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Visual evoked potentials in subgroups of migraine with aura patients

BACKGROUND: Patients suffering from migraine with aura can have either pure visual auras or complex auras with sensory disturbances and dysphasia, or both. Few studies have searched for possible pathophysiological differences between these two subgroups of patients. METHODS: Methods - Forty-seven mi...

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Autores principales: Coppola, Gianluca, Bracaglia, Martina, Di Lenola, Davide, Di Lorenzo, Cherubino, Serrao, Mariano, Parisi, Vincenzo, Di Renzo, Antonio, Martelli, Francesco, Fadda, Antonello, Schoenen, Jean, Pierelli, Francesco
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer Milan 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4630240/
https://www.ncbi.nlm.nih.gov/pubmed/26527348
http://dx.doi.org/10.1186/s10194-015-0577-6
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author Coppola, Gianluca
Bracaglia, Martina
Di Lenola, Davide
Di Lorenzo, Cherubino
Serrao, Mariano
Parisi, Vincenzo
Di Renzo, Antonio
Martelli, Francesco
Fadda, Antonello
Schoenen, Jean
Pierelli, Francesco
author_facet Coppola, Gianluca
Bracaglia, Martina
Di Lenola, Davide
Di Lorenzo, Cherubino
Serrao, Mariano
Parisi, Vincenzo
Di Renzo, Antonio
Martelli, Francesco
Fadda, Antonello
Schoenen, Jean
Pierelli, Francesco
author_sort Coppola, Gianluca
collection PubMed
description BACKGROUND: Patients suffering from migraine with aura can have either pure visual auras or complex auras with sensory disturbances and dysphasia, or both. Few studies have searched for possible pathophysiological differences between these two subgroups of patients. METHODS: Methods - Forty-seven migraine with aura patients were subdivided in a subgroup with exclusively visual auras (MA, N = 27) and another with complex neurological auras (MA+, N = 20). We recorded pattern-reversal visual evoked potentials (VEP: 15 min of arc cheques, 3.1 reversal per second, 600 sweeps) and measured amplitude and habituation (slope of the linear regression line of amplitude changes from the 1st to 6th block of 100 sweeps) for the N1-P1 and P1-N2 components in patients and, for comparison, in 30 healthy volunteers (HV) of similar age and gender distribution. RESULTS: VEP N1-P1 habituation, i.e. amplitude decrement between 1st and 6th block, which was obvious in most HV (mean slope −0.50), was deficient in both MA (slope +0.01, p = 0.0001) and MA+ (−0.0049, p = 0.001) patients. However, VEP N1-P1 amplitudes across blocks were normal in MA patients, while they were significantly greater in MA+ patients than in HVs. CONCLUSIONS: Our findings suggest that in migraine with aura patients different aura phenotypes may be underpinned by different pathophysiological mechanisms. Pre-activation cortical excitability could be higher in patients with complex neurological auras than in those having pure visual auras or in healthy volunteers.
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spelling pubmed-46302402015-11-10 Visual evoked potentials in subgroups of migraine with aura patients Coppola, Gianluca Bracaglia, Martina Di Lenola, Davide Di Lorenzo, Cherubino Serrao, Mariano Parisi, Vincenzo Di Renzo, Antonio Martelli, Francesco Fadda, Antonello Schoenen, Jean Pierelli, Francesco J Headache Pain Research Article BACKGROUND: Patients suffering from migraine with aura can have either pure visual auras or complex auras with sensory disturbances and dysphasia, or both. Few studies have searched for possible pathophysiological differences between these two subgroups of patients. METHODS: Methods - Forty-seven migraine with aura patients were subdivided in a subgroup with exclusively visual auras (MA, N = 27) and another with complex neurological auras (MA+, N = 20). We recorded pattern-reversal visual evoked potentials (VEP: 15 min of arc cheques, 3.1 reversal per second, 600 sweeps) and measured amplitude and habituation (slope of the linear regression line of amplitude changes from the 1st to 6th block of 100 sweeps) for the N1-P1 and P1-N2 components in patients and, for comparison, in 30 healthy volunteers (HV) of similar age and gender distribution. RESULTS: VEP N1-P1 habituation, i.e. amplitude decrement between 1st and 6th block, which was obvious in most HV (mean slope −0.50), was deficient in both MA (slope +0.01, p = 0.0001) and MA+ (−0.0049, p = 0.001) patients. However, VEP N1-P1 amplitudes across blocks were normal in MA patients, while they were significantly greater in MA+ patients than in HVs. CONCLUSIONS: Our findings suggest that in migraine with aura patients different aura phenotypes may be underpinned by different pathophysiological mechanisms. Pre-activation cortical excitability could be higher in patients with complex neurological auras than in those having pure visual auras or in healthy volunteers. Springer Milan 2015-11-02 /pmc/articles/PMC4630240/ /pubmed/26527348 http://dx.doi.org/10.1186/s10194-015-0577-6 Text en © Coppola et al. 2015 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made.
spellingShingle Research Article
Coppola, Gianluca
Bracaglia, Martina
Di Lenola, Davide
Di Lorenzo, Cherubino
Serrao, Mariano
Parisi, Vincenzo
Di Renzo, Antonio
Martelli, Francesco
Fadda, Antonello
Schoenen, Jean
Pierelli, Francesco
Visual evoked potentials in subgroups of migraine with aura patients
title Visual evoked potentials in subgroups of migraine with aura patients
title_full Visual evoked potentials in subgroups of migraine with aura patients
title_fullStr Visual evoked potentials in subgroups of migraine with aura patients
title_full_unstemmed Visual evoked potentials in subgroups of migraine with aura patients
title_short Visual evoked potentials in subgroups of migraine with aura patients
title_sort visual evoked potentials in subgroups of migraine with aura patients
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4630240/
https://www.ncbi.nlm.nih.gov/pubmed/26527348
http://dx.doi.org/10.1186/s10194-015-0577-6
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