MEG sensor and source measures of visually induced gamma-band oscillations are highly reliable

High frequency brain oscillations are associated with numerous cognitive and behavioral processes. Non-invasive measurements using electro-/magnetoencephalography (EEG/MEG) have revealed that high frequency neural signals are heritable and manifest changes with age as well as in neuropsychiatric illnesses. Despite the extensive use of EEG/MEG-measured neural oscillations in basic and clinical research, studies demonstrating test–retest reliability of power and frequency measures of neural signals remain scarce. Here, we evaluated the test–retest reliability of visually induced gamma (30–100 Hz) oscillations derived from sensor and source signals acquired over two MEG sessions. The study required participants (N = 13) to detect the randomly occurring stimulus acceleration while viewing a moving concentric grating. Sensor and source MEG measures of gamma-band activity yielded comparably strong reliability (average intraclass correlation, ICC = 0.861). Peak stimulus-induced gamma frequency (53–72 Hz) yielded the highest measures of stability (ICCsensor = 0.940; ICCsource = 0.966) followed by spectral signal change (ICCsensor = 0.890; ICCsource = 0.893) and peak frequency bandwidth (ICCsensor = 0.856; ICCsource = 0.622). Furthermore, source-reconstruction significantly improved signal-to-noise for spectral amplitude of gamma activity compared to sensor estimates. Our assessments highlight that both sensor and source derived estimates of visually induced gamma-band oscillations from MEG signals are characterized by high test–retest reliability, with source derived oscillatory measures conferring an improvement in the stability of peak-frequency estimates. Importantly, our finding of high test–retest reliability supports the feasibility of pharma-MEG studies and longitudinal aging or clinical studies

High-frequency neural oscillations and visual processing deficits in schizophrenia

Visual information is fundamental to how we understand our environment, make predictions, and interact with others. Recent research has underscored the importance of visuo-perceptual dysfunctions for cognitive deficits and pathophysiological processes in schizophrenia. In the current paper, we review evidence for the relevance of high frequency (beta/gamma) oscillations towards visuo-perceptual dysfunctions in schizophrenia. In the first part of the paper, we examine the relationship between beta/gamma band oscillations and visual processing during normal brain functioning. We then summarize EEG/MEG-studies which demonstrate reduced amplitude and synchrony of high-frequency activity during visual stimulation in schizophrenia. In the final part of the paper, we identify neurobiological correlates as well as offer perspectives for future research to stimulate further inquiry into the role of high-frequency oscillations in visual processing impairments in the disorder

Magnetoencephalography as a tool in psychiatric research: current status and perspective

The application of neuroimaging to provide mechanistic insights into circuit dysfunctions in major psychiatric conditions and the development of biomarkers are core challenges in current psychiatric research. In this review, we propose that recent technological and analytic advances in Magnetoencephalography (MEG), a technique which allows the measurement of neuronal events directly and non-invasively with millisecond resolution, provides novel opportunities to address these fundamental questions. Because of its potential in delineating normal and abnormal brain dynamics, we propose that MEG provides a crucial tool to advance our understanding of pathophysiological mechanisms of major neuropsychiatric conditions, such as Schizophrenia, Autism Spectrum Disorders, and the dementias. In our paper, we summarize the mechanisms underlying the generation of MEG signals and the tools available to reconstruct generators and underlying networks using advanced source-reconstruction techniques. We then survey recent studies that have utilized MEG to examine aberrant rhythmic activity in neuropsychiatric disorders. This is followed by links with preclinical research, which have highlighted possible neurobiological mechanisms, such as disturbances in excitation/inhibition parameters, which could account for measured changes in neural oscillations. In the final section of the paper, challenges as well as novel methodological developments are discussed which could pave the way for a widespread application of MEG in translational research with the aim of developing biomarkers for early detection and diagnosis

Peak visual gamma frequency is modified across the healthy menstrual cycle

Fluctuations in gonadal hormones over the course of the menstrual cycle are known to cause functional brain changes and are thought to modulate changes in the balance of cortical excitation and inhibition. Animal research has shown this occurs primarily via the major metabolite of progesterone, allopregnanolone, and its action as a positive allosteric modulator of the GABAA receptor. Our study used EEG to record gamma oscillations induced in the visual cortex using stationary and moving gratings. Recordings took place during twenty females’ mid‐luteal phase when progesterone and estradiol are highest, and early follicular phase when progesterone and estradiol are lowest. Significantly higher (∼5 Hz) gamma frequency was recorded during the luteal compared to the follicular phase for both stimuli types. Using dynamic causal modeling, these changes were linked to stronger self‐inhibition of superficial pyramidal cells in the luteal compared to the follicular phase. In addition, the connection from inhibitory interneurons to deep pyramidal cells was found to be stronger in the follicular compared to the luteal phase. These findings show that complex functional changes in synaptic microcircuitry occur across the menstrual cycle and that menstrual cycle phase should be taken into consideration when including female participants in research into gamma‐band oscillations

