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Enhanced pre-ictal cortical responsivity in migraine patients assessed by visual chirp stimulation

BACKGROUND: Migraine is associated with altered sensory processing and cortical responsivity that may contribute to susceptibility to attacks by changing brain network excitability dynamics. To gain better insight into cortical responsivity changes in migraine we subjected patients to a short series...

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Autores principales: Perenboom, Matthijs JL, van de Ruit, Mark, Zielman, Ronald, van den Maagdenberg, Arn MJM, Ferrari, Michel D, Carpay, Johannes A, Tolner, Else A
Formato: Online Artículo Texto
Lenguaje:English
Publicado: SAGE Publications 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7412874/
https://www.ncbi.nlm.nih.gov/pubmed/32188264
http://dx.doi.org/10.1177/0333102420912725
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author Perenboom, Matthijs JL
van de Ruit, Mark
Zielman, Ronald
van den Maagdenberg, Arn MJM
Ferrari, Michel D
Carpay, Johannes A
Tolner, Else A
author_facet Perenboom, Matthijs JL
van de Ruit, Mark
Zielman, Ronald
van den Maagdenberg, Arn MJM
Ferrari, Michel D
Carpay, Johannes A
Tolner, Else A
author_sort Perenboom, Matthijs JL
collection PubMed
description BACKGROUND: Migraine is associated with altered sensory processing and cortical responsivity that may contribute to susceptibility to attacks by changing brain network excitability dynamics. To gain better insight into cortical responsivity changes in migraine we subjected patients to a short series of light inputs over a broad frequency range (“chirp” stimulation), designed to uncover dynamic features of visual cortex responsivity. METHODS: EEG responses to visual chirp stimulation (10–40 Hz) were measured in controls (n = 24) and patients with migraine with aura (n = 19) or migraine without aura (n = 20). Average EEG responses were assessed at (i) all EEG frequencies between 5 and 125 Hz, (ii) stimulation frequencies, and (iii) harmonic frequencies. We compared average responses in a low (10–18 Hz), medium (19–26 Hz) and high (27–40 Hz) frequency band. RESULTS: Responses to chirp stimulation were similar in controls and migraine subtypes. Eight measurements (n = 3 migraine with aura; n = 5 without aura) were assigned as “pre-ictal”, based on reported headache within 48 hours after investigation. Pre-ictally, an increased harmonic response to 22–32 Hz stimulation (beta band) was observed (p = 0.001), compared to interictal state measurements. CONCLUSIONS: We found chirp responses to be enhanced in the 48 hours prior to migraine headache onset. Visual chirp stimulation proved a simple and reliable technique with potential to detect changes in cortical responsivity associated with the onset of migraine attacks.
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spelling pubmed-74128742020-08-19 Enhanced pre-ictal cortical responsivity in migraine patients assessed by visual chirp stimulation Perenboom, Matthijs JL van de Ruit, Mark Zielman, Ronald van den Maagdenberg, Arn MJM Ferrari, Michel D Carpay, Johannes A Tolner, Else A Cephalalgia Original Articles BACKGROUND: Migraine is associated with altered sensory processing and cortical responsivity that may contribute to susceptibility to attacks by changing brain network excitability dynamics. To gain better insight into cortical responsivity changes in migraine we subjected patients to a short series of light inputs over a broad frequency range (“chirp” stimulation), designed to uncover dynamic features of visual cortex responsivity. METHODS: EEG responses to visual chirp stimulation (10–40 Hz) were measured in controls (n = 24) and patients with migraine with aura (n = 19) or migraine without aura (n = 20). Average EEG responses were assessed at (i) all EEG frequencies between 5 and 125 Hz, (ii) stimulation frequencies, and (iii) harmonic frequencies. We compared average responses in a low (10–18 Hz), medium (19–26 Hz) and high (27–40 Hz) frequency band. RESULTS: Responses to chirp stimulation were similar in controls and migraine subtypes. Eight measurements (n = 3 migraine with aura; n = 5 without aura) were assigned as “pre-ictal”, based on reported headache within 48 hours after investigation. Pre-ictally, an increased harmonic response to 22–32 Hz stimulation (beta band) was observed (p = 0.001), compared to interictal state measurements. CONCLUSIONS: We found chirp responses to be enhanced in the 48 hours prior to migraine headache onset. Visual chirp stimulation proved a simple and reliable technique with potential to detect changes in cortical responsivity associated with the onset of migraine attacks. SAGE Publications 2020-03-18 2020-08 /pmc/articles/PMC7412874/ /pubmed/32188264 http://dx.doi.org/10.1177/0333102420912725 Text en © International Headache Society 2020 https://creativecommons.org/licenses/by-nc/4.0/ This article is distributed under the terms of the Creative Commons Attribution-NonCommercial 4.0 License (https://creativecommons.org/licenses/by-nc/4.0/) which permits non-commercial use, reproduction and distribution of the work without further permission provided the original work is attributed as specified on the SAGE and Open Access pages (https://us.sagepub.com/en-us/nam/open-access-at-sage).
spellingShingle Original Articles
Perenboom, Matthijs JL
van de Ruit, Mark
Zielman, Ronald
van den Maagdenberg, Arn MJM
Ferrari, Michel D
Carpay, Johannes A
Tolner, Else A
Enhanced pre-ictal cortical responsivity in migraine patients assessed by visual chirp stimulation
title Enhanced pre-ictal cortical responsivity in migraine patients assessed by visual chirp stimulation
title_full Enhanced pre-ictal cortical responsivity in migraine patients assessed by visual chirp stimulation
title_fullStr Enhanced pre-ictal cortical responsivity in migraine patients assessed by visual chirp stimulation
title_full_unstemmed Enhanced pre-ictal cortical responsivity in migraine patients assessed by visual chirp stimulation
title_short Enhanced pre-ictal cortical responsivity in migraine patients assessed by visual chirp stimulation
title_sort enhanced pre-ictal cortical responsivity in migraine patients assessed by visual chirp stimulation
topic Original Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7412874/
https://www.ncbi.nlm.nih.gov/pubmed/32188264
http://dx.doi.org/10.1177/0333102420912725
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