Department of Pediatric Pulmonology and Pediatric Allergy, Beatrix Children's Hospital, University Medical Center Groningen, University of Groningen, Groningen, The Netherlands; Gronigen Research Institute for Asthma and COPD, University Medical Center Groningen, University of Groningen, Groningen, The Netherlands.
Division of Pulmonary Medicine, UPMC Children's Hospital of Pittsburgh, Pittsburgh, Pa; Department of Pediatrics, University of Pittsburgh School of Medicine, Pittsburgh, Pa; School of Medicine, Tsinghua University, Beijing, China.
J Allergy Clin Immunol. 2020 Jun;145(6):1655-1663. doi: 10.1016/j.jaci.2019.12.911. Epub 2020 Jan 14.
Epigenetic signatures in the nasal epithelium, which is a primary interface with the environment and an accessible proxy for the bronchial epithelium, might provide insights into mechanisms of allergic disease.
We aimed to identify and interpret methylation signatures in nasal epithelial brushes associated with rhinitis and asthma.
Nasal epithelial brushes were obtained from 455 children at the 16-year follow-up of the Dutch Prevention and Incidence of Asthma and Mite Allergy birth cohort study. Epigenome-wide association studies were performed on children with asthma, rhinitis, and asthma and/or rhinitis (AsRh) by using logistic regression, and the top results were replicated in 2 independent cohorts of African American and Puerto Rican children. Significant CpG sites were related to environmental exposures (pets, active and passive smoking, and molds) during secondary school and were correlated with gene expression by RNA-sequencing (n = 244).
The epigenome-wide association studies identified CpG sites significantly associated with rhinitis (n = 81) and AsRh (n = 75), but not with asthma. We significantly replicated 62 of 81 CpG sites with rhinitis and 60 of 75 with AsRh, as well as 1 CpG site with asthma. Methylation of cg03565274 was negatively associated with AsRh and positively associated with exposure to pets during secondary school. DNA methylation signals associated with AsRh were mainly driven by specific IgE-positive subjects. DNA methylation related to gene transcripts that were enriched for immune pathways and expressed in immune and epithelial cells. Nasal CpG sites performed well in predicting AsRh.
We identified replicable DNA methylation profiles of asthma and rhinitis in nasal brushes. Exposure to pets may affect nasal epithelial methylation in relation to asthma and rhinitis.
鼻腔上皮细胞的表观遗传特征是与环境的主要界面,也是支气管上皮细胞的一种可及的替代物,可能为过敏疾病的机制提供见解。
我们旨在确定和解释与鼻炎和哮喘相关的鼻腔上皮刷状缘的甲基化特征。
在荷兰预防和过敏症与尘螨过敏的哮喘与过敏症发生和发病研究的 16 年随访中,从 455 名儿童中获取鼻腔上皮刷状缘。通过逻辑回归对哮喘、鼻炎、哮喘和/或鼻炎(AsRh)的儿童进行全基因组关联研究,并在 2 个独立的非裔美国人和波多黎各儿童队列中复制了顶级结果。在中学期间与环境暴露(宠物、主动和被动吸烟、霉菌)相关的显著 CpG 位点与 RNA 测序的基因表达相关(n=244)。
全基因组关联研究确定了与鼻炎(n=81)和 AsRh(n=75)显著相关的 CpG 位点,但与哮喘无关。我们显著复制了 81 个鼻炎和 75 个 AsRh 中有 62 个 CpG 位点,以及 1 个哮喘 CpG 位点。cg03565274 的甲基化与 AsRh 呈负相关,与中学期间接触宠物呈正相关。与 AsRh 相关的 DNA 甲基化信号主要由特定 IgE 阳性的患者驱动。与免疫途径相关的基因转录物的 DNA 甲基化表达在免疫和上皮细胞中。鼻腔 CpG 位点在预测 AsRh 方面表现良好。
我们在鼻腔刷状缘中确定了可重复的哮喘和鼻炎的 DNA 甲基化谱。接触宠物可能会影响与哮喘和鼻炎相关的鼻腔上皮细胞甲基化。