Lin Qi Fang, Chen Zi Chun, Fu Xian Guo, Yang Jing, Cao Luo Yuan, Yao Long Teng, Xin Yong Tong, Huang Gen Bin
Department of Internal Neurology, Ningde Municipal Hospital, Fujian Medical University, Ningde, Fujian, China.
Clinical Pharmacy, Ningde Municipal Hospital, Fujian Medical University, Ningde, Fujian, China.
J Clin Neurol. 2017 Jan;13(1):71-76. doi: 10.3988/jcn.2017.13.1.71.
Five single-nucleotide polymorphisms (SNPs) (rs4379368, rs10504861, rs10915437, rs12134493 and rs13208321) were recently identified in a Western population with migraine. These migraine-associated SNPs have not been evaluated in a Han Chinese population. This study investigated the associations of specific SNPs with migraine in a Han population.
This was a case-control study of Han Chinese residing in Fujian Province. Polymerase chain reaction-restriction-fragment-length polymorphism analysis and direct sequencing were used to characterize the relationships of SNPs in a control group of 200 subjects and in a migraine group of 201 patients.
The frequencies of the five SNPs did not differ between patients with migraine and healthy non migraine controls. However, subgroup analysis indicated certain SNPs were more strongly associated with migraine with aura or migraine without aura than with controls. The CT genotype of rs4379368 was more common in migraine patients with aura (75%) than in migraine patients without aura (47.9%) and controls (48.5%) (p<0.05), and the TT genotype of rs10504861 was more common in migraine patients with aura than in controls (8.3% vs. 0.5%) (p<0.05). Meanwhile, the CC genotype of rs12134493 was less common in migraine patients without aura than in controls (80.6% vs. 88%) (p<0.05).
Our findings suggest that the rs4379368 and rs10504861 SNPs are markers for susceptibility to migraine with aura and that rs12134493 is a marker for the risk of migraine without aura in this Han population. Future studies should further explore if these associations vary by ethnicity.
最近在西方偏头痛人群中发现了五个单核苷酸多态性(SNP)(rs4379368、rs10504861、rs10915437、rs12134493和rs13208321)。这些与偏头痛相关的SNP尚未在汉族人群中进行评估。本研究调查了特定SNP与汉族人群偏头痛的关联。
这是一项针对居住在福建省的汉族人群的病例对照研究。采用聚合酶链反应-限制性片段长度多态性分析和直接测序来确定200名对照组受试者和201名偏头痛患者组中SNP的关系。
偏头痛患者与健康非偏头痛对照组之间这五个SNP的频率没有差异。然而,亚组分析表明,某些SNP与有先兆偏头痛或无先兆偏头痛的关联比与对照组更强。rs4379368的CT基因型在有先兆偏头痛患者中(75%)比在无先兆偏头痛患者中(47.9%)和对照组中(48.5%)更常见(p<0.05),rs10504861的TT基因型在有先兆偏头痛患者中比在对照组中更常见(8.3%对0.5%)(p<0.05)。同时,rs12134493的CC基因型在无先兆偏头痛患者中比在对照组中更少见(80.6%对88%)(p<0.05)。
我们的研究结果表明,rs4379368和rs10504861 SNP是有先兆偏头痛易感性的标志物,而rs12134493是该汉族人群无先兆偏头痛风险的标志物。未来的研究应进一步探讨这些关联是否因种族而异。