Evidence map›Paper›PMID 41912483›Full record

SynthesisTranslational psychiatry2026

Prospective biomarkers of posttraumatic stress disorder in children and adolescents: a systematic review and meta-analysis.

T H Sharp, M Bailey, C Burke, A Giuliani, L V Hiscox, E Alisic, R Kumsta, S Seedat, S L Halligan

Abstract readSystematic ReviewMeta-Analysis
In one paragraph

Synthesis in Translational psychiatry, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed, 1 pooled it
–field-weighted citation impact
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

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

2 citing papers in PubMed, 1 synthesis or guideline pooled it.

  1. Pooled it
  2. Article
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

9 authors.

T H SharpDepartment of Psychology, University of Bath, Bath, UK. Tamsin.sharp@bristol.ac.uk.ORCID http://orcid.org/0000-0002-7334-0503
M BaileyDepartment of Psychology, University of Bath, Bath, UK.
C BurkeDepartment of Psychology, University of Bath, Bath, UK.
A GiulianiDepartment of Psychology, University of Bath, Bath, UK.ORCID http://orcid.org/0009-0002-4199-3611
L V HiscoxCardiff University Brain Research Imaging Centre (CUBRIC), School of Psychology, Cardiff University, Cardiff, UK.
E AlisicMelbourne School of Population and Global Health, University of Melbourne, Carlton, VIC, Australia.
R KumstaDepartment of Behavioural and Cognitive Sciences, Faculty of Humanities, Education and Social Sciences, University of Luxemburg, Esch-sur-Alzette, Luxemburg.ORCID http://orcid.org/0000-0001-6006-6958
S SeedatSouth African Medical Research Council Unit on the Genomics of Brain Disorders, Department of Psychiatry, Faculty of Medicine and Health Sciences, Stellenbosch University, Cape Town, South Africa.ORCID http://orcid.org/0000-0002-5118-786X
S L HalliganDepartment of Psychology, University of Bath, Bath, UK.ORCID http://orcid.org/0000-0002-3436-3358

Funding

RCUK | Economic and Social Research Council (ESRC) ESV0026431
6 · The paper itself

Abstract

Trauma exposure in children and young people (CYP) can lead to the development of posttraumatic stress disorder (PTSD). Identification of biomarkers prospectively associated with PTSD can provide critical insight into the mechanisms underpinning this disorder and potentially aid in identifying CYP vulnerable to persistent symptoms. A systematic search of databases was conducted up until February 2024 to identify studies testing associations of prospective biomarkers with PTSD outcomes in CYP. A narrative synthesis of study characteristics, quality, and findings was conducted. Meta-analysis using a random-effects model was performed when two or more comparable studies were identified. Searches yielded 2039 articles, with 283 identified as relevant after title/abstract screening. Twenty-one studies met eligibility criteria in the following biological domains: hormonal, immunological, cardiovascular, and multisystem. The majority of studies focussed on naturalistic recovery of CYP exposed to acute trauma. Significant heterogeneity was observed, including in trauma type, selection, and biomarker measurement. Across biomarkers, relatively consistent evidence was observed for a prospective association between elevated heart rate post-trauma and increased risk of PTSD persistence only, with limited evidence in other domains. Our review highlights a limited evidence base for prospective biomarkers of the development of PTSD in CYP, with methodological issues limiting inferences that can be drawn. A notable lack of evidence from low-and-middle income countries, despite chronic and severe trauma being endemic in these settings, was identified. Further research using standardised protocols from large, representative samples will be critical in the identification of biomarkers of PTSD risk and resilience.

Indexed as

BiomarkersStress Disorders, Post-TraumaticAdolescentChildHumansBiomarkers

Identifiers

PMID41912483
PMCPMC13039113

What OpenQuestion holds

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Registered trials

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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.