Literature DB >> 17559350

Pharmacogenetics of migraine: genetic variants and their potential role in migraine therapy.

F Fernandez1, N J Colson, L R Griffiths.   

Abstract

Migraine is a paroxysmal neurological disorder affecting up to 6% of males and 18% of females in the general population, and has been demonstrated to have a strong, but complex, genetic component. Genetic investigation of migraine provides hope that new targets for medications and individual specific therapy will be developed. The identification of polymorphisms or genetic biomarkers for disease susceptibility and treatment should aid in providing a better understanding of migraine pathology and, consequently, more appropriate and efficient treatment for migraineurs. In this review, we will discuss results investigating genetic biomarkers for migraine and their potential role in future therapy planning.

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Year:  2007        PMID: 17559350     DOI: 10.2217/14622416.8.6.609

Source DB:  PubMed          Journal:  Pharmacogenomics        ISSN: 1462-2416            Impact factor:   2.533


  3 in total

1.  Association of endothelial nitric oxide synthase gene polymorphisms (894G/T, -786T/C, G10T) and clinical findings in patients with migraine.

Authors:  Recep Eröz; Anzel Bahadir; Suber Dikici; Sener Tasdemir
Journal:  Neuromolecular Med       Date:  2014-05-22       Impact factor: 3.843

2.  The effects of body mass index on the treatment of the patients with migraine headaches.

Authors:  Siamak Afshinmajd; Ali Davati; Farnaz Akbari
Journal:  Iran J Neurol       Date:  2011

Review 3.  Genetics of migraine and pharmacogenomics: some considerations.

Authors:  Maria Piane; Patrizia Lulli; Ivano Farinelli; Simona Simeoni; Sergio De Filippis; Francesca Romana Patacchioli; Paolo Martelletti
Journal:  J Headache Pain       Date:  2007-12-05       Impact factor: 7.277

  3 in total

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