Social Cognitive Dysfunction Following Pediatric Arterial Ischemic Stroke: Evidence From a Prospective Cohort Study.


Journal

Stroke
ISSN: 1524-4628
Titre abrégé: Stroke
Pays: United States
ID NLM: 0235266

Informations de publication

Date de publication:
05 2021
Historique:
pubmed: 9 4 2021
medline: 7 1 2022
entrez: 8 4 2021
Statut: ppublish

Résumé

Childhood and adolescence coincide with rapid maturation of distributed brain networks supporting social cognition; however, little is known about the impact of early ischemic brain insult on the acquisition of these skills. This study aimed to examine the influence of arterial ischemic stroke (AIS) on facial emotion recognition and theory of mind (ToM) abilities of children and adolescents initially recruited to a single-center, prospective longitudinal study of recovery following AIS. The study involved 67 participants, including 30 children with AIS (mean time since stroke=5 years) and 37 age-matched typically developing controls who were assessed on measures of cognitive ToM, facial emotion recognition, and affective ToM. Acute clinical magnetic resonance imaging, including diffusion-weighted imaging sequences, were used to evaluate prospective structure-function relationships between acute lesion characteristics (size, location, and arterial territories affected) and long-term social cognitive abilities. Relative to age-matched typically developing controls, children with AIS showed significantly worse performance on measures of basic facial emotion processing, cognitive ToM, and affective ToM. In univariate models, poorer ToM was associated with larger infarcts, combined cortical-subcortical pathology, and involvement of multiple arterial territories. In multivariate analyses, larger lesions and multiterritory infants were predictive of ToM processing but not facial emotion recognition. Poorer cognitive ToM predicted less frequent prosocial behavior and increased peer problems. Social cognitive skills appear vulnerable to disruption from early ischemic brain insult. In the first study to examine social cognition in a prospective cohort of children with AIS, our findings suggest that acute magnetic resonance imaging-based lesion characteristics may have predictive value for long-term social cognitive outcomes and may assist to identify children at elevated risk for social cognitive dysfunction.

Sections du résumé

Background and Purpose
Childhood and adolescence coincide with rapid maturation of distributed brain networks supporting social cognition; however, little is known about the impact of early ischemic brain insult on the acquisition of these skills. This study aimed to examine the influence of arterial ischemic stroke (AIS) on facial emotion recognition and theory of mind (ToM) abilities of children and adolescents initially recruited to a single-center, prospective longitudinal study of recovery following AIS.
Methods
The study involved 67 participants, including 30 children with AIS (mean time since stroke=5 years) and 37 age-matched typically developing controls who were assessed on measures of cognitive ToM, facial emotion recognition, and affective ToM. Acute clinical magnetic resonance imaging, including diffusion-weighted imaging sequences, were used to evaluate prospective structure-function relationships between acute lesion characteristics (size, location, and arterial territories affected) and long-term social cognitive abilities.
Results
Relative to age-matched typically developing controls, children with AIS showed significantly worse performance on measures of basic facial emotion processing, cognitive ToM, and affective ToM. In univariate models, poorer ToM was associated with larger infarcts, combined cortical-subcortical pathology, and involvement of multiple arterial territories. In multivariate analyses, larger lesions and multiterritory infants were predictive of ToM processing but not facial emotion recognition. Poorer cognitive ToM predicted less frequent prosocial behavior and increased peer problems.
Conclusions
Social cognitive skills appear vulnerable to disruption from early ischemic brain insult. In the first study to examine social cognition in a prospective cohort of children with AIS, our findings suggest that acute magnetic resonance imaging-based lesion characteristics may have predictive value for long-term social cognitive outcomes and may assist to identify children at elevated risk for social cognitive dysfunction.

