Mother adversity and co-residence time impact mother–child similarity in genome-wide and gene-specific methylation profiles

IF 4.8 2区 医学 Q1 GENETICS & HEREDITY Clinical Epigenetics Pub Date : 2024-03-20 DOI:10.1186/s13148-024-01655-5
Lucía Labaut, Agustín Lage-Castellanos, María José Rodrigo, Silvia Herrero-Roldán, Colter Mitchell, Jonah Fisher, Inmaculada León
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引用次数: 0

Abstract

The effects of adverse life events on physical and psychological health, with DNA methylation (DNAm) as a critical underlying mechanism, have been extensively studied. However, the epigenetic resemblance between mother and child in the context of neglectful caregiving, and whether it may be shaped by the emotional impact of maternal stressful events and the duration of co-residence (indexed by child age), remains unknown. The present study examined mother–child similarity in methylation profiles, considering the potential effect of mother adversity, mother empathy, neglect-control group, child age (an index of years of mother–child co-residence), and mother age. Using Illumina Epic arrays, we quantified DNAm in 115 mother–child saliva samples. We obtained a methylation similarity index by computing correlation coefficients between methylation profiles within dyads, for the entire epigenome, and five specific genes related to stress and empathy: NR3C1, FKPB5, OXTR, SCL6A4, and BDNF. The methylation profiles of the mother–child familial pairs significantly correlated as compared to mother–child random pairs for the entire epigenome and NR3C1, FKBP5, OXTR and BDNF genes. Next, multiple linear regression models observed associations of mother adversity, child age, and neglect-control group on mother–child methylation similarity, only significant in mother–child familial pairs, after correcting for multiple comparisons. Higher mother adversity was associated with lower mother–child methylation similarity for the epigenome-wide analysis, for the BDNF gene, and in the neglect-control group for the OXTR gene. In turn, being an older child (longer co-residence) was associated with higher mother–child methylation similarity. Mother adversity and co-residence time are modulating factors in the intergenerational methylation process that offer a window into development-dependent adaptations that can be affected by both hereditary and environmental factors, significantly observed only in biological dyads. A twofold implication for child well-being emerges, one is positive in that children of mothers exposed to life adversity or neglect did not necessarily inherit their methylation patterns. The other is concerning due to the influence of time spent living together, which affects similarity with the mother and potentially increases the risk of inheriting an epigenetic profile associated with future dysfunctional parenting patterns. This underscores the importance of the 'the earlier, the better' recommendation by the Child Protection System, which is not always followed.
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母亲的逆境和共同居住时间影响全基因组和特异基因甲基化图谱的母子相似性
以 DNA 甲基化(DNAm)为重要基础机制的不良生活事件对身心健康的影响已得到广泛研究。然而,在疏于照顾的情况下,母亲和孩子之间的表观遗传相似性,以及这种相似性是否会受到母亲压力事件的情绪影响和共同居住时间(以孩子年龄为指标)的影响,目前仍是未知数。本研究考察了母子甲基化图谱的相似性,考虑了母亲逆境、母亲移情、忽视对照组、儿童年龄(母子共同居住年限的指标)和母亲年龄的潜在影响。我们使用 Illumina Epic 阵列对 115 份母子唾液样本中的 DNAm 进行了量化。通过计算整个表观基因组和五个与压力和移情相关的特定基因(NR3C1、FKPB5、OXTR、SCL6A4 和 BDNF)的甲基化图谱之间的相关系数,我们得出了甲基化相似性指数。在整个表观基因组和 NR3C1、FKBP5、OXTR 和 BDNF 基因方面,与母子随机配对相比,母子家族配对的甲基化图谱具有显著的相关性。接下来,多元线性回归模型观察了母亲逆境、儿童年龄和忽视对照组对母子甲基化相似性的影响,经多重比较校正后,仅在母子家族配对中具有显著性。在整个表观基因组分析中,母亲逆境程度越高,BDNF 基因的母子甲基化相似度越低,而在忽视对照组中,OXTR 基因的母子甲基化相似度越低。反过来,孩子年龄越大(共同居住时间越长),母子甲基化相似度越高。母亲的逆境和共同居住时间是代际甲基化过程中的调节因素,为了解依赖于发育的适应性提供了一个窗口。这对儿童的福祉产生了两方面的影响,一方面是积极的,因为遭受生活逆境或忽视的母亲的子女并不一定会遗传其甲基化模式。另一个令人担忧的问题是,共同生活的时间会影响与母亲的相似性,并有可能增加遗传与未来功能失调的养育模式相关的表观遗传特征的风险。这强调了儿童保护系统提出的 "越早越好 "建议的重要性,但这一建议并不总是得到遵守。
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来源期刊
自引率
5.30%
发文量
150
期刊介绍: Clinical Epigenetics, the official journal of the Clinical Epigenetics Society, is an open access, peer-reviewed journal that encompasses all aspects of epigenetic principles and mechanisms in relation to human disease, diagnosis and therapy. Clinical trials and research in disease model organisms are particularly welcome.
期刊最新文献
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