Abstract

Phase synchronization of neuronal oscillations in specific frequency bands coordinates anatomically distributed neuronal processing and communication. Typically, oscillations and synchronization take place concurrently in many distinct frequencies, which serve separate computational roles in cognitive functions. While within-frequency phase synchronization has been studied extensively, less is known about the mechanisms that govern neuronal processing distributed across frequencies and brain regions. Such integration of processing between frequencies could be achieved via cross-frequency coupling (CFC), either by phase–amplitude coupling (PAC) or by n:m-cross–frequency phase synchrony (CFS). So far, studies have mostly focused on local CFC in individual brain regions, whereas the presence and functional organization of CFC between brain areas have remained largely unknown. We posit that interareal CFC may be essential for large-scale coordination of neuronal activity and investigate here whether genuine CFC networks are present in human resting-state (RS) brain activity. To assess the functional organization of CFC networks, we identified brain-wide CFC networks at mesoscale resolution from stereoelectroencephalography (SEEG) and at macroscale resolution from source-reconstructed magnetoencephalography (MEG) data. We developed a novel, to our knowledge, graph-theoretical method to distinguish genuine CFC from spurious CFC that may arise from nonsinusoidal signals ubiquitous in neuronal activity. We show that genuine interareal CFC is present in human RS activity in both SEEG and MEG data. Both CFS and PAC networks coupled theta and alpha oscillations with higher frequencies in large-scale networks connecting anterior and posterior brain regions. CFS and PAC networks had distinct spectral patterns and opposing distribution of low- and high-frequency network hubs, implying that they constitute distinct CFC mechanisms. The strength of CFS networks was also predictive of cognitive performance in a separate neuropsychological assessment. In conclusion, these results provide evidence for interareal CFS and PAC being 2 distinct mechanisms for coupling oscillations across frequencies in large-scale brain networks.

Highlights

  • Human electrophysiological activity is characterized by neuronal oscillations, i.e., rhythmic excitability fluctuations in a wide range of frequencies, at least from 0.01 to over 150 Hz

  • In order to systematically address the possibility that observations of cross-frequency coupling (CFC) might be spuriously caused by filtering artifacts stemming from nonsinusoidal or non-zero–mean waveforms, we advance here a new, to our knowledge, method to control for spurious connections

  • Our method is based on the core assumption that any genuine CFC interaction takes place between 2 distinct processes, whereas spurious CFC is a property of a single process with signal components distributed to distinct frequency bands because of filter artifacts from nonsinusoidal or non-zero–mean signal properties

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Summary

Introduction

Human electrophysiological activity is characterized by neuronal oscillations, i.e., rhythmic excitability fluctuations in a wide range of frequencies, at least from 0.01 to over 150 Hz. Interareal synchronization of alpha (α, 7–14 Hz) and beta (β, 14–30 Hz) oscillations in humans and nonhuman primates, respectively, is thought to regulate top-down or feedback communication [14,15,16,17,18,19]. Both β and gamma-band (γ, 30–100 Hz) oscillations and synchronization have been associated with bottom-up sensory processing and representation of object-specific sensory information [15, 20,21,22], and β oscillations are associated with sensorimotor processing [23, 24]. It has been proposed that RSNs form the basis of task-state large-scale networks [8, 32]

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