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Migraine and Genetic Polymorphisms: An Overview

The relationship between genetic polymorphisms and migraine as a cause of an increased risk of thrombotic disorders development is still debated In this respect, factor V Leiden, factor V (H1299R), prothrombin G20210A, factor XIII (V34L), β-fibrinogen, MTHFR (C677T), MTHFR (A1298C), APO E, PAI-1, HP...

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Detalles Bibliográficos
Autores principales: Pizza, Vincenzo, Agresta, Anella, Agresta, Antonio, Lamaida, Eros, Lamaida, Norman, Infante, Francesco, Capasso, Anna
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Bentham Open 2012
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3434423/
https://www.ncbi.nlm.nih.gov/pubmed/22962564
http://dx.doi.org/10.2174/1874205X01206010065
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author Pizza, Vincenzo
Agresta, Anella
Agresta, Antonio
Lamaida, Eros
Lamaida, Norman
Infante, Francesco
Capasso, Anna
author_facet Pizza, Vincenzo
Agresta, Anella
Agresta, Antonio
Lamaida, Eros
Lamaida, Norman
Infante, Francesco
Capasso, Anna
author_sort Pizza, Vincenzo
collection PubMed
description The relationship between genetic polymorphisms and migraine as a cause of an increased risk of thrombotic disorders development is still debated In this respect, factor V Leiden, factor V (H1299R), prothrombin G20210A, factor XIII (V34L), β-fibrinogen, MTHFR (C677T), MTHFR (A1298C), APO E, PAI-1, HPA-1 and ACE I/D seem to play a determinant role in vascular diseases related to migraine. The present review analyzes both the incidence of the above genetic vascular mutations in migraineurs and the most re-cent developments related to genetic polymorphisms and migraine.
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spelling pubmed-34344232012-09-07 Migraine and Genetic Polymorphisms: An Overview Pizza, Vincenzo Agresta, Anella Agresta, Antonio Lamaida, Eros Lamaida, Norman Infante, Francesco Capasso, Anna Open Neurol J Article The relationship between genetic polymorphisms and migraine as a cause of an increased risk of thrombotic disorders development is still debated In this respect, factor V Leiden, factor V (H1299R), prothrombin G20210A, factor XIII (V34L), β-fibrinogen, MTHFR (C677T), MTHFR (A1298C), APO E, PAI-1, HPA-1 and ACE I/D seem to play a determinant role in vascular diseases related to migraine. The present review analyzes both the incidence of the above genetic vascular mutations in migraineurs and the most re-cent developments related to genetic polymorphisms and migraine. Bentham Open 2012-08-17 /pmc/articles/PMC3434423/ /pubmed/22962564 http://dx.doi.org/10.2174/1874205X01206010065 Text en © Finsterer and Stöllberger; Licensee Bentham Open. http://creativecommons.org/licenses/by-nc/3.0/ This is an open access article licensed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/3.0/) which permits unrestricted, non-commercial use, distribution and reproduction in any medium, provided the work is properly cited.
spellingShingle Article
Pizza, Vincenzo
Agresta, Anella
Agresta, Antonio
Lamaida, Eros
Lamaida, Norman
Infante, Francesco
Capasso, Anna
Migraine and Genetic Polymorphisms: An Overview
title Migraine and Genetic Polymorphisms: An Overview
title_full Migraine and Genetic Polymorphisms: An Overview
title_fullStr Migraine and Genetic Polymorphisms: An Overview
title_full_unstemmed Migraine and Genetic Polymorphisms: An Overview
title_short Migraine and Genetic Polymorphisms: An Overview
title_sort migraine and genetic polymorphisms: an overview
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3434423/
https://www.ncbi.nlm.nih.gov/pubmed/22962564
http://dx.doi.org/10.2174/1874205X01206010065
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