Migraine and genetic polymorphisms: an overview
- PMID: 22962564
- PMCID: PMC3434423
- DOI: 10.2174/1874205X01206010065
Migraine and genetic polymorphisms: an overview
Abstract
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.
Keywords: Genetic Polymorphisms; Migraine; Thrombosis; Vascular Disease..
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References
-
- Chiodini BD, Barlera S, Franzosi MG, Rognoni G. I geni di suscettibilità all’infarto: una revisione della letteratura. Ital Heart J. 2001;2:935–944. - PubMed
-
- C Colucci D’Amato V, Alfano E, Giordano T, Marmolo V. Pizza: Le Cefalee. Napoli: Idelson. 1997. p. 129.
-
- Bianchi A, Pitari GM, Amenta V, et al. Endothelial, Haemostatic and haemorheological modifications in migraineurs. Artery. 1996;22:93–100. - PubMed
-
- Corral J, Iniesta JA, Gonzà-Conejero R, Lozano ML, Rivera J, Vicente V. Migraine and prothrombotic genetic risk factors. Cephalalgia. 1998;18:257. - PubMed
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