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新生儿甲基化与6个月和18个月大时的社会情感发展

Neonatal Methylation and Social-Emotional Development at 6 and 18 Months of Age.

作者信息

Folger Alonzo T, Ding Lili, Ji Hong, Yolton Kimberly, Ammerman Robert T, Van Ginkel Judith B, Bowers Katherine

机构信息

Cincinnati Children's Hospital Medical Center, Department of Pediatrics, Division of Biostatistics and Epidemiology, University of Cincinnati College of Medicine, Cincinnati, OH, United States.

Department of Anatomy, Physiology and Cell Biology, School of Veterinary Medicine, University of California, Davis, Davis, CA, United States.

出版信息

Front Behav Neurosci. 2019 Feb 5;13:14. doi: 10.3389/fnbeh.2019.00014. eCollection 2019.

DOI:10.3389/fnbeh.2019.00014
PMID:30804765
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC6371639/
Abstract

The variation in childhood social-emotional development within at-risk populations may be attributed in part to epigenetic mechanisms such as DNA methylation (DNAm) that respond to environmental stressors. These mechanisms may partially underlie the degree of vulnerability (and resilience) to negative social-emotional development within adverse psychosocial environments. Extensive research supports an association between maternal adversity and offspring DNAm of the gene, which encodes the glucocorticoid receptor (GR). A gap in knowledge remains regarding the relationship between DNAm, measured in neonatal (1-month of age) buccal cells, and subsequent social-emotional development during infancy and early childhood. We conducted a longitudinal cohort study of = 53 mother-child dyads ( = 30 with developmental outcomes formed the basis of current study) who were enrolled in a home visiting (HV) program. Higher mean DNAm of the exon 1 promoter was significantly associated with lower 6-month Ages and Stages Questionnaire: Social-Emotional (ASQ:SE) scores-more positive infant social-emotional functioning. A similar trend was observed at 18-months of age in a smaller sample ( = 12). The findings of this pilot study indicate that in a diverse and disadvantaged population, the level of neonatal DNAm is related to later social-emotional development. Limitations and implications for future research are discussed.

摘要

高危人群儿童社会情感发展的差异可能部分归因于表观遗传机制,如对环境应激源产生反应的DNA甲基化(DNAm)。这些机制可能部分解释了在不良心理社会环境中负面社会情感发展的脆弱程度(和恢复力)。大量研究支持母体逆境与编码糖皮质激素受体(GR)的基因的后代DNAm之间存在关联。关于新生儿(1月龄)颊细胞中测量的DNAm与婴儿期和幼儿期随后的社会情感发展之间的关系,仍存在知识空白。我们对53对母婴(其中30对有发育结果构成了当前研究的基础)进行了一项纵向队列研究,这些母婴参加了家访(HV)项目。外显子1启动子的平均DNAm水平较高与6个月龄时较低的《年龄与阶段问卷:社会情感》(ASQ:SE)得分显著相关——婴儿社会情感功能更积极。在一个较小的样本(n = 12)中,18个月龄时也观察到了类似趋势。这项初步研究的结果表明,在一个多样化且处于不利地位的人群中,新生儿DNAm水平与后期社会情感发展有关。讨论了本研究的局限性及对未来研究的启示。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/acb6/6371639/3fe90cb80db0/fnbeh-13-00014-g0002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/acb6/6371639/92d3d3cad2d7/fnbeh-13-00014-g0001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/acb6/6371639/3fe90cb80db0/fnbeh-13-00014-g0002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/acb6/6371639/92d3d3cad2d7/fnbeh-13-00014-g0001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/acb6/6371639/3fe90cb80db0/fnbeh-13-00014-g0002.jpg

