Spatial and temporal correlations in human cortex are inherently linked and predicted by functional hierarchy, vigilance state as well as antiepileptic drug load

PLoS Comput Biol. 2023 Mar 3;19(3):e1010919. doi: 10.1371/journal.pcbi.1010919. eCollection 2023 Mar.

Abstract

The ability of neural circuits to integrate information over time and across different cortical areas is believed an essential ingredient for information processing in the brain. Temporal and spatial correlations in cortex dynamics have independently been shown to capture these integration properties in task-dependent ways. A fundamental question remains if temporal and spatial integration properties are linked and what internal and external factors shape these correlations. Previous research on spatio-temporal correlations has been limited in duration and coverage, thus providing only an incomplete picture of their interdependence and variability. Here, we use long-term invasive EEG data to comprehensively map temporal and spatial correlations according to cortical topography, vigilance state and drug dependence over extended periods of time. We show that temporal and spatial correlations in cortical networks are intimately linked, decline under antiepileptic drug action, and break down during slow-wave sleep. Further, we report temporal correlations in human electrophysiology signals to increase with the functional hierarchy in cortex. Systematic investigation of a neural network model suggests that these dynamical features may arise when dynamics are poised near a critical point. Our results provide mechanistic and functional links between specific measurable changes in the network dynamics relevant for characterizing the brain's changing information processing capabilities.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Anticonvulsants* / pharmacology
  • Brain / physiology
  • Brain Mapping / methods
  • Humans
  • Magnetic Resonance Imaging / methods
  • Wakefulness*

Substances

  • Anticonvulsants

Grants and funding

PM and CM are funded by Charité — Universitätsmedizin Berlin. CM and PM are supported by NeuroCure Cluster of Excellence, funded by the Deutsche Forschungsgemeinschaft (DFG, German Research Foundation) under Germany´s Excellence Strategy EXC 2049-89829218. CM acknowledges support from a NARSAD Young Investigator Grant. The funders had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript.