Department of Psychology, Faculty of Medicine and Psychology, Sapienza University of Rome, Italy.
Department of Psychological Medicine, Institute of Psychiatry, Psychology and Neuroscience, King's College London, London, UK.
J Affect Disord. 2024 Jul 15;357:85-96. doi: 10.1016/j.jad.2024.04.072. Epub 2024 Apr 25.
Exposure to adverse childhood experiences (ACEs) confers a higher risk of developing depression in adulthood, yet the mediation of inflammation remains under debate. To test this model, we conducted a systematic review and two-stage structural equation modelling meta-analysis of studies reporting correlations between ACEs before age 18, inflammatory markers and depression severity in adulthood. Scopus, Pubmed, Medline, PsycInfo, and CINAHL were searched up to 2 October 2023. Twenty-two studies reporting data on C-reactive protein (CRP, n = 12,935), interleukin-6 (IL-6, n = 4108), tumour necrosis factor-α (TNF-α, n = 2256) and composite measures of inflammation (n = 1674) were included. Unadjusted models revealed that CRP (β = 0.003, 95 % LBCI 0.0002 to 0.0068), IL-6 (β = 0.003, 95 % LBCI 0.001 to 0.006), and composite inflammation (β = 0.009, 95 % LBCI 0.004 to 0.018) significantly mediated the association between ACEs and adult depression. The mediation effects no longer survived after adjusting for BMI; however, a serial mediation model revealed that BMI and IL-6 sequentially mediated the association between ACEs and depression (β = 0.002, 95 % LBCI 0.0005 to 0.0046), accounting for 14.59 % and 9.94 % of the variance of IL-6 and depressive symptoms, respectively. Due to the cross-sectional nature of assessment of inflammation and depression findings should be approached with caution; however, results suggest that complex interactions of psychoneuroimmunological and metabolic factors underlie the association between ACEs and adulthood depression.
暴露于不良的童年经历 (ACEs) 会增加成年后患抑郁症的风险,但炎症的中介作用仍存在争议。为了检验这一模型,我们对截至 2023 年 10 月 2 日报告 ACEs(18 岁前)与成年期炎症标志物和抑郁严重程度之间相关性的研究进行了系统综述和两阶段结构方程模型荟萃分析。检索了 Scopus、Pubmed、Medline、PsycInfo 和 CINAHL。共纳入 22 项报告 C 反应蛋白 (CRP,n=12935)、白细胞介素-6 (IL-6,n=4108)、肿瘤坏死因子-α (TNF-α,n=2256) 和炎症综合指标 (n=1674) 的研究数据。未调整模型显示 CRP(β=0.003,95%LBCI 0.0002 至 0.0068)、IL-6(β=0.003,95%LBCI 0.001 至 0.006)和炎症综合指标(β=0.009,95%LBCI 0.004 至 0.018)显著介导 ACEs 与成人抑郁之间的关联。调整 BMI 后,中介效应不再存在;然而,串联中介模型显示 BMI 和 IL-6 依次介导 ACEs 与抑郁之间的关联(β=0.002,95%LBCI 0.0005 至 0.0046),分别解释了 IL-6 和抑郁症状变异的 14.59%和 9.94%。由于炎症和抑郁评估的横断面性质,结果应谨慎对待;然而,结果表明,心理神经免疫学和代谢因素的复杂相互作用是 ACEs 与成年期抑郁症之间关联的基础。