Significant reductions in human visual gamma frequency by the GABA reuptake inhibitor tiagabine revealed by robust peak frequency estimation

The frequency of visual gamma oscillations is determined by both the neuronal excitation–inhibition balance and the time constants of GABAergic processes. The gamma peak frequency has been linked to sensory processing, cognitive function, cortical structure, and may have a genetic contribution. To disentangle the intricate relationship among these factors, accurate and reliable estimates of peak frequency are required. Here, a bootstrapping approach that provides estimates of peak frequency reliability, thereby increasing the robustness of the inferences made on this parameter was developed. The method using both simulated data and real data from two previous pharmacological MEG studies of visual gamma with alcohol and tiagabine was validated. In particular, the study by Muthukumaraswamy et al. [2013a] (Neuropsychopharmacology 38(6):1105–1112), in which GABAergic enhancement by tiagabine had previously demonstrated a null effect on visual gamma oscillations, contrasting with strong evidence from both animal models and very recent human studies was re-evaluated. After improved peak frequency estimation and additional exclusion of unreliably measured data, it was found that the GABA reuptake inhibitor tiagabine did produce, as predicted, a marked decrease in visual gamma oscillation frequency. This result demonstrates the potential impact of objective approaches to data quality control, and provides additional translational evidence for the mechanisms of GABAergic transmission generating gamma oscillations in humans

Significant reductions in human visual gamma frequency by the gaba reuptake inhibitor tiagabine revealed by robust peak frequency estimation

The frequency of visual gamma oscillations is determined by both the neuronal excitation-inhibition balance and the time constants of GABAergic processes. The gamma peak frequency has been linked to sensory processing, cognitive function, cortical structure, and may have a genetic contribution. To disentangle the intricate relationship among these factors, accurate and reliable estimates of peak frequency are required. Here, a bootstrapping approach that provides estimates of peak frequency reliability, thereby increasing the robustness of the inferences made on this parameter was developed. The method using both simulated data and real data from two previous pharmacological MEG studies of visual gamma with alcohol and tiagabine was validated. In particular, the study by Muthukumaraswamy et al. [] (Neuropsychopharmacology 38(6):1105-1112), in which GABAergic enhancement by tiagabine had previously demonstrated a null effect on visual gamma oscillations, contrasting with strong evidence from both animal models and very recent human studies was re-evaluated. After improved peak frequency estimation and additional exclusion of unreliably measured data, it was found that the GABA reuptake inhibitor tiagabine did produce, as predicted, a marked decrease in visual gamma oscillation frequency. This result demonstrates the potential impact of objective approaches to data quality control, and provides additional translational evidence for the mechanisms of GABAergic transmission generating gamma oscillations in humans. Hum Brain Mapp, 2016. © 2016 Wiley Periodicals, Inc

Stimulus-induced gamma power predicts the amplitude of the subsequent visual evoked response

The efficiency of neuronal information transfer in activated brain networks may affect behavioral performance. Gamma-band synchronization has been proposed to be a mechanism that facilitates neuronal processing of behaviorally relevant stimuli. In line with this, it has been shown that strong gamma-band activity in visual cortical areas leads to faster responses to a visual go cue. We investigated whether there are directly observable consequences of trial-by-trial fluctuations in non-invasively observed gamma-band activity on the neuronal response. Specifically, we hypothesized that the amplitude of the visual evoked response to a go cue can be predicted by gamma power in the visual system, in the window preceding the evoked response. Thirty-three human subjects (22 female) performed a visual speeded response task while their magnetoencephalogram (MEG) was recorded. The participants had to respond to a pattern reversal of a concentric moving grating. We estimated single trial stimulus-induced visual cortical gamma power, and correlated this with the estimated single trial amplitude of the most prominent event-related field (ERF) peak within the first 100 ms after the pattern reversal. In parieto-occipital cortical areas, the amplitude of the ERF correlated positively with gamma power, and correlated negatively with reaction times. No effects were observed for the alpha and beta frequency bands, despite clear stimulus onset induced modulation at those frequencies. These results support a mechanistic model, in which gamma-band synchronization enhances the neuronal gain to relevant visual input, thus leading to more efficient downstream processing and to faster responses

Transcranial modulation of brain oscillatory responses: A concurrent tDCS–MEG investigation

