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Meta-regression detected associations between heterogeneous treatment effects and study-level, but not patient-level, factors

Authors :
Christopher H. Schmid
Paul Stark
Jesse A. Berlin
Paul Landais
Joseph Lau
Source :
Journal of Clinical Epidemiology. 57:683-697
Publication Year :
2004
Publisher :
Elsevier BV, 2004.

Abstract

Objective Two investigations evaluate Bayesian meta-regression for detecting treatment interactions. Study design and setting The first compares analyses of aggregate and individual patient data on 1,860 subjects from 11 trials testing angiotensin converting enzyme (ACE) inhibitors for nondiabetic kidney disease. The second explores meta-regression for detecting treatment interaction on 671 covariates, including the baseline risk, from 232 meta-analyses of binary outcomes compiled from the Cochrane Collaboration and the medical literature. Results In the ACE inhibitor study, treatment effects were homogeneous so meta-regression identified no interactions. Analysis of individual patient data using a multilevel model, however, discovered that treatment reduced glomerular filtration rate (GFR) more among patients with higher baseline proteinuria. The second investigation found meta-regression most effective for detecting treatment interactions with study-level factors in meta-analyses with >10 studies, heterogeneous treatment effects, or significant overall treatment effects. Under all three conditions, 46% of meta-regressions produced strong interactions (posterior probability >0.995) compared with 6% otherwise. Baseline risk was associated with the odds ratio in 6% of meta-analyses, half the rate found using maximum likelihood. Conclusion Meta-regression can detect interactions of treatment with study-level factors when treatment effects are heterogeneous. Individual patient data are needed for patient-level factors and homogeneous effects.

Details

ISSN :
08954356
Volume :
57
Database :
OpenAIRE
Journal :
Journal of Clinical Epidemiology
Accession number :
edsair.doi.dedup.....ba98fe38d88ac84600e644bb5bc75d52
Full Text :
https://doi.org/10.1016/j.jclinepi.2003.12.001