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儿童食欲特征与 DNA 甲基化的全基因组关联研究。

An epigenome-wide association study of child appetitive traits and DNA methylation.

机构信息

Department of Child & Adolescent Psychiatry/Psychology, Erasmus MC, University Medical Center, Rotterdam, the Netherlands; The Generation R Study Group, Erasmus MC, University Medical Center Rotterdam, Rotterdam, the Netherlands; Erasmus University Rotterdam, Department of Psychology, Education & Child Studies, Rotterdam, the Netherlands.

Department of Epidemiology, Colorado School of Public Health, University of Colorado Anschutz Medical Campus, Aurora, CO, USA; Lifecourse Epidemiology of Adiposity and Diabetes (LEAD) Center, University of Colorado Anschutz Medical Campus, Aurora, CO, USA.

出版信息

Appetite. 2023 Dec 1;191:107086. doi: 10.1016/j.appet.2023.107086. Epub 2023 Oct 14.

Abstract

The etiology of childhood appetitive traits is poorly understood. Early-life epigenetic processes may be involved in the developmental programming of appetite regulation in childhood. One such process is DNA methylation (DNAm), whereby a methyl group is added to a specific part of DNA, where a cytosine base is next to a guanine base, a CpG site. We meta-analyzed epigenome-wide association studies (EWASs) of cord blood DNAm and early-childhood appetitive traits. Data were from two independent cohorts: the Generation R Study (n = 1,086, Rotterdam, the Netherlands) and the Healthy Start study (n = 236, Colorado, USA). DNAm at autosomal methylation sites in cord blood was measured using the Illumina Infinium HumanMethylation450 BeadChip. Parents reported on their child's food responsiveness, emotional undereating, satiety responsiveness and food fussiness using the Children's Eating Behaviour Questionnaire at age 4-5 years. Multiple regression models were used to examine the association of DNAm (predictor) at the individual site- and regional-level (using DMRff) with each appetitive trait (outcome), adjusting for covariates. Bonferroni-correction was applied to adjust for multiple testing. There were no associations of DNAm and any appetitive trait when examining individual CpG-sites. However, when examining multiple CpGs jointly in so-called differentially methylated regions, we identified 45 associations of DNAm with food responsiveness, 7 associations of DNAm with emotional undereating, 13 associations of DNAm with satiety responsiveness, and 9 associations of DNAm with food fussiness. This study shows that DNAm in the newborn may partially explain variation in appetitive traits expressed in early childhood and provides preliminary support for early programming of child appetitive traits through DNAm. Investigating differential DNAm associated with appetitive traits could be an important first step in identifying biological pathways underlying the development of these behaviors.

摘要

儿童食欲特质的病因尚不清楚。早期的表观遗传过程可能参与了儿童时期食欲调节的发育编程。其中一个过程是 DNA 甲基化 (DNAm),即在特定的 DNA 部分添加一个甲基基团,其中一个胞嘧啶碱基紧挨着一个鸟嘌呤碱基,即 CpG 位点。我们对脐带血 DNAm 与儿童早期食欲特质的全基因组关联研究 (EWAS) 进行了荟萃分析。数据来自两个独立的队列:荷兰鹿特丹的 Generation R 研究(n=1086)和美国科罗拉多的 Healthy Start 研究(n=236)。使用 Illumina Infinium HumanMethylation450 BeadChip 测量脐带血中的常染色体甲基化位点的 DNAm。父母在孩子 4-5 岁时使用儿童饮食行为问卷报告孩子的食物反应性、情绪性少食、饱腹感反应性和食物挑剔性。使用多元回归模型,在调整协变量后,在个体位点和区域水平(使用 DMRff),检查 DNAm(预测因子)与每个食欲特质(结果)之间的关联。采用 Bonferroni 校正法进行多重检验校正。当检查个体 CpG 位点时,DNAm 与任何食欲特质均无关联。然而,当联合检查所谓的差异甲基化区域中的多个 CpG 时,我们鉴定出 45 个 DNAm 与食物反应性相关,7 个 DNAm 与情绪性少食相关,13 个 DNAm 与饱腹感反应性相关,9 个 DNAm 与食物挑剔性相关。本研究表明,新生儿的 DNAm 可能部分解释了儿童早期表现出的食欲特质的变异性,并为通过 DNAm 对儿童食欲特质进行早期编程提供了初步支持。研究与食欲特质相关的差异 DNAm 可能是确定这些行为发展背后的生物学途径的重要第一步。

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Wellcome Open Res. 2022 May 31;7:41. doi: 10.12688/wellcomeopenres.17598.2. eCollection 2022.

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