Thomsen L L, Oestergaard E, Bjornsson A, Stefansson H, Fasquel A C, Gulcher J, Stefansson K, Olesen J
Danish Headache Centre, University of Copenhagen, Department of Neurology, Glostrup Hospital, Glostrup, Denmark.
Cephalalgia. 2008 Sep;28(9):914-21. doi: 10.1111/j.1468-2982.2008.01599.x. Epub 2008 May 30.
The aim of this study was to investigate the involvement of the CACNA1A and ATP1A2 gene in a population-based sample of sporadic hemiplegic migraine (SHM). Patients with SHM (n = 105) were identified in a nationwide search in the Danish population. We sequenced all exons and promoter regions of the CACNA1A and ATP1A2 genes in 100 patients with SHM to search for possible SHM mutations. Novel DNA variants were discovered in eight SHM patients, four in exons of the CACNA1A gene and four in exons of the ATP1A2 gene. Six of the variants were considered non-pathogenic. The causal role of the two remaining DNA variants is unknown until functional studies have been made or independent genetic evidence is discovered. Only very few DNA variants were identified in 100 SHM patients, and regardless of whether the identified variants are causal the CACNA1A and ATP1A2 genes are not major genes in SHM.
本研究的目的是在散发性偏瘫性偏头痛(SHM)的基于人群的样本中调查CACNA1A和ATP1A2基因的参与情况。在丹麦人群的全国性搜索中识别出SHM患者(n = 105)。我们对100例SHM患者的CACNA1A和ATP1A2基因的所有外显子和启动子区域进行测序,以寻找可能的SHM突变。在8例SHM患者中发现了新的DNA变异,其中4例在CACNA1A基因的外显子中,4例在ATP1A2基因的外显子中。其中6个变异被认为是非致病性的。在进行功能研究或发现独立的遗传证据之前,其余两个DNA变异的因果作用尚不清楚。在100例SHM患者中仅鉴定出极少数DNA变异,并且无论所鉴定的变异是否具有因果关系,CACNA1A和ATP1A2基因都不是SHM的主要基因。