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Autonomic manifestations of epilepsy: emerging pathways to sudden death?

Authors :
Philippe Ryvlin
Rainer Surges
Roland D. Thijs
Source :
Nature Reviews Neurology, 17(12), 774-788. NATURE PORTFOLIO
Publication Year :
2021
Publisher :
Springer Science and Business Media LLC, 2021.

Abstract

Epileptic networks are intimately connected with the autonomic nervous system, as exemplified by a plethora of ictal (during a seizure) autonomic manifestations, including epigastric sensations, palpitations, goosebumps and syncope (fainting). Ictal autonomic changes might serve as diagnostic clues, provide targets for seizure detection and help us to understand the mechanisms that underlie sudden unexpected death in epilepsy (SUDEP). Autonomic alterations are generally more prominent in focal seizures originating from the temporal lobe, demonstrating the importance of limbic structures to the autonomic nervous system, and are particularly pronounced in focal-to-bilateral and generalized tonic–clonic seizures. The presence, type and severity of autonomic features are determined by the seizure onset zone, propagation pathways, lateralization and timing of the seizures, and the presence of interictal autonomic dysfunction. Evidence is mounting that not all autonomic manifestations are linked to SUDEP. In addition, experimental and clinical data emphasize the heterogeneity of SUDEP and its infrequent overlap with sudden cardiac death. Here, we review the spectrum and diagnostic value of the mostly benign and self-limiting autonomic manifestations of epilepsy. In particular, we focus on presentations that are likely to contribute to SUDEP and discuss how wearable devices might help to prevent SUDEP. The close connection between epileptic networks and the autonomic nervous system is illustrated by a range of autonomic manifestations during a seizure. This article reviews the spectrum and diagnostic value of these manifestations, focusing on presentations that could contribute to sudden unexpected death in epilepsy.

Details

ISSN :
17594766 and 17594758
Volume :
17
Database :
OpenAIRE
Journal :
Nature Reviews Neurology
Accession number :
edsair.doi.dedup.....507a0345ce9f6d6cd9084696d36d578c
Full Text :
https://doi.org/10.1038/s41582-021-00574-w