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Erschienen in: The Journal of Headache and Pain 1/2015

Open Access 01.12.2015 | Invited speaker presentation

Migraine and epilepsy: what value today?

verfasst von: Cinzia Costa, Paolo Prontera, Stefano Caproni, Letizia M Cupini, Paola Sarchielli, Paolo Calabresi

Erschienen in: The Journal of Headache and Pain | Sonderheft 1/2015

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More than 100 years of investigation have found that seizures and migraine co-occur in some affected individuals and families, and there is much evidence that these diseases share genetic susceptibility. In particular, in a recent review, the prevalence of migraine in epileptic patients was about 12%[1]. On the other hand, epilepsy exhibits a prevalence of about 6% in migraineurs[2]. Moreover, epilepsy has also been reported in patients with familial hemiplegic migraine (FHM). Although few studies showed a prevalence of epilepsy of about 7% in FHM, currently no conclusive data are available.
Certainly, epilepsy and migraine share common characteristics that the underlying pathophysiology relates to alterations in ion channels or ion transporters. In these episodic functional diseases, in which susceptible brain regions are hyperexcitable, the attacks begin with hypersynchronous neuronal firing[3]. In epilepsy, α-amino-3-hydroxy-5-methyl-4-isoxazolepropionic acid (AMPA) receptors play a predominant role in mediating the generation and spread of seizure activity whereas in migraine mainly N-methyl-D-aspartate (NMDA) receptors are involved in triggering CSD. However, the nature of the ionic conductance changes leading to the massive but transitory neuronal depolarization underlying CSD has not yet been define[4].
Genetically determined dysfunction of ion transporters seems to point at a common underlying mechanism for both paroxysmal disorders. In the last two decades the mutations in the ion transportation genes CACNA1A, ATP1A2 and SCN1A have been identified for FHM. Conversely, only a few CACNA1A and ATP1A2 mutations have been reported in patients with sporadic hemiplegic migraine (SHM). These cases can be caused by a de novo mutation or by inheritance of a gene mutation from asymptomatic carrier and are usually characterized by early-onset, severe and complex disorders.
Certainly, genetic analysis can provide greater insight into the potential causes of both disorders and it could contribute to better treatment choices.
Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (https://​creativecommons.​org/​licenses/​by/​4.​0), which permits use, duplication, adaptation, distribution, and reproduction in any medium or format, as long as 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.
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Literatur
1.
Zurück zum Zitat Selassie AW, Wilson DA, Martz GU, Smith GG, Wagner JL, Wannamaker BB: Epilepsy beyond seizure: a population-based study of comorbidities. Epilepsy Behav. 2014, 32: 42-48.CrossRefPubMed Selassie AW, Wilson DA, Martz GU, Smith GG, Wagner JL, Wannamaker BB: Epilepsy beyond seizure: a population-based study of comorbidities. Epilepsy Behav. 2014, 32: 42-48.CrossRefPubMed
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Zurück zum Zitat Bellini B, Arruda M, Cescut A, Saulle C, Persico A, Carotenuto M, Gatta M, Nacinovich R, Piazza FP, Termine C, Tozzi E, Lucchese F, Guidetti V: Headache and comorbidity in children and adolescents. J Headache Pain. 2013, 14: 79-10.1186/1129-2377-14-79.PubMedCentralCrossRefPubMed Bellini B, Arruda M, Cescut A, Saulle C, Persico A, Carotenuto M, Gatta M, Nacinovich R, Piazza FP, Termine C, Tozzi E, Lucchese F, Guidetti V: Headache and comorbidity in children and adolescents. J Headache Pain. 2013, 14: 79-10.1186/1129-2377-14-79.PubMedCentralCrossRefPubMed
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Zurück zum Zitat Rogawski MA: Common pathophysiologic mechanisms in migraine and epilepsy. Arch Neurol. 2008, 65 (6): 709-14.CrossRefPubMed Rogawski MA: Common pathophysiologic mechanisms in migraine and epilepsy. Arch Neurol. 2008, 65 (6): 709-14.CrossRefPubMed
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Zurück zum Zitat Rogawski MA: Migraine and epilepsy-shared mechanisms within the family of episodic disorders. Jasper's Basic Mechanisms of the Epilepsies. Edited by: Noebels JL, Avoli M, Rogawski MA, Olsen RW, Delgado-Escueta AV. 2012, Bethesda (MD): National Center for Biotechnology Information (US), 4 Rogawski MA: Migraine and epilepsy-shared mechanisms within the family of episodic disorders. Jasper's Basic Mechanisms of the Epilepsies. Edited by: Noebels JL, Avoli M, Rogawski MA, Olsen RW, Delgado-Escueta AV. 2012, Bethesda (MD): National Center for Biotechnology Information (US), 4
Metadaten
Titel
Migraine and epilepsy: what value today?
verfasst von
Cinzia Costa
Paolo Prontera
Stefano Caproni
Letizia M Cupini
Paola Sarchielli
Paolo Calabresi
Publikationsdatum
01.12.2015
Verlag
Springer Milan
Erschienen in
The Journal of Headache and Pain / Ausgabe Sonderheft 1/2015
Print ISSN: 1129-2369
Elektronische ISSN: 1129-2377
DOI
https://doi.org/10.1186/1129-2377-16-S1-A44

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