The Association of Childhood Allergic Diseases with Prenatal Exposure to Pollen Grains Through At-Birth DNA Methylation.

IF 2.5 Q3 GENETICS & HEREDITY
Rajesh Melaram, Hongmei Zhang, James Adefisoye, Hasan Arshad
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引用次数: 0

Abstract

Background: Pollen exposure in early life is shown to be associated with allergy and asthma. DNA methylation (DNAm), an epigenetic marker, potentially reacts to pollen. However, the role of at-birth DNAm between prenatal pollen grain (PPG) exposure and childhood asthma and allergic rhinitis is unknown.

Methods: Data in a birth cohort study on the Isle of Wight, UK, were analyzed (n = 236). Newborn DNAm was measured in cord blood or blood spots on Guthrie cards and screened for potential association with PPG exposure using the R package ttScreening. CpGs that passed screening were further assessed for such associations via linear regressions with adjusting covariates included. Finally, DNAm at PPG-associated CpGs were evaluated for their association with asthma and allergic rhinitis using logistic regressions, adjusting for covariates. The impact of cell heterogeneity on the findings was assessed. Statistical significance was set at p < 0.05.

Results: In total, 42 CpGs passed screening, with 41 remaining statistically significant after adjusting for covariates and cell types (p < 0.05). High PPG exposure was associated with lower DNAm at cg12318501 (ZNF99, β = -0.029, p = 0.032) and cg00929606 (ADM2, β = -0.023, p = 0.008), which subsequently was associated with decreased odds of asthma (OR = 0.11, 95% CI 0.02-0.53, p = 0.006; OR = 0.14, 95% CI 0.02-1.00, p = 0.049). For rhinitis, cg15790214 (HCG11) was shown to play such a role as a mediator (β = -0.027, p ≤ 0.0001; OR = 0.22, 95% CI 0.07-0.72, p = 0.01).

Conclusions: The association of PPG exposure with childhood asthma and allergic rhinitis incidence is potentially mediated by DNAm at birth.

通过出生时DNA甲基化,儿童过敏性疾病与产前暴露于花粉粒的关系。
背景:生命早期接触花粉被证明与过敏和哮喘有关。DNA甲基化(DNAm)是一种表观遗传标记,可能对花粉产生反应。然而,出生时dna在产前花粉粒(PPG)暴露与儿童哮喘和过敏性鼻炎之间的作用尚不清楚。方法:对英国怀特岛出生队列研究的数据进行分析(n = 236)。新生儿dna在脐带血或Guthrie卡片上的血斑中测量,并使用R包筛选与PPG暴露的潜在关联。通过筛选的CpGs通过包括调整协变量在内的线性回归进一步评估这种关联。最后,利用logistic回归对ppg相关CpGs的DNAm与哮喘和变应性鼻炎的相关性进行评估,调整协变量。评估了细胞异质性对结果的影响。p < 0.05为差异有统计学意义。结果:共有42个CpGs通过筛选,校正协变量和细胞类型后,有41个CpGs具有统计学意义(p < 0.05)。高PPG暴露与cg12318501 (ZNF99, β = -0.029, p = 0.032)和cg00929606 (ADM2, β = -0.023, p = 0.008)较低的DNAm相关,随后与哮喘发生率降低相关(OR = 0.11, 95% CI 0.02-0.53, p = 0.006;OR = 0.14, 95% CI 0.02-1.00, p = 0.049)。对于鼻炎,cg15790214 (HCG11)被证明发挥了这样的中介作用(β = -0.027, p≤0.0001;OR = 0.22, 95% CI 0.07-0.72, p = 0.01)。结论:PPG暴露与儿童哮喘和变应性鼻炎发病率的关联可能是由出生时的dna介导的。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Epigenomes
Epigenomes GENETICS & HEREDITY-
CiteScore
3.80
自引率
0.00%
发文量
38
审稿时长
11 weeks
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