Papasavva Maria, Vikelis Michail, Siokas Vasileios, Katsarou Martha-Spyridoula, Dermitzakis Emmanouil V, Raptis Athanasios, Kalliantasi Aikaterini, Dardiotis Efthimios, Drakoulis Nikolaos
Research Group of Clinical Pharmacology and Pharmacogenomics, Faculty of Pharmacy, School of Health Sciences, National and Kapodistrian University of Athens, Athens, Greece.
Headache Clinic, Mediterraneo Hospital, Glyfada, Greece.
Front Neurol. 2023 Jan 9;13:1054333. doi: 10.3389/fneur.2022.1054333. eCollection 2022.
Migraine is a complex disorder with genetic and environmental inputs. Cumulative evidence implicates oxidative stress (OS) in migraine pathophysiology while genetic variability may influence an individuals' oxidative/antioxidant capacity. Aim of the current study was to investigate the impact of eight common OS-related genetic variants [rs4880 (), rs1001179 (), rs1050450 (), rs1695 (), rs1138272 (), rs1799983 (), rs6721961 (), rs660339 ()] in migraine susceptibility and clinical features in a South-eastern European Caucasian population.
Genomic DNA samples from 221 unrelated migraineurs and 265 headache-free controls were genotyped for the selected genetic variants using real-time PCR (melting curve analysis).
Although allelic and genotypic frequency distribution analysis did not support an association between migraine susceptibility and the examined variants in the overall population, subgroup analysis indicated significant correlation between rs1799983 and migraine susceptibility in males. Furthermore, significant associations of rs1001179 and rs1050450 with disease age-at-onset and migraine attack duration, respectively, were revealed. Lastly, variability in the and genes were associated with sleep/weather changes, alcohol consumption and physical exercise, respectively, as migraine triggers.
Hence, the current findings possibly indicate an association of OS-related genetic variants with migraine susceptibility and clinical features, further supporting the involvement of OS and genetic susceptibility in migraine.
偏头痛是一种受遗传和环境因素影响的复杂疾病。越来越多的证据表明氧化应激(OS)在偏头痛的病理生理学中起作用,而基因变异可能会影响个体的氧化/抗氧化能力。本研究的目的是调查8种常见的与OS相关的基因变异[rs4880()、rs1001179()、rs1050450()、rs1695()、rs1138272()、rs1799983()、rs6721961()、rs660339()]对东南欧高加索人群偏头痛易感性和临床特征的影响。
使用实时PCR(熔解曲线分析)对221名无亲缘关系的偏头痛患者和265名无头痛的对照者的基因组DNA样本进行所选基因变异的基因分型。
虽然等位基因和基因型频率分布分析不支持偏头痛易感性与总体人群中所检测变异之间的关联,但亚组分析表明rs1799983与男性偏头痛易感性之间存在显著相关性。此外,还分别揭示了rs1001179和rs1050450与疾病发病年龄和偏头痛发作持续时间之间存在显著关联。最后, 基因和 基因的变异性分别与睡眠/天气变化、饮酒和体育锻炼作为偏头痛触发因素有关。
因此,目前的研究结果可能表明与OS相关的基因变异与偏头痛易感性和临床特征之间存在关联,进一步支持了OS和遗传易感性在偏头痛中的作用。