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J Headache Pain. 2015;16:553. doi: 10.1186/s10194-015-0553-1. Epub 2015 Aug 1.
2
Replication study of previous migraine genome-wide association study findings in a Spanish sample of migraine with aura.既往偏头痛全基因组关联研究结果在西班牙有先兆偏头痛样本中的重复研究。
Cephalalgia. 2015 Aug;35(9):776-82. doi: 10.1177/0333102414557841. Epub 2014 Nov 11.
3
Diagnosis, pathophysiology and management of chronic migraine: a proposal of the Belgian Headache Society.慢性偏头痛的诊断、病理生理学与管理:比利时头痛协会的提议
Acta Neurol Belg. 2015 Mar;115(1):1-17. doi: 10.1007/s13760-014-0313-z. Epub 2014 Jun 27.
4
Selectivity in genetic association with sub-classified migraine in women.女性偏头痛亚分类的基因关联选择性。
PLoS Genet. 2014 May 22;10(5):e1004366. doi: 10.1371/journal.pgen.1004366. eCollection 2014 May.
5
Studies on the pathophysiology and genetic basis of migraine.偏头痛的病理生理学和遗传学基础研究。
Curr Genomics. 2013 Aug;14(5):300-15. doi: 10.2174/13892029113149990007.
6
Genome-wide-associated variants in migraine susceptibility: a replication study from North India.偏头痛易感性的全基因组关联变异:来自印度北部的一项复制研究。
Headache. 2013 Nov-Dec;53(10):1583-94. doi: 10.1111/head.12240. Epub 2013 Oct 29.
7
Genome-wide meta-analysis identifies new susceptibility loci for migraine.全基因组荟萃分析确定偏头痛的新易感位点。
Nat Genet. 2013 Aug;45(8):912-917. doi: 10.1038/ng.2676. Epub 2013 Jun 23.
8
Association between the G252A Tumor Necrosis Factor-β Gene Polymorphism and Medication-Overuse Headache.肿瘤坏死因子-β基因 G252A 多态性与药物过度使用性头痛的关联。
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9
Replication and meta-analysis of common variants identifies a genome-wide significant locus in migraine.常见变异的复制和荟萃分析确定了偏头痛的全基因组显著位置。
Eur J Neurol. 2013 May;20(5):765-72. doi: 10.1111/ene.12055. Epub 2013 Jan 7.
10
Neurovascular changes in prolonged migraine aura in FHM with a novel ATP1A2 gene mutation.伴有新型 ATP1A2 基因突变的家族性偏瘫性偏头痛持续性偏头痛先兆的神经血管变化。
J Neurol Neurosurg Psychiatry. 2012 Feb;83(2):205-12. doi: 10.1136/jnnp-2011-300843. Epub 2011 Oct 19.

福建省汉族人群中的偏头痛易感基因。

Migraine Susceptibility Genes in Han Chinese of Fujian Province.

作者信息

Lin Qi Fang, Chen Zi Chun, Fu Xian Guo, Yang Jing, Cao Luo Yuan, Yao Long Teng, Xin Yong Tong, Huang Gen Bin

机构信息

Department of Internal Neurology, Ningde Municipal Hospital, Fujian Medical University, Ningde, Fujian, China.

Clinical Pharmacy, Ningde Municipal Hospital, Fujian Medical University, Ningde, Fujian, China.

出版信息

J Clin Neurol. 2017 Jan;13(1):71-76. doi: 10.3988/jcn.2017.13.1.71.

DOI:10.3988/jcn.2017.13.1.71
PMID:28079315
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC5242144/
Abstract

BACKGROUND AND PURPOSE

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.

METHODS

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.

RESULTS

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).

CONCLUSIONS

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.

摘要

背景与目的

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。

方法

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。

结果

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)。

结论

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。