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1.
Eur J Neurosci ; 57(8): 1317-1334, 2023 04.
Article in English | MEDLINE | ID: mdl-36878869

ABSTRACT

Binocular rivalry is an example of bistable visual perception extensively examined in neuroimaging. Magnetoencephalography can track brain responses to phasic visual stimulations of predetermined frequency and phase to advance our understanding of perceptual dominance and suppression in binocular rivalry. We used left and right eye stimuli that flickered at two tagging frequencies to track their respective oscillatory cortical evoked responses. We computed time-resolved measures of coherence to track brain responses phase locked with stimulus frequencies and with respect to the participants' indications of alternations of visual rivalry they experienced. We compared the brain maps obtained to those from a non-rivalrous control replay condition that used physically changing stimuli to mimic rivalry. We found stronger coherence within a posterior cortical network of visual areas during rivalry dominance compared with rivalry suppression and replay control. This network extended beyond the primary visual cortex to several retinotopic visual areas. Moreover, network coherence with dominant percepts in primary visual cortex peaked at least 50 ms prior to the suppressed percept nadir, consistent with the escape theory of alternations. Individual alternation rates were correlated with the rate of change in dominant evoked peaks, but not for the slope of response to suppressed percepts. Effective connectivity measures revealed that dominant (respectively, suppressed) percepts were expressed in dorsal (respectively ventral) streams. We thus demonstrate that binocular rivalry dominance and suppression engage distinct mechanisms and brain networks. These findings advance neural models of rivalry and may relate to more general aspects of selection and suppression in natural vision.


Subject(s)
Magnetoencephalography , Vision, Binocular , Humans , Vision, Binocular/physiology , Visual Perception/physiology , Brain , Brain Mapping , Photic Stimulation , Vision Disparity
2.
Brain Sci ; 12(1)2022 Jan 13.
Article in English | MEDLINE | ID: mdl-35053848

ABSTRACT

In this paper, we study the performance of a source montage corresponding to 29 brain regions reconstructed from whole-head magnetoencephalographic (MEG) recordings, with the aim of facilitating the review of MEG data containing epileptiform discharges. Test data were obtained by superposing simulated signals from 100-nAm dipolar sources to a resting state MEG recording from a healthy subject. Simulated sources were placed systematically to different cortical locations for defining the optimal regularization for the source montage reconstruction and for assessing the detectability of the source activity from the 29-channel MEG source montage. The signal-to-noise ratio (SNR), computed for each source from the sensor-level and source-montage signals, was used as the evaluation parameter. Without regularization, the SNR from the simulated sources was larger in the sensor-level signals than in the source montage reconstructions. Setting the regularization to 2% increased the source montage SNR to the same level as the sensor-level SNR, improving the detectability of the simulated events from the source montage reconstruction. Sources producing a SNR of at least 15 dB were visually detectable from the source-montage signals. Such sources are located closer than about 75 mm from the MEG sensors, in practice covering all areas in the grey matter. The 29-channel source montage creates more focal signals compared to the sensor space and can significantly shorten the detection time of epileptiform MEG discharges for focus localization.

3.
Cereb Cortex ; 32(7): 1379-1389, 2022 03 30.
Article in English | MEDLINE | ID: mdl-34496021

ABSTRACT

There is substantial evidence of age-related declines in anatomical connectivity during adulthood, with associated alterations in functional connectivity. But the relation of those functional alterations to the structural reductions is unclear. The complexities of both the structural and the functional connectomes make it difficult to determine such relationships. We pursue this question with methods, based on animal research, that specifically target the interhemispheric connections between the visual cortices. We collect t1- and diffusion-weighted imaging data from which we assess the integrity of the white matter interconnecting the bilateral visual cortices. Functional connectivity between the visual cortices is measured with electroencephalography during the presentation of drifting sinusoidal gratings that agree or conflict across hemifields. Our results show age-related reductions in the integrity of the white matter interconnecting the visual cortices, and age-related increases in the difference in functional interhemispheric lagged coherence between agreeing versus disagreeing visual stimuli. We show that integrity of the white matter in the splenium of the corpus callosum predicts the differences in lagged coherence for the agreeing versus disagreeing stimuli; and that this relationship is mediated by age. These results give new insight into the causal relationship between age and functional connectivity.


