One-stage individual participant data meta-analysis models for continuous and binary outcomes: Comparison of treatment coding options and estimation methods.

IPD estimation methods individual participant data maximum likelihood meta-analysis treatment coding

Journal

Statistics in medicine
ISSN: 1097-0258
Titre abrégé: Stat Med
Pays: England
ID NLM: 8215016

Informations de publication

Date de publication:
30 08 2020
Historique:
received: 20 02 2019
revised: 09 12 2019
accepted: 03 04 2020
pubmed: 13 5 2020
medline: 22 6 2021
entrez: 13 5 2020
Statut: ppublish

Résumé

A one-stage individual participant data (IPD) meta-analysis synthesizes IPD from multiple studies using a general or generalized linear mixed model. This produces summary results (eg, about treatment effect) in a single step, whilst accounting for clustering of participants within studies (via a stratified study intercept, or random study intercepts) and between-study heterogeneity (via random treatment effects). We use simulation to evaluate the performance of restricted maximum likelihood (REML) and maximum likelihood (ML) estimation of one-stage IPD meta-analysis models for synthesizing randomized trials with continuous or binary outcomes. Three key findings are identified. First, for ML or REML estimation of stratified intercept or random intercepts models, a t-distribution based approach generally improves coverage of confidence intervals for the summary treatment effect, compared with a z-based approach. Second, when using ML estimation of a one-stage model with a stratified intercept, the treatment variable should be coded using "study-specific centering" (ie, 1/0 minus the study-specific proportion of participants in the treatment group), as this reduces the bias in the between-study variance estimate (compared with 1/0 and other coding options). Third, REML estimation reduces downward bias in between-study variance estimates compared with ML estimation, and does not depend on the treatment variable coding; for binary outcomes, this requires REML estimation of the pseudo-likelihood, although this may not be stable in some situations (eg, when data are sparse). Two applied examples are used to illustrate the findings.

Identifiants

pubmed: 32394498
doi: 10.1002/sim.8555
doi:

Types de publication

Journal Article Meta-Analysis Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

2536-2555

Subventions

Organisme : Medical Research Council
ID : MC_UU_12023/21
Pays : United Kingdom
Organisme : Medical Research Council
ID : MC_UU_12023/29
Pays : United Kingdom

Informations de copyright

© 2020 The Authors. Statistics in Medicine published by John Wiley & Sons, Ltd.

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Auteurs

Richard D Riley (RD)

Centre for Prognosis Research, School of Primary, Community and Social Care, Keele University, Keele, UK.

Amardeep Legha (A)

Centre for Prognosis Research, School of Primary, Community and Social Care, Keele University, Keele, UK.

Dan Jackson (D)

Statistical Innovation Group, Advanced Analytics Centre, AstraZeneca, Cambridge, UK.

Tim P Morris (TP)

Institute of Clinical Trials and Methodology, MRC Clinical Trials Unit at UCL, London, UK.

Joie Ensor (J)

Centre for Prognosis Research, School of Primary, Community and Social Care, Keele University, Keele, UK.

Kym I E Snell (KIE)

Centre for Prognosis Research, School of Primary, Community and Social Care, Keele University, Keele, UK.

Ian R White (IR)

Institute of Clinical Trials and Methodology, MRC Clinical Trials Unit at UCL, London, UK.

Danielle L Burke (DL)

Centre for Prognosis Research, School of Primary, Community and Social Care, Keele University, Keele, UK.

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