Identifiants

pubmed: 33827249
doi: 10.1161/STROKEAHA.120.032955
doi:

Types de publication

Clinical Trial Journal Article Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

1609-1617

Auteurs

Nicholas P Ryan (NP)

Clinical Sciences, Murdoch Children's Research Institute, Melbourne, Australia (N.P.R., M.G., L.C., A.C, L.C., R.W.H., P.M., M.T.M., V.A.).
School of Psychology, Deakin University, Geelong, Australia (N.P.R.).
Department of Paediatrics, The University of Melbourne, Australia (N.P.R., A.C., R.W.H., P.M., M.T.M., V.A.).

Mardee Greenham (M)

Clinical Sciences, Murdoch Children's Research Institute, Melbourne, Australia (N.P.R., M.G., L.C., A.C, L.C., R.W.H., P.M., M.T.M., V.A.).

Anne L Gordon (AL)

Paediatric Neuroscience Department, Evelina London Children's Hospital, Guy's & St Thomas' NHS Foundation Trust, London, United Kingdom (A.L.G.).
Department of Population Health Sciences, Kings College London, United Kingdom (A.L.G.).

Michael Ditchfield (M)

Paediatric Imaging, Monash Children's Hospital, Melbourne, Australia (M.D.).
Department of Radiology and Paediatrics, Monash University, Melbourne, Australia (M.D.).

Lee Coleman (L)

Clinical Sciences, Murdoch Children's Research Institute, Melbourne, Australia (N.P.R., M.G., L.C., A.C, L.C., R.W.H., P.M., M.T.M., V.A.).
Department of Medical Imaging (L.C.), The Royal Children's Hospital, Melbourne, Australia.

Anna Cooper (A)

Clinical Sciences, Murdoch Children's Research Institute, Melbourne, Australia (N.P.R., M.G., L.C., A.C, L.C., R.W.H., P.M., M.T.M., V.A.).
Department of Paediatrics, The University of Melbourne, Australia (N.P.R., A.C., R.W.H., P.M., M.T.M., V.A.).

Louise Crowe (L)

Clinical Sciences, Murdoch Children's Research Institute, Melbourne, Australia (N.P.R., M.G., L.C., A.C, L.C., R.W.H., P.M., M.T.M., V.A.).

Rod W Hunt (RW)

Clinical Sciences, Murdoch Children's Research Institute, Melbourne, Australia (N.P.R., M.G., L.C., A.C, L.C., R.W.H., P.M., M.T.M., V.A.).
Department of Paediatrics, The University of Melbourne, Australia (N.P.R., A.C., R.W.H., P.M., M.T.M., V.A.).
Department of Neonatal Medicine (R.W.H.), The Royal Children's Hospital, Melbourne, Australia.

Paul Monagle (P)

Clinical Sciences, Murdoch Children's Research Institute, Melbourne, Australia (N.P.R., M.G., L.C., A.C, L.C., R.W.H., P.M., M.T.M., V.A.).
Department of Paediatrics, The University of Melbourne, Australia (N.P.R., A.C., R.W.H., P.M., M.T.M., V.A.).
Department of Haematology (P.M.), The Royal Children's Hospital, Melbourne, Australia.

Mark T Mackay (MT)

Clinical Sciences, Murdoch Children's Research Institute, Melbourne, Australia (N.P.R., M.G., L.C., A.C, L.C., R.W.H., P.M., M.T.M., V.A.).
Department of Paediatrics, The University of Melbourne, Australia (N.P.R., A.C., R.W.H., P.M., M.T.M., V.A.).
Department of Neurology (M.T.M.), The Royal Children's Hospital, Melbourne, Australia.

Vicki Anderson (V)

Clinical Sciences, Murdoch Children's Research Institute, Melbourne, Australia (N.P.R., M.G., L.C., A.C, L.C., R.W.H., P.M., M.T.M., V.A.).
Department of Paediatrics, The University of Melbourne, Australia (N.P.R., A.C., R.W.H., P.M., M.T.M., V.A.).
Department of Psychology (V.A.), The Royal Children's Hospital, Melbourne, Australia.

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