Universidad de Extremadura, University Institute of Molecular Pathology Biomarkers, Cáceres, Spain.
Section of Neurology, Hospital La Mancha-Centro, Alcázar de San Juan, Spain.
Ann Clin Transl Neurol. 2023 Oct;10(10):1824-1832. doi: 10.1002/acn3.51872. Epub 2023 Aug 8.
BACKGROUND/OBJECTIVES: Several studies have shown a relationship between vitamin D and migraine, including the association between decreased serum 25-hydroxyvitamin D in patients with migraine and the positive effects of vitamin D supplementations in the therapy of this disease. Two single-nucleotide variants (SNVs) vitamin D receptor (VDR) gene, VDR rs2228570, and VDR rs731236 have shown an association with migraine risk in a previous case-control association study, while an exome sequencing study identified a rare variant in GC vitamin D binding protein gene. This study aims to look for the association between several common variants in these two genes and the risk for migraine.
We genotyped 290 patients diagnosed with migraine and 300 age-matched controls using specific TaqMan assays for VDR rs2228570, VDR rs731236, VDR rs7975232, VDR rs739837, VDR rs78783628, GC rs7041, and GC rs4588 SNVs.
We did not find an association between these SNVs and the risk for migraine. None of these SNVs were related to the positivity of a family history of migraine or with the presence of aura. The VDR rs731236A allele showed a significant association with the triggering of migraine attacks by ethanol (Pc = 0.007).
In summary, the results of the current study suggest a lack of association between common SNVs in the VDR and GC gene and the risk of developing migraine. The possible relationship between VDR rs731236 and the triggering of migraine episodes with ethanol deserves future studies.
背景/目的:多项研究表明维生素 D 与偏头痛之间存在关联,包括偏头痛患者血清 25-羟维生素 D 水平降低与维生素 D 补充治疗该疾病的有效性之间的关联。维生素 D 受体 (VDR) 基因的两个单核苷酸变异 (SNV),VDR rs2228570 和 VDR rs731236,在前瞻性病例对照关联研究中显示与偏头痛风险相关,而外显子组测序研究则在 GC 维生素 D 结合蛋白基因中发现了一种罕见变异。本研究旨在寻找这两个基因中的几个常见变异与偏头痛风险之间的关联。
我们使用特定的 TaqMan 检测法对 290 名确诊为偏头痛的患者和 300 名年龄匹配的对照者进行了 VDR rs2228570、VDR rs731236、VDR rs7975232、VDR rs739837、VDR rs78783628、GC rs7041 和 GC rs4588 SNV 的基因分型。
我们没有发现这些 SNV 与偏头痛风险之间存在关联。这些 SNV 均与偏头痛家族史的阳性或先兆的存在无关。VDR rs731236A 等位基因与偏头痛发作由乙醇触发之间存在显著关联(Pc=0.007)。
综上所述,本研究结果表明 VDR 和 GC 基因中的常见 SNV 与偏头痛发病风险之间缺乏关联。VDR rs731236 与偏头痛发作与乙醇触发之间的可能关系值得进一步研究。