首页> 外文会议>Joint annual meeting of the International Society of Exposure Science and the International Society for Environmental Epidemiology >Methylation Marks to Inform Association between Early-Life Air Pollution Exposures and Child Body Mass Index: An Analysis Based on A Priori Selected Pathways
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Methylation Marks to Inform Association between Early-Life Air Pollution Exposures and Child Body Mass Index: An Analysis Based on A Priori Selected Pathways

机译:甲基化标记可告知生命早期空气污染暴露与儿童体重指数之间的关联:基于先验选择途径的分析

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Background: Early-life exposure to air pollution has been suggested to influence childhood growth and Body Mass Index (BMI). DNA methylation changes might explain part of this effect. Yet, methylome-wide studies with population sizes under 1000 generally suffer from lack of power. Using a priori information to reduce data dimension is an option to face this challenge. Aim: To identify genes whose methylation level is possibly implied in air pollution effect on child BMI, with a 'Meet in the middle' approach, using a priori information from functional pathways. Methods: Among 1173 mother-infant pairs from Helix cohorts, exposures to 4 outdoor air pollutants were assessed during pregnancy and at age 7-9 years (total 16 exposures). Genome-wide DNA methylation levels in peripheral blood at 7-9 years was measured using HumanMethylation450 BeadChip, with quality control, batch and cell types adjustments. We a priori considered only 2276 CpGs from genes belonging to 16 growth or obesity-relevant pathways according to KEGG pathway database. Stabilized Elasticnet regression (ENet) was used to independently assess associations of DNA methylation with exposures and BMI. We identified exposures sharing associated CpG sites with BMI and assessed their direct association with BMI using ENet. Results: Exposures were associated with 358 CpG loci; 12 exposures were associated with CpGs also associated with BMI (total, 22 CpGs). One of these exposures, PM10 level the day before blood collection, was associated with BMI. This exposure was associated with 62 CpGs, 2 of which being also associated with BMI, on PIK3CA (thyroid hormone signaling pathway) and ELOVL3 genes (fatty acid elongation pathway). Conclusion: Our hypothesis-generating approach identified 358 CpGs from BMI-relevant pathways associated with air pollutants, including 22 related to child BMI. These CpGs provide hints as to which genes may be implied in mechanisms underlying air pollution effects on child growth.
机译:背景:已经提出生命早期暴露于空气污染会影响儿童的成长和体重指数(BMI)。 DNA甲基化的变化可能部分解释了这种作用。然而,人口规模小于1000的全基因组研究普遍缺乏能力。使用先验信息来减少数据维度是面对这一挑战的一种选择。目的:利用“功能相遇”方法,通过功能途径的先验信息,鉴定甲基化水平可能暗示对儿童BMI的空气污染影响的基因。方法:在Helix队列的1173对母婴中,评估了在怀孕期间和7-9岁时暴露于4种室外空气污染物的暴露(总共16次暴露)。使用HumanMethylation450 BeadChip测量7-9岁时外周血全基因组DNA甲基化水平,并进行质量控制,批次和细胞类型调整。根据KEGG途径数据库,我们先验地认为来自属于16种生长或肥胖相关途径的基因的2276 CpGs。稳定的Elasticnet回归(ENet)用于独立评估DNA甲基化与暴露和BMI的关联。我们确定了与BMI共享关联的CpG网站的暴露,并使用ENet评估了它们与BMI的直接关联。结果:暴露与358个CpG基因座有关。 12次暴露与CpG也与BMI有关(总计22个CpG)。其中一种暴露,即采血前一天的PM10水平与BMI有关。该暴露与PIK3CA(甲状腺激素信号途径)和ELOVL3基因(脂肪酸延长途径)上的62个CpGs相关,其中2个也与BMI相关。结论:我们的假设产生方法从与空气污染物相关的BMI相关途径中鉴定了358 CpG,其中22与儿童BMI有关。这些CpG暗示了空气污染对儿童成长的潜在机制中可能隐含哪些基因。

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