Accurately Modeling the Resting Brain Functional Correlations Using Wave Equation With Spatiotemporal Varying Hypergraph Laplacian
How spontaneous brain neural activities emerge from the underlying anatomical architecture, characterized by structural connectivity (SC), has puzzled researchers for a long time. Over the past decades, much effort has been directed toward the graph modeling of SC, in which the brain SC is generally...
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| Published in: | IEEE transactions on medical imaging Vol. 41; no. 12; pp. 3787 - 3798 |
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| Main Authors: | , , , |
| Format: | Journal Article |
| Language: | English |
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IEEE
01.12.2022
The Institute of Electrical and Electronics Engineers, Inc. (IEEE) |
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| ISSN: | 0278-0062, 1558-254X, 1558-254X |
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| Abstract | How spontaneous brain neural activities emerge from the underlying anatomical architecture, characterized by structural connectivity (SC), has puzzled researchers for a long time. Over the past decades, much effort has been directed toward the graph modeling of SC, in which the brain SC is generally considered as relatively invariant. However, the graph representation of SC is unable to directly describe the connections between anatomically unconnected brain regions and fail to model the negative functional correlations. Here, we extend the static graph model to a spatiotemporal varying hypergraph Laplacian diffusion (STV-HGLD) model to describe the propagation of the spontaneous neural activity in human brain by incorporating the Laplacian of the hypergraph representation of the structural connectome (<inline-formula> <tex-math notation="LaTeX">{h} </tex-math></inline-formula>SC) into the regular wave equation. Theoretical solution shows that the dynamic functional couplings between brain regions fluctuate in the form of an exponential wave regulated by the spatiotemporal varying Laplacian of <inline-formula> <tex-math notation="LaTeX">{h} </tex-math></inline-formula>SC. Empirical study suggests that the cortical wave might give rise to resonance with SC during the self-organizing interplay between excitation and inhibition among brain regions, which orchestrates the cortical waves propagating with harmonics emanating from the <inline-formula> <tex-math notation="LaTeX">{h} </tex-math></inline-formula>SC while being bound by the natural frequencies of SC. Besides, the average statistical dependencies between brain regions, normally defined as the functional connectivity (FC), arises just at the moment before the cortical wave reaches the steady state after the wave spreads across all the brain regions. Comprehensive tests on four extensively studied empirical brain connectome datasets with different resolutions confirm our theory and findings. |
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| AbstractList | How spontaneous brain neural activities emerge from the underlying anatomical architecture, characterized by structural connectivity (SC), has puzzled researchers for a long time. Over the past decades, much effort has been directed toward the graph modeling of SC, in which the brain SC is generally considered as relatively invariant. However, the graph representation of SC is unable to directly describe the connections between anatomically unconnected brain regions and fail to model the negative functional correlations. Here, we extend the static graph model to a spatiotemporal varying hypergraph Laplacian diffusion (STV-HGLD) model to describe the propagation of the spontaneous neural activity in human brain by incorporating the Laplacian of the hypergraph representation of the structural connectome ([Formula Omitted]SC) into the regular wave equation. Theoretical solution shows that the dynamic functional couplings between brain regions fluctuate in the form of an exponential wave regulated by the spatiotemporal varying Laplacian of [Formula Omitted]SC. Empirical study suggests that the cortical wave might give rise to resonance with SC during the self-organizing interplay between excitation and inhibition among brain regions, which orchestrates the cortical waves propagating with harmonics emanating from the [Formula Omitted]SC while being bound by the natural frequencies of SC. Besides, the average statistical dependencies between brain regions, normally defined as the functional connectivity (FC), arises just at the moment before the cortical wave reaches the steady state after the wave spreads across all the brain regions. Comprehensive tests on four extensively studied empirical brain connectome datasets with different resolutions confirm our theory and findings. How spontaneous brain neural activities emerge from the underlying anatomical architecture, characterized by structural connectivity (SC), has puzzled researchers for a long time. Over the past decades, much effort has been directed toward the graph modeling of SC, in which the brain SC is generally considered as relatively invariant. However, the graph representation of SC is unable to directly describe the connections between anatomically unconnected brain regions and fail to model the negative functional correlations. Here, we extend the static graph model to a spatiotemporal varying hypergraph Laplacian diffusion (STV-HGLD) model to describe the propagation of the spontaneous neural activity in human brain by incorporating the Laplacian of the hypergraph representation of the structural connectome ( h SC) into the regular wave equation. Theoretical solution shows that the dynamic functional couplings between brain regions fluctuate in the form of an exponential wave regulated by the spatiotemporal varying Laplacian of h SC. Empirical study suggests that the cortical wave might give rise to resonance with SC during the self-organizing interplay between excitation and inhibition among brain regions, which orchestrates the cortical waves