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本文引用的文献

1
Genome-wide DNA methylation comparison between live human brain and peripheral tissues within individuals.个体活人脑与外周组织的全基因组 DNA 甲基化比较。
Transl Psychiatry. 2019 Jan 31;9(1):47. doi: 10.1038/s41398-019-0376-y.
2
Agreement in DNA methylation levels from the Illumina 450K array across batches, tissues, and time.Illumina 450K 芯片在不同批次、组织和时间的 DNA 甲基化水平的一致性。
Epigenetics. 2018;13(1):19-32. doi: 10.1080/15592294.2017.1411443. Epub 2018 Jan 30.
3
Methylation of the glucocorticoid receptor gene, nuclear receptor subfamily 3, group C, member 1 (NR3C1), in maltreated and nonmaltreated children: Associations with behavioral undercontrol, emotional lability/negativity, and externalizing and internalizing symptoms.
新生儿甲基化与子宫内暴露于母亲吸烟环境
Toxics. 2023 Oct 13;11(10):855. doi: 10.3390/toxics11100855.
4
Epigenome-wide association of neonatal methylation and trimester-specific prenatal PM exposure.新生儿甲基化与孕期特定阶段产前颗粒物暴露的全表观基因组关联研究
Environ Epidemiol. 2022 Oct 3;6(5):e227. doi: 10.1097/EE9.0000000000000227. eCollection 2022 Oct.
5
Association Between Maternal Adverse Childhood Experiences and Neonatal SCG5 DNA Methylation-Effect Modification by Prenatal Home Visiting.母亲不良童年经历与新生儿 SCG5 DNA 甲基化的关联-产前家访的影响修饰作用。
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6
Epigenetic Modifications Associated with Maternal Anxiety during Pregnancy and Children's Behavioral Measures.孕期母亲焦虑相关的表观遗传修饰与儿童行为测量。
Cells. 2021 Sep 14;10(9):2421. doi: 10.3390/cells10092421.
7
Biobehavioral organization shapes the immune epigenome in infant rhesus Macaques (Macaca mulatta).生物行为组织塑造了婴儿恒河猴(Macaca mulatta)的免疫表观基因组。
Brain Behav Immun. 2021 Aug;96:256-270. doi: 10.1016/j.bbi.2021.06.006. Epub 2021 Jun 16.
8
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9
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Ann Epidemiol. 2020 Dec;52:26-34. doi: 10.1016/j.annepidem.2020.09.015. Epub 2020 Oct 1.
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Dev Psychopathol. 2017 Dec;29(5):1795-1806. doi: 10.1017/S0954579417001407.
4
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Dev Psychopathol. 2017 Dec;29(5):1635-1648. doi: 10.1017/S0954579417001298.
5
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Nat Rev Genet. 2017 Jul;18(7):441-451. doi: 10.1038/nrg.2017.32. Epub 2017 May 30.
6
Prenatal stress and epigenetics.产前应激与表观遗传学。
Neurosci Biobehav Rev. 2020 Oct;117:198-210. doi: 10.1016/j.neubiorev.2017.05.016. Epub 2017 May 18.
7
Maternal Interpersonal Trauma and Child Social-Emotional Development: An Intergenerational Effect.母亲的人际创伤与儿童社会情感发展:一种代际效应。
Paediatr Perinat Epidemiol. 2017 Mar;31(2):99-107. doi: 10.1111/ppe.12341. Epub 2017 Jan 31.
8
Medical morbidities and DNA methylation of NR3C1 in preterm infants.早产儿的医学发病率与NR3C1的DNA甲基化
Pediatr Res. 2017 Jan;81(1-1):68-74. doi: 10.1038/pr.2016.185. Epub 2016 Sep 21.
9
Waddington, Dynamic Systems, and Epigenetics.沃丁顿、动态系统与表观遗传学
Front Behav Neurosci. 2016 Jun 10;10:107. doi: 10.3389/fnbeh.2016.00107. eCollection 2016.
10
The dynamic epigenome and its implications for behavioral interventions: a role for epigenetics to inform disorder prevention and health promotion.动态表观基因组及其对行为干预的影响:表观遗传学在疾病预防和健康促进中的作用。
Transl Behav Med. 2016 Mar;6(1):55-62. doi: 10.1007/s13142-016-0387-7.