Subject(s)
Corpus Callosum , White Matter , Aging , Animals , Corpus Callosum/diagnostic imaging , Diffusion Magnetic Resonance Imaging , Electroencephalography , White Matter/diagnostic imaging
4.
PLoS One ; 14(7): e0218529, 2019.
Article in English | MEDLINE | ID: mdl-31295259

ABSTRACT

Binocular rivalry (BR) is a dynamic visual illusion that provides insight into the cortical mechanisms of visual awareness, stimulus selection, and object identification. When dissimilar binocular images cannot be fused, perception switches every few seconds between the left and right eye images. The speed at which individuals switch between alternatives is a stable, partially heritable trait. In order to isolate the monocular and binocular processes that determine the speed of rivalry, we presented stimuli tagged with a different flicker frequency in each eye and applied stimulus-phase locked MEG source imaging. We hypothesized that the strength of the evoked fundamental or intermodulation frequencies would vary when comparing Fast and Slow Switchers. Ten subjects reported perceptual alternations, with mean dominance durations between 1.2-4.0 sec. During BR, event-related monocular input in V1, and broadly in higher-tier ventral temporal cortex, waxed and waned with the periods of left or right eye dominance/suppression. In addition, we show that Slow Switchers produce greater evoked intermodulation frequency responses in a cortical network composed of V1, lateral occipital, posterior STS, retrosplenial & superior parietal cortices. Importantly, these dominance durations were not predictable from the brain responses to either of the fundamental tagging frequencies in isolation, nor from any responses to a pattern rivalry control condition, or a non-rivalrous control. The novel cortical network isolated, which overlaps with the default-mode network, may contain neurons that compute the level of endogenous monocular difference, and monitor accumulation of this conflict over extended periods of time. These findings are the first to relate the speed of rivalry across observers to the 'efficient coding' theory of computing binocular differences that may apply to binocular vision generally.


Subject(s)
Cerebral Cortex/physiology , Models, Neurological , Nerve Net/physiology , Vision, Binocular/physiology , Vision, Monocular/physiology , Adult , Female , Humans , Male , Photic Stimulation
5.
Front Neurosci ; 13: 284, 2019.
Article in English | MEDLINE | ID: mdl-31024228

ABSTRACT

We present a simple, reproducible analysis pipeline applied to resting-state magnetoencephalography (MEG) data from the Open MEG Archive (OMEGA). The data workflow was implemented with Brainstorm, which like OMEGA is free and openly accessible. The proposed pipeline produces group maps of ongoing brain activity decomposed in the typical frequency bands of electrophysiology. The procedure is presented as a technical proof of concept for streamlining a broader range and more sophisticated studies of resting-state electrophysiological data. It also features the recently introduced extension of the brain imaging data structure (BIDS) to MEG data, highlighting the scalability and generalizability of Brainstorm analytical pipelines to other, and potentially larger data volumes.

6.
Front Neurosci ; 13: 76, 2019.
Article in English | MEDLINE | ID: mdl-30804744

ABSTRACT

Brainstorm is a free, open-source Matlab and Java application for multimodal electrophysiology data analytics and source imaging [primarily MEG, EEG and depth recordings, and integration with MRI and functional near infrared spectroscopy (fNIRS)]. We also provide a free, platform-independent executable version to users without a commercial Matlab license. Brainstorm has a rich and intuitive graphical user interface, which facilitates learning and augments productivity for a wider range of neuroscience users with little or no knowledge of scientific coding and scripting. Yet, it can also be used as a powerful scripting tool for reproducible and shareable batch processing of (large) data volumes. This article describes these Brainstorm interactive and scripted features via illustration through the complete analysis of group data from 16 participants in a MEG vision study.

