Fernandez F, Colson N J, Griffiths L R
Genomics Research Centre, School of Medical Science, Griffith University, Gold Coast, Queensland, 9726 Australia.
Pharmacogenomics. 2007 Jun;8(6):609-22. doi: 10.2217/14622416.8.6.609.
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.
偏头痛是一种发作性神经疾病,普通人群中高达6%的男性和18%的女性受其影响,并且已证明其具有强大但复杂的遗传成分。偏头痛的基因研究为开发新的药物靶点和个体化特异性疗法带来了希望。识别疾病易感性和治疗的多态性或基因生物标志物应有助于更好地理解偏头痛的病理机制,从而为偏头痛患者提供更合适、更有效的治疗。在本综述中,我们将讨论偏头痛基因生物标志物的研究结果及其在未来治疗规划中的潜在作用。