Literature DB >> 25501253

Migraine genetics: current findings and future lines of research.

A M Persico1, M Verdecchia, V Pinzone, V Guidetti.   

Abstract

In the last two decades, migraine research has greatly advanced our current knowledge of the genetic contributions and the pathophysiology of this common and debilitating disorder. Nonetheless, this knowledge still needs to grow further and to translate into more effective treatments. To date, several genes involved in syndromic and monogenic forms of migraine have been identified, allowing the generation of animal models which have significantly contributed to current knowledge of the mechanisms underlying these rare forms of migraine. Common forms of migraine are instead posing a greater challenge, as they may most often stem from complex interactions between multiple common genetic variants, with environmental triggers. This paper reviews our current understanding of migraine genetics, moving from syndromic and monogenic forms to oligogenic/polygenic migraines most recently addressed with some success through genome-wide association studies. Methodological issues in study design and future perspectives opened by biomarker research will also be briefly addressed.

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Year:  2014        PMID: 25501253     DOI: 10.1007/s10048-014-0433-x

Source DB:  PubMed          Journal:  Neurogenetics        ISSN: 1364-6745            Impact factor:   2.660


  200 in total

1.  Multilocus analyses reveal involvement of the ESR1, ESR2, and FSHR genes in migraine.

Authors:  Agustin Oterino; Maria Toriello; Amalia Cayón; Jesus Castillo; Rafael Colas; Ana Alonson-Arranz; Carlos Ruiz-Alegria; Estrella Quintela; Fernando Monton; Nuria Ruiz-Lavilla; Felix Gonzalez; Julio Pascual
Journal:  Headache       Date:  2008 Nov-Dec       Impact factor: 5.887

2.  A genome-wide scan provides evidence for loci influencing a severe heritable form of common migraine.

Authors:  R A Lea; D R Nyholt; R P Curtain; M Ovcaric; R Sciascia; C Bellis; J Macmillan; S Quinlan; R A Gibson; L C McCarthy; J H Riley; Y J Smithies; S Kinrade; L R Griffiths
Journal:  Neurogenetics       Date:  2005-04-14       Impact factor: 2.660

Review 3.  Endogenous mechanisms underlying the activation and sensitization of meningeal nociceptors: the role of immuno-vascular interactions and cortical spreading depression.

Authors:  Dan Levy
Journal:  Curr Pain Headache Rep       Date:  2012-06

4.  The impact of migraine on patients with major depressive disorder.

Authors:  Ching-I Hung; Chia-Yih Liu; Yeong-Yuh Juang; Shuu-Jiun Wang
Journal:  Headache       Date:  2006-03       Impact factor: 5.887

5.  Localization of a gene for migraine without aura to chromosome 4q21.

Authors:  Asgeir Björnsson; Grétar Gudmundsson; Einar Gudfinnsson; María Hrafnsdóttir; John Benedikz; Svanhildur Skúladóttir; Kristleifur Kristjánsson; Michael L Frigge; Augustine Kong; Kári Stefánsson; Jeffrey R Gulcher
Journal:  Am J Hum Genet       Date:  2003-09-25       Impact factor: 11.025

6.  Association of oestrogen-receptor gene (ESR1) polymorphisms with migraine in the large Norfolk Island pedigree.

Authors:  Astrid J Rodriguez-Acevedo; Bridget H Maher; Rodney A Lea; Miles Benton; Lyn R Griffiths
Journal:  Cephalalgia       Date:  2013-05-14       Impact factor: 6.292

7.  The novel p.L1649Q mutation in the SCN1A epilepsy gene is associated with familial hemiplegic migraine: genetic and functional studies. Mutation in brief #957. Online.

Authors:  Kaate R J Vanmolkot; Elena Babini; Boukje de Vries; Anine H Stam; Tobias Freilinger; Gisela M Terwindt; Lisa Norris; Joost Haan; Rune R Frants; Nabih M Ramadan; Michel D Ferrari; Michael Pusch; Arn M J M van den Maagdenberg; Martin Dichgans
Journal:  Hum Mutat       Date:  2007-05       Impact factor: 4.878

Review 8.  Hereditary cerebral small vessel diseases: a review.

Authors:  Antonio Federico; Ilaria Di Donato; Silvia Bianchi; Chiara Di Palma; Ilaria Taglia; Maria Teresa Dotti
Journal:  J Neurol Sci       Date:  2012-08-04       Impact factor: 3.181

9.  Association of the C677T and A1298C polymorphisms in the 5,10 methylenetetrahydrofolate reductase gene in patients with migraine risk.

Authors:  Ihsan Kara; Ali Sazci; Emel Ergul; Guner Kaya; Gamze Kilic
Journal:  Brain Res Mol Brain Res       Date:  2003-03-17

10.  A new autosomal dominant vascular retinopathy syndrome.

Authors:  C W Storimans; M J Van Schooneveld; J A Oosterhuis; P J Bos
Journal:  Eur J Ophthalmol       Date:  1991 Apr-Jun       Impact factor: 1.922

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  3 in total

Review 1.  Comorbidity of Alcohol Use Disorder and Chronic Pain: Genetic Influences on Brain Reward and Stress Systems.

Authors:  Ellen W Yeung; Jason G Craggs; Ian R Gizer
Journal:  Alcohol Clin Exp Res       Date:  2017-10-19       Impact factor: 3.455

2.  Artificial intelligence analysis to explore synchronize exercise, cobalamin, and magnesium as new actors to therapeutic of migraine symptoms: a randomized, placebo-controlled trial.

Authors:  Hanie Matin; Farzaneh Taghian; Ahmad Chitsaz
Journal:  Neurol Sci       Date:  2022-02-03       Impact factor: 3.307

Review 3.  Genetic and biochemical changes of the serotonergic system in migraine pathobiology.

Authors:  Claudia Francesca Gasparini; Robert Anthony Smith; Lyn Robyn Griffiths
Journal:  J Headache Pain       Date:  2017-02-13       Impact factor: 7.277

  3 in total

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