Long-term cognitive outcomes in term newborns with watershed injury caused by neonatal encephalopathy.


Journal

Pediatric research
ISSN: 1530-0447
Titre abrégé: Pediatr Res
Pays: United States
ID NLM: 0100714

Informations de publication

Date de publication:
08 2022
Historique:
received: 16 11 2020
accepted: 29 03 2021
revised: 10 03 2021
pubmed: 28 10 2021
medline: 4 10 2022
entrez: 27 10 2021
Statut: ppublish

Résumé

We previously reported that increasing severity of watershed (WS) injury in neonatal magnetic resonance imaging (MRI) is associated with worse language outcomes in early childhood. In the present study, we investigated the relationship between neonatal injury patterns and cognitive profile in adolescents with neonatal encephalopathy. Term neonates with encephalopathy were prospectively enrolled and imaged using brain MRI from 1999 to 2008. Neonatal brain injury was scored according to the degree of injury in WS and basal ganglia/thalamus (BG/T) areas. The children underwent a neurocognitive assessment and follow-up brain MRI at the age of 10-16 years. The relationship between neonatal brain injury patterns and adolescent cognitive outcomes was assessed. In a cohort of 16 children, neonatal MRI showed WS injury in 7, BG/T injury in 2, and normal imaging in 7. Children with WS injury had lower estimated overall cognitive ability than those with normal imaging. Increasing WS injury score was associated with decreasing estimated overall cognitive ability, Perceptual Reasoning Index, and digit span score. Children with the WS injury are at an increased risk of having problems in long-term intellectual ability. These cognitive outcomes may underlie early language difficulties seen in children with neonatal WS injury. Adolescents with a history of neonatal encephalopathy and watershed pattern of injury on neonatal brain magnetic resonance imaging (MRI) had lower overall cognitive ability, perceptual reasoning skills, and auditory working memory than those with normal neonatal imaging. Children with post-neonatal epilepsy and cerebral palsy had the worst cognitive outcomes. Watershed pattern of injury confers high long-term differences in intellectual ability.

Sections du résumé

BACKGROUND
We previously reported that increasing severity of watershed (WS) injury in neonatal magnetic resonance imaging (MRI) is associated with worse language outcomes in early childhood. In the present study, we investigated the relationship between neonatal injury patterns and cognitive profile in adolescents with neonatal encephalopathy.
METHODS
Term neonates with encephalopathy were prospectively enrolled and imaged using brain MRI from 1999 to 2008. Neonatal brain injury was scored according to the degree of injury in WS and basal ganglia/thalamus (BG/T) areas. The children underwent a neurocognitive assessment and follow-up brain MRI at the age of 10-16 years. The relationship between neonatal brain injury patterns and adolescent cognitive outcomes was assessed.
RESULTS
In a cohort of 16 children, neonatal MRI showed WS injury in 7, BG/T injury in 2, and normal imaging in 7. Children with WS injury had lower estimated overall cognitive ability than those with normal imaging. Increasing WS injury score was associated with decreasing estimated overall cognitive ability, Perceptual Reasoning Index, and digit span score.
CONCLUSIONS
Children with the WS injury are at an increased risk of having problems in long-term intellectual ability. These cognitive outcomes may underlie early language difficulties seen in children with neonatal WS injury.
IMPACT
Adolescents with a history of neonatal encephalopathy and watershed pattern of injury on neonatal brain magnetic resonance imaging (MRI) had lower overall cognitive ability, perceptual reasoning skills, and auditory working memory than those with normal neonatal imaging. Children with post-neonatal epilepsy and cerebral palsy had the worst cognitive outcomes. Watershed pattern of injury confers high long-term differences in intellectual ability.

Identifiants

pubmed: 34702974
doi: 10.1038/s41390-021-01526-2
pii: 10.1038/s41390-021-01526-2
pmc: PMC9038956
mid: NIHMS1690035
doi:

Types de publication

Journal Article Research Support, Non-U.S. Gov't Research Support, N.I.H., Extramural

Langues

eng

Sous-ensembles de citation

IM

Pagination

505-512

Subventions

Organisme : NINDS NIH HHS
ID : P01 NS082330
Pays : United States
Organisme : NINDS NIH HHS
ID : P50 NS035902
Pays : United States

Informations de copyright

© 2021. The Author(s).

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Auteurs

Bo Lyun Lee (BL)

Department of Pediatrics, Busan Paik Hospital, Inje University College of Medicine, Busan, Korea.

Dawn Gano (D)

Department of Neurology, University of California San Francisco, San Francisco, CA, USA.
Department of Pediatrics, University of California San Francisco, San Francisco, CA, USA.

Elizabeth E Rogers (EE)

Department of Pediatrics, University of California San Francisco, San Francisco, CA, USA.

Duan Xu (D)

Department of Radiology and Biomedical Imaging, University of California San Francisco, San Francisco, CA, USA.

Stephany Cox (S)

Department of Pediatrics, University of California San Francisco, San Francisco, CA, USA.

A James Barkovich (A)

Department of Radiology and Biomedical Imaging, University of California San Francisco, San Francisco, CA, USA.

Yi Li (Y)

Department of Radiology and Biomedical Imaging, University of California San Francisco, San Francisco, CA, USA.

Donna M Ferriero (DM)

Department of Neurology, University of California San Francisco, San Francisco, CA, USA.
Department of Pediatrics, University of California San Francisco, San Francisco, CA, USA.

Hannah C Glass (HC)

Department of Neurology, University of California San Francisco, San Francisco, CA, USA. Hannah.Glass@ucsf.edu.
Department of Pediatrics, University of California San Francisco, San Francisco, CA, USA. Hannah.Glass@ucsf.edu.
Department of Epidemiology and Biostatistics, University of California San Francisco, San Francisco, CA, USA. Hannah.Glass@ucsf.edu.

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