TY - JOUR
T1 - A generative network model of neurodevelopmental diversity in structural brain organization
AU - Akarca, Danyal
AU - Vértes, Petra E.
AU - Bullmore, Edward T.
AU - Baker, Kate
AU - Gathercole, Susan E.
AU - Holmes, Joni
AU - Kievit, Rogier A.
AU - Manly, Tom
AU - Bathelt, Joe
AU - Bennett, Marc
AU - Bignardi, Giacomo
AU - Bishop, Sarah
AU - Bottacin, Erica
AU - Bridge, Lara
AU - Brkic, Diandra
AU - Bryant, Annie
AU - Butterfield, Sally
AU - Byrne, Elizabeth M.
AU - Crickmore, Gemma
AU - Dalmaijer, Edwin S.
AU - Daly, Fánchea
AU - Emery, Tina
AU - Forde, Laura
AU - Franckel, Grace
AU - Fuhrmann, Delia
AU - Gadie, Andrew
AU - Gharooni, Sara
AU - Guy, Jacalyn
AU - Hawkins, Erin
AU - Jaroslawska, Agnieszka
AU - Joeghan, Sara
AU - Johnson, Amy
AU - Jones, Jonathan
AU - Mareva, Silvana
AU - Ng-Cordell, Elise
AU - O’Brien, Sinead
AU - O’Leary, Cliodhna
AU - Rennie, Joseph P.
AU - Simpson-Kent, Ivan
AU - Siugzdaite, Roma
AU - Smith, Tess A.
AU - Uh, Stephani
AU - Vedechkina, Maria
AU - Woolgar, Francesca
AU - Zdorovtsova, Natalia
AU - Zhang, Mengya
AU - Astle, Duncan E.
AU - The CALM Team
N1 - Funding Information: D.A. is supported by the Medical Research Council Doctoral Training Programme and Cambridge Trust Vice Chancellor’s Award Scholarship. D.E.A. is supported by Medical Research Council Program Grant MC-A0606-5PQ41, respectively. Both D.E.A. and D.A. are supported by The James S. McDonnell Foundation Opportunity Award. P.E.V. is a fellow of MQ: Transforming Mental Health (MQF17_24) and of the Alan Turing Institute funded by EPSRC grant EP/N510129/1. E. T.B. is an NIHR Senior Investigator, supported by the NIHR Cambridge Biomedical Research Centre. The views expressed are those of the authors, and not necessarily those of the NHS, the NIHR, or the Department of Health and Social Care. All opinions expressed in this publication are those of the authors and do not necessarily reflect the views of the funding agencies.
PY - 2021/7/9
Y1 - 2021/7/9
N2 - The formation of large-scale brain networks, and their continual refinement, represent crucial developmental processes that can drive individual differences in cognition and which are associated with multiple neurodevelopmental conditions. But how does this organization arise, and what mechanisms drive diversity in organization? We use generative network modeling to provide a computational framework for understanding neurodevelopmental diversity. Within this framework macroscopic brain organization, complete with spatial embedding of its organization, is an emergent property of a generative wiring equation that optimizes its connectivity by renegotiating its biological costs and topological values continuously over time. The rules that govern these iterative wiring properties are controlled by a set of tightly framed parameters, with subtle differences in these parameters steering network growth towards different neurodiverse outcomes. Regional expression of genes associated with the simulations converge on biological processes and cellular components predominantly involved in synaptic signaling, neuronal projection, catabolic intracellular processes and protein transport. Together, this provides a unifying computational framework for conceptualizing the mechanisms and diversity in neurodevelopment, capable of integrating different levels of analysis—from genes to cognition.
AB - The formation of large-scale brain networks, and their continual refinement, represent crucial developmental processes that can drive individual differences in cognition and which are associated with multiple neurodevelopmental conditions. But how does this organization arise, and what mechanisms drive diversity in organization? We use generative network modeling to provide a computational framework for understanding neurodevelopmental diversity. Within this framework macroscopic brain organization, complete with spatial embedding of its organization, is an emergent property of a generative wiring equation that optimizes its connectivity by renegotiating its biological costs and topological values continuously over time. The rules that govern these iterative wiring properties are controlled by a set of tightly framed parameters, with subtle differences in these parameters steering network growth towards different neurodiverse outcomes. Regional expression of genes associated with the simulations converge on biological processes and cellular components predominantly involved in synaptic signaling, neuronal projection, catabolic intracellular processes and protein transport. Together, this provides a unifying computational framework for conceptualizing the mechanisms and diversity in neurodevelopment, capable of integrating different levels of analysis—from genes to cognition.
UR - http://www.scopus.com/inward/record.url?scp=85112123565&partnerID=8YFLogxK
U2 - 10.1038/s41467-021-24430-z
DO - 10.1038/s41467-021-24430-z
M3 - Article
C2 - 34244490
AN - SCOPUS:85112123565
VL - 12
JO - Nature Communications
JF - Nature Communications
SN - 2041-1723
IS - 1
M1 - 4216
ER -