Chen Yinxian, Abrishamcar Sarina, Johnson Sheroi, Aqua Jasmine, Dye Christian, Llabre Maria M, Gallo Linda C, Pereira Krista M, Daviglus Martha, Argos Maria, Cai Jianwen, Thyagarajan Bharat, Baccarelli Andrea, Isasi Carmen R, Kaplan Robert C, Conneely Karen N, Suglia Shakira F
Department of Epidemiology, Rollins School of Public Health, Emory University, Atlanta, GA, USA.
Department of Epidemiology, Rollins School of Public Health, Emory University, Atlanta, GA, USA.
Psychoneuroendocrinology. 2025 Mar;173:107369. doi: 10.1016/j.psyneuen.2025.107369. Epub 2025 Jan 28.
Whether adverse childhood experiences (ACEs) are associated with accelerated epigenetic aging over time among the Hispanic/Latino population remains unknown. This study examined the longitudinal association between ACEs and epigenetic age acceleration (EAA), as well as potential effect modifiers, among a sample of Hispanic/Latino adults.
We analyzed 960 Hispanic/Latino adults with DNA methylation (DNAm) profile data from two visits (approximately six years apart) sampled from the Hispanic Community Health Study/Study of Latinos (HCHS/SOL). We used PhenoAge, GrimAge, and DunedinPace, a biomarker for the pace of biological aging, to calculate epigenetic aging deviations. Linear mixed models were fit to estimate the association between ACEs and EAA measured by each epigenetic aging measure, adjusting for sex, age, and parental highest education level. Sex and nativity were also assessed as potential effect modifiers.
A one-unit increase in ACE score was associated with a 0.16-year (95 %CI: 0.06, 0.26, p = 0.002) higher GrimAge acceleration (AgeAccelGrim) at Visit 1. Among US-born individuals, a one-unit increase in ACE score was associated with a 0.35-year (95 %CI: 0.12, 0.58, p = 0.003) higher AgeAccelGrim and 0.01-biological year/calendar year (95 %CI: 0.01, 0.02, p = 0.0003) higher DunedinPACE at Visit 1, but statistically significantly weaker associations were found among foreign/US-territory born individuals (p for interaction=0.039 in AgeAccelGrim and 0.001 in DuendinPACE). No association was found between ACEs and the rate of change in EAA between two visits.
ACEs are associated with a higher EAA over time among Hispanic/Latino adults at a constant rate. Hispanic/Latino born in the US are more susceptible to the increased EAA related to ACEs compared with those born in a foreign country or US territory.
童年不良经历(ACEs)是否与西班牙裔/拉丁裔人群随时间推移的表观遗传衰老加速相关仍不清楚。本研究在一组西班牙裔/拉丁裔成年人样本中,考察了ACEs与表观遗传年龄加速(EAA)之间的纵向关联以及潜在的效应修饰因素。
我们分析了960名西班牙裔/拉丁裔成年人,他们来自西班牙裔社区健康研究/拉丁裔研究(HCHS/SOL),有两次访视(间隔约六年)的DNA甲基化(DNAm)谱数据。我们使用PhenoAge、GrimAge和达尼丁PACE(一种生物衰老速度的生物标志物)来计算表观遗传衰老偏差。采用线性混合模型来估计ACEs与每种表观遗传衰老指标所测量的EAA之间的关联,并对性别、年龄和父母最高教育水平进行了调整。性别和出生地也被评估为潜在的效应修饰因素。
在第一次访视时,ACE评分每增加一个单位,与GrimAge加速(AgeAccelGrim)高0.16岁(95%CI:0.06,0.26,p = 0.002)相关。在美国出生的个体中,ACE评分每增加一个单位,在第一次访视时与AgeAccelGrim高0.35岁(95%CI:0.12,0.58,p = 0.003)以及达尼丁PACE高0.01个生物学年/日历年(95%CI:0.01,0.02,p = 0.0003)相关,但在外国/美国领土出生的个体中发现的关联在统计学上显著较弱(AgeAccelGrim的交互作用p = 0.039,达尼丁PACE的交互作用p = 0.001)。未发现ACEs与两次访视之间EAA的变化率有关联。
ACEs与西班牙裔/拉丁裔成年人随时间推移以恒定速率出现的较高EAA相关。与在国外或美国领土出生的人相比,在美国出生的西班牙裔/拉丁裔更容易受到与ACEs相关的EAA增加的影响。