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Journal article

Association between a selective 5-HT4 receptor agonist and incidence of major depressive disorder: emulated target trial

Abstract:

Background

The serotonin 4 receptor (5-HT4R) is a promising target for the treatment of depression. Highly selective 5-HT4R agonists, such as prucalopride, have antidepressant-like and procognitive effects in preclinical models, but their clinical effects are not yet established.

Aims

To determine whether prucalopride (a 5-HT4R agonist and licensed treatment for constipation) is associated with reduced incidence of depression in individuals with no past history of mental illness, compared with anti-constipation agents with no effect on the central nervous system.

Method

Using anonymised routinely collected data from a large-scale USA electronic health records network, we conducted an emulated target trial comparing depression incidence over 1 year in individuals without prior diagnoses of major mental illness, who initiated treatment with prucalopride versus two alternative anti-constipation agents that act by different mechanisms (linaclotide and lubiprostone). Cohorts were matched for 121 covariates capturing sociodemographic factors, and historical and/or concurrent comorbidities and medications. The primary outcome was a first diagnosis of major depressive disorder (ICD-10 code F32) within 1 year of the index date. Robustness of the results to changes in model and population specification was tested. Secondary outcomes included a first diagnosis of six other neuropsychiatric disorders.

Results

Treatment with prucalopride was associated with significantly lower incidence of depression in the following year compared with linaclotide (hazard ratio 0.87, 95% CI 0.76–0.99; P = 0.038; n = 8572 in each matched cohort) and lubiprostone (hazard ratio 0.79, 95% CI 0.69–0.91; P < 0.001; n = 8281). Significantly lower risks of all mood disorders and psychosis were also observed. Results were similar across robustness analyses. Conclusions These findings support preclinical data and suggest a role for 5-HT4R agonists as novel agents in the prevention of major depression. These findings should stimulate randomised controlled trials to confirm if these agents can serve as a novel class of antidepressant within a clinical setting.
Publication status:
Published
Peer review status:
Peer reviewed

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Publisher copy:
10.1192/bjp.2024.97

Authors


More by this author
Role:
Author
ORCID:
0000-0001-7848-1295
More by this author
Institution:
University of Oxford
Division:
MSD
Department:
Psychiatry
Role:
Author
More by this author
Institution:
University of Oxford
Division:
MSD
Department:
Psychiatry
Oxford college:
Wolfson College
Role:
Author
ORCID:
0000-0002-6719-1126
More by this author
Institution:
University of Oxford
Division:
MSD
Department:
Psychiatry
Role:
Author


More from this funder
Funder identifier:
https://ror.org/029chgv08
Grant:
216430/Z/19/Z
Programme:
Wellcome Trust Clinical Doctoral Fellowship


Publisher:
Cambridge University Press
Journal:
British Journal of Psychiatry More from this journal
Volume:
225
Issue:
3
Pages:
371-378
Publication date:
2024-08-07
Acceptance date:
2024-05-05
DOI:
EISSN:
1472-1465
ISSN:
0007-1250


Language:
English
Keywords:
Pubs id:
2020814
Local pid:
pubs:2020814
Deposit date:
2024-08-09

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