Laboratory of Epidemiology and Population Sciences, NIA/NIH/IRP, Baltimore, MD 21224, USA.
Department of Research Programs, Fort Belvoir Community Hospital, Fort Belvoir, VA 22060, USA.
Aging (Albany NY). 2022 Jul 1;14(13):5311-5344. doi: 10.18632/aging.204150.
Perceived discrimination may be associated with accelerated aging later in life, with depressive symptoms acting as potential mediator.
A nationally representative sample of older adults was used [Health and Retirement Study 2010-2016, Age: 50-100 y in 2016, = 2,806, 55.6% female, 82.3% Non-Hispanic White (NHW)] to evaluate associations of perceived discrimination measures [Experience of discrimination or EOD; and Reasons for Perceived discrimination or RPD) and depressive symptoms (DEP)] with 13 DNAm-based measures of epigenetic aging. Group-based trajectory and four-way mediation analyses were used.
Overall, and mostly among female and NHW participants, greater RPD in 2010-2012 had a significant adverse total effect on epigenetic aging [2016: DNAm GrimAge, DunedinPoAm38 (MPOA), Levine (PhenoAge) and Horvath 2], with 20-50% of this effect being explained by a pure indirect effect through DEP in 2014-2016. Among females, sustained elevated DEP (2010-2016) was associated with greater LIN DNAm age (β ± SE: +1.506 ± 0.559, = 0.009, reduced model), patterns observed for elevated DEP (high vs. low) for GrimAge and MPOA DNAm markers. Overall and in White adults, the relationship of the Levine clock with perceived discrimination in general (both EOD and RPD) was mediated through elevated DEP.
Sustained elevations in DEP and RPD were associated with select biological aging measures, consistently among women and White adults, with DEP acting as mediator in several RPD-EPICLOCK associations.
感知歧视可能与晚年加速衰老有关,抑郁症状是潜在的中介因素。
使用全国代表性的老年人样本[健康与退休研究 2010-2016 年,2016 年年龄:50-100 岁,n=2806,女性占 55.6%,非西班牙裔白人占 82.3%(NHW)]评估感知歧视测量([歧视经历或 EOD;感知歧视原因或 RPD)]和抑郁症状(DEP)与 13 个基于 DNAm 的表观遗传衰老测量值的关联。使用基于群组的轨迹和四向中介分析。
总体而言,在女性和 NHW 参与者中,2010-2012 年 RPD 较高对表观遗传衰老有显著的不利总效应[2016 年:DNAm GrimAge、DunedinPoAm38(MPOA)、Levine(PhenoAge)和 Horvath 2],其中 20-50%的效应通过 2014-2016 年的 DEP 产生纯间接效应。在女性中,持续升高的 DEP(2010-2016 年)与 LIN DNAm 年龄增加相关(β±SE:+1.506±0.559,P=0.009,简化模型),观察到 GrimAge 和 MPOA DNAm 标志物中 DEP 升高(高 vs. 低)的模式。总体而言,在白人成年人中,感知歧视与 Levine 时钟的关系(EOD 和 RPD 都包括在内)通过升高的 DEP 起中介作用。
持续升高的 DEP 和 RPD 与特定的生物衰老测量值有关,在女性和白人成年人中一致存在,DEP 在几个 RPD-EPICLOCK 关联中充当中介。