Your browser doesn't support javascript.
loading
Atypical measures of diffusion at the gray-white matter boundary in autism spectrum disorder in adulthood.
Bletsch, Anke; Schäfer, Tim; Mann, Caroline; Andrews, Derek S; Daly, Eileen; Gudbrandsen, Maria; Ruigrok, Amber N V; Dallyn, Robert; Romero-Garcia, Rafael; Lai, Meng-Chuan; Lombardo, Michael V; Craig, Michael C; Suckling, John; Bullmore, Edward T; Baron-Cohen, Simon; Murphy, Declan G M; Dell'Acqua, Flavio; Ecker, Christine.
Affiliation
  • Bletsch A; Department of Child and Adolescent Psychiatry, Psychosomatics and Psychotherapy, University Hospital, Goethe University, Frankfurt, Germany.
  • Schäfer T; Department of Child and Adolescent Psychiatry, Psychosomatics and Psychotherapy, University Hospital, Goethe University, Frankfurt, Germany.
  • Mann C; Department of Child and Adolescent Psychiatry, Psychosomatics and Psychotherapy, University Hospital, Goethe University, Frankfurt, Germany.
  • Andrews DS; Department of Psychiatry and Behavioral Sciences at the M.I.N.D. Institute, University of California, Davis, California, USA.
  • Daly E; Department of Forensic and Neurodevelopmental Sciences, and the Sackler Institute for Translational Neurodevelopmental Sciences, Institute of Psychiatry, Psychology and Neuroscience, King's College, London, UK.
  • Gudbrandsen M; Department of Forensic and Neurodevelopmental Sciences, and the Sackler Institute for Translational Neurodevelopmental Sciences, Institute of Psychiatry, Psychology and Neuroscience, King's College, London, UK.
  • Ruigrok ANV; Autism Research Centre, Department of Psychiatry, University of Cambridge, Cambridge, UK.
  • Dallyn R; Department of Forensic and Neurodevelopmental Sciences, and the Sackler Institute for Translational Neurodevelopmental Sciences, Institute of Psychiatry, Psychology and Neuroscience, King's College, London, UK.
  • Romero-Garcia R; Brain Mapping Unit, Department of Psychiatry, University of Cambridge, Cambridge, UK.
  • Lai MC; Autism Research Centre, Department of Psychiatry, University of Cambridge, Cambridge, UK.
  • Lombardo MV; Centre for Addiction and Mental Health and The Hospital for Sick Children, Department of Psychiatry, University of Toronto, Toronto, Canada.
  • Craig MC; Department of Psychiatry, National Taiwan University Hospital and College of Medicine, Taipei, Taiwan.
  • Suckling J; Autism Research Centre, Department of Psychiatry, University of Cambridge, Cambridge, UK.
  • Bullmore ET; Laboratory for Autism and Neurodevelopmental Disorders, Center for Neuroscience and Cognitive Systems, Istituto Italiano di Tecnologia, Rovereto, Italy.
  • Baron-Cohen S; Department of Forensic and Neurodevelopmental Sciences, and the Sackler Institute for Translational Neurodevelopmental Sciences, Institute of Psychiatry, Psychology and Neuroscience, King's College, London, UK.
  • Murphy DGM; Brain Mapping Unit, Department of Psychiatry, University of Cambridge, Cambridge, UK.
  • Dell'Acqua F; Brain Mapping Unit, Department of Psychiatry, University of Cambridge, Cambridge, UK.
  • Ecker C; Autism Research Centre, Department of Psychiatry, University of Cambridge, Cambridge, UK.
Hum Brain Mapp ; 42(2): 467-484, 2021 02 01.
Article in En | MEDLINE | ID: mdl-33094897
Autism spectrum disorder (ASD) is a highly complex neurodevelopmental condition that is accompanied by neuroanatomical differences on the macroscopic and microscopic level. Findings from histological, genetic, and more recently in vivo neuroimaging studies converge in suggesting that neuroanatomical abnormalities, specifically around the gray-white matter (GWM) boundary, represent a crucial feature of ASD. However, no research has yet characterized the GWM boundary in ASD based on measures of diffusion. Here, we registered diffusion tensor imaging data to the structural T1-weighted images of 92 adults with ASD and 92 matched neurotypical controls in order to examine between-group differences and group-by-sex interactions in fractional anisotropy and mean diffusivity sampled at the GWM boundary, and at different sampling depths within the superficial white and into the gray matter. As hypothesized, we observed atypical diffusion at and around the GWM boundary in ASD, with between-group differences and group-by-sex interactions depending on tissue class and sampling depth. Furthermore, we identified that altered diffusion at the GWM boundary partially (i.e., ~50%) overlapped with atypical gray-white matter tissue contrast in ASD. Our study thus replicates and extends previous work highlighting the GWM boundary as a crucial target of neuropathology in ASD, and guides future work elucidating etiological mechanisms.
Subject(s)
Key words

Full text: 1 Database: MEDLINE Main subject: Brain / Diffusion Tensor Imaging / Gray Matter / White Matter / Autism Spectrum Disorder Type of study: Clinical_trials / Prognostic_studies Limits: Adolescent / Adult / Female / Humans / Male / Middle aged Language: En Journal: Hum Brain Mapp Journal subject: CEREBRO Year: 2021 Type: Article Affiliation country: Germany

Full text: 1 Database: MEDLINE Main subject: Brain / Diffusion Tensor Imaging / Gray Matter / White Matter / Autism Spectrum Disorder Type of study: Clinical_trials / Prognostic_studies Limits: Adolescent / Adult / Female / Humans / Male / Middle aged Language: En Journal: Hum Brain Mapp Journal subject: CEREBRO Year: 2021 Type: Article Affiliation country: Germany