Division of Infection, Immunity and Respiratory Medicine, School of Biological Sciences, The University of Manchester, Manchester Academic Health Science Centre, and Manchester University NHS Foundation Trust, Manchester, United Kingdom.
MRC Integrative Epidemiology Unit, Department of Population Health Sciences, Bristol Medical School, University of Bristol, Bristol, United Kingdom.
J Allergy Clin Immunol. 2023 Feb;151(2):423-430. doi: 10.1016/j.jaci.2022.10.012. Epub 2022 Oct 20.
Asthma-associated single nucleotide polymorphisms from large genome-wide association studies only explain a fraction of genetic heritability. Likely causes of the missing heritability include broad phenotype definitions and gene-environment interactions (GxE). The mechanisms underlying GxE in asthma are poorly understood. Previous GxE studies on pet ownership showed discordant results.
We sought to study the GxE between the 17q12-21 locus and pet ownership in infancy in relation to wheeze.
Wheezing classes derived from 5 UK-based birth cohorts (latent class analysis) were used to study GxE between the 17q12-21 asthma-risk variant rs2305480 and dog and cat ownership in infancy, using multinomial logistic regression. A total of 9149 children had both pet ownership and genotype data available. Summary statistics from individual analyses were meta-analyzed.
rs2305480 G allele was associated with increased risk of persistent wheeze (additive model odds ratio, 1.37; 95% CI, 1.25-1.51). There was no evidence of an association between dog or cat ownership and wheeze. We found significant evidence of a GxE interaction between rs2305480 and dog ownership (P = 8.3 × 10) on persistent wheeze; among dog owners, the G allele was no longer associated with an increased risk of persistent wheeze (additive model odds ratio, 0.95; 95% CI, 0.73-1.24). For those without pets, G allele was associated with increased risk of persistent wheeze (odds ratio, 1.61; 95% CI, 1.40-1.86). Among cat owners, no such dampening of the genetic effect was observed.
Among dog owners, rs2305480 G was no longer associated with an increased risk of persistent wheeze (or asthma). Early-life environmental exposures may therefore attenuate likelihood of asthma in those carrying 17q12-21 risk alleles.
来自大型全基因组关联研究的哮喘相关单核苷酸多态性仅解释了遗传可遗传性的一部分。遗传缺失的可能原因包括广泛的表型定义和基因-环境相互作用(GxE)。哮喘中 GxE 的机制尚不清楚。以前关于宠物拥有的 GxE 研究结果不一致。
我们旨在研究 17q12-21 基因座与婴儿期宠物拥有之间的 GxE 与喘息之间的关系。
使用潜在类别分析,来自 5 个英国出生队列的喘息类别用于研究 17q12-21 哮喘风险变异 rs2305480 与婴儿期狗和猫拥有之间的 GxE,使用多项逻辑回归。共有 9149 名儿童既有宠物拥有数据又有基因型数据。对个体分析的汇总统计数据进行了荟萃分析。
rs2305480 G 等位基因与持续性喘息的风险增加相关(加性模型优势比,1.37;95%CI,1.25-1.51)。没有证据表明狗或猫的拥有与喘息有关。我们发现 rs2305480 与狗的拥有之间存在 GxE 相互作用的显著证据(P=8.3×10)对持续性喘息;在狗的拥有者中,G 等位基因不再与持续性喘息的风险增加相关(加性模型优势比,0.95;95%CI,0.73-1.24)。对于那些没有宠物的人,G 等位基因与持续性喘息的风险增加相关(比值比,1.61;95%CI,1.40-1.86)。在猫的拥有者中,没有观察到这种遗传效应的减弱。
在狗的拥有者中,rs2305480 G 不再与持续性喘息(或哮喘)的风险增加相关。因此,生命早期的环境暴露可能会降低携带 17q12-21 风险等位基因的人患哮喘的可能性。