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一项基于全基因组关联研究的、与吸烟状态相关的哮喘频繁恶化研究。

A genome-wide association study on frequent exacerbation of asthma depending on smoking status.

机构信息

Department of Interdisciplinary Program in Biomedical Science Major, Graduate School, Soonchunhyang University, Asan, South Korea.

Division of Allergy and Respiratory Medicine, Department of Internal Medicine, Soonchunhyang Univ. Bucheon Hospital, Bucheon, South Korea.

出版信息

Respir Med. 2022 Aug;199:106877. doi: 10.1016/j.rmed.2022.106877. Epub 2022 May 17.

Abstract

PURPOSE

Exacerbation of asthma is affected by genetic and environmental factors, but little is known about genetic differences according to smoking status. We evaluated genetic factors associated with asthma exacerbations in smokers and non-smokers, and identified the underlying mechanisms via a genome-wide association study (GWAS) and gene-level analyses according to smoking status.

METHODS

A GWAS on the annual frequency of asthma exacerbations was performed in 420 non-smoking and 188 smoking patients with asthma. Gene-wise associations were analyzed by Multi-marker Analysis of GenoMic Annotation (MAGMA); Gene Ontology analysis was also performed.

RESULTS

In the non-smoker group, 189 genes showed significant associations with the annual frequency of exacerbations (permutated P < 0.001). The top 10 genes were F5, KLRC1, TAFA2, AIRE, IER3IP1, CHMP2A, IL31RA, ZNF497, DNMT3L, and MYT1L (permutated P = 1.0 × 10 - 1.7 × 10). In smoking asthmatics, 140 genes-including KANK1, ZMYND12, ZNF34, ANXA11, VAV2, CCDC150, CCDC30, CATSPER3, ARMH2, and MPRIP (permutated P = 9.23 × 10 - 5.50 × 10)-were associated with asthma exacerbations. Genes participating in the innate immune response in non-smokers and the regulation of cell fate (including apoptosis) in smokers were the major causal genes of asthma exacerbation (FDR q < 0.05).

CONCLUSIONS

Our findings not only suggest novel genetic candidates for predicting asthma exacerbations, but also that asthma treatment strategies should take into account smoking behavior.

摘要

目的

哮喘加重受遗传和环境因素的影响,但根据吸烟状况,遗传差异知之甚少。我们评估了吸烟和不吸烟哮喘患者哮喘加重与遗传因素的关系,并通过全基因组关联研究(GWAS)和根据吸烟状况进行基因水平分析,确定了潜在机制。

方法

对 420 名不吸烟和 188 名吸烟哮喘患者的哮喘加重年频率进行了 GWAS。通过多标记分析基因组注释(MAGMA)进行基因水平关联分析;还进行了基因本体论分析。

结果

在不吸烟组中,有 189 个基因与每年哮喘加重的频率有显著关联(置换 P<0.001)。前 10 个基因是 F5、KLRC1、TAFA2、AIRE、IER3IP1、CHMP2A、IL31RA、ZNF497、DNMT3L 和 MYT1L(置换 P=1.0×10 - 1.7×10)。在吸烟哮喘患者中,有 140 个基因-包括 KANK1、ZMYND12、ZNF34、ANXA11、VAV2、CCDC150、CCDC30、CATSPER3、ARMH2 和 MPRIP(置换 P=9.23×10 - 5.50×10)与哮喘加重有关。在不吸烟者中参与先天免疫反应的基因和在吸烟者中参与细胞命运调节(包括细胞凋亡)的基因是哮喘加重的主要致病基因(FDR q<0.05)。

结论

我们的研究结果不仅为预测哮喘加重提供了新的遗传候选基因,而且还表明哮喘治疗策略应考虑吸烟行为。

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