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Novel Noninvasive Identification of Patient-specific Epileptic Networks in Focal Epilepsies: Linking Single-photon Emission Computed Tomography Perfusion During Seizures with Resting-state Magnetoencephalography Dynamics

Overview
Journal Hum Brain Mapp
Publisher Wiley
Specialty Neurology
Date 2022 Dec 8
PMID 36480260
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Abstract

Single-photon emission computed tomography (SPECT) during seizures and magnetoencephalography (MEG) during the interictal state are noninvasive modalities employed in the localization of the epileptogenic zone in patients with drug-resistant focal epilepsy (DRFE). The present study aims to investigate whether there exists a preferentially high MEG functional connectivity (FC) among those regions of the brain that exhibit hyperperfusion or hypoperfusion during seizures. We studied MEG and SPECT data in 30 consecutive DRFE patients who had resective epilepsy surgery. We parcellated each ictal perfusion map into 200 regions of interest (ROIs) and generated ROI time series using source modeling of MEG data. FC between ROIs was quantified using coherence and phase-locking value. We defined a generalized linear model to relate the connectivity of each ROI, ictal perfusion z score, and distance between ROIs. We compared the coefficients relating perfusion z score to FC of each ROI and estimated the connectivity within and between resected and unresected ROIs. We found that perfusion z scores were strongly correlated with the FC of hyper-, and separately, hypoperfused ROIs across patients. High interictal connectivity was observed between hyperperfused brain regions inside and outside the resected area. High connectivity was also observed between regions of ictal hypoperfusion. Importantly, the ictally hypoperfused regions had a low interictal connectivity to regions that became hyperperfused during seizures. We conclude that brain regions exhibiting hyperperfusion during seizures highlight a preferentially connected interictal network, whereas regions of ictal hypoperfusion highlight a separate, discrete and interconnected, interictal network.

Citing Articles

The Role of Neuroinflammation and Network Anomalies in Drug-Resistant Epilepsy.

Shi J, Xie J, Li Z, He X, Wei P, Sander J Neurosci Bull. 2025; .

PMID: 39992353 DOI: 10.1007/s12264-025-01348-w.


Novel noninvasive identification of patient-specific epileptic networks in focal epilepsies: Linking single-photon emission computed tomography perfusion during seizures with resting-state magnetoencephalography dynamics.

Krishnan B, Tousseyn S, Wang Z, Murakami H, Wu G, Burgess R Hum Brain Mapp. 2022; 44(4):1695-1710.

PMID: 36480260 PMC: 9921232. DOI: 10.1002/hbm.26168.

References
1.
Shin W, Bong Hong S, Tae W, Kim S . Ictal hyperperfusion patterns according to the progression of temporal lobe seizures. Neurology. 2002; 58(3):373-80. DOI: 10.1212/wnl.58.3.373. View

2.
Bartolomei F, Wendling F, Vignal J, Kochen S, Bellanger J, Badier J . Seizures of temporal lobe epilepsy: identification of subtypes by coherence analysis using stereo-electro-encephalography. Clin Neurophysiol. 1999; 110(10):1741-54. DOI: 10.1016/s1388-2457(99)00107-8. View

3.
Dale A, Fischl B, Sereno M . Cortical surface-based analysis. I. Segmentation and surface reconstruction. Neuroimage. 1999; 9(2):179-94. DOI: 10.1006/nimg.1998.0395. View

4.
Krishnan B, Tousseyn S, Nayak C, Aung T, Kheder A, Wang Z . Neurovascular networks in epilepsy: Correlating ictal blood perfusion with intracranial electrophysiology. Neuroimage. 2021; 231:117838. DOI: 10.1016/j.neuroimage.2021.117838. View

5.
Tousseyn S, Krishnan B, Wang Z, Wongwiangjunt S, Nayak C, Mosher J . Connectivity in ictal single photon emission computed tomography perfusion: a cortico-cortical evoked potential study. Brain. 2017; 140(7):1872-1884. PMC: 6915825. DOI: 10.1093/brain/awx123. View