AI Article Synopsis

  • Genetic generalized epilepsies (GGEs) involve generalized spike-wave discharges (GSWDs) in EEGs, with unclear origins but potential connections to the thalamus and default mode network (DMN).
  • Researchers studied 12 GGE patients using EEG-fMRI to identify brain networks involved in GSWD generation and their activation sequences.
  • Findings revealed activity changes in several brain areas, with the DMN playing a central role in regulating GSWDs, suggesting a link to consciousness downregulation and significant variability among patients' activation patterns.

Article Abstract

Objective: Genetic generalized epilepsies (GGEs) are characterized by generalized spike-wave discharges (GSWDs) in electroencephalography (EEG) recordings without underlying structural brain lesions. The origin of the epileptic activity remains unclear, although several studies have reported involvement of thalamus and default mode network (DMN). The aim of the current study was to investigate the networks involved in the generation and temporal evolution of GSWDs to elucidate the origin and propagation of the underlying generalized epileptic activity.

Methods: We examined 12 patients with GGE and GSWDs using EEG-functional magnetic resonance imaging (fMRI) and identified involved brain areas on the basis of a classical general linear model (GLM) analysis. The activation time courses of these areas were further investigated to reveal their temporal sequence of activations and deactivations. Dynamic causal modeling (DCM) was used to determine the generator of GSWDs in GGE.

Results: We observed activity changes in the thalamus, DMN, dorsal attention network (DAN), salience network (SN), basal ganglia, dorsolateral prefrontal cortex, and motor cortex with supplementary motor area, however, with a certain heterogeneity between patients. Investigation of the temporal sequence of activity changes showed deactivations in the DMN and DAN and activations in the SN and thalamus preceding the onset of GSWDs on EEG by several seconds. DCM analysis indicated that the DMN gates GSWDs in GGE.

Significance: The observed interplay between DMN, DAN, SN, and thalamus may indicate a downregulation of consciousness. The DMN seems to play a leading role as a driving force behind these changes. Overall, however, there were also clear differences in activation patterns between patients, reflecting a certain heterogeneity in this cohort of GGE patients.

Download full-text PDF

Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC6276776PMC
http://dx.doi.org/10.1002/epi4.12252DOI Listing

Publication Analysis

Top Keywords

spike-wave discharges
8
genetic generalized
8
temporal sequence
8
activity changes
8
dmn dan
8
gswds
6
dmn
6
unravelling brain
4
brain networks
4
networks driving
4

Similar Publications

In the present study, the effects of the acetylcholinesterase (AChE) enzyme inhibitor rivastigmine (RIVA) on spike-wave discharges (SWDs), memory impairment, anxiety-like behavior, and the transient receptor potential vanilloid 1 (TRPV1) gene expression were investigated in genetic absence epileptic Wistar Albino Glaxo/Rijswijk (WAG/Rij) rats. After tripolar electrodes were implanted on the WAG/Rij rats' skulls, single doses of 0.125, 0.

View Article and Find Full Text PDF

We presented a 7-year-old boy with refractory Epileptic Encephalopathy with Spike-and-Wave Activation in Sleep (EE-SWAS) successfully managed with a combination of propofol and midazolam. His seizures began at age 2, initially controlled by multiple antiseizure medications (ASMs) for almost three years. At age 5, seizures recurred with electroencephalography (EEG) showing electrical status epilepticus in sleep (ESES) and a spike-wave index (SWI) of 85 %.

View Article and Find Full Text PDF

Spike-wave-discharges (SWD) are the electrophysiological hallmark of absence epilepsy. SWD are generated in the thalamo-cortical network and a seizure onset zone was identified in the somatosensory cortex (S1). We have shown before that inhibition of the centromedian thalamic nucleus (CM) in GAERS rats resulted in a selective suppression of the spike component while rhythmic cortical 5-9 Hz oscillations remained present.

View Article and Find Full Text PDF

Dynamic prediction of nonlinear waveform transitions in a thalamo-cortical neural network under a square sensory control.

Cogn Neurodyn

December 2024

School of Aerospace Engineering, Xi'an Jiaotong University, Xi'an, 710049 Shaanxi People's Republic of China.

Waveform transitions have high correlation to spike wave discharges and polyspike wave discharges in seizure dynamics. This research adopts nonlinear dynamics to study the waveform transitions in a cerebral thalamo-coritcal neural network subjected to a square sensory control via discretization and mappings. The continuous non-smooth network outputs are discretized to establish implicit mapping chains or loops for stable and unstable waveform solutions.

View Article and Find Full Text PDF

Modelling the effect of allopregnanolone on the resolution of spike-wave discharges.

J Comput Neurosci

December 2024

Department of Applied Mathematics, and Centre for Theoretical Neuroscience, University of Waterloo, 200 University Avenue W, Waterloo, N2L 3G1, ON, Canada.

Article Synopsis
  • Childhood absence epilepsy (CAE) is a children's epilepsy that often resolves during adolescence, and this study investigates how the hormone allopregnanolone affects brain circuits involved in this disorder.
  • The research used a computational model of various brain neurons and found that allopregnanolone can help reduce spike-wave discharges linked to absence seizures, particularly in the thalamus.
  • The study suggests that the beneficial effects of allopregnanolone may vary among individuals based on their brain's connectivity and inhibition levels, paving the way for future research on remission in CAE patients.
View Article and Find Full Text PDF

Want AI Summaries of new PubMed Abstracts delivered to your In-box?

Enter search terms and have AI summaries delivered each week - change queries or unsubscribe any time!