propagating with harmonics emanating from the h SC while being bound by the natural frequencies of SC. Besides, the average statistical dependencies between brain regions, normally defined as the functional connectivity (FC), arises just at the moment before the cortical wave reaches the steady state after the wave spreads across all the brain regions. Comprehensive tests on four extensively studied empirical brain connectome datasets with different resolutions confirm our theory and findings.How spontaneous brain neural activities emerge from the underlying anatomical architecture, characterized by structural connectivity (SC), has puzzled researchers for a long time. Over the past decades, much effort has been directed toward the graph modeling of SC, in which the brain SC is generally considered as relatively invariant. However, the graph representation of SC is unable to directly describe the connections between anatomically unconnected brain regions and fail to model the negative functional correlations. Here, we extend the static graph model to a spatiotemporal varying hypergraph Laplacian diffusion (STV-HGLD) model to describe the propagation of the spontaneous neural activity in human brain by incorporating the Laplacian of the hypergraph representation of the structural connectome ( h SC) into the regular wave equation. Theoretical solution shows that the dynamic functional couplings between brain regions fluctuate in the form of an exponential wave regulated by the spatiotemporal varying Laplacian of h SC. Empirical study suggests that the cortical wave might give rise to resonance with SC during the self-organizing interplay between excitation and inhibition among brain regions, which orchestrates the cortical waves propagating with harmonics emanating from the h SC while being bound by the natural frequencies of SC. Besides, the average statistical dependencies between brain regions, normally defined as the functional connectivity (FC), arises just at the moment before the cortical wave reaches the steady state after the wave spreads across all the brain regions. Comprehensive tests on four extensively studied empirical brain connectome datasets with different resolutions confirm our theory and findings. How spontaneous brain neural activities emerge from the underlying anatomical architecture, characterized by structural connectivity (SC), has puzzled researchers for a long time. Over the past decades, much effort has been directed toward the graph modeling of SC, in which the brain SC is generally considered as relatively invariant. However, the graph representation of SC is unable to directly describe the connections between anatomically unconnected brain regions and fail to model the negative functional correlations. Here, we extend the static graph model to a spatiotemporal varying hypergraph Laplacian diffusion (STV-HGLD) model to describe the propagation of the spontaneous neural activity in human brain by incorporating the Laplacian of the hypergraph representation of the structural connectome (<inline-formula> <tex-math notation="LaTeX">{h} </tex-math></inline-formula>SC) into the regular wave equation. Theoretical solution shows that the dynamic functional couplings between brain regions fluctuate in the form of an exponential wave regulated by the spatiotemporal varying Laplacian of <inline-formula> <tex-math notation="LaTeX">{h} </tex-math></inline-formula>SC. Empirical study suggests that the cortical wave might give rise to resonance with SC during the self-organizing interplay between excitation and inhibition among brain regions, which orchestrates the cortical waves propagating with harmonics emanating from the <inline-formula> <tex-math notation="LaTeX">{h} </tex-math></inline-formula>SC while being bound by the natural frequencies of SC. Besides, the average statistical dependencies between brain regions, normally defined as the functional connectivity (FC), arises just at the moment before the cortical wave reaches the steady state after the wave spreads across all the brain regions. Comprehensive tests on four extensively studied empirical brain connectome datasets with different resolutions confirm our theory and findings. |
| Author | Wang, Yanjiang Liu, Baodi Ma, Jichao Chen, Xue |
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| Cites_doi | 10.1007/s13311-018-0663-y 10.1038/44730 10.1177/1073858417728032 10.1038/nrn2201 10.1103/PhysRevE.90.012707 10.1016/j.neucom.2019.06.068 10.1371/journal.pbio.0060159 10.1073/pnas.0701519104 10.1523/JNEUROSCI.1091-13.2013 10.1109/TGRS.2018.2867570 10.3390/math9182345 10.1016/j.ijpsycho.2015.02.011 10.1002/hbm.20737 10.1109/JAS.2017.7510880 10.1016/j.neuroimage.2013.12.039 10.1016/j.media.2020.101799 10.1016/j.neuroimage.2009.10.003 10.1126/science.1238411 10.1038/s41598-017-18769-x 10.1038/s41467-018-04614-w 10.1016/j.neuroimage.2007.02.012 10.1038/s41467-019-12765-7 10.1002/hbm.460020107 10.1089/brain.2015.0408 10.1523/JNEUROSCI.4423-13.2014 10.1073/pnas.0811168106 10.1016/j.neucom.2020.11.021 10.1016/j.neuroimage.2013.09.071 10.1371/journal.pcbi.1005325 10.1016/j.neuroimage.2018.02.016 10.1093/cercor/bhr234 10.1073/pnas.1219562110 10.1038/nrn2575 10.1073/pnas.1315529111 10.1016/j.neuroimage.2016.04.050 10.1016/j.neuroimage.2014.04.038 10.1109/TMI.2014.2341732 10.1371/journal.pcbi.1008310 10.1038/srep10532 10.1038/nature18933 10.1038/ncomms10340 10.1109/ACCESS.2020.3039837 |
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| SubjectTerms | Brain Brain connectivity Brain modeling Correlation Couplings Formulas (mathematics) Graph representations Graph theory Graphical representations Laplace equations Mathematical models Modelling Neural activity Neural networks Predictive models Propagation resonance Resonant frequencies spatiotemporal varying hypergraph Laplacian structure-function relation wave equation Wave equations Wave propagation |
| Title | Accurately Modeling the Resting Brain Functional Correlations Using Wave Equation With Spatiotemporal Varying Hypergraph Laplacian |
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