Differences in MEG and EEG power-law scaling explained by a coupling between spatial coherence and frequency: a simulation study

International audienceElectrophysiological signals (electroencephalography, EEG, and magnetoencephalography , MEG), as many natural processes, exhibit scale-invariance properties resulting in a power-law (1/f) spectrum. Interestingly, EEG and MEG differ in their slopes, which could be explained by several mechanisms, including non-resistive properties of tissues. Our goal in the present study is to estimate the impact of space/frequency structure of source signals as a putative mechanism to explain spectral scaling properties of neuroimaging signals. We performed simulations based on the summed contribution of cortical patches with different sizes (ranging from 0.4 to 104.2 cm 2). Small patches were attributed signals of high frequencies, whereas large patches were associated with signals of low frequencies, on a logarithmic scale. The tested parameters included i) the space/frequency structure (range of patch sizes and frequencies) and ii) the amplitude factor c parametrizing the spatial scale ratios. We found that the space/frequency structure may cause differences between EEG and MEG scale-free spectra that are compatible with real data findings reported in previous studies. We also found that below a certain spatial scale, there were no more differences between EEG and MEG, suggesting a limit for the resolution of both methods. Our work provides an explanation of experimental findings. This does not rule out other mechanisms for differences between EEG and MEG, but suggests an important role of spatio-temporal structure of neural dynamics. This can help the analysis and interpretation of power-law measures in EEG and MEG, and we believe our results can also impact computational modeling of brain dynamics, where different local connectivity structures could be used at different frequencies

Design of MRI Structured Spiking Neural Networks and Learning Algorithms for Personalized Modelling, Analysis, and Prediction of EEG Signals

Abstract This paper proposes a novel method and algorithms for the design of MRI structured personalized 3D spiking neural network models (MRI-SNN) for a better analysis, modeling, and prediction of EEG signals. It proposes a novel gradient-descent learning algorithm integrated with a spike-time-dependent-plasticity algorithm. The models capture informative personal patterns of interaction between EEG channels, contrary to single EEG signal modeling methods or to spike-based approaches which do not use personal MRI data to pre-structure a model. The proposed models can not only learn and model accurately measured EEG data, but they can also predict signals at 3D model locations that correspond to non-monitored brain areas, e.g. other EEG channels, from where data has not been collected. This is the first study in this respect. As an illustration of the method, personalized MRI-SNN models are created and tested on EEG data from two subjects. The models result in better prediction accuracy and a better understanding of the personalized EEG signals than traditional methods due to the MRI and EEG information integration. The models are interpretable and facilitate a better understanding of related brain processes. This approach can be applied for personalized modeling, analysis, and prediction of EEG signals across brain studies such as the study and prediction of epilepsy, peri-perceptual brain activities, brain-computer interfaces, and others

Variable Anisotropic Brain Electrical Conductivities in Epileptogenic Foci

Source localization models assume brain electrical conductivities are isotropic at about 0.33 S/m. These assumptions have not been confirmed ex vivo in humans. This study determined bidirectional electrical conductivities from pediatric epilepsy surgery patients. Electrical conductivities perpendicular and parallel to the pial surface of neocortex and subcortical white matter (n = 15) were measured using the 4-electrode technique and compared with clinical variables. Mean (±SD) electrical conductivities were 0.10 ± 0.01 S/m, and varied by 243% from patient to patient. Perpendicular and parallel conductivities differed by 45%, and the larger values were perpendicular to the pial surface in 47% and parallel in 40% of patients. A perpendicular principal axis was associated with normal, while isotropy and parallel principal axes were linked with epileptogenic lesions by MRI. Electrical conductivities were decreased in patients with cortical dysplasia compared with non-dysplasia etiologies. The electrical conductivity values of freshly excised human brain tissues were approximately 30% of assumed values, varied by over 200% from patient to patient, and had erratic anisotropic and isotropic shapes if the MRI showed a lesion. Understanding brain electrical conductivity and ways to non-invasively measure them are probably necessary to enhance the ability to localize EEG sources from epilepsy surgery patients

Interictal Functional Connectivity of Human Epileptic Networks Assessed by Intracerebral EEG and BOLD Signal Fluctuations

In this study, we aimed to demonstrate whether spontaneous fluctuations in the blood oxygen level dependent (BOLD) signal derived from resting state functional magnetic resonance imaging (fMRI) reflect spontaneous neuronal activity in pathological brain regions as well as in regions spared by epileptiform discharges. This is a crucial issue as coherent fluctuations of fMRI signals between remote brain areas are now widely used to define functional connectivity in physiology and in pathophysiology. We quantified functional connectivity using non-linear measures of cross-correlation between signals obtained from intracerebral EEG (iEEG) and resting-state functional MRI (fMRI) in 5 patients suffering from intractable temporal lobe epilepsy (TLE). Functional connectivity was quantified with both modalities in areas exhibiting different electrophysiological states (epileptic and non affected regions) during the interictal period. Functional connectivity as measured from the iEEG signal was higher in regions affected by electrical epileptiform abnormalities relative to non-affected areas, whereas an opposite pattern was found for functional connectivity measured from the BOLD signal. Significant negative correlations were found between the functional connectivities of iEEG and BOLD signal when considering all pairs of signals (theta, alpha, beta and broadband) and when considering pairs of signals in regions spared by epileptiform discharges (in broadband signal). This suggests differential effects of epileptic phenomena on electrophysiological and hemodynamic signals and/or an alteration of the neurovascular coupling secondary to pathological plasticity in TLE even in regions spared by epileptiform discharges. In addition, indices of directionality calculated from both modalities were consistent showing that the epileptogenic regions exert a significant influence onto the non epileptic areas during the interictal period. This study shows that functional connectivity measured by iEEG and BOLD signals give complementary but sometimes inconsistent information in TLE

AnyWave: A cross-platform and modular software for visualizing and processing electrophysiological signals

International audienceBACKGROUND: The importance of digital signal processing in clinical neurophysiology is growing steadily, involving clinical researchers and methodologists. There is a need for crossing the gap between these communities by providing efficient delivery of newly designed algorithms to end users. We have developed such a tool which both visualizes and processes data and, additionally, acts as a software development platform.NEW METHOD: AnyWave was designed to run on all common operating systems. It provides access to a variety of data formats and it employs high fidelity visualization techniques. It also allows using external tools as plug-ins, which can be developed in languages including C++, MATLAB and Python. RESULTS In the current version, plug-ins allow computation of connectivity graphs (non-linear correlation h2) and time-frequency representation (Morlet wavelets). The software is freely available under the LGPL3 license.COMPARISON WITH EXISTING METHODS: AnyWave is designed as an open, highly extensible solution, with an architecture that permits rapid delivery of new techniques to end users.CONCLUSIONS: We have developed AnyWave software as an efficient neurophysiological data visualizer able to integrate state of the art techniques. AnyWave offers an interface well suited to the needs of clinical research and an architecture designed for integrating new tools. We expect this software to strengthen the collaboration between clinical neurophysiologists and researchers in biomedical engineering and signal processing

A Mesoscopic Biophysical Model for Multimodal Brain Activity Data.

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Personalized multichannel transcranial direct current electrical stimulation guided by SEEG in drug resistant focal epilepsies

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Personalized multichannel transcranial direct current electrical stimulation guided by SEEG in drug resistant focal epilepsies

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Personalized multichannel transcranial direct current electrical stimulation guided by SEEG in drug resistant focal epilepsies

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