Using in silico perturbational approach to identify critical areas in schizophrenia

Author:

Mana Ludovica12ORCID,Vila-Vidal Manel3456ORCID,Köckeritz Charlotte12,Aquino Kevin7ORCID,Fornito Alex7ORCID,Kringelbach Morten L891011ORCID,Deco Gustavo1212ORCID

Affiliation:

1. Center for Brain and Cognition , Computational Neuroscience Group, Department of Information and Communication Technologies, , Barcelona 08018 , Spain

2. Universitat Pompeu Fabra , Computational Neuroscience Group, Department of Information and Communication Technologies, , Barcelona 08018 , Spain

3. Center for Brain and Cognition , Computational Neuroscience Group, Department of Information and Communication Technologies, , Barcelona 08018 , Spain , m@vila-vidal.com

4. Universitat Pompeu Fabra , Computational Neuroscience Group, Department of Information and Communication Technologies, , Barcelona 08018 , Spain , m@vila-vidal.com

5. Computational Biology and Complex Systems Group , Department of Physics, , Barcelona 08028 , Spain

6. Universitat Politècnica de Catalunya , Department of Physics, , Barcelona 08028 , Spain

7. School of Psychological Sciences and Monash Biomedical Imaging, Turner Institute for Brain and Mental Health, Monash University , Clayton, Melbourne, state of Victoria 3800 , Australia

8. Department of Psychiatry, University of Oxford , Oxford OX1 4BH , United Kingdom

9. Centre for Eudaimonia and Human Flourishing, Linacre College, University of Oxford , Oxford OX1 4BH , United Kingdom

10. Center for Music in the Brain , Department of Clinical Medicine, , Aarhus 8000 , Denmark

11. Aarhus University , Department of Clinical Medicine, , Aarhus 8000 , Denmark

12. Institució Catalana de la Recerca i Estudis Avancats (ICREA) , Passeig Lluis Companys 23, Barcelona 08010 , Spain

Abstract

Abstract Schizophrenia is a debilitating neuropsychiatric disorder whose underlying correlates remain unclear despite decades of neuroimaging investigation. One contentious topic concerns the role of global signal (GS) fluctuations and how they affect more focal functional changes. Moreover, it has been difficult to pinpoint causal mechanisms of circuit disruption. Here, we analyzed resting-state fMRI data from 47 schizophrenia patients and 118 age-matched healthy controls and used dynamical analyses to investigate how global fluctuations and other functional metastable states are affected by this disorder. We found that brain dynamics in the schizophrenia group were characterized by an increased probability of globally coherent states and reduced recurrence of a substate dominated by coupled activity in the default mode and limbic networks. We then used the in silico perturbation of a whole-brain model to identify critical areas involved in the disease. Perturbing a set of temporo-parietal sensory and associative areas in a model of the healthy brain reproduced global pathological dynamics. Healthy brain dynamics were instead restored by perturbing a set of medial fronto-temporal and cingulate regions in the model of pathology. These results highlight the relevance of GS alterations in schizophrenia and identify a set of vulnerable areas involved in determining a shift in brain state.

Funder

Human Brain Project Specific Grant Agreement 3

Danish National Research Foundation

Centre for Eudaimonia and Human Flourishing at Linacre College

Pettit and Carlsberg Foundations

Publisher

Oxford University Press (OUP)

Subject

Cellular and Molecular Neuroscience,Cognitive Neuroscience

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