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利用孟德尔随机化研究环境因素与哮喘之间的关联:体重指数对成人起病的中重度哮喘亚型影响增强

Association Between Environmental Factors and Asthma Using Mendelian Randomization: Increased Effect of Body Mass Index on Adult-Onset Moderate-to-Severe Asthma Subtypes.

作者信息

Ha Tae-Woong, Jung Hae-Un, Kim Dong Jun, Baek Eun Ju, Lee Won Jun, Lim Ji Eun, Kim Han Kyul, Kang Ji-One, Oh Bermseok

机构信息

Department of Biochemistry and Molecular Biology, School of Medicine, Kyung Hee University, Seoul, South Korea.

Department of Biomedical Science, Graduate School, Kyung Hee University, Seoul, South Korea.

出版信息

Front Genet. 2021 May 20;12:639905. doi: 10.3389/fgene.2021.639905. eCollection 2021.

DOI:10.3389/fgene.2021.639905
PMID:34093643
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC8172971/
Abstract

Although asthma is one of the most common chronic diseases throughout all age groups, its etiology remains unknown, primarily due to its heterogeneous characteristics. We examined the causal effects of various environmental factors on asthma using Mendelian randomization and determined whether the susceptibility to asthma due to the causal effect of a risk factor differs between asthma subtypes, based on age of onset, severity of asthma, and sex. We performed Mendelian randomization analyses (inverse variance weighted, weighted median, and generalized summary-data-based Mendelian randomization) using UK Biobank data to estimate the causal effects of 69 environmental factors on asthma. Additional sensitivity analyses (MR-Egger regression, Cochran's Q test, clumping, and reverse Mendelian randomization) were performed to ensure minimal or no pleiotropy. For confirmation, two-sample setting analyses were replicated using BMI SNPs that had been reported by a meta-genome-wide association study in Japanese and European (GIANT) populations and a genome-wide association study in control individuals from the UK Biobank. We found that BMI causally affects the development of asthma and that the adult-onset moderate-to-severe asthma subtype is the most susceptible to causal inference by BMI. Further, it is likely that the female subtype is more susceptible to BMI than males among adult asthma cases. Our findings provide evidence that obesity is a considerable risk factor in asthma patients, particularly in adult-onset moderate-to-severe asthma cases, and that weight loss is beneficial for reducing the burden of asthma.

摘要

尽管哮喘是所有年龄组中最常见的慢性疾病之一,但其病因仍不清楚,主要是由于其具有异质性特征。我们使用孟德尔随机化方法研究了各种环境因素对哮喘的因果效应,并根据发病年龄、哮喘严重程度和性别,确定了危险因素因果效应导致的哮喘易感性在哮喘亚型之间是否存在差异。我们使用英国生物银行的数据进行了孟德尔随机化分析(逆方差加权、加权中位数和基于广义汇总数据的孟德尔随机化),以估计69种环境因素对哮喘的因果效应。进行了额外的敏感性分析(MR-Egger回归、 Cochr an's Q检验、聚类和反向孟德尔随机化),以确保最小程度的多效性或无多效性。为了进行验证,我们使用了在日本和欧洲人群的一项元全基因组关联研究以及英国生物银行对照个体的一项全基因组关联研究中报告的BMI单核苷酸多态性,重复进行了两样本设定分析。我们发现BMI对哮喘的发展有因果影响,并且成人发病的中度至重度哮喘亚型最容易受到BMI的因果推断。此外,在成人哮喘病例中,女性亚型可能比男性更容易受到BMI的影响。我们的研究结果提供了证据,表明肥胖是哮喘患者的一个重要危险因素,特别是在成人发病的中度至重度哮喘病例中,并且减肥有利于减轻哮喘负担。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/05c6/8172971/710eb0e9887e/fgene-12-639905-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/05c6/8172971/673fb4236f29/fgene-12-639905-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/05c6/8172971/8b9e20fce1ab/fgene-12-639905-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/05c6/8172971/ae190e5f5e8d/fgene-12-639905-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/05c6/8172971/bb05c29f1159/fgene-12-639905-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/05c6/8172971/710eb0e9887e/fgene-12-639905-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/05c6/8172971/673fb4236f29/fgene-12-639905-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/05c6/8172971/8b9e20fce1ab/fgene-12-639905-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/05c6/8172971/ae190e5f5e8d/fgene-12-639905-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/05c6/8172971/bb05c29f1159/fgene-12-639905-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/05c6/8172971/710eb0e9887e/fgene-12-639905-g005.jpg

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J Epidemiol Community Health. 2021 Mar;75(3):277-281. doi: 10.1136/jech-2020-213745. Epub 2020 Oct 13.
2
Novel loci for childhood body mass index and shared heritability with adult cardiometabolic traits.儿童体重指数的新位点及其与成人心脏代谢特征的共享遗传度。
PLoS Genet. 2020 Oct 12;16(10):e1008718. doi: 10.1371/journal.pgen.1008718. eCollection 2020 Oct.
3
Guidelines for performing Mendelian randomization investigations: update for summer 2023.
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Commun Biol. 2022 Oct 17;5(1):1098. doi: 10.1038/s42003-022-04070-9.
4
Asthma and the Missing Heritability Problem: Necessity for Multiomics Approaches in Determining Accurate Risk Profiles.哮喘与遗传缺失问题:确定准确风险概况需要多组学方法。
Front Immunol. 2022 May 25;13:822324. doi: 10.3389/fimmu.2022.822324. eCollection 2022.
5
Mendelian Randomization Study of Causal Relationship between Omega-3 Fatty Acids and Risk of Lung Cancer.基于孟德尔随机化研究的ω-3 脂肪酸与肺癌风险的因果关系。
Biomed Res Int. 2022 May 31;2022:2786567. doi: 10.1155/2022/2786567. eCollection 2022.
孟德尔随机化研究实施指南:2023年夏季更新版
Wellcome Open Res. 2023 Aug 4;4:186. doi: 10.12688/wellcomeopenres.15555.3. eCollection 2019.
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