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Giant early components of somatosensory evoked potentials to tibial nerve stimulation in cortical myoclonus

Enlarged cortical components of somatosensory evoked potentials (giant SEPs) recorded by electroencephalography (EEG) and abnormal somatosensory evoked magnetic fields (SEFs) recorded by magnetoencephalography (MEG) are observed in the majority of patients with cortical myoclonus (CM). Studies on si...

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Autores principales: Anzellotti, Francesca, Onofrj, Marco, Bonanni, Laura, Saracino, Antonio, Franciotti, Raffaella
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4949734/
https://www.ncbi.nlm.nih.gov/pubmed/27489768
http://dx.doi.org/10.1016/j.nicl.2016.07.001
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author Anzellotti, Francesca
Onofrj, Marco
Bonanni, Laura
Saracino, Antonio
Franciotti, Raffaella
author_facet Anzellotti, Francesca
Onofrj, Marco
Bonanni, Laura
Saracino, Antonio
Franciotti, Raffaella
author_sort Anzellotti, Francesca
collection PubMed
description Enlarged cortical components of somatosensory evoked potentials (giant SEPs) recorded by electroencephalography (EEG) and abnormal somatosensory evoked magnetic fields (SEFs) recorded by magnetoencephalography (MEG) are observed in the majority of patients with cortical myoclonus (CM). Studies on simultaneous recordings of SEPs and SEFs showed that generator mechanism of giant SEPs involves both primary sensory and motor cortices. However the generator sources of giant SEPs have not been fully understood as only one report describes clearly giant SEPs following lower limb stimulation. In our study we performed a combined EEG-MEG recording on responses elicited by electric median and tibial nerve stimulation in a patient who developed consequently to methyl bromide intoxication CM with giant SEPs to median and tibial nerve stimuli. SEPs wave shapes were identified on the basis of polarity-latency components (e.g. P15-N20-P25) as defined by earlier studies and guidelines. At EEG recording, the SEP giant component did not appear in the latency range of the first cortical component for median nerve SEP (N20), but appeared instead in the range of the P37 tibial nerve SEP, which is currently identified as the first cortical component elicited by tibial nerve stimuli. Our MEG and EEG SEPs recordings also showed that components in the latency range of P37 were preceded by other cortical components. These findings suggest that lower limb P37 does not correspond to upper limb N20. MEG results confirmed that giant SEFs are the second component from both tibial (N43m-P43m) and median (N27m-P27m) nerve stimulation. MEG dipolar sources of these giant components were located in the primary sensory and motor area.
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spelling pubmed-49497342016-08-03 Giant early components of somatosensory evoked potentials to tibial nerve stimulation in cortical myoclonus Anzellotti, Francesca Onofrj, Marco Bonanni, Laura Saracino, Antonio Franciotti, Raffaella Neuroimage Clin Regular Article Enlarged cortical components of somatosensory evoked potentials (giant SEPs) recorded by electroencephalography (EEG) and abnormal somatosensory evoked magnetic fields (SEFs) recorded by magnetoencephalography (MEG) are observed in the majority of patients with cortical myoclonus (CM). Studies on simultaneous recordings of SEPs and SEFs showed that generator mechanism of giant SEPs involves both primary sensory and motor cortices. However the generator sources of giant SEPs have not been fully understood as only one report describes clearly giant SEPs following lower limb stimulation. In our study we performed a combined EEG-MEG recording on responses elicited by electric median and tibial nerve stimulation in a patient who developed consequently to methyl bromide intoxication CM with giant SEPs to median and tibial nerve stimuli. SEPs wave shapes were identified on the basis of polarity-latency components (e.g. P15-N20-P25) as defined by earlier studies and guidelines. At EEG recording, the SEP giant component did not appear in the latency range of the first cortical component for median nerve SEP (N20), but appeared instead in the range of the P37 tibial nerve SEP, which is currently identified as the first cortical component elicited by tibial nerve stimuli. Our MEG and EEG SEPs recordings also showed that components in the latency range of P37 were preceded by other cortical components. These findings suggest that lower limb P37 does not correspond to upper limb N20. MEG results confirmed that giant SEFs are the second component from both tibial (N43m-P43m) and median (N27m-P27m) nerve stimulation. MEG dipolar sources of these giant components were located in the primary sensory and motor area. Elsevier 2016-07-02 /pmc/articles/PMC4949734/ /pubmed/27489768 http://dx.doi.org/10.1016/j.nicl.2016.07.001 Text en © 2016 Published by Elsevier Inc. http://creativecommons.org/licenses/by-nc-nd/4.0/ This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).
spellingShingle Regular Article
Anzellotti, Francesca
Onofrj, Marco
Bonanni, Laura
Saracino, Antonio
Franciotti, Raffaella
Giant early components of somatosensory evoked potentials to tibial nerve stimulation in cortical myoclonus
title Giant early components of somatosensory evoked potentials to tibial nerve stimulation in cortical myoclonus
title_full Giant early components of somatosensory evoked potentials to tibial nerve stimulation in cortical myoclonus
title_fullStr Giant early components of somatosensory evoked potentials to tibial nerve stimulation in cortical myoclonus
title_full_unstemmed Giant early components of somatosensory evoked potentials to tibial nerve stimulation in cortical myoclonus
title_short Giant early components of somatosensory evoked potentials to tibial nerve stimulation in cortical myoclonus
title_sort giant early components of somatosensory evoked potentials to tibial nerve stimulation in cortical myoclonus
topic Regular Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4949734/
https://www.ncbi.nlm.nih.gov/pubmed/27489768
http://dx.doi.org/10.1016/j.nicl.2016.07.001
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