• 文献检索
  • 文档翻译
  • 深度研究
  • 学术资讯
  • Suppr Zotero 插件Zotero 插件
  • 邀请有礼
  • 套餐&价格
  • 历史记录
应用&插件
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
定价
高级版会员购买积分包购买API积分包
服务
文献检索文档翻译深度研究API 文档MCP 服务
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利:CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2026

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验

多态性与偏头痛风险关联的定量评估。

Quantitative assessment of the association between polymorphisms and migraine risk.

机构信息

Department of Pediatric Endocrinology/Genetics, Shanghai Institute for Pediatric Research, Xinhua Hospital, School of Medicine, Shanghai Jiao Tong University, Shanghai 200092, China

Department of Pediatric Endocrinology/Genetics, Shanghai Institute for Pediatric Research, Xinhua Hospital, School of Medicine, Shanghai Jiao Tong University, Shanghai 200092, China.

出版信息

Biosci Rep. 2018 Dec 14;38(6). doi: 10.1042/BSR20181347. Print 2018 Dec 21.

DOI:10.1042/BSR20181347
PMID:30446525
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC6294621/
Abstract

PURPOSE

The association between rs548294 G>A and rs2195450 C>T polymorphisms and migraine risk has been reported in several case-control studies. However, the results of studies are inconsistent. Thus, we conducted a meta-analysis to more precisely estimate the association of the two polymorphisms with migraine risk.

METHODS

Eligible studies were retrieved and screened from the online databases (EMBASE, PubMed, Web of Science, Wanfang, and Chinese National Knowledge Infrastructure). The pooled odds ratio (OR) with corresponding 95.0% confidence intervals (CIs) was assessed using random- or fixed-effects model.

RESULTS

A total of 1233 cases and 1374 controls from four eligible studies were included. The pooled analysis showed that rs548294 G>A polymorphism was not significantly associated with migraine risk. rs2195450 C>T polymorphism was significantly associated with migraine risk under heterozygous model (CT vs. CC, OR = 1.23, 95%CI = 1.02-1.48, = 0.03). Further subgroup analysis based on ethnicity showed a significant association of rs2195450 C>T polymorphism with migraine risk in Asian population, but not in Caucasian population.

CONCLUSIONS

Our results indicates that rs2195450 C>T polymorphism is significantly associated with migraine risk. However, the number of studies included in the meta-analysis was small. Thus, more high quality case-control studies with a large sample size are still required to confirm these findings.

摘要

目的

rs548294 G>A 和 rs2195450 C>T 多态性与偏头痛风险的关联已在几项病例对照研究中报道。然而,研究结果并不一致。因此,我们进行了荟萃分析,以更准确地估计这两种多态性与偏头痛风险的关联。

方法

从在线数据库(EMBASE、PubMed、Web of Science、万方和中国国家知识基础设施)中检索和筛选符合条件的研究。使用随机或固定效应模型评估合并的优势比(OR)及其相应的 95.0%置信区间(CI)。

结果

共有四项符合条件的研究纳入了 1233 例病例和 1374 例对照。荟萃分析显示,rs548294 G>A 多态性与偏头痛风险无显著相关性。rs2195450 C>T 多态性在杂合子模型下(CT 与 CC,OR=1.23,95%CI=1.02-1.48, = 0.03)与偏头痛风险显著相关。基于种族的亚组分析进一步表明,rs2195450 C>T 多态性与亚洲人群的偏头痛风险显著相关,但在白人群体中则无显著相关性。

结论

我们的研究结果表明,rs2195450 C>T 多态性与偏头痛风险显著相关。然而,纳入荟萃分析的研究数量较少。因此,仍需要更多高质量的、大样本量的病例对照研究来验证这些发现。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3ade/6294621/d245fe4ea788/bsr-38-bsr20181347-g3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3ade/6294621/0b051bda7085/bsr-38-bsr20181347-g1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3ade/6294621/61b707525693/bsr-38-bsr20181347-g2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3ade/6294621/d245fe4ea788/bsr-38-bsr20181347-g3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3ade/6294621/0b051bda7085/bsr-38-bsr20181347-g1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3ade/6294621/61b707525693/bsr-38-bsr20181347-g2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3ade/6294621/d245fe4ea788/bsr-38-bsr20181347-g3.jpg

