Literature DB >> 34009846

Electrocorticography Analysis in Patients With Dual Neurostimulators Supports Desynchronization as a Mechanism of Action for Acute Vagal Nerve Stimulator Stimulation.

Lia D Ernst1, Paul J Steffan, Priya Srikanth, Jack Wiedrick, David C Spencer, Proleta Datta, Navya M Joseph, Magda Wernovsky, Danielle A Becker.   

Abstract

PURPOSE: Both vagal nerve stimulation (VNS) and responsive neurostimulation (RNS System) are treatment options for medically refractory focal epilepsy. The mechanism of action of both devices remains poorly understood. Limited prior evidence suggests that acute VNS stimulation may reduce epileptiform activity and cause EEG desynchronization on electrocorticography (ECoG). Our study aims to isolate effects of VNS on ECoG as recorded by RNS System in patients who have both devices, by comparing ECoG samples with and without acute VNS stimulation.
METHODS: Ten 60-second ECoGs each from 22 individuals at 3 epilepsy centers were obtained-5 ECoGs with VNS "off" and 5 ECoGs with VNS "on." Electrocorticograps containing seizures or loss of telemetry connection artifact were excluded from analysis (total of 169 ECoGs were included). Electrocorticographs were analyzed for differences in spectral content by generating average spectrograms for "on" and "off" states and using a linear mixed-effects model to isolate effects of VNS stimulation.
RESULTS: Acute VNS stimulation reduced average power in the theta band by 4.9%, beta band by 3.8%, and alpha band by 2.5%. The reduction in theta power reached statistical significance with a P value of <0.05.
CONCLUSIONS: Our results provide evidence that acute VNS stimulation results in desynchronization of specific frequency bands (salient decrease in theta and beta bands, smaller decrease in alpha band) in ECoGs recorded by the RNS device in patients with dual (VNS and RNS) neurostimulators. This finding offers support for desynchronization as a theorized mechanism of action of VNS. Further research may lead to future improved neurostimulator efficacy by informing optimal stimulation programming parameters.
Copyright © 2021 by the American Clinical Neurophysiology Society.

Entities:  

Year:  2021        PMID: 34009846     DOI: 10.1097/WNP.0000000000000847

Source DB:  PubMed          Journal:  J Clin Neurophysiol        ISSN: 0736-0258            Impact factor:   2.177


  4 in total

1.  Vagus Nerve Stimulation Elicits Sleep EEG Desynchronization and Network Changes in Responder Patients in Epilepsy.

Authors:  Simone Vespa; Jolan Heyse; Lars Stumpp; Giulia Liberati; Susana Ferrao Santos; Herbert Rooijakkers; Antoine Nonclercq; André Mouraux; Pieter van Mierlo; Riëm El Tahry
Journal:  Neurotherapeutics       Date:  2021-10-19       Impact factor: 6.088

2.  Human intracranial recordings reveal distinct cortical activity patterns during invasive and non-invasive vagus nerve stimulation.

Authors:  William L Schuerman; Kirill V Nourski; Ariane E Rhone; Matthew A Howard; Edward F Chang; Matthew K Leonard
Journal:  Sci Rep       Date:  2021-11-23       Impact factor: 4.379

3.  Concurrent brain-responsive and vagus nerve stimulation for treatment of drug-resistant focal epilepsy.

Authors:  Mesha-Gay Brown; Stefan Sillau; Danielle McDermott; Lia D Ernst; David C Spencer; Dario J Englot; Hernán F J González; Proleta Datta; Ioannis Karakis; Danielle Becker; John D Rolston; Amir Arain; Vikram R Rao; Michael Doherty; Alexandra Urban; Cornelia Drees
Journal:  Epilepsy Behav       Date:  2022-03-16       Impact factor: 3.337

Review 4.  Evolution of the Vagus Nerve Stimulation (VNS) Therapy System Technology for Drug-Resistant Epilepsy.

Authors:  Pegah Afra; Bola Adamolekun; Seyhmus Aydemir; Glenn David Robert Watson
Journal:  Front Med Technol       Date:  2021-08-26
  4 in total

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