IBRO WORKSHOP

29-30 January, 2020 - Szeged, Hungary

 
 

Abstract details

INTERICTAL EPILEPTIC DISCHARGES ASSOCIATED WITH SLEEP SPINDLES IN THE ANTERIOR AND MEDIODORSAL THALAMUS

01/29/2020

Orsolya Szalárdy12, Péter Simor13, Péter Przemyslaw Ujma14, Zsófia Jordán4, Csaba Borbély4, László Halász4, Loránd Erőss4, László Entz4, Péter Halász4, Dániel Fabó4, Róbert Bódizs14

1 Institute of Behavioural Sciences, Faculty of Medicine, Semmelweis University, Budapest

2 Institute of Cognitive Neuroscience and Psychology, RCNS, Budapest

3 Eötvös Loránd University, Faculty of Education and Psychology, Budapest

4 National Institute of Clinical Neurosciences, Budapest

Sleep spindles are major oscillatory components of Non-Rapid Eye Movement (NREM) sleep, reflecting hyperpolarization-rebound sequences of thalamocortical neurons, the inhibition of which is caused by the NREM-dependent activation of GABAergic neurons in the reticular thalamic nucleus. Reports suggest a link between sleep spindles and several forms of interictal epileptic discharges (IEDs) which are considered as expressions of pathological off-line neural plasticity in the central nervous system. Here we investigated the relationship between sleep spindles and IEDs in the anterior and mediodorsal nuclei of the thalamus (ANT and MD) of epilepsy patients. Whole-night scalp EEG, and LFP from the ANT MD were recorded from 15 epilepsy patients undergoing Deep Brain Stimulation protocol. ANT and MD slow and fast spindles have been detected using the Individual Adjustment Method (IAM). A subgroup of thalamic, but not scalp spindles was associated with prominent high frequency activity (>30 Hz) in the time-frequency spectra reflecting visually verifiable IED-like waveforms. IED-associated spindles were longer irrespective of frequency (slow or fast). Furthermore, IEDs were more frequently coupled with spindles than with non-spindle NREM segments. The relationship between neuropsychological data and IED-associated spindles was not straightforward. Our findings indicate the involvement of the human thalamus in sleep spindle-related IEDs.