| Literature DB >> 30511174 |
M Rubega1, M Carboni2,3, M Seeber2, D Pascucci4, S Tourbier5, G Toscano3,6, P Van Mierlo3,7, P Hagmann5, G Plomp4, S Vulliemoz3, C M Michel2,8.
Abstract
In the last decade, the use of high-density electrode arrays for EEG recordings combined with the improvements of source reconstruction algorithms has allowed the investigation of brain networks dynamics at a sub-second scale. One powerful tool for investigating large-scale functional brain networks with EEG is time-varying effective connectivity applied to source signals obtained from electric source imaging. Due to computational and interpretation limitations, the brain is usually parcelled into a limited number of regions of interests (ROIs) before computing EEG connectivity. One specific need and still open problem is how to represent the time- and frequency-content carried by hundreds of dipoles with diverging orientation in each ROI with one unique representative time-series. The main aim of this paper is to provide a method to compute a signal that explains most of the variability of the data contained in each ROI before computing, for instance, time-varying connectivity. As the representative time-series for a ROI, we propose to use the first singular vector computed by a singular-value decomposition of all dipoles belonging to the same ROI. We applied this method to two real datasets (visual evoked potentials and epileptic spikes) and evaluated the time-course and the frequency content of the obtained signals. For each ROI, both the time-course and the frequency content of the proposed method reflected the expected time-course and the scalp-EEG frequency content, representing most of the variability of the sources (~ 80%) and improving connectivity results in comparison to other procedures used so far. We also confirm these results in a simulated dataset with a known ground truth.Entities:
Keywords: Dipole orientation; EEG; Epilepsy; Source space activity; Visual evoked potentials
Mesh:
Year: 2018 PMID: 30511174 DOI: 10.1007/s10548-018-0691-2
Source DB: PubMed Journal: Brain Topogr ISSN: 0896-0267 Impact factor: 3.020