Childhood trauma and hippocampal-dependent memory across the psychosis spectrum: a systematic review and meta-analysis.

IF 3.3 2区 医学 Q2 NEUROSCIENCES
Journal of Psychiatry & Neuroscience Pub Date : 2025-08-14 Print Date: 2025-07-01 DOI:10.1503/jpn.240150
Ava J C Mason, Mia Harada-Laszlo, Max Wanduragala, Rui Tang, Paul Jung, Sherin Oommen, Chris Brewin, Neil Burgess, James Bisby, Michael Bloomfield
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引用次数: 0

Abstract

Background: Although the processes underlying the relationship between developmental trauma and psychosis remain to be elucidated, alterations in hippocampal-dependent memory (HDM) processing may underlie this relationship. We hypothesized that exposure to developmental trauma would be negatively associated with HDM and hippocampal volume and positively associated with intrusive memories among people with psychosis.

Methods: We conducted a systematic search of studies published from Dec. 18, 2020, to Nov. 14, 2023, using the search terms "childhood," "trauma," "psychosis," and "memory processing" in Embase, PsycINFO, MEDLINE, OpenGrey, Google Scholar, and PTSDpubs. We conducted meta-analyses of studies that measured developmental trauma (self-report questionnaires or interviews), HDM (episodic memory performance and trauma-memory intrusions), semantic and recognition-memory performance, and hippocampal volume among people with psychosis. Subsample analysis determined whether these associations differed across the psychosis spectrum or for specific abuse types.

Results: We included 26 studies. Meta-analyses found that developmental trauma was not associated with total hippocampal volume (n = 4, outcomes = 6, d = -0.12, standard error [SE] = 0.20, p = 0.2), episodic memory performance (n = 10, outcomes = 42, d = 0.11, SE = 0.19, p = 0.5), recognition (n = 3, outcomes = 4, d = -0.55, SE = 0.58, p = 0.3), or semantic memory performance (n = 4, outcomes = 6, d = 0.08, SE = 0.13, p = 0.6) in participants across the psychosis spectrum. One study found that developmental trauma was associated with impaired episodic memory performance in participants with schizotypal disorder and participants with a mixed phenotype of affective and psychotic symptoms. Two studies found developmental trauma to be associated with increased involuntary memory intrusions in a sample of people with psychosis.

Limitations: We did not control for age of trauma, sex, or chronicity of trauma. Results should be considered with caution, given the high publication bias and study heterogeneity seen within meta-analyses.

Conclusion: The association between developmental trauma and memory processing may not affect HDM more than the psychotic symptoms already experienced by affected individuals. However, future studies should focus on the effects of developmental trauma on involuntary memory among people with psychosis.

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童年创伤和海马体依赖记忆跨越精神病谱:系统回顾和荟萃分析。
背景:尽管发育性创伤和精神病之间的关系背后的过程仍有待阐明,海马依赖性记忆(HDM)加工的改变可能是这种关系的基础。我们假设,在精神病患者中,暴露于发展性创伤与HDM和海马体积负相关,与侵入性记忆正相关。方法:我们在Embase、PsycINFO、MEDLINE、OpenGrey、谷歌Scholar和ptsdbars中使用“童年”、“创伤”、“精神病”和“记忆处理”等搜索词,对2020年12月18日至2023年11月14日发表的研究进行了系统检索。我们对一些研究进行了荟萃分析,这些研究测量了精神病患者的发展性创伤(自我报告问卷或访谈)、HDM(情景记忆表现和创伤记忆侵入)、语义和识别记忆表现以及海马体体积。亚样本分析确定了这些关联是否在精神病谱系或特定滥用类型中有所不同。结果:我们纳入了26项研究。荟萃分析发现,发展创伤与海马总量无关(n = 4,结果= 6,d = -0.12,标准误差(SE) = 0.20, p = 0.2),情景记忆性能(n = 10,结果= 42 d = 0.11, = 0.19, p = 0.5),识别(n = 3,结果= 4 d = -0.55, = 0.58, p = 0.3),或语义记忆性能(n = 4,结果= 6,d = 0.08, = 0.13, p = 0.6)参与者的精神病。一项研究发现,在患有分裂型障碍的参与者和患有情感和精神症状混合表型的参与者中,发展性创伤与情景记忆表现受损有关。两项研究发现,在精神病患者的样本中,发展性创伤与非自愿记忆入侵的增加有关。局限性:我们没有控制创伤的年龄、性别或创伤的慢性性。考虑到meta分析中的高发表偏倚和研究异质性,应谨慎考虑结果。结论:发展性创伤与记忆加工之间的关联对HDM的影响可能小于受影响个体已经经历的精神病症状。然而,未来的研究应该集中在发展性创伤对精神病患者非自愿记忆的影响上。
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来源期刊
CiteScore
6.80
自引率
2.30%
发文量
51
审稿时长
2 months
期刊介绍: The Journal of Psychiatry & Neuroscience publishes papers at the intersection of psychiatry and neuroscience that advance our understanding of the neural mechanisms involved in the etiology and treatment of psychiatric disorders. This includes studies on patients with psychiatric disorders, healthy humans, and experimental animals as well as studies in vitro. Original research articles, including clinical trials with a mechanistic component, and review papers will be considered.
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