Ictal Bradycardia and Asystole in Sleep-Related Hypermotor Epilepsy: A Study of 200 Patients

: Ictal bradycardia (IB) and asystole (IA) represent a rare but potentially harmful feature of epileptic seizures. The aim of this study was to study IB/IA in patients with sleep-related hypermotor epilepsy (SHE). : We retrospectively included cases with video-EEG-confirmed SHE who attended our Inst...

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Veröffentlicht in:Journal of clinical medicine 2024-03, Vol.13 (6), p.1767
Hauptverfasser: Muccioli, Lorenzo, Bruschi, Giulia, Ferri, Lorenzo, Scarabello, Anna, Taruffi, Lisa, Di Vito, Lidia, Mostacci, Barbara, Provini, Federica, Calandra-Buonaura, Giovanna, Tinuper, Paolo, Licchetta, Laura, Bisulli, Francesca
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Sprache:eng
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Zusammenfassung:: Ictal bradycardia (IB) and asystole (IA) represent a rare but potentially harmful feature of epileptic seizures. The aim of this study was to study IB/IA in patients with sleep-related hypermotor epilepsy (SHE). : We retrospectively included cases with video-EEG-confirmed SHE who attended our Institute up to January 2021. We reviewed the ictal polysomnography recordings focusing on ECG and identified cases with IB (R-R interval ≥ 2 s or a ≥10% decrease of baseline heart rate) and IA (R-R interval ≥ 4 s). : We included 200 patients (123 males, 61.5%), with a mean age of 42 ± 16 years. Twenty patients (20%) had focal cortical dysplasia (FCD) on brain MRI. Eighteen (out of 104 tested, 17.3%) carried pathogenic variants (mTOR pathway, = 10, nAchR subunits, = 4, KCNT1, = 4). We identified IB/IA in four cases (2%): three had IA (mean 10 s) and one had IB. Three patients had FCD (left fronto-insular region, left amygdala, right mid-temporal gyrus) and two had pathogenic variants in ; both features were more prevalent in patients with IB/IA than those without ( = 0.003 and = 0.037, respectively). : We identified IB/IA in 2% of patients with SHE and showed that this subgroup more frequently had FCD on brain MRI and pathogenic variants in genes related to the mTOR pathway.
ISSN:2077-0383
2077-0383
DOI:10.3390/jcm13061767