Evidence map›Paper›PMID 38710907›Full record

ArticleMolecular psychiatry2024

A transdiagnostic prodrome for severe mental disorders: an electronic health record study.

Maite Arribas, Dominic Oliver, Rashmi Patel, Daisy Kornblum, Hitesh Shetty, Stefano Damiani, Kamil Krakowski, Umberto Provenzani, Daniel Stahl, Nikolaos Koutsouleris and 2 more

Abstract read
In one paragraph

Article in Molecular psychiatry, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 16 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
16citing 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

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

  1. Pooled it
  2. Article
  3. [Diagnostic transitions in adolescent inpatients with mental disorders: a retrospective cohort study].Zhejiang da xue xue bao. Yi xue ban = Journal of Zhejiang University. Medical sciences · 2026
    Article
  4. Article
  5. Article
  6. Observational
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  8. Characterisation of serious mental illness trajectories through transdiagnostic clinical features.The British journal of psychiatry : the journal of mental science · 2026
    Article
  9. Article
  10. Article
  11. Article
  12. Article
  13. Article
  14. ADHD symptom trajectories across childhood and early adolescence and risk for hypomanic symptoms in young adulthood.European psychiatry : the journal of the Association of European Psychiatrists · 2025
    Observational
  15. Article
  16. 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

12 authors.

Maite Arribas *Early Psychosis: Interventions and Clinical-Detection (EPIC) Lab, Department of Psychosis Studies, Institute of Psychiatry, Psychology & Neuroscience, King's College London, London, SE5 8AF, UK. maite.arribas@kcl.ac.uk.ORCID 0000-0002-0182-3493
Dominic Oliver *Early Psychosis: Interventions and Clinical-Detection (EPIC) Lab, Department of Psychosis Studies, Institute of Psychiatry, Psychology & Neuroscience, King's College London, London, SE5 8AF, UK.ORCID 0000-0002-8920-3407
Rashmi PatelDepartment of Psychological Medicine, Institute of Psychiatry, Psychology & Neuroscience, King's College London, London, SE5 8AF, UK.ORCID 0000-0002-9259-8788
Daisy KornblumNIHR Maudsley Biomedical Research Centre, London, UK.
Hitesh ShettyNIHR Maudsley Biomedical Research Centre, London, UK.
Stefano DamianiDepartment of Brain and Behavioral Sciences, University of Pavia, Pavia, Italy.
Kamil KrakowskiEarly Psychosis: Interventions and Clinical-Detection (EPIC) Lab, Department of Psychosis Studies, Institute of Psychiatry, Psychology & Neuroscience, King's College London, London, SE5 8AF, UK.
Umberto ProvenzaniDepartment of Brain and Behavioral Sciences, University of Pavia, Pavia, Italy.
Daniel StahlNIHR Maudsley Biomedical Research Centre, London, UK.ORCID 0000-0001-7987-6619
Nikolaos KoutsoulerisDepartment of Psychosis Studies, Institute of Psychiatry, Psychology and Neuroscience, King's College London, London, SE5 8AF, UK.
Philip McGuireDepartment of Psychiatry, University of Oxford, Oxford, OX3 7JX, UK.ORCID 0000-0003-4381-0532
Paolo Fusar-PoliEarly Psychosis: Interventions and Clinical-Detection (EPIC) Lab, Department of Psychosis Studies, Institute of Psychiatry, Psychology & Neuroscience, King's College London, London, SE5 8AF, UK.ORCID 0000-0003-3582-6788

Funding

Medical Research Council MR/N013700/1Medical Research Council MR/S003118/ 1Wellcome TrustWellcome Trust 215793/Z/19/ZWellcome Trust (Wellcome) 215793/Z/19/Z
6 · The paper itself

Abstract

Effective prevention of severe mental disorders (SMD), including non-psychotic unipolar mood disorders (UMD), non-psychotic bipolar mood disorders (BMD), and psychotic disorders (PSY), rely on accurate knowledge of the duration, first presentation, time course and transdiagnosticity of their prodromal stages. Here we present a retrospective, real-world, cohort study using electronic health records, adhering to RECORD guidelines. Natural language processing algorithms were used to extract monthly occurrences of 65 prodromal features (symptoms and substance use), grouped into eight prodromal clusters. The duration, first presentation, and transdiagnosticity of the prodrome were compared between SMD groups with one-way ANOVA, Cohen's f and d. The time course (mean occurrences) of prodromal clusters was compared between SMD groups with linear mixed-effects models. 26,975 individuals diagnosed with ICD-10 SMD were followed up for up to 12 years (UMD = 13,422; BMD = 2506; PSY = 11,047; median[IQR] age 39.8[23.7] years; 55% female; 52% white). The duration of the UMD prodrome (18[36] months) was shorter than BMD (26[35], d = 0.21) and PSY (24[38], d = 0.18). Most individuals presented with multiple first prodromal clusters, with the most common being non-specific ('other'; 88% UMD, 85% BMD, 78% PSY). The only first prodromal cluster that showed a medium-sized difference between the three SMD groups was positive symptoms (f = 0.30). Time course analysis showed an increase in prodromal cluster occurrences approaching SMD onset. Feature occurrence across the prodromal period showed small/negligible differences between SMD groups, suggesting that most features are transdiagnostic, except for positive symptoms (e.g. paranoia, f = 0.40). Taken together, our findings show minimal differences in the duration and first presentation of the SMD prodromes as recorded in secondary mental health care. All the prodromal clusters intensified as individuals approached SMD onset, and all the prodromal features other than positive symptoms are transdiagnostic. These results support proposals to develop transdiagnostic preventive services for affective and psychotic disorders detected in secondary mental healthcare.

Indexed as

Bipolar DisorderElectronic Health RecordsProdromal SymptomsPsychotic DisordersAdultCohort StudiesFemaleHumansMaleMental DisordersMiddle AgedMood DisordersNatural Language ProcessingRetrospective StudiesYoung Adult

Identifiers

PMID38710907
PMCPMC11540905

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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.