Division of Epidemiology, Biostatistics, and Environmental Health Sciences, School of Public Health, University of Memphis, Memphis, TN.
Center for Precision Environmental Health, Baylor College of Medicine, Houston, Texas.
Allergy. 2019 Jun;74(6):1166-1175. doi: 10.1111/all.13746. Epub 2019 Mar 5.
The presence of allergic sensitization has a major influence on the development and course of common childhood conditions such as asthma and rhinitis. The etiology of allergic sensitization is poorly understood, and its underlying biological mechanisms are not well established. Several studies showed that DNA methylation (DNAm) at some CpGs is associated with allergic sensitization. However, no studies have focused on the critical adolescence period.
We assessed the association of pre- and postadolescence genome-wide DNAm with allergic sensitization against indoor, outdoor and food allergens, using linear mixed models. We hypothesized that DNAm is associated with sensitization in general, and with poly-sensitization status, and these associations are age- and gender-specific. We tested these hypotheses in the IoW cohort (n = 376) and examined the findings in the BAMSE cohort (n = 267).
Via linear mixed models, we identified 35 CpGs in IoW associated with allergic sensitization (at false discovery rate of 0.05), of which 33 were available in BAMSE and replicated with respect to the direction of associations with allergic sensitization. At the 35 CpGs except for cg19210306 on C13orf27, a reduction in methylation among atopic subjects was observed, most notably for cg21220721 and cg11699125 (ACOT7). DNAm at cg10159529 was strongly correlated with expression of IL5RA in peripheral blood (P-value = 6.76 × 10 ). Three CpGs (cg14121142, cg23842695, and cg26496795) were identified in IoW with age-specific association between DNAm and allergic sensitization.
In adolescence, the status of allergic sensitization was associated with DNAm differentiation and at some CpGs the association is likely to be age-specific.
过敏致敏的存在对哮喘和鼻炎等常见儿童疾病的发展和进程有重大影响。过敏致敏的病因尚不清楚,其潜在的生物学机制也尚未确定。一些研究表明,一些 CpG 上的 DNA 甲基化 (DNAm) 与过敏致敏有关。然而,尚无研究关注关键的青春期。
我们使用线性混合模型评估了青春期前和青春期后全基因组 DNAm 与室内、室外和食物过敏原过敏致敏的关联。我们假设 DNAm 与过敏致敏有关,与多敏状态有关,这些关联具有年龄和性别特异性。我们在 IoW 队列(n=376)中检验了这些假设,并在 BAMSE 队列(n=267)中检验了这些发现。
通过线性混合模型,我们在 IoW 中确定了 35 个与过敏致敏相关的 CpG(错误发现率为 0.05),其中 33 个在 BAMSE 中可用,并根据与过敏致敏的关联方向进行了复制。在除 C13orf27 上的 cg19210306 以外的 35 个 CpG 中,观察到过敏患者的甲基化水平降低,尤其是 cg21220721 和 cg11699125(ACOT7)。cg10159529 处的 DNAm 与外周血中 IL5RA 的表达密切相关(P 值=6.76×10-8)。在 IoW 中确定了 3 个 CpG(cg14121142、cg23842695 和 cg26496795),其 DNAm 与过敏致敏之间存在与年龄相关的特异性关联。
在青春期,过敏致敏状态与 DNAm 分化有关,在某些 CpG 中,这种关联可能具有年龄特异性。