Tikka-Kleemola P, Kaunisto M A, Hämäläinen E, Todt U, Göbel H, Kaprio J, Kubisch C, Färkkilä M, Palotie A, Wessman M, Kallela M
Institute of Molecular Medicine in Finland, University of Helsinki, 00014 Helsinki, Finland.
Cephalalgia. 2009 Nov;29(11):1224-31. doi: 10.1111/j.1468-2982.2009.01855.x. Epub 2009 Apr 9.
The effect of endothelin-1 and its receptors EDNRA and EDNRB in migraine with aura (MA) susceptibility is not established yet. We studied the association between the MA end-diagnosis and three migraine trait components and 32 single nucleotide polymorphisms (SNPs) capturing the variation of endothelin genes in 850 Finnish migraine patients and 890 non-migrainous individuals. The SNPs showing evidence of association were further studied in 648 German migraine patients and 651 non-migrainous individuals. No significant association was detected. However, the homozygous minor genotype (5% in cases) of the EDNRA SNP rs2048894 showed nominal association with MA both in the Finnish sample (P = 0.015) and in the pooled sample [odds ratio (OR) 1.61, 95% confidence interval (CI) 1.12-2.32, P = 0.010] when adjusted for gender and sample origin. The trait age of onset < 20 years was also associated with rs2048894 (OR 1.69, 95% CI 1.13-2.54, P = 0.011) in the pooled sample. To confirm this finding studies on even larger samples are required.
内皮素 -1及其受体EDNRA和EDNRB在伴先兆偏头痛(MA)易感性中的作用尚未明确。我们研究了850名芬兰偏头痛患者和890名非偏头痛个体中MA最终诊断与三个偏头痛特征成分以及32个捕获内皮素基因变异的单核苷酸多态性(SNP)之间的关联。在648名德国偏头痛患者和651名非偏头痛个体中对显示出关联证据的SNP进行了进一步研究。未检测到显著关联。然而,在根据性别和样本来源进行调整后,EDNRA SNP rs2048894的纯合次要基因型(病例中占5%)在芬兰样本(P = 0.015)和合并样本中均与MA显示出名义上的关联[优势比(OR)1.61,95%置信区间(CI)1.12 - 2.32,P = 0.010]。在合并样本中,发病特征年龄<20岁也与rs2048894相关(OR 1.69,95% CI 1.13 - 2.54,P = 0.011)。为证实这一发现,需要对更大样本进行研究。