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Jurkovičová, Lenka

https://orcid.org/0000-0001-5042-1119

Mayo Clinic

Masaryk University

Citations 2

Network hubs supporting memory encoding: Implications for cognitive preservation in epilepsy surgery
Matoušková, Barbora , Cimbálník, Jan , Pavel, Daniel, Kojan, Martin , Jurkovičová, L., Pail, Martin , Brázdil, Milan , Kucewicz, Michał T. , Jurkovičová, Lenka , Daniel, Pavel , Roman, Robert , Jurkovicova, Lenka , Pail, Martin , Brazdil, Milan , Kucewicz, Michal , Klimes, Petr , Román, Róbert , Kucewicz, Michał , Klimeš, Petr

Epilepsia | December 22, 2025 | Volume: 67 | Issue: 2 | Pages: 606-619

10.1111/epi.18705 Get It

Abstract Objective Memory impairments are common in neurological disorders, especially drug‐resistant epilepsy, where cognitive deficits such as accelerated long‐term forgetting may occur before surgery due to interictal/ictal discharges, antiseizure medications, and disease progression. Postsurgical memory decline affects 40%–60% of patients. Understanding the neural mechanisms of memory encoding is essential for identifying critical network hubs and guiding surgical interventions that preserve cognitive function. Methods We analyzed intracranial electroencephalographic recordings from epilepsy patients ( n = 15) performing a verbal memory encoding task to identify key structures involved in successful memory formation. Functional connectivity was computed using multiple features across several frequency bands. Temporal dynamics of connectivity were examined to characterize pre‐encoding and encoding phases. Results The middle temporal gyrus (MTG) consistently emerged as a verbal memory hub across features and frequency bands. The inferior frontal gyrus (IFG) was identified as a beta‐band‐specific hub via phase synchrony. Temporal analyses revealed that MTG exhibited stable and widespread connectivity differences across all encoding phases, suggesting a role in pre‐encoding network priming. In contrast, IFG displayed a transient decrease in connectivity and spatial extent during early encoding, indicating a more focal and dynamic contribution. Significance These findings suggest that successful memory encoding relies on widespread, frequency‐specific connectivity patterns centered on MTG, complemented by transient, localized IFG activity. Identifying such hubs may inform surgical planning by highlighting regions critical for cognitive outcomes, ultimately supporting strategies to preserve memory in epilepsy surgery.
Coincident bursts of high frequency oscillations across the human cortex coordinate large-scale memory processing
Prathapagiri, S. , Galanina, Marina, Daniel, Paul , Kojan, M., Pail, Martin , Sluzewska-Niedzwiedz, M., Cimbálník, Jan , García‐Salinas, Jesús S. , Jurkovičová, Lenka , Daniel, Pavel, Kojan, Martin , Román, Róbert , Fortuna, Wojciech , Służewska‐Niedźwiedź, Monika , Tabakow, Paweł , Czyżewski, Andrzej , Brázdil, Milan , Kucewicz, Michał T.

No container title available | March 26, 2025 | Volume: No volume available | Issue: No issue available | Pages: No page available

10.1101/2025.03.24.644989 Get It

Abstract Oscillations in the high gamma and ripple frequency ranges are known to coordinate local hippocampal and neocortical neuronal assemblies during memory encoding and recall. Here, we explored spatiotemporal dynamics and the role of global coordination of these fast oscillatory discharges across the sensory and associational cortical areas in distinct phases of memory processing. Individual bursts of high frequency oscillations were detected in intracranial recordings from epilepsy patients remembering word lists for immediate free recall. We found constant coincident bursting across visual and higher order processing areas, peaking before recall and elevated during encoding of words. This global co-bursting was modulated by memory processing, engaged approximately half of the recorded electrode sites, and clustered into a sequence of multiple consecutive bursting discharges. Our results suggest a general role of global coincident high frequency oscillations in organizing large-scale information processing across the brain necessary especially, but not exclusively, for memory functions.