Department of Psychology, School of Behavioral and Brain Sciences, University of Texas at Dallas, Richardson, TX, USA; Department of Psychology, Northwestern University, Evanston, IL, USA; Institute for Innovations in Developmental Sciences (DevSci), Northwestern University, Evanston and Chicago, IL, USA; Department of Psychiatry, Northwestern University, Chicago, IL, USA.
Department of Psychology, Northwestern University, Evanston, IL, USA; Institute for Innovations in Developmental Sciences (DevSci), Northwestern University, Evanston and Chicago, IL, USA.
Psychoneuroendocrinology. 2024 Nov;169:107149. doi: 10.1016/j.psyneuen.2024.107149. Epub 2024 Jul 26.
Stress is associated with increased vulnerability to psychosis, yet the mechanisms that contribute to these effects are poorly understood. Substantial literature has linked reduced hippocampal volume to both psychosis risk and early life stress. However, less work has explored the direct and indirect effects of stress on psychosis through the hippocampus in preclinical samples- when vulnerability for psychosis is accumulating. The current paper leverages the Adolescent Brain Cognitive Development (ABCD) Study sample to examine whether objective psychosocial stressors, specifically adverse childhood experiences (ACE), are linked to vulnerability for psychosis, measured by psychotic-like experiences (PLE) severity, in late childhood and early adolescence, both directly and indirectly through the deleterious effects of stress on the hippocampus. Baseline data from 11,728 individuals included previously examined and validated items to assess ACE exposure, hippocampal volume, and PLE severity - a developmentally appropriate metric of risk for psychosis. Objective psychosocial stress exposure in childhood was associated with elevated PLE severity during the transition from childhood to adolescence. Hippocampal volume was significantly reduced in individuals with greater PLE severity and greater childhood stress exposure compared to peers with low symptoms or low stress exposure. These findings are consistent with a hippocampal vulnerability model of psychosis risk. Stress exposure may cumulatively impact hippocampal volume and may also reflect a direct pathway of psychosis risk. Objective psychosocial stress should be considered as a treatment target that may impact neurodevelopment and psychosis risk.
压力与增加精神病易感性有关,但导致这些影响的机制还不清楚。大量文献将海马体体积减少与精神病风险和生命早期压力联系起来。然而,在临床前样本中,当精神病易感性增加时,很少有工作探索压力通过海马体对精神病的直接和间接影响。本文利用青少年大脑认知发展 (ABCD) 研究样本,检验客观心理社会压力源,特别是不良童年经历 (ACE),是否与晚期儿童和青少年的精神病易感性(通过类精神病体验 (PLE) 严重程度来衡量)有关,以及是否通过压力对海马体的有害影响直接或间接相关。11728 名个体的基线数据包括先前检查和验证的项目,以评估 ACE 暴露、海马体体积和 PLE 严重程度——这是一种适合发展的精神病风险指标。童年时期的客观心理社会压力暴露与从儿童期到青春期的 PLE 严重程度升高有关。与低症状或低压力暴露的同龄人相比,PLE 严重程度较高和童年压力暴露较大的个体的海马体体积明显减少。这些发现与精神病风险的海马体脆弱性模型一致。压力暴露可能会累积性地影响海马体体积,也可能反映出精神病风险的直接途径。客观心理社会压力应被视为一种治疗目标,可能会影响神经发育和精神病风险。