Division of Epidemiology, Biostatistics and Environmental Health, School of Public Health, University of Memphis, Memphis, TN, USA.
Department of Mathematical Sciences, University of Memphis, Memphis, TN, USA.
Clin Exp Allergy. 2021 Feb;51(2):318-328. doi: 10.1111/cea.13776. Epub 2020 Nov 25.
Underlying biological mechanisms involved in sex differences in asthma status changes from pre- to post-adolescence are unclear. DNA methylation (DNAm) has been shown to be associated with the risk of asthma.
We hypothesized that asthma acquisition from pre- to post-adolescence was associated with changes in DNAm during this period at asthma-associated cytosine-phosphate-guanine (CpG) sites and such an association was sex-specific.
Subjects from the Isle of Wight birth cohort (IOWBC) with DNAm in blood at ages 10 and 18 years (n = 124 females, 151 males) were studied. Using a training-testing approach, epigenome-wide CpGs associated with asthma were identified. Logistic regression was used to examine sex-specific associations of DNAm changes with asthma acquisition between ages 10 and 18 at asthma-associated CpGs. The ALSPAC birth cohort was used for independent replication. To assess functional relevance of identified CpGs, association of DNAm with gene expression in blood was assessed.
We identified 535 CpGs potentially associated with asthma. Significant interaction effects of DNAm changes and sex on asthma acquisition in adolescence were found at 13 of the 535 CpGs in IOWBC (P-values <1.0 × 10 ). In the replication cohort, consistent interaction effects were observed at 10 of the 13 CpGs. At 7 of these 10 CpGs, opposite DNAm changes across adolescence were observed between sexes in both cohorts. In both cohorts, cg20891917, located on IFRD1 linked to asthma, shows strong sex-specific effects on asthma transition (P-values <.01 in both cohorts).
Gender reversal in asthma acquisition is associated with opposite changes in DNAm (males vs females) from pre- to post-adolescence at asthma-associated CpGs. These CpGs are potential biomarkers of sex-specific asthma acquisition in adolescence.
青春期前至青春期后哮喘状态变化的潜在生物学机制在性别上存在差异,但目前尚不清楚。DNA 甲基化(DNAm)已被证明与哮喘风险相关。
我们假设从青春期前到青春期后发生哮喘的过程与该时期哮喘相关胞嘧啶-磷酸-鸟嘌呤(CpG)位点的 DNAm 变化有关,并且这种关联具有性别特异性。
研究对象来自怀特岛出生队列(IOWBC),在 10 岁和 18 岁时的血液中具有 DNAm(n=124 名女性,151 名男性)。使用训练-测试方法,鉴定与哮喘相关的全基因组 CpG。使用逻辑回归检验在哮喘相关 CpG 上,10 岁至 18 岁之间 DNAm 变化与哮喘发病之间的性别特异性关联。ALSPAC 出生队列用于独立验证。为了评估鉴定 CpG 的功能相关性,评估了血液中 DNAm 与基因表达的关联。
我们鉴定出 535 个可能与哮喘相关的 CpG。在 IOWBC 中,在 535 个 CpG 中有 13 个观察到 DNAm 变化与性别对青春期哮喘发病的显著交互作用(P 值均<1.0×10-4)。在复制队列中,在 13 个 CpG 中有 10 个观察到一致的交互作用。在这 10 个 CpG 中,有 7 个 CpG 在两个队列中观察到青春期男女之间的 DNAm 变化相反。在两个队列中,位于与哮喘相关的 IFRD1 上的 cg20891917 均表现出对哮喘转变的强烈性别特异性影响(两个队列的 P 值均<.01)。
哮喘发病的性别逆转与哮喘相关 CpG 从青春期前到青春期的 DNAm 变化(男性与女性)相反。这些 CpG 可能是青春期性别特异性哮喘发病的生物标志物。