Ran Caroline, Fourier Carmen, Arafa Donia, Liesecke Franziska, Sjöstrand Christina, Waldenlind Elisabet, Steinberg Anna, Belin Andrea Carmine
Department of Neuroscience, Karolinska Institutet, Biomedicum D7, Solnavägen 9, 171 65 Stockholm, Sweden.
Department of Clinical Neuroscience, Karolinska University Hospital, Tomtebodavägen 18A, 171 77 Stockholm, Sweden.
Brain Sci. 2019 Jul 30;9(8):184. doi: 10.3390/brainsci9080184.
Cluster headache is a severe primary headache characterized by extremely painful attacks of unilateral headache. Verapamil is commonly used as a prophylactic treatment with good effect. In order to search for new pathways involved in the pathophysiology of cluster headache, we analyzed genetic variants that were previously linked to verapamil response in migraine in a Swedish cluster headache case-control sample. We used TaqMan qPCR for genetic screening and performed a gene expression analysis on associated genes in patient-derived fibroblasts, and further investigated which reference genes were suitable for analysis in fibroblasts from cluster headache patients. We discovered a significant association between , a gene encoding a calcium-activated ion channel, and cluster headache. The association was not dependent on verapamil treatment since the associated variant, rs1531394, was also overrepresented in patients not using verapamil. No difference was found in the gene expression between controls and patients. Also, we determined that , and were suitable reference genes in cluster headache fibroblasts. This finding is the first report of an association between a variant in a gene encoding an ion-channel and cluster headache, and the first significant genetic evidence of calcium involvement in cluster headache pathophysiology.
丛集性头痛是一种严重的原发性头痛,其特征为单侧头痛的极度疼痛发作。维拉帕米通常用作预防性治疗,效果良好。为了寻找丛集性头痛病理生理学中涉及的新途径,我们在瑞典丛集性头痛病例对照样本中分析了先前与偏头痛中维拉帕米反应相关的基因变异。我们使用TaqMan qPCR进行基因筛查,并对患者来源的成纤维细胞中的相关基因进行基因表达分析,并进一步研究哪些参考基因适合用于丛集性头痛患者成纤维细胞的分析。我们发现编码钙激活离子通道的基因与丛集性头痛之间存在显著关联。该关联不依赖于维拉帕米治疗,因为相关变体rs1531394在未使用维拉帕米的患者中也过度表达。对照组和患者之间未发现该基因表达存在差异。此外,我们确定,和是丛集性头痛成纤维细胞中合适的参考基因。这一发现是关于编码离子通道的基因变体与丛集性头痛之间关联的首次报告,也是钙参与丛集性头痛病理生理学的首个重要遗传证据。