Andrew S Moriarty
Development and validation of a prognostic model to predict relapse in adults with remitted depression in primary care: secondary analysis of pooled individual participant data from multiple studies
Moriarty, Andrew S; Paton, Lewis W; Snell, Kym IE; Archer, Lucinda; Riley, Richard D; Buckman, Joshua EJ; Chew Graham, Carolyn A; Gilbody, Simon; Ali, Shehzad; Pilling, Stephen; Meader, Nick; Phillips, Bob; Coventry, Peter A; Delgadillo, Jaime; Richards, David A; Salisbury, Chris; McMillan, Dean
Authors
Lewis W Paton
Kym IE Snell
Lucinda Archer
Richard D Riley
Joshua EJ Buckman
Carolyn Chew-Graham c.a.chew-graham@keele.ac.uk
Simon Gilbody
Shehzad Ali
Stephen Pilling
Nick Meader
Bob Phillips
Peter A Coventry
Jaime Delgadillo
David A Richards
Chris Salisbury
Dean McMillan
Abstract
Background: Relapse of depression is common and contributes to the overall associated morbidity and burden. We lack evidence-based tools to estimate an individual’s risk of relapse after treatment in primary care, which may help us more effectively target relapse prevention. Objective: The objective was to develop and validate a prognostic model to predict risk of relapse of depression in primary care. Methods: Multilevel logistic regression models were developed, using individual participant data from seven primary care-based studies (n=1244), to predict relapse of depression. The model was internally validated using bootstrapping, and generalisability was explored using internal–external cross-validation. Findings: Residual depressive symptoms (OR: 1.13 (95% CI: 1.07 to 1.20), p<0.001) and baseline depression severity (OR: 1.07 (1.04 to 1.11), p<0.001) were associated with relapse. The validated model had low discrimination (C-statistic 0.60 (0.55–0.65)) and miscalibration concerns (calibration slope 0.81 (0.31–1.31)). On secondary analysis, being in a relationship was associated with reduced risk of relapse (OR: 0.43 (0.28–0.67), p<0.001); this remained statistically significant after correction for multiple significance testing. Conclusions: We could not predict risk of depression relapse with sufficient accuracy in primary care data, using routinely recorded measures. Relationship status warrants further research to explore its role as a prognostic factor for relapse. Clinical implications: Until we can accurately stratify patients according to risk of relapse, a universal approach to relapse prevention may be most beneficial, either during acute-phase treatment or post remission. Where possible, this could be guided by the presence or absence of known prognostic factors (eg, residual depressive symptoms) and targeted towards these. Trial registration number: NCT04666662.
Citation
Moriarty, A. S., Paton, L. W., Snell, K. I., Archer, L., Riley, R. D., Buckman, J. E., …McMillan, D. (2024). Development and validation of a prognostic model to predict relapse in adults with remitted depression in primary care: secondary analysis of pooled individual participant data from multiple studies. BMJ Mental Health, 27(1), https://doi.org/10.1136/bmjment-2024-301226
Journal Article Type | Article |
---|---|
Acceptance Date | Oct 9, 2024 |
Online Publication Date | Oct 28, 2024 |
Publication Date | Oct 28, 2024 |
Journal | BMJ Mental Health |
Volume | 27 |
Issue | 1 |
DOI | https://doi.org/10.1136/bmjment-2024-301226 |
Keywords | Data Interpretation, Statistical, Depression, Adult psychiatry |
Public URL | https://keele-repository.worktribe.com/output/919234 |
Publisher URL | https://www.medrxiv.org/content/10.1101/2024.06.25.24309402v1 |
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Development and validation of a prognostic model to predict relapse in adults with remitted depression in primary care: secondary analysis of pooled individual participant data from multiple studies
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This is an open access article distributed in accordance with the Creative Commons Attribution Non Commercial (CC BY-NC 4.0) license, which permits others to distribute, remix, adapt, build upon this work non-commercially, and license their derivative works on different terms, provided the original work is properly cited, appropriate credit is given, any changes made indicated, and the use is non-commercial. See: http://creativecommons.org/licenses/by-nc/4.0/.
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