TY - JOUR
T1 - Model-based whole-brain perturbational landscape of neurodegenerative diseases
AU - Perl, Yonatan Sanz
AU - Fittipaldi, Sol
AU - Campo, Cecilia Gonzalez
AU - Moguilner, Sebastián
AU - Cruzat, Josephine
AU - Fraile-Vazquez, Matias E.
AU - Herzog, Rubén
AU - Kringelbach, Morten L.
AU - Deco, Gustavo
AU - Prado, Pavel
AU - Ibanez, Agustin
AU - Tagliazucchi, Enzo
N1 - Publisher Copyright:
© Sanz Perl et al.
PY - 2023
Y1 - 2023
N2 - 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 repro-ducing 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.
AB - 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 repro-ducing 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.
UR - http://www.scopus.com/inward/record.url?scp=85151508830&partnerID=8YFLogxK
U2 - 10.7554/elife.83970
DO - 10.7554/elife.83970
M3 - Article
C2 - 36995213
AN - SCOPUS:85151508830
SN - 2050-084X
VL - 12
JO - eLife
JF - eLife
M1 - e83970
ER -