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偏头痛中多巴胺β羟化酶基因多态性的分析

Analysis of dopamine beta hydroxylase gene polymorphisms in migraine.

作者信息

Sezer Saime, Kurt Semiha, Ates Omer

机构信息

Department of Medical Biology, Gaziosmanpasa University, Tokat, Turkey.

Department ofNeurology, Medical Faculty, Gaziosmanpasa University, Tokat, Turkey.

出版信息

Clin Neurol Neurosurg. 2016 Jun;145:96-100. doi: 10.1016/j.clineuro.2016.02.002. Epub 2016 Feb 3.

Abstract

BACKGROUND

Migraine is a complex neurological disorder characterized by severe recurrent headache, nausea, vomiting, photophobia, and phonophobia. The frequency and duration of these symptoms varies among individuals. Dopaminergic systems are believed to be involved in migraine pathophysiology. We aimed to look for association of polymorphisms in dopaminergic genes in genetic susceptibility to migraine in Turkey population.

METHODS

The present study was designed to explore possible association of three polymorphisms, (1021C>T (Rs1611115), +1603C>T (Rs6271; C535R) and +444G>A (rs1108580), of Dopamin Beta Hydroxylase gene in migraine patients. 200 migraine patients and 267 healthy controls were included in the study. Genomic DNA was extracted from blood and genotypes were analyzed using polymerase chain reaction-restriction fragment length polymorphism methods (PCR-RFLP).

RESULTS

Statistical evaluation of data results showed a significant association for allelic and genotypic frequency distribution between the Dopamin Beta Hydroxylase gene +1603C>T polymorphism and migraine (p=0.000, OR: 4.36, 95% CI: 2.73-7.16). There was no association observed between the -1021C>T and +444 G>A polymorphisms of the Dopamin Beta Hydroxylase gene and migraine (p=0.8731 and p=0.7584).

CONCLUSIONS

This study reflects that Dopamin Beta Hydroxylase gene +1603C>T polymorphism may be one of the many genetic factors for migraine susceptibility in the Turkish population.

摘要

背景

偏头痛是一种复杂的神经系统疾病,其特征为严重的复发性头痛、恶心、呕吐、畏光和畏声。这些症状的频率和持续时间因人而异。多巴胺能系统被认为参与了偏头痛的病理生理过程。我们旨在寻找土耳其人群中多巴胺能基因多态性与偏头痛遗传易感性之间的关联。

方法

本研究旨在探讨多巴胺β羟化酶基因的三种多态性(1021C>T(Rs1611115)、+1603C>T(Rs6271;C535R)和+444G>A(rs1108580))与偏头痛患者的可能关联。200名偏头痛患者和267名健康对照者纳入研究。从血液中提取基因组DNA,并使用聚合酶链反应-限制性片段长度多态性方法(PCR-RFLP)分析基因型。

结果

数据结果的统计评估显示,多巴胺β羟化酶基因+1603C>T多态性与偏头痛之间的等位基因和基因型频率分布存在显著关联(p=0.000,OR:4.36,95%CI:2.73-7.16)。未观察到多巴胺β羟化酶基因的-1021C>T和+444G>A多态性与偏头痛之间存在关联(p=0.8731和p=0.7584)。

结论

本研究表明,多巴胺β羟化酶基因+1603C>T多态性可能是土耳其人群中偏头痛易感性的众多遗传因素之一。

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