CLOCK和ADH4基因中的SNPs与丛集性头痛易感性之间没有显著关联:一项系统综述和荟萃分析

IF 1 4区 生物学 Q4 GENETICS & HEREDITY Annals of Human Genetics Pub Date : 2022-04-18 DOI:10.1111/ahg.12467
Jiarui Cui, Wei Peng, Ting Yi, Ping Gao, Mingze Zhou, Tianmin Zhu
{"title":"CLOCK和ADH4基因中的SNPs与丛集性头痛易感性之间没有显著关联:一项系统综述和荟萃分析","authors":"Jiarui Cui,&nbsp;Wei Peng,&nbsp;Ting Yi,&nbsp;Ping Gao,&nbsp;Mingze Zhou,&nbsp;Tianmin Zhu","doi":"10.1111/ahg.12467","DOIUrl":null,"url":null,"abstract":"<div>\n \n \n <section>\n \n <h3> Background</h3>\n \n <p>The circadian locomotor output cycles kaput (<i>CLOCK</i>) gene and the alcohol dehydrogenase 4 (<i>ADH4</i>) gene are promising candidates for susceptibility to cluster headaches (CH). Associations of the three single nucleotide polymorphisms (SNPs)—<i>CLOCK</i> SNP rs1801260 and <i>ADH4</i> SNPs rs1800759, and rs1126671—with CH were studied previously, but the results were inconsistent.</p>\n </section>\n \n <section>\n \n <h3> Methods</h3>\n \n <p>Associations between the three SNPs (rs1801260, rs1126671, and rs1800759) and CH risk were separately assessed by pooled odds ratios (ORs) along with 95% confidence intervals (95% CIs) based on five different genetic models. Methodological quality was assessed using the Newcastle–Ottawa Quality Assessment Scale (NOS). All statistical analyses were carried out with RevMan 5.3 software.</p>\n </section>\n \n <section>\n \n <h3> Results</h3>\n \n <p>Eight studies involving 1437 CH patients and 2541 healthy controls were selected for quantitative synthesis, from five studies on <i>CLOCK</i> rs1801260, five on <i>ADH4</i> rs1800759, and three on <i>ADH4</i> rs1126671. Our pooled data did not support associations between the three SNPs (rs1801260 in the <i>CLOCK</i> gene, rs1800759 and rs1126671 in the <i>ADH4</i> gene) and susceptibility to CH (rs1801260: OR 1.10, 95% CI: 0.95–1.28; <i>p</i> = 0.19; rs1800759: OR 1.06, 95% CI: 0.93–1.22; <i>p</i> = 0.37; and rs1126671: OR 1.09, 95% CI: 0.92–1.28; <i>p</i> = 0.32).</p>\n </section>\n \n <section>\n \n <h3> Conclusion</h3>\n \n <p>We found no significant associations between the three SNPs (rs1801260 in the <i>CLOCK</i> gene and rs1800759 and rs1126671 in the <i>ADH4</i> gene) and the susceptibility to CH across both Caucasian and Asian ethnicities in our meta-analysis.</p>\n </section>\n </div>","PeriodicalId":8085,"journal":{"name":"Annals of Human Genetics","volume":"86 4","pages":"159-170"},"PeriodicalIF":1.0000,"publicationDate":"2022-04-18","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"1","resultStr":"{\"title\":\"No significant association between SNPs in the CLOCK and ADH4 genes and susceptibility to cluster headaches: A systematic review and meta-analysis\",\"authors\":\"Jiarui Cui,&nbsp;Wei Peng,&nbsp;Ting Yi,&nbsp;Ping Gao,&nbsp;Mingze Zhou,&nbsp;Tianmin Zhu\",\"doi\":\"10.1111/ahg.12467\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<div>\\n \\n \\n <section>\\n \\n <h3> Background</h3>\\n \\n <p>The circadian locomotor output cycles kaput (<i>CLOCK</i>) gene and the alcohol dehydrogenase 4 (<i>ADH4</i>) gene are promising candidates for susceptibility to cluster headaches (CH). Associations of the three single nucleotide polymorphisms (SNPs)—<i>CLOCK</i> SNP rs1801260 and <i>ADH4</i> SNPs rs1800759, and rs1126671—with CH were studied previously, but the results were inconsistent.</p>\\n </section>\\n \\n <section>\\n \\n <h3> Methods</h3>\\n \\n <p>Associations between the three SNPs (rs1801260, rs1126671, and rs1800759) and CH risk were separately assessed by pooled odds ratios (ORs) along with 95% confidence intervals (95% CIs) based on five different genetic models. Methodological quality was assessed using the Newcastle–Ottawa Quality Assessment Scale (NOS). All statistical analyses were carried out with RevMan 5.3 software.</p>\\n </section>\\n \\n <section>\\n \\n <h3> Results</h3>\\n \\n <p>Eight studies involving 1437 CH patients and 2541 healthy controls were selected for quantitative synthesis, from five studies on <i>CLOCK</i> rs1801260, five on <i>ADH4</i> rs1800759, and three on <i>ADH4</i> rs1126671. Our pooled data did not support associations between the three SNPs (rs1801260 in the <i>CLOCK</i> gene, rs1800759 and rs1126671 in the <i>ADH4</i> gene) and susceptibility to CH (rs1801260: OR 1.10, 95% CI: 0.95–1.28; <i>p</i> = 0.19; rs1800759: OR 1.06, 95% CI: 0.93–1.22; <i>p</i> = 0.37; and rs1126671: OR 1.09, 95% CI: 0.92–1.28; <i>p</i> = 0.32).</p>\\n </section>\\n \\n <section>\\n \\n <h3> Conclusion</h3>\\n \\n <p>We found no significant associations between the three SNPs (rs1801260 in the <i>CLOCK</i> gene and rs1800759 and rs1126671 in the <i>ADH4</i> gene) and the susceptibility to CH across both Caucasian and Asian ethnicities in our meta-analysis.</p>\\n </section>\\n </div>\",\"PeriodicalId\":8085,\"journal\":{\"name\":\"Annals of Human Genetics\",\"volume\":\"86 4\",\"pages\":\"159-170\"},\"PeriodicalIF\":1.0000,\"publicationDate\":\"2022-04-18\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"1\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Annals of Human Genetics\",\"FirstCategoryId\":\"99\",\"ListUrlMain\":\"https://onlinelibrary.wiley.com/doi/10.1111/ahg.12467\",\"RegionNum\":4,\"RegionCategory\":\"生物学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q4\",\"JCRName\":\"GENETICS & HEREDITY\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Annals of Human Genetics","FirstCategoryId":"99","ListUrlMain":"https://onlinelibrary.wiley.com/doi/10.1111/ahg.12467","RegionNum":4,"RegionCategory":"生物学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q4","JCRName":"GENETICS & HEREDITY","Score":null,"Total":0}
引用次数: 1

