Functional connectivity of neural oscillations (oscillation-based FC) is thought to afford dynamic information exchange across task-relevant neural ensembles. Although oscillation-based FC is classically defined relative to a prestimulus baseline, giving rise to rapid, context-dependent changes in individual connections, studies of distributed spatial patterns show that oscillation-based FC is omnipresent, occurring even in the absence of explicit cognitive demands. Thus, the issue of whether oscillation-based FC is primarily shaped by cognitive state or is intrinsic in nature remains open. Accordingly, we sought to reconcile these observations by interrogating the ECoG recordings of 18 presurgical human patients (8 females) for state dependence of oscillation-based FC in five canonical frequency bands across an array of six task states. FC analysis of phase and amplitude coupling revealed a highly similar, largely state-invariant (i.e., intrinsic) spatial component across cognitive states. This spatial organization was shared across all frequency bands. Crucially, however, each band also exhibited temporally independent FC dynamics capable of supporting frequency-specific information exchange. In conclusion, the spatial organization of oscillation-based FC is largely stable over cognitive states (i.e., primarily intrinsic in nature) and shared across frequency bands. Together, our findings converge with previous observations of spatially invariant patterns of FC derived from extremely slow and aperiodic fluctuations in fMRI signals. Our observations indicate that "background" FC should be accounted for in conceptual frameworks of oscillation-based FC targeting task-related changes.
Functional connectivity (FC) of neural oscillations (~1-150Hz) is thought to facilitate neural information exchange across brain areas by forming malleable neural ensembles in the service of cognitive processes. However, neural oscillations and their FC are not restricted to certain cognitive demands and continuously unfold in all cognitive states. To what degree is the spatial organization of oscillation-based FC affected by cognitive state or governed by an intrinsic architecture? And what is the impact of oscillation frequency and FC mode (phase-versus amplitude coupling)? Using ECoG recordings of 18 presurgical patients, we quantified the state-dependency of oscillation-based FC in five canonical frequency bands and across an array of 6 task states. For both phase- and amplitude coupling, static FC analysis revealed a spatially largely state-invariant (i.e. intrinsic) component in all frequency bands. Further, the observed intrinsic FC pattern was spatially similar across all frequency bands. However, temporally independent FC dynamics in each frequency band allow for frequency-specific malleability in information exchange. In conclusion, the spatial organization of oscillation-based FC is largely stable over cognitive states, i.e. primarily intrinsic in nature, and shared across frequency bands. The state-invariance is in line with prior findings at the other temporal extreme of brain activity, the infraslow range (~<0.1Hz) observed in fMRI. Our observations have implications for conceptual frameworks of oscillation-based FC and the analysis of task-related FC changes.
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