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Cerebral metabolism before and after external trigeminal nerve stimulation in episodic migraine

BACKGROUND AND AIM: A recent sham-controlled trial showed that external trigeminal nerve stimulation (eTNS) is effective in episodic migraine (MO) prevention. However, its mechanism of action remains unknown. We performed 18-fluorodeoxyglucose positron emission tomography (FDG-PET) to evaluate brain...

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Autores principales: Magis, Delphine, D’Ostilio, Kevin, Thibaut, Aurore, De Pasqua, Victor, Gerard, Pascale, Hustinx, Roland, Laureys, Steven, Schoenen, Jean
Formato: Online Artículo Texto
Lenguaje:English
Publicado: SAGE Publications 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5560481/
https://www.ncbi.nlm.nih.gov/pubmed/27342225
http://dx.doi.org/10.1177/0333102416656118
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author Magis, Delphine
D’Ostilio, Kevin
Thibaut, Aurore
De Pasqua, Victor
Gerard, Pascale
Hustinx, Roland
Laureys, Steven
Schoenen, Jean
author_facet Magis, Delphine
D’Ostilio, Kevin
Thibaut, Aurore
De Pasqua, Victor
Gerard, Pascale
Hustinx, Roland
Laureys, Steven
Schoenen, Jean
author_sort Magis, Delphine
collection PubMed
description BACKGROUND AND AIM: A recent sham-controlled trial showed that external trigeminal nerve stimulation (eTNS) is effective in episodic migraine (MO) prevention. However, its mechanism of action remains unknown. We performed 18-fluorodeoxyglucose positron emission tomography (FDG-PET) to evaluate brain metabolic changes before and after eTNS in episodic migraineurs. METHODS: Twenty-eight individuals were recruited: 14 with MO and 20 healthy volunteers (HVs). HVs underwent a single FDG-PET, whereas patients were scanned at baseline, directly after a first prolonged session of eTNS (Cefaly®) and after three months of treatment (uncontrolled study). RESULTS: The frequency of migraine attacks significantly decreased in compliant patients (N = 10). Baseline FDG-PET revealed a significant hypometabolism in fronto-temporal areas, especially in the orbitofrontal (OFC) and rostral anterior cingulate cortices (rACC) in MO patients. This hypometabolism was reduced after three months of eTNS treatment. CONCLUSION: Our study shows that metabolic activity of OFC and rACC, which are pivotal areas in central pain and behaviour control, is decreased in migraine. This hypometabolism is reduced after three months of eTNS. eTNS might thus exert its beneficial effects via slow neuromodulation of central pain-controlling areas, a mechanism also previously reported in chronic migraine and cluster headache after percutaneous occipital nerve stimulation. However, this finding needs to be confirmed by further studies using a sham condition.
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spelling pubmed-55604812017-08-31 Cerebral metabolism before and after external trigeminal nerve stimulation in episodic migraine Magis, Delphine D’Ostilio, Kevin Thibaut, Aurore De Pasqua, Victor Gerard, Pascale Hustinx, Roland Laureys, Steven Schoenen, Jean Cephalalgia Original Articles BACKGROUND AND AIM: A recent sham-controlled trial showed that external trigeminal nerve stimulation (eTNS) is effective in episodic migraine (MO) prevention. However, its mechanism of action remains unknown. We performed 18-fluorodeoxyglucose positron emission tomography (FDG-PET) to evaluate brain metabolic changes before and after eTNS in episodic migraineurs. METHODS: Twenty-eight individuals were recruited: 14 with MO and 20 healthy volunteers (HVs). HVs underwent a single FDG-PET, whereas patients were scanned at baseline, directly after a first prolonged session of eTNS (Cefaly®) and after three months of treatment (uncontrolled study). RESULTS: The frequency of migraine attacks significantly decreased in compliant patients (N = 10). Baseline FDG-PET revealed a significant hypometabolism in fronto-temporal areas, especially in the orbitofrontal (OFC) and rostral anterior cingulate cortices (rACC) in MO patients. This hypometabolism was reduced after three months of eTNS treatment. CONCLUSION: Our study shows that metabolic activity of OFC and rACC, which are pivotal areas in central pain and behaviour control, is decreased in migraine. This hypometabolism is reduced after three months of eTNS. eTNS might thus exert its beneficial effects via slow neuromodulation of central pain-controlling areas, a mechanism also previously reported in chronic migraine and cluster headache after percutaneous occipital nerve stimulation. However, this finding needs to be confirmed by further studies using a sham condition. SAGE Publications 2016-06-23 2017-08 /pmc/articles/PMC5560481/ /pubmed/27342225 http://dx.doi.org/10.1177/0333102416656118 Text en © International Headache Society 2016 http://creativecommons.org/licenses/by-nc/3.0/ This article is distributed under the terms of the Creative Commons Attribution-NonCommercial 3.0 License (http://www.creativecommons.org/licenses/by-nc/3.0/) 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
Magis, Delphine
D’Ostilio, Kevin
Thibaut, Aurore
De Pasqua, Victor
Gerard, Pascale
Hustinx, Roland
Laureys, Steven
Schoenen, Jean
Cerebral metabolism before and after external trigeminal nerve stimulation in episodic migraine
title Cerebral metabolism before and after external trigeminal nerve stimulation in episodic migraine
title_full Cerebral metabolism before and after external trigeminal nerve stimulation in episodic migraine
title_fullStr Cerebral metabolism before and after external trigeminal nerve stimulation in episodic migraine
title_full_unstemmed Cerebral metabolism before and after external trigeminal nerve stimulation in episodic migraine
title_short Cerebral metabolism before and after external trigeminal nerve stimulation in episodic migraine
title_sort cerebral metabolism before and after external trigeminal nerve stimulation in episodic migraine
topic Original Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5560481/
https://www.ncbi.nlm.nih.gov/pubmed/27342225
http://dx.doi.org/10.1177/0333102416656118
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