Table · dataset · 2026
Supplementary file 1_Tensor decomposition reveals discrete cortical reorganization under graded propofol anesthesia.docx
Listed in figshare and Loughborough Research Repository and GRANTS Data and UP Research Data Repository — shown once because both records carry DOI 10.3389/fnins.2026.1950745.s001
Background<p>Although propofol-induced anesthesia is known to suppress consciousness by promoting low-frequency frontal oscillations through thalamocortical circuits, a comprehensive understanding of its whole-brain coupling feature set remains elusive.
Description
Specifically, the global reorganization of nonlinear cross-frequency coupling remains poorly characterized due to analytical limitations.</p>Methods<p>We analyzed 64-channel EEG data from 17 participants across five states (awake and target propofol concentrations of 1, 2, 3, and 4 mcg/ml, defined as States 1 to 5).
After computing time-frequency representation (TFR) and bicoherence, Parallel Factor Analysis (PARAFAC) was used to extract unbiased spatio-spectral components from both linear and nonlinear measures.</p>Results<p>PARAFAC decomposition isolated distinct linear and nonlinear neurodynamic components driving the anesthetic transition. While linear spectral features and signal complexity transitioned in a gradual, monotonic manner.
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PARAFAC tensor decomposition of high-dimensional whole-brain bicoherence identified two robust, intrinsically decoupled nonlinear components with distinct spatial-spectral profiles. Model comparison demonstrated that frontal slow-wave self-coupling (Component 1) undergoes a discrete, stepwise state-space reconfiguration during loss of consciousness, whereas posterior alpha coupling (Component 2) exhibits a smooth, continuous decay with propofol titration.
Phase-space kinetic trajectories confirmed a highly directed transition at unconsciousness onset, followed by confined local oscillations during deep anesthesia.</p>Conclusion<p>This multi-dimensional decomposition framework captures discrete versus continuous neural dynamics, providing objective, state-sensitive biomarkers for precisely monitoring anesthesia depth and cortical state transitions.</p>
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Where it is published
- DOI doi.org/10.3389/fnins.2026.1950745.s001 ↗
DOI / persistent id · from figshare com
Catalogue records · 1
- OAI-PMH record api.figshare.com/v2/oai?verb=GetRecord&metadataPrefix=oai_dc&identifier=oai%3Af… ↗
metadata API · from figshare com
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Provenance · 4 source records, 35 field assertions
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|---|---|---|---|
| figshare | oai:figshare.com:article/34054644 | 12 d ago | JSON v1 |
| Loughborough Research Repository | oai:figshare.com:article/34054644 | 12 d ago | JSON v1 |
| GRANTS Data | oai:figshare.com:article/34054644 | 12 d ago | JSON v1 |
| UP Research Data Repository | oai:figshare.com:article/34054644 | 12 d ago | JSON v1 |
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