相似文献

1
Quantitative assessment of the association between polymorphisms and migraine risk.多态性与偏头痛风险关联的定量评估。
Biosci Rep. 2018 Dec 14;38(6). doi: 10.1042/BSR20181347. Print 2018 Dec 21.
2
Case-control study of GRIA1 and GRIA3 gene variants in migraine.偏头痛中GRIA1和GRIA3基因变异的病例对照研究。
J Headache Pain. 2015;17:2. doi: 10.1186/s10194-016-0592-2. Epub 2016 Jan 22.
3
Lack of association between GRIA1 polymorphisms and haplotypes with migraine without aura or response to triptans.GRIA1 多态性与无先兆偏头痛或曲坦类药物反应之间缺乏关联。
Neurol Sci. 2014 Mar;35(3):421-7. doi: 10.1007/s10072-013-1535-1. Epub 2013 Sep 13.
4
Common variants in the regulative regions of GRIA1 and GRIA3 receptor genes are associated with migraine susceptibility.常见的 GRIA1 和 GRIA3 受体基因调节区变异与偏头痛易感性相关。
BMC Med Genet. 2010 Jun 25;11:103. doi: 10.1186/1471-2350-11-103.
5
The association between eating behavior and polymorphisms in GRIN2B, GRIK3, GRIA1 and GRIN1 genes in people with type 2 diabetes mellitus.2 型糖尿病患者的饮食行为与 GRIN2B、GRIK3、GRIA1 和 GRIN1 基因多态性之间的关联。
Mol Biol Rep. 2020 Mar;47(3):2035-2046. doi: 10.1007/s11033-020-05304-x. Epub 2020 Feb 10.
6
Association of TLR4 (896A/G and 1196C/T) Gene Polymorphisms with Asthma Risk: A Meta-Analysis.TLR4(896A/G和1196C/T)基因多态性与哮喘风险的关联:一项荟萃分析。
Med Sci Monit. 2015 Nov 20;21:3591-9. doi: 10.12659/msm.895380.
7
Effects of MTHFR C677T and A1298C Polymorphisms on Migraine Susceptibility: A Meta-Analysis of 26 Studies.MTHFR C677T 和 A1298C 多态性对偏头痛易感性的影响:26 项研究的荟萃分析。
Headache. 2019 Jun;59(6):891-905. doi: 10.1111/head.13540. Epub 2019 May 2.
8
Association of a GRIA3 gene polymorphism with migraine in an Australian case-control cohort.GRIA3 基因多态性与澳大利亚病例对照队列中偏头痛的关联。
Headache. 2013 Sep;53(8):1245-9. doi: 10.1111/head.12151. Epub 2013 Jun 14.
9
5-HTTLPR polymorphism in the serotonin transporter gene and migraine: a systematic review and meta-analysis.5-羟色胺转运体基因中的 5-HTTLPR 多态性与偏头痛:系统评价和荟萃分析。
Cephalalgia. 2010 Nov;30(11):1296-305. doi: 10.1177/0333102410362929. Epub 2010 Mar 26.
10
A meta-analysis of the relationship between MTHFR gene A1298C polymorphism and the risk of adult stroke.MTHFR基因A1298C多态性与成人中风风险关系的荟萃分析。
Cerebrovasc Dis. 2014;38(6):425-32. doi: 10.1159/000369122. Epub 2014 Dec 3.

引用本文的文献

1
Glutamate receptor genetic variants affected peripheral glutamatergic transmission and treatment induced improvement of Indian ADHD probands.谷氨酸受体基因变异影响外周谷氨酸能传递,并且改善了印度 ADHD 先证者的治疗效果。
Sci Rep. 2023 Nov 14;13(1):19922. doi: 10.1038/s41598-023-47117-5.
2
Clinical M2 Macrophage-Related Genes Can Serve as a Reliable Predictor of Lung Adenocarcinoma.临床M2巨噬细胞相关基因可作为肺腺癌的可靠预测指标。
Front Oncol. 2022 Jul 22;12:919899. doi: 10.3389/fonc.2022.919899. eCollection 2022.
3
Association of GRIA1 polymorphisms with ovarian response to human menopausal gonadotropin in Iranian women.

