Lowry Elaine, McInerney Amy, Schmitz Norbert, Deschênes Sonya S
UCD School of Psychology, University College Dublin, Dublin, Ireland.
Department of Psychiatry, McGill University, Montreal, QC, Canada.
Soc Psychiatry Psychiatr Epidemiol. 2022 Dec;57(12):2367-2377. doi: 10.1007/s00127-022-02315-w. Epub 2022 Jun 26.
Adverse childhood experiences (ACEs) have been associated with cognitive decline in adulthood. However, the underlying mechanisms implicated remain unclear. This study investigated depressive symptoms and systemic inflammation as potential mediators of the association between ACEs and later cognitive function.
Participants were adults aged 50 + from the English Longitudinal Study of Ageing (N = 3029; 54.8% female). Measures included self-reported ACEs at wave 3 (2006-2007), C-reactive protein (CRP) and depressive symptoms at wave 4 (2008-2009), and cognitive function at waves 3 and 7 (2014-2015). Mediation analyses examined the direct associations between ACEs and cognitive function at wave 7 and the indirect associations via depressive symptoms and CRP at wave 4. In a first set of analyses, models were adjusted for sociodemographic factors and baseline cognitive function. In a second set of analyses, models were additionally adjusted for BMI and health behaviours (n = 1915).
Cumulative ACEs exposure positively predicted depressive symptoms (b = 0.184, s.e. = 0.034, p < .001), which in turn predicted poorer cognitive function at wave 7 (b = - 0.035, s.e. = 0.008, p < .001). ACEs also positively predicted systemic inflammation as measured by CRP (b = 0.031, s.e. = 0.01, p = 0.0016). However, CRP did not mediate the association between ACEs and later cognitive function (b = - 0.0002, 95% CI: - 0.002, 0.002).
These findings suggest that ACEs may be related to cognitive decline partly via depressive symptoms and corroborate prior research linking ACEs with systemic inflammation in adulthood.
童年不良经历(ACEs)与成年后的认知衰退有关。然而,其中潜在的机制仍不清楚。本研究调查了抑郁症状和全身炎症作为ACEs与后期认知功能之间关联的潜在中介因素。
参与者为来自英国老龄化纵向研究的50岁及以上成年人(N = 3029;54.8%为女性)。测量指标包括第3轮(2006 - 2007年)自我报告的ACEs、第4轮(2008 - 2009年)的C反应蛋白(CRP)和抑郁症状,以及第3轮和第7轮(2014 - 2015年)的认知功能。中介分析检验了第7轮时ACEs与认知功能之间的直接关联,以及通过第4轮的抑郁症状和CRP的间接关联。在第一组分析中,模型对社会人口学因素和基线认知功能进行了调整。在第二组分析中,模型还额外对体重指数和健康行为进行了调整(n = 1915)。
累积ACEs暴露正向预测抑郁症状(b = 0.184,标准误 = 0.034,p <.001),而抑郁症状反过来又预测第7轮时较差的认知功能(b = - 0.035,标准误 = 0.008,p <.001)。ACEs也正向预测以CRP衡量的全身炎症(b = 0.031,标准误 = 0.01,p = 0.0016)。然而,CRP并未介导ACEs与后期认知功能之间的关联(b = - 0.0002,95%置信区间:- 0.002,0.002)。
这些发现表明,ACEs可能部分通过抑郁症状与认知衰退有关,并证实了先前将ACEs与成年期全身炎症联系起来的研究。