Alternatives)-Saclay, 91191 Gif sur Yvette, France.

Philippe Vo Van (P)

Department of Neonatology, Hospices Civils de Lyon, Femme Mère Enfant Hospital, Pinel, 69500 Bron, France.

Thierry Debillon (T)

Neonatal Intensive Care Unit CHU (Centre Hospital-Universitaire) Grenoble Alpes, 38000 Grenoble, France.
Grenoble INP (Institut d'Ingénierie et de Management), TIMC (Techniques de l'Ingénierie Médicale et de la Complexité)-IMAG (Informatique, Mathématiques et Applications, Grenoble), CNRS (Centre National de la Recherche Scientifique), University Grenoble Alpes, 38000 Grenoble, France.

Nathalie Bednarek (N)

Department of Neonatology, Reims University Hospital Alix de Champagne, 51100 Reims, France.
CReSTIC EA (Centre de Recherche en Traitement du Signal Informatique) 3804, Université de Reims Champagne Ardenne, 51097 Reims, France.

Classifications MeSH