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Multifractal formalism introduces an invaluable framework for the investigation of nonlinear, scale-invariant features across multiple time scales in non-stationary time series data.In this context, we sought to explore multifractal features defining spatiotemporal correlations in seizure activity, by applying multifractal detrended fluctuation analysis (MFDFA) to stereoelectroencephalography (sEEG) recordings from five patients with refractory, focal temporal epilepsy, who underwent subsequent surgical removal of the temporal lobe and achieved seizure freedom.To the best of our knowledge, we are the first to report evidence for a multifractal architecture underscoring sEEG-recorded epileptiform signals, suggesting a fundamental propensity for scale-invariance in electrophysiological human brain recordings. Importantly, dynamical MFDFA-derived features captured altered spatiotemporal trends through the pre-ictal, ictal and post-ictal states, and also across anatomical brain regions. Larger fluctuations (deviations) in these metrics were observed to varying extents across resected temporal lobe structures, as compared to more constrained dynamics in non-resected networks.MFDFA-derived metrics were statistically analyzed and found to capture unique features from the sEEG data, with temporal variations across anatomical brain networks offering a potentially useful tool for the visualization, quantification and interpretation of network involvement in the onset and evolution of seizure activity. These results underscore the importance of investigating high-complexity dynamics in intracranial sEEG recordings and their potential utility towards surgical decision-making in patients with medically intractable epilepsy.
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http://dx.doi.org/10.1088/1741-2552/adf66a | DOI Listing |
J Neurophysiol
September 2025
Department of Neurosurgery, University of Utah School of Medicine, Salt Lake City, UT, USA.
Although glutamatergic and GABAergic synapses are important in seizure generation, the contribution of non-synaptic ionic and electrical mechanisms to synchronization of seizure-prone hippocampal neurons remains unclear. Here, we developed a physiologically relevant model to study these mechanisms by inducing prolonged seizure-like discharges (SLDs) in hippocampal slices from male rats through modest, sustained ionic manipulations. Specifically, we reduced extracellular calcium to 0.
View Article and Find Full Text PDFJCI Insight
September 2025
Department of Physiology and Neurobiology, University of Connecticut, Storrs, United States of America.
Dravet syndrome (DS) is an early-onset epilepsy caused by loss of function mutations in the SCN1A gene, which encodes Nav1.1 channels that preferentially regulate activity of inhibitory neurons early in development. DS is associated with a high incidence of sudden unexpected death in epilepsy (SUDEP) by a mechanism that may involve respiratory failure.
View Article and Find Full Text PDFAdv Mater
September 2025
State Key Laboratory of Crystal Materials, Shandong University, Jinan, Shandong, 250100, P. R. China.
Electrical deep brain stimulation is effective for epilepsy suppression, but will lead to neural tissue damage and inflammation due to implantation of electrodes and a pulse generator. Transcranial magnetic and transcranial ultrasound stimulation cannot directly generate effective electrical signals in deep brain regions. Here, the use of piezoelectric nanoparticles is proposed as wireless nanostimulators for deep brain electrical stimulation and minimally invasive suppression of epilepsy.
View Article and Find Full Text PDFArq Neuropsiquiatr
September 2025
Pontifícia Universidade Católica de Campinas, Campinas SP, Brazil.
Symptoms in the postictal period are often neglected by professionals and patients/family members.To relate the characteristics of the postictal period with the clinical variables of adult patients with epilepsy.Prospectively, the clinical characteristics of the postictal period were related to the clinical variables and the scores on the Hospital Anxiety and Depression Scale (HADS) and Mini-Mental State Examination (MMSE) of 70 patients with epilepsy.
View Article and Find Full Text PDFJ Child Neurol
September 2025
Department of Neurology, Nationwide Children's Hospital, Columbus, OH, USA.
This case report describes the use of doxazosin (Cardura) as a treatment for a patient with an autosomal dominant , single-nucleotide R398Q pathogenic variant, which has not previously been described in the literature. The patient has gain-of-function pathogenic genetic variant. Because of the patient's continued seizure burden with the use of traditional antiseizure medications and failed invasive antiseizure interventions, an oocyte cell line with the specific genetic variant was created to test efficacy of various medications.
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