Your browser doesn't support javascript.
loading
Increased persuadability and credulity in people with corpus callosum dysgenesis.
Barnby, Joseph M; Dean, Ryan J; Burgess, Henry; Kim, Jeffrey; Teunisse, Alessa K; Mackenzie, Lisa; Robinson, Gail A; Dayan, Peter; Richards, Linda J.
Afiliação
  • Barnby JM; Queensland Brain Institute, University of Queensland, Brisbane, Australia; Department of Psychology, Royal Holloway, University of London, London, United Kingdom. Electronic address: Joseph.Barnby@rhul.ac.uk.
  • Dean RJ; Queensland Brain Institute, University of Queensland, Brisbane, Australia; Department of Neuroscience, Washington University in St Louis School of Medicine, St. Louis, Missouri, USA. Electronic address: ryan.dean@wustl.edu.
  • Burgess H; Queensland Brain Institute, University of Queensland, Brisbane, Australia; Department of Neuroscience, Washington University in St Louis School of Medicine, St. Louis, Missouri, USA. Electronic address: henry.burgess@wustl.edu.
  • Kim J; Queensland Brain Institute, University of Queensland, Brisbane, Australia. Electronic address: jeffrey.kim@uq.net.au.
  • Teunisse AK; Department of Psychology, Macquarie University, New South Wales, Australia.
  • Mackenzie L; Queensland Brain Institute, University of Queensland, Brisbane, Australia; Department of Neuroscience, Washington University in St Louis School of Medicine, St. Louis, Missouri, USA. Electronic address: lisa.mackenzie@wustl.edu.
  • Robinson GA; Queensland Brain Institute, University of Queensland, Brisbane, Australia; School of Psychology, University of Queensland, Brisbane, Australia. Electronic address: gail.robinson@uq.edu.au.
  • Dayan P; Max Planck Institute for Biological Cybernetics, Tübingen, DE, Germany; University of Tübingen, Tübingen, DE, Germany. Electronic address: dayan@tue.mpg.de.
  • Richards LJ; Queensland Brain Institute, University of Queensland, Brisbane, Australia; Department of Neuroscience, Washington University in St Louis School of Medicine, St. Louis, Missouri, USA. Electronic address: linda.richards@wustl.edu.
Cortex ; 155: 251-263, 2022 10.
Article em En | MEDLINE | ID: mdl-36041321
ABSTRACT
Corpus callosum dysgenesis is one of the most common congenital neurological malformations. Despite being a clear and identifiable structural alteration of the brain's white matter connectivity, the impact of corpus callosum dysgenesis on cognition and behaviour has remained unclear. Here we build upon past clinical observations in the literature to define the clinical phenotype of corpus callosum dysgenesis better using unadjusted and adjusted group differences compared with a neurotypical sample on a range of social and cognitive measures that have been previously reported to be impacted by a corpus callosum dysgenesis diagnosis. Those with a diagnosis of corpus callosum dysgenesis (n = 22) demonstrated significantly higher persuadability, credulity, and insensitivity to social trickery than neurotypical (n = 86) participants, after controlling for age, sex, education, autistic-like traits, social intelligence, and general cognition. To explore this further, we examined the covariance structure of our psychometric variables using a machine learning algorithm trained on a neurotypical dataset. The algorithm was then used to test whether these dimensions possessed the capability to discriminate between a test-set of neurotypical and corpus callosum dysgenesis participants. After controlling for age and sex, and with Leave-One-Out-Cross-Validation across 250 training-set bootstrapped iterations, we found that participants with a diagnosis of corpus callosum dysgenesis were best classed within dimension space along the same axis as persuadability, credulity, and insensitivity to social trickery, with a mean accuracy of 71.7%. These results have implications for a) the characterisation of corpus callosum dysgenesis, and b) the role of the corpus callosum in social inference.
Assuntos
Palavras-chave

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Transtorno Autístico / Substância Branca Tipo de estudo: Prognostic_studies Limite: Humans Idioma: En Ano de publicação: 2022 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Transtorno Autístico / Substância Branca Tipo de estudo: Prognostic_studies Limite: Humans Idioma: En Ano de publicação: 2022 Tipo de documento: Article