Suppr超能文献

在敏感时期经历逆境会导致儿童的表观遗传衰老加速。

Adversity exposure during sensitive periods predicts accelerated epigenetic aging in children.

机构信息

Center for Genomic Medicine, Massachusetts General Hospital, Boston, MA, 02114, USA.

Center for Genomic Medicine, Massachusetts General Hospital, Boston, MA, 02114, USA; Stanley Center for Psychiatric Research, The Broad Institute of Harvard and MIT, Cambridge, MA, 02142, USA; Department of Psychiatry, Harvard Medical School, Boston, MA, 02115, USA.

出版信息

Psychoneuroendocrinology. 2020 Mar;113:104484. doi: 10.1016/j.psyneuen.2019.104484. Epub 2019 Nov 6.

Abstract

OBJECTIVES

Exposure to adversity has been linked to accelerated biological aging, which in turn has been shown to predict numerous physical and mental health problems. In recent years, measures of DNA methylation-based epigenetic age--known as "epigenetic clocks"--have been used to estimate accelerated epigenetic aging. Although a small number of studies have found an effect of adversity exposure on epigenetic age in children, none have investigated if there are "sensitive periods" when adversity is most impactful.

METHODS

Using data from the Avon Longitudinal Study of Parents and Children (ALSPAC; n = 973), we tested the prospective association between repeated measures of childhood exposure to seven types of adversity on epigenetic age assessed at age 7.5 using the Horvath and Hannum epigenetic clocks. With a Least Angle Regression variable selection procedure, we evaluated potential sensitive period effects.

RESULTS

We found that exposure to abuse, financial hardship, or neighborhood disadvantage during sensitive periods in early and middle childhood best explained variability in the deviation of Hannum-based epigenetic age from chronological age, even after considering the role of adversity accumulation and recency. Secondary sex-stratified analyses identified particularly strong sensitive period effects. These effects were undetected in analyses comparing children "exposed" versus "unexposed" to adversity. We did not identify any associations between adversity and epigenetic age using the Horvath epigenetic clock.

CONCLUSIONS

Our results suggest that adversity may alter methylation processes in ways that either directly or indirectly perturb normal cellular aging and that these effects may be heightened during specific life stages.

摘要

目的

逆境暴露与生物衰老加速有关,而衰老加速又与许多身心健康问题相关。近年来,基于 DNA 甲基化的表观遗传年龄(称为“表观遗传时钟”)已被用于估计加速的表观遗传衰老。尽管少数研究发现逆境暴露对儿童的表观遗传年龄有影响,但尚无研究探讨逆境影响最大的“敏感时期”。

方法

利用阿冯纵向父母与子女研究(ALSPAC;n=973)的数据,我们测试了在儿童期经历的七种逆境的重复测量与 7.5 岁时基于 Horvath 和 Hannum 的表观遗传时钟评估的表观遗传年龄之间的前瞻性关联。通过最小角回归变量选择程序,我们评估了潜在的敏感时期效应。

结果

我们发现,在儿童早期和中期的敏感时期,暴露于虐待、经济困难或邻里劣势中,最能解释基于 Hannum 的表观遗传年龄与实际年龄之间的偏差的可变性,即使考虑到逆境积累和最近的作用也是如此。二级性别分层分析确定了特别强烈的敏感时期效应。在比较暴露于逆境和未暴露于逆境的儿童的分析中,未发现这些效应。我们使用 Horvath 表观遗传时钟未发现逆境与表观遗传年龄之间的任何关联。

结论

我们的结果表明,逆境可能会以直接或间接干扰正常细胞衰老的方式改变甲基化过程,并且这些影响在特定的生命阶段可能会加剧。

相似文献

1
Adversity exposure during sensitive periods predicts accelerated epigenetic aging in children.
Psychoneuroendocrinology. 2020 Mar;113:104484. doi: 10.1016/j.psyneuen.2019.104484. Epub 2019 Nov 6.
4
Examining the epigenetic mechanisms of childhood adversity and sensitive periods: A gene set-based approach.
Psychoneuroendocrinology. 2022 Oct;144:105854. doi: 10.1016/j.psyneuen.2022.105854. Epub 2022 Jun 27.
5
Sensitive Periods for the Effect of Childhood Adversity on DNA Methylation: Results From a Prospective, Longitudinal Study.
Biol Psychiatry. 2019 May 15;85(10):838-849. doi: 10.1016/j.biopsych.2018.12.023. Epub 2019 Jan 21.
8
Exposure to childhood adversity and deficits in emotion recognition: results from a large, population-based sample.
J Child Psychol Psychiatry. 2018 Aug;59(8):845-854. doi: 10.1111/jcpp.12881. Epub 2018 Mar 7.
9
Early life adversity and age acceleration at mid-life and older ages indexed using the next-generation GrimAge and Pace of Aging epigenetic clocks.
Psychoneuroendocrinology. 2022 Mar;137:105643. doi: 10.1016/j.psyneuen.2021.105643. Epub 2021 Dec 23.
10
Childhood trauma is linked to epigenetic age deceleration in young adults with previous youth residential care placements.
Eur J Psychotraumatol. 2024;15(1):2379144. doi: 10.1080/20008066.2024.2379144. Epub 2024 Jul 25.

