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This study applies a graph-neural-network surrogate to model the human motor cortex as a port-Hamiltonian system, aiming to create physically principled substrates for closed-loop neuromodulation. While it successfully reconstructs kinematics and reproduces near-critical avalanche branching in EEG data, the authors identify specific gaps regarding $1/f$ spectral slopes that require further theoretical upgrades. The work represents a significant intersection of machine learning methods with non-equilibrium thermodynamics to decode complex neural dynamics.
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Learning the Brain's Dynamics as a Port-Hamiltonian System: A GNN-Surrogate Metriplectic Twin for Non-Equilibrium Cortical Dynamics and Closed-Loop Neuromodulation

arXiv3 min read

arXiv:2607.10439v2 Announce Type: replace-cross Abstract: We model human motor cortex, recorded during rest and motor-imagery BCI conditions, as a port-Hamiltonian system: a conservative interconnection (skew-symmetric coupling between band-limited neural phasors) together with a dissipative port whose state-dependent decay is set by a graph-neural-network surrogate. The Hamiltonian is resolved into five interpretable frequency sub-energies, and a phase-locking prior measured from the recordings gates the learned functional connectome so that coupling is admitted only where phase coherence is present. A metriplectic formulation places the resting cortex at a non-equilibrium steady state sustained by an explicit metabolic port, with a fluctuation-dissipation-consistent noise channel governed by a single arousal temperature. Fitting the model to 'FitTrainN' phasor samples from the PhysioNet EEG Motor Movement/Imagery database, under a leakage-free split with three subjects held out entirely, yields a held-out kinematic reconstruction error of 'FitTestMSE' that is stable across random seeds. We then score the free-running model against model-independent dynamical invariants it did not author: it reproduces near-critical avalanche branching ($\sigma\approx1$) but not yet the aperiodic $1/f$ spectral slope or the long-range temporal correlations of real cortex a concrete, falsifiable gap that we trace to specific, testable upgrades. The port-Hamiltonian structure supplies neuroanatomically grounded stimulation ports with stability guarantees, positioning the model as a physically principled, structure-preserving substrate for closed-loop neuromodulation.

Abstract:We model human motor cortex, recorded during rest and motor-imagery BCI conditions, as a port-Hamiltonian system: a conservative interconnection (skew-symmetric coupling between band-limited neural phasors) together with a dissipative port whose state-dependent decay is set by a graph-neural-network surrogate. The Hamiltonian is resolved into five interpretable frequency sub-energies, and a phase-locking prior measured from the recordings gates the learned functional connectome so that coupling is admitted only where phase coherence is present. A metriplectic formulation places the resting cortex at a non-equilibrium steady state sustained by an explicit metabolic port, with a fluctuation-dissipation-consistent noise channel governed by a single arousal temperature. Fitting the model to 'FitTrainN' phasor samples from the PhysioNet EEG Motor Movement/Imagery database, under a leakage-free split with three subjects held out entirely, yields a held-out kinematic reconstruction error of 'FitTestMSE' that is stable across random seeds. We then score the free-running model against model-independent dynamical invariants it did not author: it reproduces near-critical avalanche branching ($\sigma\approx1$) but not yet the aperiodic $1/f$ spectral slope or the long-range temporal correlations of real cortex a concrete, falsifiable gap that we trace to specific, testable upgrades. The port-Hamiltonian structure supplies neuroanatomically grounded stimulation ports with stability guarantees, positioning the model as a physically principled, structure-preserving substrate for closed-loop neuromodulation.

Neurons and Cognition (q-bio.NC); Artificial Intelligence (cs.AI)

arXiv:2607.10439 [q-bio.NC]

(or arXiv:2607.10439v2 [q-bio.NC] for this version)

https://doi.org/10.48550/arXiv.2607.10439 Focus to learn more arXiv-issued DOI via DataCite

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Full text under the publisher's open licence · 305 words

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