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Adolescence is associated with genomically patterned consolidation of the hubs of the human brain connectome.
Whitaker, Kirstie J; Vértes, Petra E; Romero-Garcia, Rafael; Vása, Frantisek; Moutoussis, Michael; Prabhu, Gita; Weiskopf, Nikolaus; Callaghan, Martina F; Wagstyl, Konrad; Rittman, Timothy; Tait, Roger; Ooi, Cinly; Suckling, John; Inkster, Becky; Fonagy, Peter; Dolan, Raymond J; Jones, Peter B; Goodyer, Ian M; Bullmore, Edward T.
Afiliación
  • Whitaker KJ; Department of Psychiatry, University of Cambridge, Cambridge CB2 0SZ, United Kingdom; kw401@cam.ac.uk.
  • Vértes PE; Department of Psychiatry, University of Cambridge, Cambridge CB2 0SZ, United Kingdom;
  • Romero-Garcia R; Department of Psychiatry, University of Cambridge, Cambridge CB2 0SZ, United Kingdom;
  • Vása F; Department of Psychiatry, University of Cambridge, Cambridge CB2 0SZ, United Kingdom;
  • Moutoussis M; Wellcome Trust Centre for Neuroimaging, University College London, London WC1N 3BG, United Kingdom;
  • Prabhu G; Wellcome Trust Centre for Neuroimaging, University College London, London WC1N 3BG, United Kingdom;
  • Weiskopf N; Wellcome Trust Centre for Neuroimaging, University College London, London WC1N 3BG, United Kingdom; Department of Neurophysics, Max Planck Institute for Human Cognitive and Brain Sciences, 04103 Leipzig, Germany;
  • Callaghan MF; Wellcome Trust Centre for Neuroimaging, University College London, London WC1N 3BG, United Kingdom;
  • Wagstyl K; Department of Psychiatry, University of Cambridge, Cambridge CB2 0SZ, United Kingdom;
  • Rittman T; Department of Clinical Neurosciences, University of Cambridge, Cambridge CB2 3EB, United Kingdom;
  • Tait R; Department of Psychiatry, University of Cambridge, Cambridge CB2 0SZ, United Kingdom;
  • Ooi C; Department of Psychiatry, University of Cambridge, Cambridge CB2 0SZ, United Kingdom;
  • Suckling J; Department of Psychiatry, University of Cambridge, Cambridge CB2 0SZ, United Kingdom; Cambridgeshire and Peterborough National Health Service Foundation Trust, Cambridge, CB21 5EF, United Kingdom; Medical Research Council/Wellcome Trust Behavioural and Clinical Neuroscience Institute, University of
  • Inkster B; Department of Psychiatry, University of Cambridge, Cambridge CB2 0SZ, United Kingdom;
  • Fonagy P; Research Department of Clinical, Educational and Health Psychology, University College London, London WC1E 6BT, United Kingdom;
  • Dolan RJ; Wellcome Trust Centre for Neuroimaging, University College London, London WC1N 3BG, United Kingdom; Max Planck University College London Centre for Computational Psychiatry and Ageing Research, University College London, London WC1B 5EH, United Kingdom;
  • Jones PB; Department of Psychiatry, University of Cambridge, Cambridge CB2 0SZ, United Kingdom; Cambridgeshire and Peterborough National Health Service Foundation Trust, Cambridge, CB21 5EF, United Kingdom;
  • Goodyer IM; Department of Psychiatry, University of Cambridge, Cambridge CB2 0SZ, United Kingdom; Cambridgeshire and Peterborough National Health Service Foundation Trust, Cambridge, CB21 5EF, United Kingdom;
  • Bullmore ET; Department of Psychiatry, University of Cambridge, Cambridge CB2 0SZ, United Kingdom; Cambridgeshire and Peterborough National Health Service Foundation Trust, Cambridge, CB21 5EF, United Kingdom; Medical Research Council/Wellcome Trust Behavioural and Clinical Neuroscience Institute, University of
Proc Natl Acad Sci U S A ; 113(32): 9105-10, 2016 08 09.
Article en En | MEDLINE | ID: mdl-27457931
ABSTRACT
How does human brain structure mature during adolescence? We used MRI to measure cortical thickness and intracortical myelination in 297 population volunteers aged 14-24 y old. We found and replicated that association cortical areas were thicker and less myelinated than primary cortical areas at 14 y. However, association cortex had faster rates of shrinkage and myelination over the course of adolescence. Age-related increases in cortical myelination were maximized approximately at the internal layer of projection neurons. Adolescent cortical myelination and shrinkage were coupled and specifically associated with a dorsoventrally patterned gene expression profile enriched for synaptic, oligodendroglial- and schizophrenia-related genes. Topologically efficient and biologically expensive hubs of the brain anatomical network had greater rates of shrinkage/myelination and were associated with overexpression of the same transcriptional profile as cortical consolidation. We conclude that normative human brain maturation involves a genetically patterned process of consolidating anatomical network hubs. We argue that developmental variation of this consolidation process may be relevant both to normal cognitive and behavioral changes and the high incidence of schizophrenia during human brain adolescence.
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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Corteza Cerebral / Conectoma Tipo de estudio: Risk_factors_studies Límite: Adolescent / Adult / Female / Humans / Male Idioma: En Revista: Proc Natl Acad Sci U S A Año: 2016 Tipo del documento: Article

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Corteza Cerebral / Conectoma Tipo de estudio: Risk_factors_studies Límite: Adolescent / Adult / Female / Humans / Male Idioma: En Revista: Proc Natl Acad Sci U S A Año: 2016 Tipo del documento: Article
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