Model-based whole-brain perturbational landscape of neurodegenerative diseases

Author:

Sanz Perl Yonatan1234ORCID,Fittipaldi Sol23,Gonzalez Campo Cecilia23,Moguilner Sebastián56,Cruzat Josephine46,Fraile-Vazquez Matias E3,Herzog Rubén6,Kringelbach Morten L78910,Deco Gustavo411121314ORCID,Prado Pavel615ORCID,Ibanez Agustin235616ORCID,Tagliazucchi Enzo1236

Affiliation:

1. Department of Physics, University of Buenos Aires

2. National Scientific and Technical Research Council (CONICET), CABA

3. Cognitive Neuroscience Center (CNC), Universidad de San Andrés

4. Center for Brain and Cognition, Computational Neuroscience Group, Universitat Pompeu Fabra

5. Global Brain Health Institute, University of California, San Francisco

6. Latin American Brain Health Institute (BrainLat), Universidad Adolfo Ibáñez

7. Department of Psychiatry, University of Oxford

8. Center for Music in the Brain, Department of Clinical Medicine, Aarhus University

9. Life and Health Sciences Research Institute (ICVS), School of Medicine, University of Minho

10. Centre for Eudaimonia and Human Flourishing, University of Oxford

11. Department of Information and Communication Technologies, Universitat Pompeu Fabra

12. Institució Catalana de la Recerca i Estudis Avancats (ICREA)

13. Department of Neuropsychology, Max Planck Institute for Human Cognitive and Brain Sciences

14. School of Psychological Sciences, Monash University

15. Escuela de Fonoaudiología, Facultad de Odontología y Ciencias de la Rehabilitación, Universidad San Sebastián

16. Trinity College Institute of Neuroscience (TCIN), Trinity College Dublin

Abstract

The treatment of neurodegenerative diseases is hindered by lack of interventions capable of steering multimodal whole-brain dynamics towards patterns indicative of preserved brain health. To address this problem, we combined deep learning with a model capable of reproducing whole-brain functional connectivity in patients diagnosed with Alzheimer’s disease (AD) and behavioral variant frontotemporal dementia (bvFTD). These models included disease-specific atrophy maps as priors to modulate local parameters, revealing increased stability of hippocampal and insular dynamics as signatures of brain atrophy in AD and bvFTD, respectively. Using variational autoencoders, we visualized different pathologies and their severity as the evolution of trajectories in a low-dimensional latent space. Finally, we perturbed the model to reveal key AD- and bvFTD-specific regions to induce transitions from pathological to healthy brain states. Overall, we obtained novel insights on disease progression and control by means of external stimulation, while identifying dynamical mechanisms that underlie functional alterations in neurodegeneration.

Funder

Marie Skłodowska-Curie Actions

Fondo Nacional de Desarrollo Científico y Tecnológico

Fondo de Financiamiento de Centros de Investigación en Áreas Prioritarias

Comisión Nacional de Investigación Científica y Tecnológica

Takeda

National Institute on Aging

Alzheimer's Association

Rainwater Charitable Foundation

Agencia Nacional de Promoción de la Investigación, el Desarrollo Tecnológico y la Innovación

Tau Consortium

Global Brain Health Institute

Publisher

eLife Sciences Publications, Ltd

Subject

General Immunology and Microbiology,General Biochemistry, Genetics and Molecular Biology,General Medicine,General Neuroscience

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