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Electro/Magneto‐EncephaloGraphy (EEG/MEG) source imaging (EMSI) of epileptic activity from deep generators is often challenging due to the higher sensitivity of EEG/MEG to superficial regions and to the spatial configuration of subcortical structures. We previously demonstrated the ability of the coherent Maximum Entropy on the Mean (cMEM) method to accurately localize the superficial cortical generators and their spatial extent. Here, we propose a depth‐weighted adaptation of cMEM to localize deep generators more accurately. These methods were evaluated using realistic MEG/high‐density EEG (HD‐EEG) simulations of epileptic activity and actual MEG/HD‐EEG recordings from patients with focal epilepsy. We incorporated depth‐weighting within the MEM framework to compensate for its preference for superficial generators. We also included a mesh of both hippocampi, as an additional deep structure in the source model. We generated 5400 realistic simulations of interictal epileptic discharges for MEG and HD‐EEG involving a wide range of spatial extents and signal‐to‐noise ratio (SNR) levels, before investigating EMSI on clinical HD‐EEG in 16 patients and MEG in 14 patients. Clinical interictal epileptic discharges were marked by visual inspection. We applied three EMSI methods: cMEM, depth‐weighted cMEM and depth‐weighted minimum norm estimate (MNE). The ground truth was defined as the true simulated generator or as a drawn region based on clinical information available for patients. For deep sources, depth‐weighted cMEM improved the localization when compared to cMEM and depth‐weighted MNE, whereas depth‐weighted cMEM did not deteriorate localization accuracy for superficial regions. For patients' data, we observed improvement in localization for deep sources, especially for the patients with mesial temporal epilepsy, for which cMEM failed to reconstruct the initial generator in the hippocampus. Depth weighting was more crucial for MEG (gradiometers) than for HD‐EEG. Similar findings were found when considering depth weighting for the wavelet extension of MEM. In conclusion, depth‐weighted cMEM improved the localization of deep sources without or with minimal deterioration of the localization of the superficial sources. This was demonstrated using extensive simulations with MEG and HD‐EEG and clinical MEG and HD‐EEG for epilepsy patients.
Electro/Magneto‐EncephaloGraphy (EEG/MEG) source imaging (EMSI) of epileptic activity from deep generators is often challenging due to the higher sensitivity of EEG/MEG to superficial regions and to the spatial configuration of subcortical structures. We previously demonstrated the ability of the coherent Maximum Entropy on the Mean (cMEM) method to accurately localize the superficial cortical generators and their spatial extent. Here, we propose a depth‐weighted adaptation of cMEM to localize deep generators more accurately. These methods were evaluated using realistic MEG/high‐density EEG (HD‐EEG) simulations of epileptic activity and actual MEG/HD‐EEG recordings from patients with focal epilepsy. We incorporated depth‐weighting within the MEM framework to compensate for its preference for superficial generators. We also included a mesh of both hippocampi, as an additional deep structure in the source model. We generated 5400 realistic simulations of interictal epileptic discharges for MEG and HD‐EEG involving a wide range of spatial extents and signal‐to‐noise ratio (SNR) levels, before investigating EMSI on clinical HD‐EEG in 16 patients and MEG in 14 patients. Clinical interictal epileptic discharges were marked by visual inspection. We applied three EMSI methods: cMEM, depth‐weighted cMEM and depth‐weighted minimum norm estimate (MNE). The ground truth was defined as the true simulated generator or as a drawn region based on clinical information available for patients. For deep sources, depth‐weighted cMEM improved the localization when compared to cMEM and depth‐weighted MNE, whereas depth‐weighted cMEM did not deteriorate localization accuracy for superficial regions. For patients' data, we observed improvement in localization for deep sources, especially for the patients with mesial temporal epilepsy, for which cMEM failed to reconstruct the initial generator in the hippocampus. Depth weighting was more crucial for MEG (gradiometers) than for HD‐EEG. Similar findings were found when considering depth weighting for the wavelet extension of MEM. In conclusion, depth‐weighted cMEM improved the localization of deep sources without or with minimal deterioration of the localization of the superficial sources. This was demonstrated using extensive simulations with MEG and HD‐EEG and clinical MEG and HD‐EEG for epilepsy patients.
Well-documented sleep datasets from healthy adults are important for sleep pattern analysis and comparison with a wide range of neuropsychiatric disorders. Currently, available sleep datasets from healthy adults are acquired using low-density arrays with a minimum of four electrodes in a typical sleep montage. The low spatial resolution is thus prohibitive for the analysis of the spatial structure of sleep. Here we introduce an open-access sleep dataset from 29 healthy adults (13 female, aged 32.17 ± 6.30 years) acquired at the Montreal Neurological Institute. The dataset includes overnight polysomnograms with high-density scalp electroencephalograms incorporating 83 electrodes, electrocardiogram, electromyogram, electrooculogram, and an average of electrode positions using manual co-registrations and sleep scoring annotations. Data characteristics and group-level analysis of sleep properties were assessed. The database can be accessed through (10.17605/OSF.IO/R26FH). This is the first high-density electroencephalogram open sleep database from healthy adults, allowing researchers to investigate sleep physiology at high spatial resolution. We expect that this database will serve as a valuable resource for studying sleep physiology and for benchmarking sleep pathology.
INTRODUCTIONEpilepsy is increasingly conceptualized as a network disorder, and advancing methods for its diagnosis and treatment requires characterizing both the epileptic generator and related networks. We combined multimodal magnetic resonance imaging (MRI) and high-density electroencephalography (HD-EEG) to interrogate alterations in cortical microstructure, morphology, and local function within and beyond spiking tissue in focal epilepsy.METHODSWe studied 25 patients with focal epilepsy (12F, mean ± SD age = 31.28 ± 9.30 years) and 55 age- and sex-matched healthy controls, subdivided into a group of 30 for imaging feature normalization (15F, 31.40 ± 8.74 years) and a group of 25 for replication (12F, 31.04 ± 5.65 years). The 3T MRI acquisition included T1-weighted, diffusion, quantitative T1 relaxometry, and resting-state functional imaging. Open-access MRI processing tools derived cortex-wide maps of morphology and microstructure (cortical thickness, mean diffusivity, and quantitative T1 relaxometry) and intrinsic local function and connectivity (timescales, connectivity distance, and node strength) for all participants. Multivariate approaches generated structural and functional alteration scores for each cortical location. Using HD-EEG, the predominant spike type was localized and we quantified MRI alterations within spike sources, as well as in proximal and connected networks.RESULTSRegions harboring spike sources showed increased structural MRI alterations (mean: 27.98%) compared to the rest of the brain (mean: 17.67%) in patients. Structural compromise extended to all regions with close functional coupling to spike sources (pairedt-tests; FDR-correctedp< 0.05), but not to anatomical neighbors of spike sources. This finding was replicated using average control functional, structural, and anatomical matrices instead of patient-specific matrices.CONCLUSIONSpiking regions contain more marked alterations in microstructure and morphology than the remaining cortex, which may help localize the epileptogenic zone non-invasively. There are nevertheless broader networks effects, which may relate to a cascading of structural changes to functionally connected cortices. These results underscore the utility of combining high-definition MRI and EEG approaches for characterizing epileptogenic tissue and assessing distributed network effects.
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