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A Bayesian dose-response meta-analysis model: A simulations study and application

期刊

STATISTICAL METHODS IN MEDICAL RESEARCH
卷 30, 期 5, 页码 1358-1372

出版社

SAGE PUBLICATIONS LTD
DOI: 10.1177/0962280220982643

关键词

Clusters; one-stage model; hierarchical model; antidepressants; random effects

资金

  1. European Union [825162]
  2. Swiss National Science Foundation [17481]
  3. National Institute for Health Research (NIHR) Oxford Cognitive Health Clinical Research Facility
  4. NIHR Research Professorship [RP-2017-08-ST2-006]
  5. NIHR Oxford and Thames Valley Applied Research Collaboration
  6. NIHR Oxford Health Biomedical Research Centre [BRC-1215-20005]

向作者/读者索取更多资源

The study proposes a hierarchical dose-response model implemented in a Bayesian framework and compares its performance with frequentist approaches in a simulation study. It finds that the Bayesian model with binomial likelihood has lower bias than the Bayesian model with normal likelihood and the frequentist one-stage model in situations with small sample size. The performance of all models is influenced by the choice of knots' location when the true underlying shape is log-log or half-sigmoid.
Dose-response models express the effect of different dose or exposure levels on a specific outcome. In meta-analysis, where aggregated-level data is available, dose-response evidence is synthesized using either one-stage or two-stage models in a frequentist setting. We propose a hierarchical dose-response model implemented in a Bayesian framework. We develop our model assuming normal or binomial likelihood and accounting for exposures grouped in clusters. To allow maximum flexibility, the dose-response association is modelled using restricted cubic splines. We implement these models in R using JAGS and we compare our approach to the one-stage dose-response meta-analysis model in a simulation study. We found that the Bayesian dose-response model with binomial likelihood has lower bias than the Bayesian model with normal likelihood and the frequentist one-stage model when studies have small sample size. When the true underlying shape is log-log or half-sigmoid, the performance of all models depends on choosing an appropriate location for the knots. In all other examined situations, all models perform very well and give practically identical results. We also re-analyze the data from 60 randomized controlled trials (15,984 participants) examining the efficacy (response) of various doses of serotonin-specific reuptake inhibitor (SSRI) antidepressant drugs. All models suggest that the dose-response curve increases between zero dose and 30-40 mg of fluoxetine-equivalent dose, and thereafter shows small decline. We draw the same conclusion when we take into account the fact that five different antidepressants have been studied in the included trials. We show that implementation of the hierarchical model in Bayesian framework has similar performance to, but overcomes some of the limitations of the frequentist approach and offers maximum flexibility to accommodate features of the data.

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