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ESR1基因多态性对偏头痛易感性的影响:一项荟萃分析。

Impact of ESR1 Gene Polymorphisms on Migraine Susceptibility: A Meta-Analysis.

作者信息

Li Li, Liu Ruozhuo, Dong Zhao, Wang Xiaolin, Yu Shengyuan

机构信息

From the Department of Neurology, Chinese PLA General Hospital, Haidan District, Beijing (LL, RL, ZD, XW, SY), and Department of Neurology, General Hospital of Jincheng Anthracite Coal Mining Group Co. Ltd, Jincheng, Shanxi Province, China (LL).

出版信息

Medicine (Baltimore). 2015 Sep;94(35):e0976. doi: 10.1097/MD.0000000000000976.

Abstract

An increasing number of studies have explored genetic associations between the functionally important polymorphisms in estrogen receptor 1 (ESR1) gene and migraine susceptibility. The previously reported associations have nevertheless been inconsistent.The present work incorporating the published data derived from 8 publications was performed to assess the impact of these polymorphisms on incident migraine. Strength of the genetic risk was estimated by means of an odds ratio along with the 95% confidence interval (OR and 95% CI).From the results, we found individuals who harbored the 325-GG genotype, compared with those harboring the CC genotype or CG and CC combined genotypes, had almost 50% greater risk of migraine. The same genetic models showed notable associations in subgroups of Caucasians and migraine with aura (MA). For 594G>A, a moderately increased risk of migraine was seen under AG versus GG. The AA + AG versus GG model, however, showed a borderline association with migraine. Subgroup analyses according to ethnicity and subtype of migraine provided statistical evidence of significantly increased risk of migraine in Caucasians and of a marginal association with MA, respectively. Both 325C>G and 594G>A polymorphisms showed no major effects either in males or in females.Based on the statistical data, we conclude some of the ESR1 gene polymorphisms may have major contributions to the pathogenesis of migraine in Caucasian populations.

摘要

越来越多的研究探讨了雌激素受体1(ESR1)基因中功能重要的多态性与偏头痛易感性之间的遗传关联。然而,先前报道的关联并不一致。本研究纳入了来自8篇出版物的已发表数据,以评估这些多态性对偏头痛发病的影响。通过优势比以及95%置信区间(OR和95%CI)来估计遗传风险强度。从结果中,我们发现携带325-GG基因型的个体,与携带CC基因型或CG和CC组合基因型的个体相比,患偏头痛的风险几乎高50%。相同的遗传模型在白种人和伴有先兆偏头痛(MA)的亚组中显示出显著关联。对于594G>A,AG与GG相比,偏头痛风险适度增加。然而,AA + AG与GG模型显示与偏头痛存在临界关联。根据种族和偏头痛亚型进行的亚组分析分别提供了白种人偏头痛风险显著增加以及与MA存在边缘关联的统计证据。325C>G和594G>A多态性在男性或女性中均未显示出主要影响。基于统计数据,我们得出结论,ESR1基因的某些多态性可能对白种人群偏头痛的发病机制有重要影响。

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