Meta-research study reveals widespread variability in dose-response modelling across depression network meta-analyses, highlighting the need for standardised methodological guidance.
OBJECTIVES: Dose can meaningfully affect the comparative effectiveness of depression treatments, yet how network meta-analyses (NMAs) in this field handle dose is not well characterised. We conducted a meta-research study to examine how current depression NMAs incorporate dosing information and identify methodological gaps in current practice. DESIGN: Meta-research study following guidance for meta-epidemiological research and incorporating relevant elements of Preferred Reporting Items for Systematic Reviews and Meta-Analyses (PRISMA) 2020. DATA SOURCES: We searched PubMed, Embase, the Cochrane Library, PsycINFO, Web of Science and Scopus for NMAs published between January 2020 and May 2025. ELIGIBILITY CRITERIA: NMAs comparing interventions, or different doses of a single intervention, in the context of depression-where an antidepressant was evaluated for depression-related indications and/or depressive symptoms were the primary clinical focus-and in which dose variation was incorporated into the evidence synthesis. DATA EXTRACTION AND SYNTHESIS: We extracted data on dose-handling strategies, analysis methods, statistical frameworks and reporting quality, and synthesised these narratively to characterise methodological practice across studies. RESULTS: to conduct a model-based NMA for secondary analyses, primarily examining exercise interventions with varied dose-response functions. Reporting of priors, consistency assessments and justifications for dose categorisation or operationalisation was inconsistent. CONCLUSIONS: Current depression NMAs demonstrate broad variability in handling dose-related heterogeneity, with dose-response modelling often absent or inconsistently applied-particularly for behavioural interventions lacking standardised dose metrics. Greater methodological clarity, practical guidance and reporting standards are needed to integrate dose-response modelling into NMAs of depression treatments, where both pharmacologic and behavioural interventions pose distinct dosing challenges.
No takes yet. Share an insight, caveat, or question.
Herder et al. (2026) studied this question.
Synapse has enriched 5 closely related papers on similar clinical questions. Consider them for comparative context: