van de Ven Rob C G, Kaja Simon, Plomp Jaap J, Frants Rune R, van den Maagdenberg Arn M J M, Ferrari Michel D
Department of Human Genetics, Leiden University Medical Centre, Leiden, the Netherlands.
Arch Neurol. 2007 May;64(5):643-6. doi: 10.1001/archneur.64.5.643.
Migraine is a common, disabling, complex brain disorder, presenting in attacks that may have up to 3 phases: a prodromal phase, the aura phase, and the headache phase. The pathogenesis of the aura and headache phases is reasonably well understood, but the mechanism by which migraine attacks are triggered is unknown. Most likely, migraineurs have a genetically determined reduced threshold for migraine triggers. Identifying "threshold genes" and deciphering their function will help to unravel the triggering mechanisms for migraine attacks. Familial hemiplegic migraine is a rare monogenic subtype of migraine with aura. Three genes have been identified for familial hemiplegic migraine. Recently, knock-in mice carrying human pathogenic FHM1 mutations were generated, which show behavioral, electrophysiological, and neurobiological characteristics in line with prevailing views of migraine physiological processes. Genetic migraine models will be useful in unraveling the triggering mechanisms for migraine attacks and in identifying novel migraine prophylactic targets and therapies.
偏头痛是一种常见的、使人衰弱的复杂脑部疾病,发作时可能有多达三个阶段:前驱期、先兆期和头痛期。先兆期和头痛期的发病机制已得到较好的理解,但偏头痛发作的触发机制尚不清楚。最有可能的是,偏头痛患者对偏头痛触发因素的阈值在基因上是降低的。识别“阈值基因”并解读其功能将有助于揭示偏头痛发作的触发机制。家族性偏瘫性偏头痛是偏头痛伴先兆的一种罕见单基因亚型。已鉴定出与家族性偏瘫性偏头痛相关的三个基因。最近,产生了携带人类致病性FHM1突变的基因敲入小鼠,其行为、电生理和神经生物学特征与偏头痛生理过程的主流观点一致。基因偏头痛模型将有助于揭示偏头痛发作的触发机制,并有助于识别新的偏头痛预防靶点和治疗方法。