A novel framework with automated horizontal pleiotropy adjustment in mendelian randomization.

IF 3.3 Q2 GENETICS & HEREDITY HGG Advances Pub Date : 2024-08-02 DOI:10.1016/j.xhgg.2024.100339
Zhaotong Lin
{"title":"A novel framework with automated horizontal pleiotropy adjustment in mendelian randomization.","authors":"Zhaotong Lin","doi":"10.1016/j.xhgg.2024.100339","DOIUrl":null,"url":null,"abstract":"<p><p>The presence of horizontal pleiotropy in Mendelian randomization (MR) analysis has long been a concern due to its potential to induce substantial bias. In recent years, many robust MR methods have been proposed to address this by relaxing the \"no horizontal pleiotropy\" assumption. Here, we propose a novel two-stage framework called CMR, which integrates a conditional analysis of multiple genetic variants to remove pleiotropy induced by linkage disequilibrium, followed by the application of robust MR methods to model the conditional genetic effect estimates. We demonstrate how the conditional analysis can reduce horizontal pleiotropy and improve the performance of existing MR methods. Extensive simulation studies covering a wide range of scenarios of horizontal pleiotropy showcased the superior performance of the proposed CMR framework over the standard MR framework in which marginal genetic effects are modeled. Moreover, the application of CMR in a negative control outcome analysis and investigation into the causal role of body mass index across various diseases highlighted its potential to deliver more reliable results in real-world applications.</p>","PeriodicalId":34530,"journal":{"name":"HGG Advances","volume":null,"pages":null},"PeriodicalIF":3.3000,"publicationDate":"2024-08-02","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11375132/pdf/","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"HGG Advances","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.1016/j.xhgg.2024.100339","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q2","JCRName":"GENETICS & HEREDITY","Score":null,"Total":0}
引用次数: 0

Abstract

The presence of horizontal pleiotropy in Mendelian randomization (MR) analysis has long been a concern due to its potential to induce substantial bias. In recent years, many robust MR methods have been proposed to address this by relaxing the "no horizontal pleiotropy" assumption. Here, we propose a novel two-stage framework called CMR, which integrates a conditional analysis of multiple genetic variants to remove pleiotropy induced by linkage disequilibrium, followed by the application of robust MR methods to model the conditional genetic effect estimates. We demonstrate how the conditional analysis can reduce horizontal pleiotropy and improve the performance of existing MR methods. Extensive simulation studies covering a wide range of scenarios of horizontal pleiotropy showcased the superior performance of the proposed CMR framework over the standard MR framework in which marginal genetic effects are modeled. Moreover, the application of CMR in a negative control outcome analysis and investigation into the causal role of body mass index across various diseases highlighted its potential to deliver more reliable results in real-world applications.

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
在孟德尔随机化中自动调整水平多效性的新框架
长期以来,孟德尔随机化(MR)分析中存在的横向多效性(horizontal pleiotropy)一直是一个令人担忧的问题,因为它有可能导致严重的偏差。近年来,人们提出了许多稳健的随机分析方法,通过放宽 "无水平多向性 "假设来解决这一问题。在这里,我们提出了一个新颖的两阶段框架--CMR,它整合了对多个遗传变异的条件分析,以去除由连锁不平衡引起的多义性,然后应用稳健的 MR 方法对条件遗传效应估计值进行建模。我们展示了条件分析如何减少水平褶状效应并提高现有 MR 方法的性能。广泛的模拟研究涵盖了水平褶状效应的各种情况,表明与建立边际遗传效应模型的标准 MR 框架相比,所提出的 CMR 框架具有更优越的性能。此外,CMR 在负对照结果分析中的应用,以及对体重指数在各种疾病中的因果作用的调查,都凸显了它在实际应用中提供更可靠结果的潜力。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
求助全文
约1分钟内获得全文 去求助
来源期刊
HGG Advances
HGG Advances Biochemistry, Genetics and Molecular Biology-Molecular Medicine
CiteScore
4.30
自引率
4.50%
发文量
69
审稿时长
14 weeks
期刊最新文献
Joint genotype and ancestry analysis identify novel loci associated with atopic dermatitis in African American population. Investigation of cryptic JAG1 splice variants as a cause of Alagille syndrome and performance evaluation of splice predictor tools. Dominantly acting variants in vacuolar ATPase subunits impair lysosomal/autophagolysosome function causing a multisystemic disorder with neurocognitive impairment and multiple congenital anomalies. Extensive co-regulation of neighbouring genes complicates the use of eQTLs in target gene prioritisation. Enhancing Personalized Gene Expression Prediction From DNA Sequences Using Genomic Foundation Models.
×
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