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Vagus Nerve Stimulation-Induced Laryngeal Motor Evoked Potentials: A Possible Biomarker of Effective Nerve Activation

Vagus nerve stimulation (VNS) therapy is associated with laryngeal muscle activation and induces voice modifications, well-known side effects of the therapy resulting from co-activation of the recurrent laryngeal nerve. In this study, we describe the non-invasive transcutaneous recording of laryngea...

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Autores principales: Vespa, Simone, Stumpp, Lars, Bouckaert, Charlotte, Delbeke, Jean, Smets, Hugo, Cury, Joaquin, Ferrao Santos, Susana, Rooijakkers, Herbert, Nonclercq, Antoine, Raedt, Robrecht, Vonck, Kristl, El Tahry, Riëm
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6718640/
https://www.ncbi.nlm.nih.gov/pubmed/31507360
http://dx.doi.org/10.3389/fnins.2019.00880
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author Vespa, Simone
Stumpp, Lars
Bouckaert, Charlotte
Delbeke, Jean
Smets, Hugo
Cury, Joaquin
Ferrao Santos, Susana
Rooijakkers, Herbert
Nonclercq, Antoine
Raedt, Robrecht
Vonck, Kristl
El Tahry, Riëm
author_facet Vespa, Simone
Stumpp, Lars
Bouckaert, Charlotte
Delbeke, Jean
Smets, Hugo
Cury, Joaquin
Ferrao Santos, Susana
Rooijakkers, Herbert
Nonclercq, Antoine
Raedt, Robrecht
Vonck, Kristl
El Tahry, Riëm
author_sort Vespa, Simone
collection PubMed
description Vagus nerve stimulation (VNS) therapy is associated with laryngeal muscle activation and induces voice modifications, well-known side effects of the therapy resulting from co-activation of the recurrent laryngeal nerve. In this study, we describe the non-invasive transcutaneous recording of laryngeal motor evoked potentials (LMEPs), which could serve as a biomarker of effective nerve activation and individual titration in patients with drug-resistant epilepsy. We recruited drug-resistant epileptic patients treated for at least 6 months with a VNS. Trains of 600–1200 VNS pulses were delivered with increasing current outputs. We placed six skin electrodes on the ventral surface of the neck, in order to record LMEPs whenever the laryngeal muscular threshold was reached. We studied the internal consistency and the variability of LMEP recordings, and compared different methods for amplitude calculation. Recruitment curves were built based on the stimulus–response relationship. We also determined the electrical axis of the LMEPs dipole in order to define the optimal electrode placement for LMEPs recording in a clinical setting. LMEPs were successfully recorded in 11/11 patients. The LMEPs threshold ranged from 0.25 to 1 mA (median 0.50 mA), and onset latency was between 5.37 and 8.77 ms. The signal-to-noise ratio was outstanding in 10/11 patients. In these cases, excellent reliability (Intraclass correlation coefficient, ICC > 0.90 across three different amplitude measurements) was achieved with 10 sample averages. Moreover, our recordings showed very good internal consistency (Cronbach’s alpha > 0.95 for 10 epochs). Area-under-the-curve and peak-to-peak measurement proved to be complementary methods for amplitude calculation. Finally, we determined that an optimal derivation requires only two recording electrodes, aligned on a horizontal axis around the laryngeal prominence. In conclusion, we describe here an optimal methodology for the recording of VNS-induced motor evoked responses from the larynx. Although further clinical validation is still necessary, LMEPs might be useful as a non-invasive marker of effective nerve activation, and as an aid for the clinician to perform a more rational titration of VNS parameters.