The physiological mechanisms underlying the effects of transcranial direct current stimulation (tDCS) are still largely unknown. To provide novel insight into the neurobiology of tDCS, stimulation was applied concurrently with Magnetoencephalography (MEG). This occurred while participants completed a visuomotor task before, during and after stimulation. Motor beta band (15–30 Hz) and visual gamma band (30–80 Hz) responses were localised using Synthetic Aperture Magnetometry (SAM). The resulting evoked and induced brain oscillatory responses were analysed. A significant reduction of average power was observed in the visual gamma band for anodal compared to sham stimulation. The magnitude of motor evoked responses was also demonstrated to be modulated by anodal tDCS. These results highlight that MEG can be used to draw inferences on the cortical mechanisms of DC stimulation

Test-retest reliability of the magnetic mismatch negativity response to sound duration and omission deviants

Mismatch negativity (MMN) is a neurophysiological measure of auditory novelty detection that could serve as a translational biomarker of psychiatric disorders, such as schizophrenia. However, the replicability of its magnetoencephalographic (MEG) counterpart (MMNm) has been insufficiently addressed. In the current study, test-retest reliability of the MMNm response to both duration and omission deviants was evaluated over two MEG sessions in 16 healthy adults. MMNm amplitudes and latencies were obtained at both sensor- and source-level using a cortically-constrained minimum-norm approach. Intraclass correlations (ICC) were derived to assess stability of MEG responses over time. In addition, signal-to-noise ratios (SNR) and within-subject statistics were obtained in order to determine MMNm detectability in individual participants. ICC revealed robust values at both sensor- and source-level for both duration and omission MMNm amplitudes (ICC = 0.81-0.90), in particular in the right hemisphere, while moderate to strong values were obtained for duration MMNm and omission MMNm peak latencies (ICC = 0.74-0.88). Duration MMNm was robustly identified in individual participants with high SNR, whereas omission MMNm responses were only observed in half of the participants. Our data indicate that MMNm to unexpected duration changes and omitted sounds are highly reproducible, providing support for the use of MEG-parameters in basic and clinical research

Assessing neural network dynamics under normal and altered states of consciousness with MEG : methodological challenges and proposed solutions for atypical power spectra

