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Pubertal stress recalibration reverses the effects of early life stress in postinstitutionalized children.青春期应激再校准可逆转被领养儿童早期生活应激的影响。
Proc Natl Acad Sci U S A. 2019 Nov 26;116(48):23984-23988. doi: 10.1073/pnas.1909699116. Epub 2019 Nov 11.
2
Adverse Childhood Experiences and Early Pubertal Timing Among Girls: A Meta-Analysis.不良童年经历与女孩青春期启动时间:一项荟萃分析。
Int J Environ Res Public Health. 2019 Aug 13;16(16):2887. doi: 10.3390/ijerph16162887.
3
The epigenetic clock as a predictor of disease and mortality risk: a systematic review and meta-analysis.表观遗传时钟作为疾病和死亡风险的预测指标:系统评价和荟萃分析。
Clin Epigenetics. 2019 Apr 11;11(1):62. doi: 10.1186/s13148-019-0656-7.
4
Agreement Between Prospective and Retrospective Measures of Childhood Maltreatment: A Systematic Review and Meta-analysis.前瞻性和回顾性儿童虐待测量之间的一致性:系统评价和荟萃分析。
JAMA Psychiatry. 2019 Jun 1;76(6):584-593. doi: 10.1001/jamapsychiatry.2019.0097.
5
The epigenetic clock: a molecular crystal ball for human aging?表观遗传时钟:人类衰老的分子水晶球?
Aging (Albany NY). 2019 Jan 21;11(2):833-835. doi: 10.18632/aging.101712.
6
DNA methylation GrimAge strongly predicts lifespan and healthspan.DNA甲基化GrimAge能有力地预测寿命和健康跨度。
Aging (Albany NY). 2019 Jan 21;11(2):303-327. doi: 10.18632/aging.101684.
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A new aging measure captures morbidity and mortality risk across diverse subpopulations from NHANES IV: A cohort study.一种新的衰老衡量标准可捕捉来自 NHANES IV 的不同亚人群的发病和死亡风险:一项队列研究。
PLoS Med. 2018 Dec 31;15(12):e1002718. doi: 10.1371/journal.pmed.1002718. eCollection 2018 Dec.
8
Early Experiences of Threat, but Not Deprivation, Are Associated With Accelerated Biological Aging in Children and Adolescents.早期的威胁经历,而不是剥夺,与儿童和青少年的生物衰老加速有关。
Biol Psychiatry. 2019 Feb 1;85(3):268-278. doi: 10.1016/j.biopsych.2018.09.008. Epub 2018 Sep 26.
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DNA Methylation Clocks in Aging: Categories, Causes, and Consequences.DNA 甲基化时钟与衰老:分类、原因和后果。
Mol Cell. 2018 Sep 20;71(6):882-895. doi: 10.1016/j.molcel.2018.08.008.
10
Epigenetic clock for skin and blood cells applied to Hutchinson Gilford Progeria Syndrome and studies.应用于哈钦森-吉尔福德早衰综合征及相关研究的皮肤和血细胞表观遗传时钟。
Aging (Albany NY). 2018 Jul 26;10(7):1758-1775. doi: 10.18632/aging.101508.

早期生活逆境、青春期时间和成年后的表观遗传年龄加速。

Early life adversity, pubertal timing, and epigenetic age acceleration in adulthood.

机构信息

University of California, San Francisco, CA, USA.

University of California, Los Angeles, CA, USA.

出版信息

Dev Psychobiol. 2021 Jul;63(5):890-902. doi: 10.1002/dev.22085. Epub 2021 Jan 10.

DOI:10.1002/dev.22085
PMID:33423276
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC8271092/
Abstract

BACKGROUND

Given associations linking early life adversity, pubertal timing, and biological aging, we examined the direct and indirect effects of early life trauma on adult biological aging (via age of menarche).

METHODS

Participants were premenopausal women (N = 183). Path models evaluated whether early life trauma predicted early pubertal timing and thereby, adult epigenetic age acceleration (indexed via four epigenetic clocks: Horvath DNAm Age, Hannum DNAm Age, DNAm PhenoAge, and DNAm GrimAge). Secondary analyses explored the effects of type of trauma (abuse and neglect) and adult chronic stress status (caregiver of child with autism and non-caregiver).

RESULTS

Early life trauma and earlier age at menarche independently predicted accelerated aging based on one of the four epigenetic clocks, DNAm GrimAge, though early life trauma was not associated with age of menarche. Childhood abuse, but not neglect, predicted faster epigenetic aging; results did not differ by chronic stress status.

CONCLUSIONS

Early trauma and early menarche appear to exert independent effects on DNAm GrimAge, which has been shown to be the strongest epigenetic predictor of mortality risk. This study identifies a potential correlate or determinant of accelerated epigenetic aging-menarcheal age. Future research should address the limitations of this study by using racially diverse samples.

摘要

背景

鉴于早期生活逆境、青春期时间和生物衰老之间的关联,我们研究了早期生活创伤对成年生物衰老(通过初潮年龄)的直接和间接影响。

方法

参与者为绝经前妇女(N=183)。路径模型评估了早期生活创伤是否预测了早期青春期时间,从而预测了成年表观遗传年龄加速(通过四个表观遗传时钟评估:Horvath DNAm 年龄、Hannum DNAm 年龄、DNAm PhenoAge 和 DNAm GrimAge)。二次分析探讨了创伤类型(虐待和忽视)和成年慢性应激状态(自闭症儿童的照顾者和非照顾者)的影响。

结果

早期生活创伤和初潮年龄较早均独立预测了基于四个表观遗传时钟之一的 DNAm GrimAge 加速老化,尽管早期生活创伤与初潮年龄无关。儿童期虐待,但不是忽视,预测了更快的表观遗传老化;结果不受慢性应激状态的影响。

结论

早期创伤和初潮年龄似乎对 DNAm GrimAge 有独立的影响,DNAm GrimAge 已被证明是死亡率风险的最强表观遗传预测因子。这项研究确定了加速表观遗传老化-初潮年龄的一个潜在相关因素或决定因素。未来的研究应通过使用种族多样化的样本来解决本研究的局限性。