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Connectome-wide Mega-analysis Reveals Robust Patterns of Atypical Functional Connectivity in Autism.
Ilioska, Iva; Oldehinkel, Marianne; Llera, Alberto; Chopra, Sidhant; Looden, Tristan; Chauvin, Roselyne; Van Rooij, Daan; Floris, Dorothea L; Tillmann, Julian; Moessnang, Carolin; Banaschewski, Tobias; Holt, Rosemary J; Loth, Eva; Charman, Tony; Murphy, Declan G M; Ecker, Christine; Mennes, Maarten; Beckmann, Christian F; Fornito, Alex; Buitelaar, Jan K.
Affiliation
  • Ilioska I; Department of Cognitive Neuroscience, Donders Institute for Brain, Cognition and Behaviour, Radboud University Medical Centre, Nijmegen, the Netherlands; Turner Institute for Brain and Mental Health, School of Psychological Science, and Monash Biomedical Imaging, Monash University, Melbourne, Victor
  • Oldehinkel M; Department of Cognitive Neuroscience, Donders Institute for Brain, Cognition and Behaviour, Radboud University Medical Centre, Nijmegen, the Netherlands; Turner Institute for Brain and Mental Health, School of Psychological Science, and Monash Biomedical Imaging, Monash University, Melbourne, Victor
  • Llera A; Department of Cognitive Neuroscience, Donders Institute for Brain, Cognition and Behaviour, Radboud University Medical Centre, Nijmegen, the Netherlands.
  • Chopra S; Turner Institute for Brain and Mental Health, School of Psychological Science, and Monash Biomedical Imaging, Monash University, Melbourne, Victoria, Australia.
  • Looden T; Department of Cognitive Neuroscience, Donders Institute for Brain, Cognition and Behaviour, Radboud University Medical Centre, Nijmegen, the Netherlands.
  • Chauvin R; Department of Cognitive Neuroscience, Donders Institute for Brain, Cognition and Behaviour, Radboud University Medical Centre, Nijmegen, the Netherlands; Department of Neurology, Washington University School of Medicine, St. Louis, Missouri.
  • Van Rooij D; Department of Cognitive Neuroscience, Donders Institute for Brain, Cognition and Behaviour, Radboud University Medical Centre, Nijmegen, the Netherlands.
  • Floris DL; Department of Cognitive Neuroscience, Donders Institute for Brain, Cognition and Behaviour, Radboud University Medical Centre, Nijmegen, the Netherlands; Methods of Plasticity Research, Department of Psychology, University of Zurich, Zurich, Switzerland.
  • Tillmann J; Department of Psychology, Institute of Psychiatry, Psychology and Neuroscience, King's College London, London, United Kingdom; Roche Pharma Research and Early Development, Neuroscience and Rare Diseases, Roche Innovation Center Basel, F. Hoffmann-La Roche Ltd., Basel, Switzerland.
  • Moessnang C; Department of Psychiatry and Psychotherapy, Central Institute of Mental Health, Medical Faculty, University of Heidelberg, Mannheim, Germany.
  • Banaschewski T; Department of Child and Adolescent Psychiatry, Central Institute of Mental Health, Medical Faculty Mannheim, University of Heidelberg, Mannheim, Germany.
  • Holt RJ; Autism Research Centre, Department of Psychiatry, University of Cambridge, Cambridge, United Kingdom.
  • Loth E; Department of Forensic and Neurodevelopmental Sciences, Institute of Psychiatry, Psychology and Neuroscience, King's College London, London, United Kingdom.
  • Charman T; Department of Psychology, Institute of Psychiatry, Psychology and Neuroscience, King's College London, London, United Kingdom.
  • Murphy DGM; Department of Forensic and Neurodevelopmental Sciences, Institute of Psychiatry, Psychology and Neuroscience, King's College London, London, United Kingdom.
  • Ecker C; Department of Forensic and Neurodevelopmental Sciences, Institute of Psychiatry, Psychology and Neuroscience, King's College London, London, United Kingdom; Department of Child and Adolescent Psychiatry, University Hospital, Goethe University, Frankfurt am Main, Germany.
  • Mennes M; Department of Cognitive Neuroscience, Donders Institute for Brain, Cognition and Behaviour, Radboud University Medical Centre, Nijmegen, the Netherlands.
  • Beckmann CF; Department of Cognitive Neuroscience, Donders Institute for Brain, Cognition and Behaviour, Radboud University Medical Centre, Nijmegen, the Netherlands; Centre for Functional MRI of the Brain, University of Oxford, Oxford, United Kingdom.
  • Fornito A; Turner Institute for Brain and Mental Health, School of Psychological Science, and Monash Biomedical Imaging, Monash University, Melbourne, Victoria, Australia.
  • Buitelaar JK; Department of Cognitive Neuroscience, Donders Institute for Brain, Cognition and Behaviour, Radboud University Medical Centre, Nijmegen, the Netherlands; Karakter Child and Adolescent Psychiatry University Centre, Nijmegen, the Netherlands.
Biol Psychiatry ; 94(1): 29-39, 2023 07 01.
Article in En | MEDLINE | ID: mdl-36925414
ABSTRACT

BACKGROUND:

Neuroimaging studies of functional connectivity (FC) in autism have been hampered by small sample sizes and inconsistent findings with regard to whether connectivity is increased or decreased in individuals with autism, whether these alterations affect focal systems or reflect a brain-wide pattern, and whether these are age and/or sex dependent.

METHODS:

The study included resting-state functional magnetic resonance imaging and clinical data from the EU-AIMS LEAP (European Autism Interventions Longitudinal European Autism Project) and the ABIDE (Autism Brain Imaging Data Exchange) 1 and 2 initiatives of 1824 (796 with autism) participants with an age range of 5-58 years. Between-group differences in FC were assessed, and associations between FC and clinical symptom ratings were investigated through canonical correlation analysis.

RESULTS:

Autism was associated with a brainwide pattern of hypo- and hyperconnectivity. Hypoconnectivity predominantly affected sensory and higher-order attentional networks and correlated with social impairments, restrictive and repetitive behavior, and sensory processing. Hyperconnectivity was observed primarily between the default mode network and the rest of the brain and between cortical and subcortical systems. This pattern was strongly associated with social impairments and sensory processing. Interactions between diagnosis and age or sex were not statistically significant.

CONCLUSIONS:

The FC alterations observed, which primarily involve hypoconnectivity of primary sensory and attention networks and hyperconnectivity of the default mode network and subcortex with the rest of the brain, do not appear to be age or sex dependent and correlate with clinical dimensions of social difficulties, restrictive and repetitive behaviors, and alterations in sensory processing. These findings suggest that the observed connectivity alterations are stable, trait-like features of autism that are related to the main symptom domains of the condition.
Subject(s)
Key words

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Autistic Disorder / Connectome / Autism Spectrum Disorder Limits: Adolescent / Adult / Child / Child, preschool / Humans / Middle aged Language: En Journal: Biol Psychiatry Year: 2023 Type: Article

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Autistic Disorder / Connectome / Autism Spectrum Disorder Limits: Adolescent / Adult / Child / Child, preschool / Humans / Middle aged Language: En Journal: Biol Psychiatry Year: 2023 Type: Article