本文引用的文献

1
Gastrointestinal disorders associated with migraine: A comprehensive review.与偏头痛相关的胃肠道疾病:综述
World J Gastroenterol. 2016 Sep 28;22(36):8149-60. doi: 10.3748/wjg.v22.i36.8149.
2
Molecular factors in migraine.偏头痛的分子因素
Oncotarget. 2016 Aug 2;7(31):50708-50718. doi: 10.18632/oncotarget.9367.
3
Plasma urotensin-2 level and Thr21Met but not Ser89Asn polymorphisms of the urotensin-2 gene are associated with migraines.血浆尾加压素-2水平以及尾加压素-2基因的Thr21Met多态性而非Ser89Asn多态性与偏头痛相关。
伊朗女性中GRIA1基因多态性与卵巢对人绝经期促性腺激素反应的相关性
Clin Exp Reprod Med. 2020 Sep;47(3):207-212. doi: 10.5653/cerm.2020.03370. Epub 2020 Aug 24.
4
Meta-analysis of the association between rs619586 A>G polymorphism and cancer risk.rs619586 A>G多态性与癌症风险关联的荟萃分析。
J Int Med Res. 2020 Jul;48(7):300060520941969. doi: 10.1177/0300060520941969.
5
Genetic variants in migraine: a field synopsis and systematic re-analysis of meta-analyses.偏头痛中的遗传变异:领域概述和荟萃分析的系统重新分析。
J Headache Pain. 2020 Feb 11;21(1):13. doi: 10.1186/s10194-020-01087-5.
J Headache Pain. 2016;17:36. doi: 10.1186/s10194-016-0623-z. Epub 2016 Apr 18.
4
Analysis of dopamine beta hydroxylase gene polymorphisms in migraine.偏头痛中多巴胺β羟化酶基因多态性的分析
Clin Neurol Neurosurg. 2016 Jun;145:96-100. doi: 10.1016/j.clineuro.2016.02.002. Epub 2016 Feb 3.
5
Case-control study of GRIA1 and GRIA3 gene variants in migraine.偏头痛中GRIA1和GRIA3基因变异的病例对照研究。
J Headache Pain. 2015;17:2. doi: 10.1186/s10194-016-0592-2. Epub 2016 Jan 22.
6
Common polygenic variation contributes to risk of migraine in the Norfolk Island population.常见的多基因变异会增加诺福克岛人群患偏头痛的风险。
Hum Genet. 2015 Oct;134(10):1079-87. doi: 10.1007/s00439-015-1587-9. Epub 2015 Jul 29.
7
Headache and facial pain: differential diagnosis and treatment.头痛和面部疼痛:鉴别诊断与治疗。
J Allergy Clin Immunol Pract. 2013 May-Jun;1(3):242-51. doi: 10.1016/j.jaip.2013.03.014. Epub 2013 Apr 29.
8
Lack of association between GRIA1 polymorphisms and haplotypes with migraine without aura or response to triptans.GRIA1 多态性与无先兆偏头痛或曲坦类药物反应之间缺乏关联。
Neurol Sci. 2014 Mar;35(3):421-7. doi: 10.1007/s10072-013-1535-1. Epub 2013 Sep 13.
9
Genome-wide meta-analysis identifies new susceptibility loci for migraine.全基因组荟萃分析确定偏头痛的新易感位点。
Nat Genet. 2013 Aug;45(8):912-917. doi: 10.1038/ng.2676. Epub 2013 Jun 23.
10
Association of a GRIA3 gene polymorphism with migraine in an Australian case-control cohort.GRIA3 基因多态性与澳大利亚病例对照队列中偏头痛的关联。
Headache. 2013 Sep;53(8):1245-9. doi: 10.1111/head.12151. Epub 2013 Jun 14.