Cette dernière décennie a vu un certain nombre d'avancées significatives en mathématiques, en apprentissage computationnel et en traitement de signal, qui n'ont pas encore été pleinement exploitées en neurosciences. En particulier, l'évaluation de la connectivité dans les réseaux neuronaux peut grandement bénéficier de ces travaux. Nous proposons ici d'exploiter ces outils pour combler partiellement le fossé considérable qui existe encore entre la recherche connectomique à grande échelle (largement centrée sur des mesures indirectes de l'activité cérébrale comme l'Imagerie par résonance magnétique fonctionnelle (IRMf)) et les mesures physiologiques plus directes de l'activité cérébrale. Il est particulièrement important de combler ce fossé pour l'étude des propriétés physiologiques associées à divers états de conscience normaux et anormaux, notamment les troubles psychiatriques, le sommeil, l'anesthésie ou les états induits par les drogues. Les travaux récents sur l'induction d'états de conscience altérés par des agonistes non sélectifs de la sérotonine, tels que la psilocybine et le Diéthyllysergamide (LSD), en sont de bons exemples. Au cours des cinq dernières années, une résurgence rapide de la recherche sur la neurobiologie des tryptamines psychédéliques s'est produite, après une interruption d'un demi-siècle. Bien que ces substances présentent un grand potentiel pour éclairer des aspects jusqu'ici non interrogés du fonctionnement normal et anormal du cerveau, l'ampleur et le caractère inhabituel des changements qu'elles provoquent posent de sérieux défis aux chercheurs. La découverte de méthodes convaincantes et évolutives pour étudier ces données est d'une grande importance si nous voulons tirer parti de la fenêtre unique que ces substances atypiques offrent sur les aspects centraux de la conscience et des fonctions cérébrales anormales. Dans la présente thèse, nous résumons l'état actuel de la neuro-imagerie électrophysiologique en ce qui concerne l'étude des tryptamines psychédéliques, et nous démontrons un certain nombre de lacunes évidentes dans la recherche électrophysiologique actuelle sur les psychédéliques. Nous offrons également quelques modestes contributions méthodologiques au domaine. L'utilité de ces contributions est soutenue par quelques résultats empiriques intrigants, bien que préliminaires. Dans le premier chapitre, nous présentons l'histoire de la recherche neuroscientifique sur le LSD. Il a été rapporté que le LSD induit des déplacements de pics dans les spectres de puissance, en même temps que des diminutions de l'amplitude des pics. Le fait que ces effets soient liés entre eux et que la plupart des recherches menées jusqu'à présent n'aient pas cherché à les distinguer est uniformément négligé dans la littérature, ce qui, selon nous, peut conduire à de fausses interprétations. Le chapitre 2 examine certains des avantages plausibles ainsi que les obstacles sérieux à la recherche sur la connectivité du cerveau entier par magnétoencéphalographie (MEG), et propose plusieurs stratégies pour surmonter ces limites méthodologiques. Celles-ci comprennent des stratégies d'imagerie de source convaincantes, des développements nouveaux et récents dans la décomposition spectrale, des mesures de connectivité insensibles à la conduction volumique, et des implémentations évolutives de métriques de couplage interfréquence bien établies. Nous montrons que ces techniques peuvent être étendues à une grille corticale et sous-corticale de plus haute résolution que celle qui existe actuellement. Nous discutons également d'une mise en œuvre allégée de statistiques non paramétriques adaptées à ces données. Le troisième chapitre a pour but de démontrer l'efficacité de ces procédures, en montrant les résultats empiriques d'une étude de la connectivité du cerveau entier sous LSD par MEG. Le quatrième et dernier chapitre discute de ces résultats, ainsi que des précautions nécessaires et des orientations futures prometteuses pour ce type de recherche. Il propose des approches computationnelles supplémentaires qui pourraient étendre la portée de ces recherches et, plus généralement, de l'électrophysiologie du cerveau entier. Dans l'ensemble, le cadre méthodologique proposé dans ce travail surmonte les limitations endémiques précédentes, non seulement dans la recherche sur les psychédéliques, mais aussi dans la recherche électrophysiologique en général, et jette une lumière nouvelle sur sur les mécanismes centraux qui sous-tendent ces états de conscience anormaux, ainsi que sur les importantes précautions à prendre dans la recherche électrophysiologique.The past decade has seen a number of significant advances in mathematics, computational learning, and signal processing, which have yet to be deployed in neuroscience. In particular the assessment of connectivity in neural networks has much to gain from this work. Here we propose these tools be leveraged to partially bridge the considerable gap that still exists between large-scale connectomics research (largely centered around indirect measures of brain activity such as fMRI), and more direct, physiological measures of brain activity. Bridging this gap is especially important to the study of physiological properties associated with various normal and abnormal states of consciousness including Psychiatric conditions, sleep, anaesthesia or drug-induced states. Exemplary of such research, is recent work surrounding the induction of altered states of consciousness by non-selective serotonin agonists such as Psilocybin and LSD. During the past five years, a rapid resurgence of research into the neurobiology of Psychedelic tryptamines has transpired, following a half-century hiatus. While these substances hold great potential to illuminate hitherto uninterrogated aspects of normal and abnormal brain function, the scope and unusual character of the changes they illicit pose serious challenges to researchers. Uncovering cogent and scalable methods for investigating such data is a matter of great importance if we are to leverage the unique window such atypical substances provide into central aspects of consciousness and abnormal brain function. In the present thesis, we summarize the current state of electrophysiological neuroimaging as it pertains to the study of Psychedelic tryptamines, and demonstrate a number of clear shortcomings in current electrophysiological research on Psychedelics. We also offer some modest methodological contributions to the field. The utility of these contributions is supported by some intriguing, albeit preliminary, empirical findings. In the first chapter, we present the history of neuroscientific research on LSD. LSD has been reported to induce peak shifts in power spectra, alongside decreases in peak amplitude. The fact that these effects are inter-related and most research so far has not sought to disambiguate them is uniformly overlooked in the literature, which we believe may lead to false interpretations. Chapter Two discusses some of the plausible advantages as well as serious barriers to whole-brain connectivity research in MEG, proposing several strategies to overcome these methodological limitations. These include cogent source imaging strategies, novel and recent developments in spectral decomposition, connectivity measures insensitive to volume conduction, and scalable implementations of well-established cross-frequency coupling metrics. We show that these techniques can be extended to a higher resolution cortical and subcortical grid than previously shown. We also discuss a lightweight implementation of non-parametric statistics suitable to such data. Chapter Three serves to demonstrate the efficacy of these procedures, showing empirical results from a whole-brain study of connectivity under LSD in MEG. The fourth and final chapter discusses these results, as well as necessary precautions and promising future directions for this kind of research. It proposes additional computational approaches that might extend the scope of such research and whole-brain electrophysiology more generally. Taken together, the methodological framework proposed in this work overcomes previous limitations endemic not only in Psychedelics research, but electrophysiological research broadly, and sheds new light on central mechanisms underlying these abnormal states of consciousness, as well as important precautions in electrophysiological research