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内皮型一氧化氮合酶基因多态性与偏头痛之间不存在关联。

Lack of association of endothelial nitric oxide synthase polymorphisms and migraine.

作者信息

Toriello María, Oterino Agustín, Pascual Julio, Castillo Jesús, Colás Rafael, Alonso-Arranz Ana, Ruiz-Alegría Carlos, Quintela Estrella, Montón Fernando, Ruiz-Lavilla Nuria

机构信息

Services of Neurology, University Hospital Marqués de Valdecilla, Santander, Spain.

出版信息

Headache. 2008 Jul;48(7):1115-9. doi: 10.1111/j.1526-4610.2008.01181.x.

Abstract

OBJECTIVE

The aim of this study was to evaluate if 2 functional endothelial nitric oxide synthase (eNOS) gene polymorphisms might be risk factors for migraine.

BACKGROUND

Nitric oxide synthase promotes the synthesis of nitric oxide (NO). NO is a potent vasodilator and mediates several processes involved in migraine pathophysiology. Only one study has suggested an association with migraine with aura.

METHODS

We performed a sex- and age-matched case-control study using 2 eNOS polymorphisms (rs1800779 and rs1799983), which are in linkage disequilibrium. Genotypes were obtained with allele-specific probes in a real-time polymerase chain reaction assay. Genotypic and allelic distributions were compared with chi(2) method. We also estimated the reconstructed haplotypes and calculated ORs for individual haplotypes.

RESULTS

A total of 337 migraine patients (188 with aura) and 341 healthy controls were recruited. We found no significant differences in the distribution of genotypes and alleles for either polymorphism among clinical subgroups. Neither rs1800779 nor rs1799983 polymorphisms increased the risk for suffering from migraine aura.

CONCLUSIONS

As others have previously reported, we failed to demonstrate genetic association of the eNOS gene with migraine.

摘要

目的

本研究旨在评估两种功能性内皮型一氧化氮合酶(eNOS)基因多态性是否可能是偏头痛的危险因素。

背景

一氧化氮合酶促进一氧化氮(NO)的合成。NO是一种强效血管舒张剂,介导偏头痛病理生理学中的多个过程。仅有一项研究提示其与伴先兆偏头痛有关。

方法

我们采用两项处于连锁不平衡状态的eNOS基因多态性(rs1800779和rs1799983)进行了一项性别和年龄匹配的病例对照研究。通过实时聚合酶链反应分析中的等位基因特异性探针获得基因型。采用卡方检验比较基因型和等位基因分布。我们还估计了重组单倍型,并计算了各个单倍型的比值比(OR)。

结果

共纳入337例偏头痛患者(188例有先兆)和341例健康对照。我们发现,在各临床亚组中,两种多态性的基因型和等位基因分布均无显著差异。rs1800779和rs1799983多态性均未增加患偏头痛先兆的风险。

结论

正如其他人之前所报道的,我们未能证明eNOS基因与偏头痛之间存在遗传关联。

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