7.
Sci Data ; 5: 180110, 2018 06 19.
Article in English | MEDLINE | ID: mdl-29917016

ABSTRACT

We present a significant extension of the Brain Imaging Data Structure (BIDS) to support the specific aspects of magnetoencephalography (MEG) data. MEG measures brain activity with millisecond temporal resolution and unique source imaging capabilities. So far, BIDS was a solution to organise magnetic resonance imaging (MRI) data. The nature and acquisition parameters of MRI and MEG data are strongly dissimilar. Although there is no standard data format for MEG, we propose MEG-BIDS as a principled solution to store, organise, process and share the multidimensional data volumes produced by the modality. The standard also includes well-defined metadata, to facilitate future data harmonisation and sharing efforts. This responds to unmet needs from the multimodal neuroimaging community and paves the way to further integration of other techniques in electrophysiology. MEG-BIDS builds on MRI-BIDS, extending BIDS to a multimodal data structure. We feature several data-analytics software that have adopted MEG-BIDS, and a diverse sample of open MEG-BIDS data resources available to everyone.


Subject(s)
Brain , Magnetoencephalography , Neuroimaging , Brain/diagnostic imaging , Brain/physiology , Humans
8.
Neuroimage ; 124(Pt B): 1182-1187, 2016 Jan 01.
Article in English | MEDLINE | ID: mdl-25896932

ABSTRACT

In contrast with other imaging modalities, there is presently a scarcity of fully open resources in magnetoencephalography (MEG) available to the neuroimaging community. Here we present a collaborative effort led by the McConnell Brain Imaging Centre of the Montreal Neurological Institute, and the Université de Montréal to build and share a centralised repository to curate MEG data in raw and processed form for open dissemination. The Open MEG Archive (OMEGA, omega.bic.mni.mcgill.ca) is bound to become a continuously expanding repository of multimodal data with a primary focus on MEG, in addition to storing anatomical MRI volumes, demographic participant data and questionnaires, and other forms of electrophysiological data such as EEG. The OMEGA initiative offers both the technological framework for multi-site MEG data aggregation, and serves as one of the largest freely available resting-state and eventually task-related MEG datasets presently available.


Subject(s)
Databases, Factual , Information Dissemination , Magnetoencephalography , Electroencephalography , Humans , Magnetic Resonance Imaging , Neuroimaging
9.
Neuroimage ; 88: 54-60, 2014 03.
Article in English | MEDLINE | ID: mdl-24211817

ABSTRACT

Biofeedback and brain-computer interfacing using EEG has been receiving continuous and increasing interest. However, the limited spatial resolution of low-density scalp recordings is a roadblock to the unequivocal monitoring and targeting of neuroanatomical regions and physiological signaling. This latter aspect is pivotal to the actual efficiency of neurofeedback procedures, which are expected to engage the modulation of well-identified components of neural activity within and between predetermined brain regions. Our group has previously contributed to demonstrate the principles of real-time magnetoencephalography (MEG) source imaging. Here we show how the technique was further developed to provide healthy subjects with region-specific neurofeedback to modulate successfully predetermined components of their brain activity in targeted brain regions. Overall, our results positively indicate that neurofeedback based on time-resolved MEG imaging has the potential to become an innovative therapeutic approach in neurology and neuropsychiatry.


Subject(s)
Brain Waves/physiology , Cerebral Cortex/physiology , Feedback, Sensory/physiology , Functional Neuroimaging/methods , Magnetoencephalography/methods , Adult , Cerebral Cortex/diagnostic imaging , Female , Humans , Magnetic Resonance Imaging , Male
10.
Neurosci Lett ; 501(3): 173-8, 2011 Sep 01.
Article in English | MEDLINE | ID: mdl-21787839

ABSTRACT

Plannexin represents a NCAM-derived peptide mimicking trans-homophilic NCAM interaction, which proved to exert neuroprotective effects in vitro. The effect of plannexin was evaluated in a rat status epilepticus model. As expected, prolonged seizure activity resulted in a pronounced cell loss in hippocampal subregions. The comparison between the vehicle- and plannexin-treated animals with status epilepticus did not reveal neuroprotective effects of plannexin on mature neurons. However, treatment with plannexin partially prevented the reduction in the number of doublecortin-labeled neuronal progenitor cells, which was evident 48h following status epilepticus. In conclusion, the data might give first evidence that plannexin can protect immature neurons in vivo. Future studies are necessary to evaluate whether disease-modifying or preventive effects are observed in models of epileptogenesis.


