Secondary thalamic dysfunction underlies abnormal large-scale neural dynamics in chronic stroke

Stroke causes pronounced and widespread slowing of neural activity. Despite decades of work exploring these abnormal neural dynamics and their associated functional impairments, their causes remain largely unclear. To close this gap in understanding, we applied a neurophysiological corticothalamic circuit model to simulate magnetoencephalography (MEG) power spectra recorded from chronic stroke patients. Comparing model-estimated physiological parameters to those of controls, patients demonstrated significantly lower intrathalamic inhibition in the lesioned hemisphere, despite the absence of direct damage to the thalamus itself. We hypothesized that this disinhibition could instead be related to secondary degeneration of the thalamus, for which growing evidence exists in the literature. Further analyses confirmed that spectral slowing correlated significantly with overall secondary degeneration of the ipsilesional thalamus, encompassing decreased thalamic volume, altered tissue microstructure, and decreased blood flow. Crucially, this relationship was mediated by model-estimated thalamic disinhibition, suggesting a causal link between secondary thalamic degeneration and abnormal brain dynamics via thalamic disinhibition. Finally, thalamic degeneration was correlated significantly with poorer cognitive and language outcomes, but not lesion volume, reinforcing that thalamus damage may account for additional individual variability in poststroke disability. Overall, our findings indicate that the frequently observed poststroke slowing reflects a disruption of corticothalamic circuit dynamics due to secondary thalamic dysfunction, and highlights the thalamus as an important target for understanding and potentially treating poststroke brain dysfunction.

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Publication Details

Journal
Proceedings of the National Academy of Sciences
Published
2024-11-06
DOI
https://doi.org/10.1073/pnas.2409345121
Citations
6
Primary Topic
Functional Brain Connectivity Studies
Type
article
Field-Weighted Citation Impact
2.06

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article

Secondary thalamic dysfunction underlies abnormal large-scale neural dynamics in chronic stroke

John D. Griffiths, Anthony R. McIntosh, Phillip R. Johnston, Jed A. Meltzer et al.
6 citations
Proceedings of the National Academy of Sciences
Functional Brain Connectivity Studies
2.06
article

Secondary thalamic dysfunction underlies abnormal large-scale neural dynamics in chronic stroke

John D. Griffiths, Anthony R. McIntosh, Phillip R. Johnston, Jed A. Meltzer, Leanne Rokos
article en
6 citations

Abstract

Stroke causes pronounced and widespread slowing of neural activity. Despite decades of work exploring these abnormal neural dynamics and their associated functional impairments, their causes remain largely unclear. To close this gap in understanding, we applied a neurophysiological corticothalamic circuit model to simulate magnetoencephalography (MEG) power spectra recorded from chronic stroke patients. Comparing model-estimated physiological parameters to those of controls, patients demonstrated significantly lower intrathalamic inhibition in the lesioned hemisphere, despite the absence of direct damage to the thalamus itself. We hypothesized that this disinhibition could instead be related to secondary degeneration of the thalamus, for which growing evidence exists in the literature. Further analyses confirmed that spectral slowing correlated significantly with overall secondary degeneration of the ipsilesional thalamus, encompassing decreased thalamic volume, altered tissue microstructure, and decreased blood flow. Crucially, this relationship was mediated by model-estimated thalamic disinhibition, suggesting a causal link between secondary thalamic degeneration and abnormal brain dynamics via thalamic disinhibition. Finally, thalamic degeneration was correlated significantly with poorer cognitive and language outcomes, but not lesion volume, reinforcing that thalamus damage may account for additional individual variability in poststroke disability. Overall, our findings indicate that the frequently observed poststroke slowing reflects a disruption of corticothalamic circuit dynamics due to secondary thalamic dysfunction, and highlights the thalamus as an important target for understanding and potentially treating poststroke brain dysfunction.

Proceedings of the National Academy of SciencesVol. 121(46)
Centre for Addiction and Mental Health (CA), Simon Fraser University (CA), University of Toronto (CA), Baycrest Hospital (CA)
Canada Research Chairs, University of Toronto, Krembil Foundation, Alliance de recherche numérique du Canada, Natural Sciences and Engineering Research Council of Canada
No poverty
Openalex Percentile: Top 13%
Functional Brain Connectivity Studies
2.06
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