TY - JOUR
T1 - Subtly altered topological asymmetry of brain structural covariance networks in autism spectrum disorder across 43 datasets from the ENIGMA consortium
AU - Sha, Zhiqiang
AU - van Rooij, Daan
AU - Anagnostou, Evdokia
AU - Arango, Celso
AU - Auzias, Guillaume
AU - Behrmann, Marlene
AU - Bernhardt, Boris
AU - Bolte, Sven
AU - Busatto, Geraldo F
AU - Calderoni, Sara
AU - Calvo, Rosa
AU - Daly, Eileen
AU - Deruelle, Christine
AU - Duan, Meiyu
AU - Duran, Fabio Luis Souza
AU - Durston, Sarah
AU - Ecker, Christine
AU - Ehrlich, Stefan
AU - Fair, Damien
AU - Fedor, Jennifer
AU - Fitzgerald, Jacqueline
AU - Floris, Dorothea L
AU - Franke, Barbara
AU - Freitag, Christine M
AU - Gallagher, Louise
AU - Glahn, David C
AU - Haar, Shlomi
AU - Hoekstra, Liesbeth
AU - Jahanshad, Neda
AU - Jalbrzikowski, Maria
AU - Janssen, Joost
AU - King, Joseph A
AU - Lazaro, Luisa
AU - Luna, Beatriz
AU - McGrath, Jane
AU - Medland, Sarah E
AU - Muratori, Filippo
AU - Murphy, Declan G M
AU - Neufeld, Janina
AU - O'Hearn, Kirsten
AU - Oranje, Bob
AU - Parellada, Mara
AU - Pariente, Jose C
AU - Postema, Merel C
AU - Remnelius, Karl Lundin
AU - Retico, Alessandra
AU - Rosa, Pedro Gomes Penteado
AU - Rubia, Katya
AU - Shook, Devon
AU - Tammimies, Kristiina
N1 - Funding Information:
We thank the participants of all studies who have contributed data to the ENIGMA-ASD working group (http://enigma.ini.usc.edu/ongoing/enigma-asd-working-group/) [23]. This research was funded by the Max Planck Society (Germany). This study was further supported by the ENIGMA Center for Worldwide Medicine, Imaging & Genomics grant (NIH U54 EB020403) to PMT, and further supported by the Innovative Medicines Initiative Joint Undertaking under grant agreement number 115300 (EU-AIMS) and 777394 (AIMS-2-TRIALS), resources of which are composed of financial contribution from the European Union’s Seventh Framework Programme and Horizon2020 programs and the European Federation of Pharmaceutical Industries and Associations (EFPIA) companies’ in-kind contribution. The Canadian samples were collected as part of the POND network funded by the Ontario Brain Institute (Anagnostou/Lerch). Boris Bernhardt acknowledges research support from the National Science and Engineering Research Council of Canada (NSERC Discovery-1304413), the Canadian Institutes of Health Research (CIHR FDN-154298, CIHR PJT-174995), SickKids Foundation (NI17-039), Azrieli Center for Autism Research (ACAR-TACC), BrainCanada, FRQ-S, and the Tier-2 Canada Research Chairs program. Neda Jahanshad is partially funded by NIH R01MH117601, P41EB015922, R01AG058854, R01MH121246, R01MH111671 and is MPI of a research grant from Biogen Inc, for work unrelated to the contents of this manuscript.
Publisher Copyright:
© 2022, The Author(s).
PY - 2022/4
Y1 - 2022/4
N2 - Small average differences in the left-right asymmetry of cerebral cortical thickness have been reported in individuals with autism spectrum disorder (ASD) compared to typically developing controls, affecting widespread cortical regions. The possible impacts of these regional alterations in terms of structural network effects have not previously been characterized. Inter-regional morphological covariance analysis can capture network connectivity between different cortical areas at the macroscale level. Here, we used cortical thickness data from 1455 individuals with ASD and 1560 controls, across 43 independent datasets of the ENIGMA consortium's ASD Working Group, to assess hemispheric asymmetries of intra-individual structural covariance networks, using graph theory-based topological metrics. Compared with typical features of small-world architecture in controls, the ASD sample showed significantly altered average asymmetry of networks involving the fusiform, rostral middle frontal, and medial orbitofrontal cortex, involving higher randomization of the corresponding right-hemispheric networks in ASD. A network involving the superior frontal cortex showed decreased right-hemisphere randomization. Based on comparisons with meta-analyzed functional neuroimaging data, the altered connectivity asymmetry particularly affected networks that subserve executive functions, language-related and sensorimotor processes. These findings provide a network-level characterization of altered left-right brain asymmetry in ASD, based on a large combined sample. Altered asymmetrical brain development in ASD may be partly propagated among spatially distant regions through structural connectivity.
AB - Small average differences in the left-right asymmetry of cerebral cortical thickness have been reported in individuals with autism spectrum disorder (ASD) compared to typically developing controls, affecting widespread cortical regions. The possible impacts of these regional alterations in terms of structural network effects have not previously been characterized. Inter-regional morphological covariance analysis can capture network connectivity between different cortical areas at the macroscale level. Here, we used cortical thickness data from 1455 individuals with ASD and 1560 controls, across 43 independent datasets of the ENIGMA consortium's ASD Working Group, to assess hemispheric asymmetries of intra-individual structural covariance networks, using graph theory-based topological metrics. Compared with typical features of small-world architecture in controls, the ASD sample showed significantly altered average asymmetry of networks involving the fusiform, rostral middle frontal, and medial orbitofrontal cortex, involving higher randomization of the corresponding right-hemispheric networks in ASD. A network involving the superior frontal cortex showed decreased right-hemisphere randomization. Based on comparisons with meta-analyzed functional neuroimaging data, the altered connectivity asymmetry particularly affected networks that subserve executive functions, language-related and sensorimotor processes. These findings provide a network-level characterization of altered left-right brain asymmetry in ASD, based on a large combined sample. Altered asymmetrical brain development in ASD may be partly propagated among spatially distant regions through structural connectivity.
UR - http://www.scopus.com/inward/record.url?scp=85124387600&partnerID=8YFLogxK
U2 - 10.1038/s41380-022-01452-7
DO - 10.1038/s41380-022-01452-7
M3 - Article
C2 - 35136228
SN - 1359-4184
VL - 27
SP - 2114
EP - 2125
JO - Molecular Psychiatry
JF - Molecular Psychiatry
IS - 4
ER -