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γ-氨基丁酸(GABA)受体Rho(Gabrr)基因多态性与偏头痛风险

Gamma-Aminobutyric Acid (Gaba) Receptors Rho (Gabrr) Gene Polymorphisms and Risk for Migraine.

作者信息

García-Martín Elena, Martínez Carmen, Serrador Mercedes, Alonso-Navarro Hortensia, Navacerrada Francisco, Esguevillas Gara, García-Albea Esteban, Agúndez José A G, Jiménez-Jiménez Félix Javier

机构信息

Department of Pharmacology, University of Extremadura, Cáceres, Spain.

Red de Investigación de reacciones adversas a alergenos y fármacos, Instituto de Salud Carlos III, Madrid, Spain.

出版信息

Headache. 2017 Jul;57(7):1118-1135. doi: 10.1111/head.13122. Epub 2017 Jun 14.

Abstract

BACKGROUND/OBJECTIVES: The possible role of gammaaminobutyric acid (GABA) in the pathogenesis of migraine has been suggested by a number of biochemical, pharmacological, neurophysiological and experimental data. We investigated the possible association between the most common single nucleotide polymorphisms (SNPs) in the GABA receptor rho1, 2, and 3 genes (GABRR1, GABRR2, and GABRR3) and the risk of developing migraine.

METHODS

The frequency of GABRR1 rs12200969, GABRR1 rs1186902, GABRR2 rs282129, and GABRR3 rs832032 genotypes and allelic variants were studied in a case-control association study involving 197 patients with migraine and 278 healthy controls by means of a TaqMan-based qPCR Assay. We also studied the possible influence of gender, age at onset of migraine, positive family history of migraine, presence or absence of aura, and triggering of migraine by ethanol on the frequency of the genotypes.

RESULTS

The frequencies of the genotypes and allelic variants of the 4 SNPs were similar in migraine patients and controls. Gender, positive family history of migraine, presence or absence of aura, and triggering of migraine attacks by ethanol did not influence the frequency of these genotypes. Carriers of the minor allele of the rs1186902 SNP showed a trend towards later onset of migraine.

CONCLUSION

The most common polymorphisms in the GABRR genes seemed to be not associated with the risk for migraine in Caucasian Spanish people, although one of them (GABRR1 rs1186902) shows a statistically significant association with the age of onset of migraine.

摘要

背景/目的:多项生化、药理学、神经生理学及实验数据提示,γ-氨基丁酸(GABA)在偏头痛发病机制中可能发挥作用。我们研究了GABA受体rho1、2和3基因(GABRR1、GABRR2和GABRR3)中最常见的单核苷酸多态性(SNP)与偏头痛发病风险之间的可能关联。

方法

采用基于TaqMan的qPCR检测法,在一项病例对照关联研究中,对197例偏头痛患者和278例健康对照者的GABRR1 rs12200969、GABRR1 rs1186902、GABRR2 rs282129和GABRR3 rs832032基因型及等位基因变异频率进行了研究。我们还研究了性别、偏头痛发病年龄、偏头痛家族史阳性、有无先兆以及乙醇诱发偏头痛对基因型频率的可能影响。

结果

4个SNP的基因型及等位基因变异频率在偏头痛患者和对照者中相似。性别、偏头痛家族史阳性、有无先兆以及乙醇诱发偏头痛发作均未影响这些基因型的频率。rs1186902 SNP次要等位基因携带者偏头痛发病有延迟趋势。

结论

在西班牙白种人中,GABRR基因中最常见的多态性似乎与偏头痛风险无关,尽管其中一个(GABRR1 rs1186902)与偏头痛发病年龄存在统计学显著关联。

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