University of California, San Francisco, CA, USA.
University of California, Los Angeles, CA, USA.
Dev Psychobiol. 2021 Jul;63(5):890-902. doi: 10.1002/dev.22085. Epub 2021 Jan 10.
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).
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).
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.
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.
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。
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。
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。
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。