4.6 Article

Graph neural fields: A framework for spatiotemporal dynamical models on the human connectome

期刊

PLOS COMPUTATIONAL BIOLOGY
卷 17, 期 1, 页码 -

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PUBLIC LIBRARY SCIENCE
DOI: 10.1371/journal.pcbi.1008310

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资金

  1. ERC Consolidator Grant: CARE-GIVING [615539]
  2. Center for Music in the Brain
  3. Danish National Research Foundation [DNRF117]
  4. Centre for Eudaimonia and Human Flourishing - Pettit and Carlsberg Foundations
  5. NWO-Wiskundeclusters grant [613.009.105]

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Tools from graph signal processing, specifically the graph Laplacian, have been successfully used to model neural activity and investigate structure-function relationships in the human brain. The models, called graph neural fields, allow for predictions of harmonic and temporal power spectra, functional connectivity, and coherence matrices. This approach, applied directly on the human connectome graph, provides insights into the organization of brain activity and potential avenues for future research.
Tools from the field of graph signal processing, in particular the graph Laplacian operator, have recently been successfully applied to the investigation of structure-function relationships in the human brain. The eigenvectors of the human connectome graph Laplacian, dubbed connectome harmonics, have been shown to relate to the functionally relevant resting-state networks. Whole-brain modelling of brain activity combines structural connectivity with local dynamical models to provide insight into the large-scale functional organization of the human brain. In this study, we employ the graph Laplacian and its properties to define and implement a large class of neural activity models directly on the human connectome. These models, consisting of systems of stochastic integrodifferential equations on graphs, are dubbed graph neural fields, in analogy with the well-established continuous neural fields. We obtain analytic predictions for harmonic and temporal power spectra, as well as functional connectivity and coherence matrices, of graph neural fields, with a technique dubbed CHAOSS (shorthand for Connectome-Harmonic Analysis Of Spatiotemporal Spectra). Combining graph neural fields with appropriate observation models allows for estimating model parameters from experimental data as obtained from electroencephalography (EEG), magnetoencephalography (MEG), or functional magnetic resonance imaging (fMRI). As an example application, we study a stochastic Wilson-Cowan graph neural field model on a high-resolution connectome graph constructed from diffusion tensor imaging (DTI) and structural MRI data. We show that the model equilibrium fluctuations can reproduce the empirically observed harmonic power spectrum of resting-state fMRI data, and predict its functional connectivity, with a high level of detail. Graph neural fields natively allow the inclusion of important features of cortical anatomy and fast computations of observable quantities for comparison with multimodal empirical data. They thus appear particularly suitable for modelling whole-brain activity at mesoscopic scales, and opening new potential avenues for connectome-graph-based investigations of structure-function relationships. Author summary The human brain can be seen as an interconnected network of many thousands neuronal populations; in turn, each population contains thousands of neurons, and each is connected both to its neighbors on the cortex, and crucially also to distant populations thanks to long-range white matter fibers. This extremely complex network, unique to each of us, is known as the human connectome graph. In this work, we develop a novel approach to investigate how the neural activity that is necessary for our life and experience of the world arises from an individual human connectome graph. For the first time, we implement a mathematical model of neuronal activity directly on a high-resolution connectome graph, and show that it can reproduce the spatial patterns of activity observed in the real brain with magnetic resonance imaging. This new kind of model, made of equations implemented directly on connectome graphs, could help us better understand how brain function is shaped by computational principles and anatomy, but also how it is affected by pathology and lesions.

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