摘要

昼夜节律运动输出周期kaput(CLOCK)基因和乙醇脱氢酶4(ADH4)基因是丛集性头痛(CH)易感性的候选基因。三种单核苷酸多态性(SNPs)——CLOCK SNP rs1801260、ADH4 SNPs rs1800759和rs1126671——与CH的相关性先前曾进行过研究,但结果不一致。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
查看原文
分享 分享
微信好友 朋友圈 QQ好友 复制链接
本刊更多论文
No significant association between SNPs in the CLOCK and ADH4 genes and susceptibility to cluster headaches: A systematic review and meta-analysis

Background

The circadian locomotor output cycles kaput (CLOCK) gene and the alcohol dehydrogenase 4 (ADH4) gene are promising candidates for susceptibility to cluster headaches (CH). Associations of the three single nucleotide polymorphisms (SNPs)—CLOCK SNP rs1801260 and ADH4 SNPs rs1800759, and rs1126671—with CH were studied previously, but the results were inconsistent.

Methods

Associations between the three SNPs (rs1801260, rs1126671, and rs1800759) and CH risk were separately assessed by pooled odds ratios (ORs) along with 95% confidence intervals (95% CIs) based on five different genetic models. Methodological quality was assessed using the Newcastle–Ottawa Quality Assessment Scale (NOS). All statistical analyses were carried out with RevMan 5.3 software.

Results

Eight studies involving 1437 CH patients and 2541 healthy controls were selected for quantitative synthesis, from five studies on CLOCK rs1801260, five on ADH4 rs1800759, and three on ADH4 rs1126671. Our pooled data did not support associations between the three SNPs (rs1801260 in the CLOCK gene, rs1800759 and rs1126671 in the ADH4 gene) and susceptibility to CH (rs1801260: OR 1.10, 95% CI: 0.95–1.28; p = 0.19; rs1800759: OR 1.06, 95% CI: 0.93–1.22; p = 0.37; and rs1126671: OR 1.09, 95% CI: 0.92–1.28; p = 0.32).

Conclusion

We found no significant associations between the three SNPs (rs1801260 in the CLOCK gene and rs1800759 and rs1126671 in the ADH4 gene) and the susceptibility to CH across both Caucasian and Asian ethnicities in our meta-analysis.

求助全文
通过发布文献求助,成功后即可免费获取论文全文。 去求助
来源期刊
Annals of Human Genetics
Annals of Human Genetics 生物-遗传学
CiteScore
4.20
自引率
0.00%
发文量
34
审稿时长
3 months
期刊介绍: Annals of Human Genetics publishes material directly concerned with human genetics or the application of scientific principles and techniques to any aspect of human inheritance. Papers that describe work on other species that may be relevant to human genetics will also be considered. Mathematical models should include examples of application to data where possible. Authors are welcome to submit Supporting Information, such as data sets or additional figures or tables, that will not be published in the print edition of the journal, but which will be viewable via the online edition and stored on the website.
期刊最新文献
Intermittent episodes of acute severe encephalomyopathy and early death in two siblings caused by biallelic likely pathogenic variants in FASTKD2: Expanding phenotype and literature review. Secondary findings in 443 exome sequencing data. Gastroesophageal reflux disease increases predisposition to severe COVID-19: Insights from integrated Mendelian randomization and genetic analysis. Clinical and immunological features of four patients with activation-induced cytidine deaminase deficiency: Renal amyloidosis and other presentations. Incorporating familial risk, lifestyle factors, and pharmacogenomic insights into personalized noncommunicable disease (NCD) reports for healthcare funder beneficiaries participating in the Open Genome Project.
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
现在去查看 取消
×
提示
确定
0
微信
客服QQ
Book学术公众号 扫码关注我们
反馈
×
意见反馈
请填写您的意见或建议
请填写您的手机或邮箱
已复制链接
已复制链接
快去分享给好友吧!
我知道了
×
扫码分享
扫码分享
Book学术官方微信
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术
文献互助 智能选刊 最新文献 互助须知 联系我们:info@booksci.cn
Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。
Copyright © 2023 Book学术 All rights reserved.
ghs 京公网安备 11010802042870号 京ICP备2023020795号-1