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spelling pubmed-67186402019-09-10 Vagus Nerve Stimulation-Induced Laryngeal Motor Evoked Potentials: A Possible Biomarker of Effective Nerve Activation Vespa, Simone Stumpp, Lars Bouckaert, Charlotte Delbeke, Jean Smets, Hugo Cury, Joaquin Ferrao Santos, Susana Rooijakkers, Herbert Nonclercq, Antoine Raedt, Robrecht Vonck, Kristl El Tahry, Riëm Front Neurosci Neuroscience Vagus nerve stimulation (VNS) therapy is associated with laryngeal muscle activation and induces voice modifications, well-known side effects of the therapy resulting from co-activation of the recurrent laryngeal nerve. In this study, we describe the non-invasive transcutaneous recording of laryngeal motor evoked potentials (LMEPs), which could serve as a biomarker of effective nerve activation and individual titration in patients with drug-resistant epilepsy. We recruited drug-resistant epileptic patients treated for at least 6 months with a VNS. Trains of 600–1200 VNS pulses were delivered with increasing current outputs. We placed six skin electrodes on the ventral surface of the neck, in order to record LMEPs whenever the laryngeal muscular threshold was reached. We studied the internal consistency and the variability of LMEP recordings, and compared different methods for amplitude calculation. Recruitment curves were built based on the stimulus–response relationship. We also determined the electrical axis of the LMEPs dipole in order to define the optimal electrode placement for LMEPs recording in a clinical setting. LMEPs were successfully recorded in 11/11 patients. The LMEPs threshold ranged from 0.25 to 1 mA (median 0.50 mA), and onset latency was between 5.37 and 8.77 ms. The signal-to-noise ratio was outstanding in 10/11 patients. In these cases, excellent reliability (Intraclass correlation coefficient, ICC > 0.90 across three different amplitude measurements) was achieved with 10 sample averages. Moreover, our recordings showed very good internal consistency (Cronbach’s alpha > 0.95 for 10 epochs). Area-under-the-curve and peak-to-peak measurement proved to be complementary methods for amplitude calculation. Finally, we determined that an optimal derivation requires only two recording electrodes, aligned on a horizontal axis around the laryngeal prominence. In conclusion, we describe here an optimal methodology for the recording of VNS-induced motor evoked responses from the larynx. Although further clinical validation is still necessary, LMEPs might be useful as a non-invasive marker of effective nerve activation, and as an aid for the clinician to perform a more rational titration of VNS parameters. Frontiers Media S.A. 2019-08-27 /pmc/articles/PMC6718640/ /pubmed/31507360 http://dx.doi.org/10.3389/fnins.2019.00880 Text en Copyright © 2019 Vespa, Stumpp, Bouckaert, Delbeke, Smets, Cury, Ferrao Santos, Rooijakkers, Nonclercq, Raedt, Vonck and El Tahry. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Neuroscience
Vespa, Simone
Stumpp, Lars
Bouckaert, Charlotte
Delbeke, Jean
Smets, Hugo
Cury, Joaquin
Ferrao Santos, Susana
Rooijakkers, Herbert
Nonclercq, Antoine
Raedt, Robrecht
Vonck, Kristl
El Tahry, Riëm
Vagus Nerve Stimulation-Induced Laryngeal Motor Evoked Potentials: A Possible Biomarker of Effective Nerve Activation
title Vagus Nerve Stimulation-Induced Laryngeal Motor Evoked Potentials: A Possible Biomarker of Effective Nerve Activation
title_full Vagus Nerve Stimulation-Induced Laryngeal Motor Evoked Potentials: A Possible Biomarker of Effective Nerve Activation
title_fullStr Vagus Nerve Stimulation-Induced Laryngeal Motor Evoked Potentials: A Possible Biomarker of Effective Nerve Activation
title_full_unstemmed Vagus Nerve Stimulation-Induced Laryngeal Motor Evoked Potentials: A Possible Biomarker of Effective Nerve Activation
title_short Vagus Nerve Stimulation-Induced Laryngeal Motor Evoked Potentials: A Possible Biomarker of Effective Nerve Activation
title_sort vagus nerve stimulation-induced laryngeal motor evoked potentials: a possible biomarker of effective nerve activation
topic Neuroscience
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6718640/
https://www.ncbi.nlm.nih.gov/pubmed/31507360
http://dx.doi.org/10.3389/fnins.2019.00880
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