Subject(s)
Molecular Mimicry/physiology , Nerve Degeneration/pathology , Neural Cell Adhesion Molecules/physiology , Oligopeptides/administration & dosage , Status Epilepticus/drug therapy , Status Epilepticus/pathology , Acute Disease , Animals , Cell Communication/drug effects , Cell Communication/physiology , Cell Differentiation/drug effects , Cell Differentiation/physiology , Disease Models, Animal , Doublecortin Protein , Female , Hippocampus/cytology , Hippocampus/drug effects , Ligands , Nerve Degeneration/drug therapy , Nerve Degeneration/etiology , Neural Cell Adhesion Molecules/administration & dosage , Neural Cell Adhesion Molecules/metabolism , Neuroprotective Agents/administration & dosage , Neuroprotective Agents/chemical synthesis , Neuroprotective Agents/metabolism , Oligopeptides/chemical synthesis , Oligopeptides/metabolism , Rats , Rats, Wistar , Status Epilepticus/complications
11.
Comput Intell Neurosci ; 2011: 327953, 2011.
Article in English | MEDLINE | ID: mdl-21687573

ABSTRACT

To date, the majority of studies using magnetoencephalography (MEG) rely on off-line analysis of the spatiotemporal properties of brain activity. Real-time MEG feedback could potentially benefit multiple areas of basic and clinical research: brain-machine interfaces, neurofeedback rehabilitation of stroke and spinal cord injury, and new adaptive paradigm designs, among others. We have developed a software interface to stream MEG signals in real time from the 306-channel Elekta Neuromag MEG system to an external workstation. The signals can be accessed with a minimal delay (≤45 ms) when data are sampled at 1000 Hz, which is sufficient for most real-time studies. We also show here that real-time source imaging is possible by demonstrating real-time monitoring and feedback of alpha-band power fluctuations over parieto-occipital and frontal areas. The interface is made available to the academic community as an open-source resource.


Subject(s)
Brain Mapping , Brain Waves/physiology , Brain/physiology , Magnetoencephalography , Software , Humans , Neurofeedback , Signal Processing, Computer-Assisted , Time Factors , User-Computer Interface
12.
IEEE Trans Biomed Eng ; 52(4): 593-8, 2005 Apr.
Article in English | MEDLINE | ID: mdl-15825861

ABSTRACT

For generations of electrocardiogram (ECG) analysis, the presence of premature ventricular beats (PVBs) has been characterized as a common event in the ECG without regard to the mechanism which has caused the PVB in the first place. At best, the coupling interval with the preceding sinus beat may be noted. This viewpoint persisted throughout the era of automated ECG analysis, as well as influencing the treatment of more life threatening events by PVB suppression strategies alone. This study proposed three hypotheses which would link the PVB to a specific mechanism or milieu. Each of these hypotheses requires significant signal processing of the continuously recorded high resolution ECG. Data are presented which demonstrate that abnormal intra-QRS potentials may be linked to a reentrant mechanism for the PVBs and that many patients have significant changes in these potentials in the sinus beats preceding the PVB. Changes in the characteristics of the repolarization as measured in the T/U wave period were also observed and could be linked to triggered activity mechanism for some PVBs. Finally, the role of subclinical ST segment changes also indicates that low grade ischemia may play a role in modulating either PVB mechanism. The data generated by this study suggest that a new view toward PVB mechanism as measured by ECG characteristics may warrant a more rational approach to renewed interest identifying the malignant PVBs and their eventual clinical management.


Subject(s)
Algorithms , Diagnosis, Computer-Assisted/methods , Electrocardiography, Ambulatory/methods , Heart Rate , Ventricular Premature Complexes/diagnosis , Ventricular Premature Complexes/physiopathology , Humans , Reproducibility of Results , Sensitivity and Specificity
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