引用本文的文献

1
Adverse Childhood Experiences, Genetic Susceptibility, and the Risk of Osteoporosis: A Cohort Study.
Medicina (Kaunas). 2025 Jul 30;61(8):1387. doi: 10.3390/medicina61081387.
2
Adolescent depression, childhood maltreatment, and the immune system; a role for epigenetic aging?
Brain Behav Immun Health. 2025 Jul 28;48:101080. doi: 10.1016/j.bbih.2025.101080. eCollection 2025 Oct.
3
Epigenetic regulation of brain development, plasticity, and response to early-life stress.
Neuropsychopharmacology. 2025 Aug 6. doi: 10.1038/s41386-025-02179-z.
4
Early-Life Adversity and Epigenetic Aging: Findings from a 17-Year Longitudinal Study.
Biomolecules. 2025 Jun 18;15(6):887. doi: 10.3390/biom15060887.
6
Precise and interpretable neural networks reveal epigenetic signatures of aging across youth in health and disease.
Front Aging. 2025 Jan 23;5:1526146. doi: 10.3389/fragi.2024.1526146. eCollection 2024.
7
Maximizing insights from longitudinal epigenetic age data: simulations, applications, and practical guidance.
Clin Epigenetics. 2024 Dec 20;16(1):187. doi: 10.1186/s13148-024-01784-x.
8
A Brief Historic Review of Research on Early Life Stress and Inflammation across the Lifespan.
Neuroimmunomodulation. 2025;32(1):24-35. doi: 10.1159/000542676. Epub 2024 Nov 27.
9
War Exposure and DNA Methylation in Syrian Refugee Children and Adolescents.
JAMA Psychiatry. 2025 Feb 1;82(2):191-200. doi: 10.1001/jamapsychiatry.2024.3714.
10
Early resilience and epigenetic ageing: Results from the prospective Young Finns Study with a 31-year follow-up.
Aging Cell. 2025 Feb;24(2):e14394. doi: 10.1111/acel.14394. Epub 2024 Oct 25.

本文引用的文献

2
Sensitive Periods for the Effect of Childhood Adversity on DNA Methylation: Results From a Prospective, Longitudinal Study.
Biol Psychiatry. 2019 May 15;85(10):838-849. doi: 10.1016/j.biopsych.2018.12.023. Epub 2019 Jan 21.
3
Editorial: Peripheral Markers of Immune Response in Major Psychiatric Disorders: Where Are We Now and Where Do We Want to Be?
Front Psychiatry. 2019 Jan 22;10:5. doi: 10.3389/fpsyt.2019.00005. eCollection 2019.
4
Early Experiences of Threat, but Not Deprivation, Are Associated With Accelerated Biological Aging in Children and Adolescents.
Biol Psychiatry. 2019 Feb 1;85(3):268-278. doi: 10.1016/j.biopsych.2018.09.008. Epub 2018 Sep 26.
5
DNA Methylation Age-Environmental Influences, Health Impacts, and Its Role in Environmental Epidemiology.
Curr Environ Health Rep. 2018 Sep;5(3):317-327. doi: 10.1007/s40572-018-0203-2.
6
The epigenetic clock and pubertal, neuroendocrine, psychiatric, and cognitive outcomes in adolescents.
Clin Epigenetics. 2018 Jul 18;10(1):96. doi: 10.1186/s13148-018-0528-6.
7
The Epigenetic Clock at Birth: Associations With Maternal Antenatal Depression and Child Psychiatric Problems.
J Am Acad Child Adolesc Psychiatry. 2018 May;57(5):321-328.e2. doi: 10.1016/j.jaac.2018.02.011. Epub 2018 Mar 15.
8
DNA methylation-based biomarkers and the epigenetic clock theory of ageing.
Nat Rev Genet. 2018 Jun;19(6):371-384. doi: 10.1038/s41576-018-0004-3.
10
Traumatic stress and accelerated DNA methylation age: A meta-analysis.
Psychoneuroendocrinology. 2018 Jun;92:123-134. doi: 10.1016/j.psyneuen.2017.12.007. Epub 2017 Dec 27.

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验