2012
DOI: 10.2174/1874205x01206010065
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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 de… Show more

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Cited by 16 publications
(12 citation statements)
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“…On the other hand, several genetic polymorphisms probably increase thrombotic disorders among the migraineurs; however, these putative genes are extremely different from those linked to IBS. For examples, migraine related candidate genes include factor V Leiden , factor V ( H1299R ), prothrombin ( G20210A ), factor XIII ( V34L ), β-fibrinoge n and lipoprotein receptor ( LRP1 ) etc, whereas IBS related candidate genes consist of serotonin transporter ( SLC6A4 ), norepinephrine transporter ( NET ), alpha-2A-adrenergic receptors ( ADRA2A ), interleukin-10 ( IL-10 ), G protein β3 subunit ( GNβ3 ) and sodium channel ( SCN5A ) etc 73,75,76. In fact, the potential functions of these genetic variants are controversial because they result in a small to moderate risk of developing migraine which means that migraine is a heterogeneous disorder.…”
Section: Pathogenesesmentioning
confidence: 99%
“…On the other hand, several genetic polymorphisms probably increase thrombotic disorders among the migraineurs; however, these putative genes are extremely different from those linked to IBS. For examples, migraine related candidate genes include factor V Leiden , factor V ( H1299R ), prothrombin ( G20210A ), factor XIII ( V34L ), β-fibrinoge n and lipoprotein receptor ( LRP1 ) etc, whereas IBS related candidate genes consist of serotonin transporter ( SLC6A4 ), norepinephrine transporter ( NET ), alpha-2A-adrenergic receptors ( ADRA2A ), interleukin-10 ( IL-10 ), G protein β3 subunit ( GNβ3 ) and sodium channel ( SCN5A ) etc 73,75,76. In fact, the potential functions of these genetic variants are controversial because they result in a small to moderate risk of developing migraine which means that migraine is a heterogeneous disorder.…”
Section: Pathogenesesmentioning
confidence: 99%
“…There are several neurological, hormonal and vascular genes that are considered as key factors in the pathophysiology of migraine [5]. It has been proposed that endothelial dysfunction, which increases oxidative stress and promotes inflammatory processes, is involved in the pathogenesis of migraine [6]. In this respect, MTHFR C677T genetic polymorphisms may play a crucial role in vascular diseases [3].…”
Section: Discussionmentioning
confidence: 99%
“…There are two common MTHFR polymorphisms, namely, C677T and A1298C [3,4]. In MTHFR C677T and A1298C polymorphisms, a point mutation occurs, which leads to the replacement of alanine by valine, while glutamine is replaced by alanine, respectively, in [5,6]. Thus, the role of MTHFR C677T gene polymorphism in migraine susceptibility needs further evaluation.…”
Section: Introductionmentioning
confidence: 99%
“…Late studies focus on the role of migraine as potential risk of endothelial dysfunction [5][6][7][8][9], which may further affect the normal function of vascular endothelial cells. Because endothelial dysfunction always occure in a situation of an increased oxidative stress and pro-inflammatory reaction, this proposed as one of pathogenesis of migraine [10]. Allergic sensitity are also considered to be one cause of migraine, in theory, allergy offers many suggestive possibilities as an etiological agent in magraine, but further study still need to be done fo prove this [11], [12].…”
Section: Introductionmentioning
confidence: 99%