Abnormal resting-state EEG phase dynamics distinguishes major depressive disorder and bipolar disorder.

Changes in EEG have been reported in both major depressive disorder (MDD) and bipolar disorder (BD). Specifically, power changes in EEG alpha and theta frequency bands during rest and task are known in both disorders. This leaves open whether there are changes in yet another component of the electrophysiological EEG signal, namely phase-related processes that may allow for distinguishing MDD and BD. For that purpose, we investigate EEG-based spontaneous phase in the resting state of MDD, BD and healthy controls. Our main findings show: (i) decreased spontaneous phase variability in frontal theta of both MDD and BD compared to HC; (ii) decreased spontaneous phase variability in central-parietal alpha in MDD compared to both BD and HC; (iii) increased delays or lags of alpha phase cycles in MDD (but not in BD), which (iv) correlate with the decreased phase variability in MDD. Together, we show similar (decreased frontal theta variability) and distinct (decreased central-parietal alpha variability with increased lags or delays) findings in the spontaneous phase dynamics of MDD and BD. This suggests potential relevance of theta and alpha phase dynamics in distinguishing MDD and BD in clinical differential-diagnosis.

Intrinsic neural timescales relate to the dynamics of infraslow neural waves.

The human brain is a highly dynamic organ that operates across a variety of timescales, the intrinsic neural timescales (INT). In addition to the INT, the neural waves featured by its phase-related processes including their cycles with peak/trough and rise/fall play a key role in shaping the brain's neural activity. However, the relationship between the brain's ongoing wave dynamics and INT remains yet unclear. In this study, we utilized functional magnetic resonance imaging (fMRI) rest and task data from the Human Connectome Project (HCP) to investigate the relationship of infraslow wave dynamics [as measured in terms of speed by changes in its peak frequency (PF)] with INT. Our findings reveal that: (i) the speed of phase dynamics (PF) is associated with distinct parts of the ongoing phase cycles, namely higher PF in peak/trough and lower PF in rise/fall; (ii) there exists a negative correlation between phase dynamics (PF) and INT such that slower PF relates to longer INT; (iii) exposure to a movie alters both PF and INT across the different phase cycles, yet their negative correlation remains intact. Collectively, our results demonstrate that INT relates to infraslow phase dynamics during both rest and task states.

Temporal imprecision and phase instability in schizophrenia resting state EEG.

Schizophrenia is characterized by temporal imprecision and irregularities on neuronal, psychological cognitive, and behavioral levels which are usually tested during task-related activity. This leaves open whether analogous temporal imprecision and irregularities can already be observed in the brain's spontaneous activity as measured during the resting state; this is the goal of our study. Building on recent task-related data, we, using EEG, aimed to investigate the temporal precision and regularity of phase coherence over time in healthy, schizophrenia, and bipolar disorder participants. To this end, we developed a novel methodology, nominal frequency phase stability (NFPS), that allows to measure stability over phase angles in selected frequencies. By applying sample entropy quantification to the time-series of the nominal frequency phase angle time series, we found increased irregularities in theta activity over a frontocentral electrode in schizophrenia but not in bipolar disorder. We therefore assume that temporal imprecision and irregularity already occur in the brain's spontaneous activity in schizophrenia.

Prolonged Intrinsic Neural Timescales Dissociate from Phase Coherence in Schizophrenia.

Input processing in the brain is mediated by phase synchronization and intrinsic neural timescales, both of which have been implicated in schizophrenia. Their relationship remains unclear, though. Recruiting a schizophrenia EEG sample from the B-SNIP consortium dataset (n = 134, 70 schizophrenia patients, 64 controls), we investigate phase synchronization, as measured by intertrial phase coherence (ITPC), and intrinsic neural timescales, as measured by the autocorrelation window (ACW) during both the rest and oddball-task states. The main goal of our paper was to investigate whether reported shifts from shorter to longer timescales are related to decreased ITPC. Our findings show (i) decreases in both theta and alpha ITPC in response to both standard and deviant tones; and (iii) a negative correlation of ITPC and ACW in healthy subjects while such correlation is no longer present in SCZ participants. Together, we demonstrate evidence of abnormally long intrinsic neural timescales (ACW) in resting-state EEG of schizophrenia as well as their dissociation from phase synchronization (ITPC). Our data suggest that, during input processing, the resting state's abnormally long intrinsic neural timescales tilt the balance of temporal segregation and integration towards the latter. That results in temporal imprecision with decreased phase synchronization in response to inputs. Our findings provide further evidence for a basic temporal disturbance in schizophrenia on the different timescales (longer ACW and shorter ITPC), which, in the future, might be able to explain common symptoms related to the temporal experience in schizophrenia, for example temporal fragmentation.