Evidence map›Paper›PMID 40556309›Full record

ArticleThe British journal of psychiatry : the journal of mental science2026

Oral glucocorticoids and risk of psychiatric and suicidal behaviour outcomes: population-based cohort study.

Tyra Lagerberg, Tapio T Gustafsson, Yasmina Molero, Julian Forton, Amir Sariaslan, Zheng Chang, Henrik Larsson, Paul Lichtenstein, Seena Fazel

Abstract read
In one paragraph

Article in The British journal of psychiatry : the journal of mental science, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
8citing 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

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

  1. Pooled it
  2. Article
  3. Review
  4. Article
  5. Review
  6. Article
  7. Review
  8. Safe Use of Corticosteroids in Non-Infectious Uveitis.Journal of inflammation research · 2025
    Review
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.

Tyra LagerbergDepartment of Psychiatry, Warneford Hospital, University of Oxford, UK.ORCID https://orcid.org/0000-0003-2480-0216
Tapio T GustafssonDepartment of Forensic Psychiatry, University of Eastern Finland, Niuvanniemi Hospital, Kuopio, Finland.
Yasmina MoleroDepartment of Medical Epidemiology and Biostatistics, Karolinska Institutet, Sweden.
Julian FortonThe Children's Hospital for Wales, Cardiff, UK.
Amir SariaslanDepartment of Psychiatry, Warneford Hospital, University of Oxford, UK.
Zheng ChangDepartment of Medical Epidemiology and Biostatistics, Karolinska Institutet, Sweden.
Henrik LarssonDepartment of Medical Epidemiology and Biostatistics, Karolinska Institutet, Sweden.
Paul LichtensteinDepartment of Medical Epidemiology and Biostatistics, Karolinska Institutet, Sweden.
Seena FazelDepartment of Psychiatry, Warneford Hospital, University of Oxford, UK.ORCID https://orcid.org/0000-0002-5383-5365

Funding

Wellcome Trust 202836
6 · The paper itself

Abstract

backgroundDespite evidence of associations between glucocorticoid treatment and adverse psychiatric and suicidal behaviour outcomes, large-scale observational evidence for serious outcomes is lacking.

aimsTo assess the risk of psychiatric and suicidal behaviour outcomes during glucocorticoid treatment.

methodUsing Swedish population registers, we identified 1 105 964 individuals aged 15-54 years who collected a glucocorticoid prescription in oral form between 2006 and 2020. We investigated associations with a range of psychiatric outcomes: unplanned specialist healthcare contacts due to depressive, bipolar, anxiety or schizophrenia-spectrum disorders; and deaths by suicide or unplanned specialist healthcare contacts due to self-harm ('suicidal behaviour'). We estimated hazard ratios from Cox proportional hazards models in a medication-only cohort by comparing outcome rates during and outside treated periods within individuals. We further identified individuals with an autoimmune or gastrointestinal autoimmune disorder diagnosis and compared hazards of the outcomes between those who did and did not initiate a glucocorticoid using a target trial emulation approach.

resultsWe found increased risks for psychiatric outcomes, with within-individual hazard ratios ranging from 1.08 (95% CI, 1.00-1.16) for depressive disorders to 1.23 (95% CI, 1.12-1.36) for bipolar disorder and 1.25 (95% CI, 1.20-1.31) for anxiety disorders. We found no clear association with suicidal behaviour (hazard ratio: 1.06; 95% CI, 0.96-1.17). These findings were similar when stratified by age and gender. Within-individual associations were attenuated in those diagnosed with an autoimmune disorder. The risk of anxiety and bipolar disorder outcomes appeared particularly elevated in the first weeks of treatment. Absolute rates were modestly elevated during treatment, and higher in those with a history of psychiatric disorders.

conclusionsGlucocorticoid treatment is associated with elevated risks of serious psychiatric outcomes, including the onset and relapse of common psychiatric disorders. Individuals with psychiatric histories may require additional monitoring during glucocorticoid treatment.

Indexed as

GlucocorticoidsMental DisordersSuicideAdministration, OralAdolescentAdultCohort StudiesFemaleHumansMaleMiddle AgedProportional Hazards ModelsRegistriesRisk FactorsSwedenYoung AdultGlucocorticoidsBipolar disordercorticosteroiddepressionpharmacoepidemiologysuicidal behaviour

Identifiers

PMID40556309
PMCPMC7617852

What Socratic holds

Textmetadata
LicenceCC BY
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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 Socratic graph.