Evidence map›Paper›PMID 41148174›Full record

ArticleSchizophrenia bulletin2026

The Effect of Developmental Trauma on Brain Structures Involved in Threat and Memory Processing and Its Relation to Psychotic Experiences in Adulthood.

Ava J C Mason, Paul G Y Jung, Kate Merritt, Arjun Sethi, Stanley Zammit, Derek K Jones, Anthony S David, Michael A P Bloomfield

Abstract read
In one paragraph

Article in Schizophrenia bulletin, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
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0citing papers in PubMed
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1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

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3 · Its place in the literature

Who cites it

0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

8 authors.

Ava J C MasonDivision of Psychiatry, UCL Institute of Mental Health, University College London, London W1T 7NF, United Kingdom.
Paul G Y JungDivision of Psychiatry, UCL Institute of Mental Health, University College London, London W1T 7NF, United Kingdom.
Kate MerrittDivision of Psychiatry, UCL Institute of Mental Health, University College London, London W1T 7NF, United Kingdom.
Arjun SethiDepartment of Forensic and Neurodevelopmental Sciences (FANS), Institute of Psychiatry, Psychology and Neuroscience, King's College London, Denmark Hill, SE5 8AB, United Kingdom.
Stanley ZammitDivision of Psychological Medicine and Clinical Neurosciences, Cardiff University, School of Medicine, UHW Main Building, Heath Park, Cardiff, CF14 4XN, United Kingdom.
Derek K JonesBrain Research Imaging Centre (CUBRIC), Cardiff University, Cardiff, CF24 4HQ, United Kingdom.
Anthony S DavidDivision of Psychiatry, UCL Institute of Mental Health, University College London, London W1T 7NF, United Kingdom.
Michael A P BloomfieldDivision of Psychiatry, UCL Institute of Mental Health, University College London, London W1T 7NF, United Kingdom.

Funding

ALSPACAstor foundation MR/S003436/1British Medical Association Margaret Temple Award for Schizophrenia ResearchNIHR Bristol Biomedical Research Centre NIHR203315UK Medical Research Council and Wellcome 217065/Z/19/ZUKRI Future Leaders FellowshipWellcome Trust
6 · The paper itself

Abstract

background and hypothesisDespite growing evidence of a causal association between developmental trauma (DT) and psychotic experiences (PEs), the precise neurobiological mechanisms underlying this association remain poorly understood. We examined the effect of DT on the structure of brain regions involved in threat and memory processing, and the role of these alterations in the association between DT and PEs. STUDY

designThis study used data from the Avon Longitudinal Study of Parents and Children, a large, population-based birth cohort in the United Kingdom. Data were available from 419 participants, including DT reported by the parents or the participants between ages 0 and 17 years, PEs at age 18, and volumes of regions involved in threat and memory processing in adulthood (mean = 21,2, SD = 1.5 years). STUDY

resultsDT exposure was associated with increased odds of PEs (odds ratio [OR] = 1.64; 95% CI, 1.04-2.59, P = .035), with evidence supporting cumulative risk effects for exposure to multiple trauma types (B = 0.160, P < .001). DT was also associated with reduced left amygdala volumes (B = -0.011, P = .02) with evidence again supporting cumulative risk effect with multiple trauma types (B = -0.006, P = .01). Reduced bilateral amygdala volume was associated with an increased odds of PEs driven by the left amygdala (OR = 0.001, 95% CI, 0.000-0.154, P = .006).

conclusionsThese findings are consistent with theories that alterations in brain regions involved in threat and memory processing lie on the neurobiological pathway from DT to PEs, offering the possibility of prevention strategies for psychosis.

Indexed as

Adverse Childhood ExperiencesAmygdalaFearMemoryPsychological TraumaPsychotic DisordersAdolescentAdultChildChild, PreschoolFemaleHumansInfantLongitudinal StudiesMagnetic Resonance ImagingMaledevelopmental traumamemory processingpsychotic experiencessMRIthreat processing

Identifiers

PMID41148174
PMCPMC13645828

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.