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5-羟色胺2A受体基因多态性与偏头痛易感性的Meta分析

Meta-analysis of 5-hydroxytryptamine type 2A receptor polymorphisms and migraine susceptibility.

作者信息

Peng Jian-Ming, Yu You-Jiang, Su Lan-Di, Luo Xue

机构信息

1Medical College of Yangzhou Polytechnic College, Yangzhou, China.

出版信息

Int J Neurosci. 2014 Dec;124(12):882-9. doi: 10.3109/00207454.2014.888425. Epub 2014 Jul 21.

Abstract

Epidemiologic studies have investigated the association of polymorphisms in 5-hydroxytryptamine type 2A receptor (5HT2A) gene and migraine susceptibility, but the results of those studies are inconclusive. To obtain a more systematic estimation of the association, we conducted a comprehensive search to examine all the eligible studies of 5HT2A polymorphisms and migraine risk. The odd ratios (ORs) with 95% confidence intervals (CIs) were used to determine the strength of the association. Publication bias was analyzed by Begg's funnel plots. Seven eligible studies regarding 5HT2A T102C and A-1438G polymorphisms with 721 cases and 713 controls were included in this meta-analysis. Overall, no significant associations were found between 5HT2A T102C (for T vs. C: OR = 1.029, 95% CI = 0.870-1.217, p = 0.739; for TT vs. CC: OR = 1.083, 95% CI = 0.760-1.544, p = 0.657; for TT + TC vs. CC: OR = 1.066, 95% CI = 0.802-1.416, p = 0.662; for TT vs. TC + CC: OR = 1.017, 95% CI = 0.774-1.336, p = 0.904) or A-1438G (for T vs. C: OR = 0.996, 95% CI = 0.726-1.365, p = 0.979; for TT vs. CC: OR = 0.983, 95% CI = 0.511-1.891, p = 0.960; for TT + TC vs. CC: OR = 1.118, 95% CI = 0.654-1.910, p = 0.684; for TT vs. TC + CC: OR = 0.890, 95% CI = 0.528-1.499, p = 0.661) polymorphisms and migraine risk. The further subgroup analysis by ethnicity, assay and disease type also found no significant association using four genetic models. Meanwhile, the publication bias analysis suggests that there is no publication bias in these studies. In conclusion, our current meta-analysis implies that 5HT2A T102C and A-1438G polymorphisms may be not risk factors in the pathogenesis of migraine.

摘要

流行病学研究调查了5-羟色胺2A受体(5HT2A)基因多态性与偏头痛易感性之间的关联,但这些研究结果尚无定论。为了更系统地评估这种关联,我们进行了全面检索,以审查所有关于5HT2A多态性与偏头痛风险的合格研究。使用具有95%置信区间(CI)的比值比(OR)来确定关联强度。通过Begg漏斗图分析发表偏倚。本荟萃分析纳入了7项关于5HT2A T102C和A - 1438G多态性的合格研究,共721例病例和713例对照。总体而言,未发现5HT2A T102C(T vs. C:OR = 1.029,95% CI = 0.870 - 1.217,p = 0.739;TT vs. CC:OR = 1.083,95% CI = 0.760 - 1.544,p = 0.657;TT + TC vs. CC:OR = 1.066,95% CI = 0.802 - 1.416,p = 0.662;TT vs. TC + CC:OR = 1.017,95% CI = 0.774 - 1.336,p = 0.904)或A - 1438G(T vs. C:OR = 0.996,95% CI = 0.726 - 1.365,p = 0.979;TT vs. CC:OR = 0.983,95% CI = 0.511 - 1.891,p = 0.960;TT + TC vs. CC:OR = 1.118,95% CI = 0.654 - 1.910,p = 0.684;TT vs. TC + CC:OR = 0.890,95% CI = 0.528 - 1.499,p = 0.661)多态性与偏头痛风险之间存在显著关联。按种族、检测方法和疾病类型进行的进一步亚组分析,在四种遗传模型下也未发现显著关联。同时,发表偏倚分析表明这些研究不存在发表偏倚。总之,我们当前的荟萃分析表明,5HT2A T102C和A - 1438G多态性可能不是偏头痛发病机制中的危险因素。

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