| Literature DB >> 28194612 |
Ben Ridley1,2, Jonathan Wirsich3,4,5, Gaelle Bettus3,4,5, Roman Rodionov6,7, Teresa Murta6,8, Umair Chaudhary6,7, David Carmichael9, Rachel Thornton6,7, Serge Vulliemoz6,7,10, Andrew McEvoy6,7,11, Fabrice Wendling12,13, Fabrice Bartolomei5,14, Jean-Philippe Ranjeva3,4, Louis Lemieux6,7, Maxime Guye3,4.
Abstract
For the first time in research in humans, we used simultaneous icEEG-fMRI to examine the link between connectivity in haemodynamic signals during the resting-state (rs) and connectivity derived from electrophysiological activity in terms of the inter-modal connectivity correlation (IMCC). We quantified IMCC in nine patients with drug-resistant epilepsy (i) within brain networks in 'healthy' non-involved cortical zones (NIZ) and (ii) within brain networks involved in generating seizures and interictal spikes (IZ1) or solely spikes (IZ2). Functional connectivity (h 2 ) estimates for 10 min of resting-state data were obtained between each pair of electrodes within each clinical zone for both icEEG and fMRI. A sliding window approach allowed us to quantify the variability over time of h 2 (vh 2) as an indicator of connectivity dynamics. We observe significant positive IMCC for h 2 and vh 2, for multiple bands in the NIZ only, with the strongest effect in the lower icEEG frequencies. Similarly, intra-modal h 2 and vh 2 were found to be differently modified as a function of different epileptic processes: compared to NIZ, [Formula: see text] was higher in IZ1, but lower in IZ2, while [Formula: see text] showed the inverse pattern. This corroborates previous observations of inter-modal connectivity discrepancies in pathological cortices, while providing the first direct invasive and simultaneous comparison in humans. We also studied time-resolved FC variability multimodally for the first time, finding that IZ1 shows both elevated internal [Formula: see text] and less rich dynamical variability, suggesting that its chronic role in epileptogenesis may be linked to greater homogeneity in self-sustaining pathological oscillatory states.Entities:
Keywords: Connectivity; Dynamic connectivity; Focal epilepsy; Multimodal imaging; Resting-state
Mesh:
Year: 2017 PMID: 28194612 DOI: 10.1007/s10548-017-0551-5
Source DB: PubMed Journal: Brain Topogr ISSN: 0896-0267 Impact factor: 3.020