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One‐stage individual participant data meta‐analysis models: estimation of treatment‐covariate interactions must avoid ecological bias by separating out within‐trial and across‐trial information
Stratified medicine utilizes individual‐level covariates that are associated with a differential treatment effect, also known as treatment‐covariate interactions. When multiple trials are available, meta‐analysis is used to help detect true treatment‐covariate interactions by combining their data. M...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5299543/ https://www.ncbi.nlm.nih.gov/pubmed/27910122 http://dx.doi.org/10.1002/sim.7171 |
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author | Hua, Hairui Burke, Danielle L. Crowther, Michael J. Ensor, Joie Tudur Smith, Catrin Riley, Richard D. |
author_facet | Hua, Hairui Burke, Danielle L. Crowther, Michael J. Ensor, Joie Tudur Smith, Catrin Riley, Richard D. |
author_sort | Hua, Hairui |
collection | PubMed |
description | Stratified medicine utilizes individual‐level covariates that are associated with a differential treatment effect, also known as treatment‐covariate interactions. When multiple trials are available, meta‐analysis is used to help detect true treatment‐covariate interactions by combining their data. Meta‐regression of trial‐level information is prone to low power and ecological bias, and therefore, individual participant data (IPD) meta‐analyses are preferable to examine interactions utilizing individual‐level information. However, one‐stage IPD models are often wrongly specified, such that interactions are based on amalgamating within‐ and across‐trial information. We compare, through simulations and an applied example, fixed‐effect and random‐effects models for a one‐stage IPD meta‐analysis of time‐to‐event data where the goal is to estimate a treatment‐covariate interaction. We show that it is crucial to centre patient‐level covariates by their mean value in each trial, in order to separate out within‐trial and across‐trial information. Otherwise, bias and coverage of interaction estimates may be adversely affected, leading to potentially erroneous conclusions driven by ecological bias. We revisit an IPD meta‐analysis of five epilepsy trials and examine age as a treatment effect modifier. The interaction is −0.011 (95% CI: −0.019 to −0.003; p = 0.004), and thus highly significant, when amalgamating within‐trial and across‐trial information. However, when separating within‐trial from across‐trial information, the interaction is −0.007 (95% CI: −0.019 to 0.005; p = 0.22), and thus its magnitude and statistical significance are greatly reduced. We recommend that meta‐analysts should only use within‐trial information to examine individual predictors of treatment effect and that one‐stage IPD models should separate within‐trial from across‐trial information to avoid ecological bias. © 2016 The Authors. Statistics in Medicine published by John Wiley & Sons Ltd. |
format | Online Article Text |
id | pubmed-5299543 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-52995432017-02-22 One‐stage individual participant data meta‐analysis models: estimation of treatment‐covariate interactions must avoid ecological bias by separating out within‐trial and across‐trial information Hua, Hairui Burke, Danielle L. Crowther, Michael J. Ensor, Joie Tudur Smith, Catrin Riley, Richard D. Stat Med Research Articles Stratified medicine utilizes individual‐level covariates that are associated with a differential treatment effect, also known as treatment‐covariate interactions. When multiple trials are available, meta‐analysis is used to help detect true treatment‐covariate interactions by combining their data. Meta‐regression of trial‐level information is prone to low power and ecological bias, and therefore, individual participant data (IPD) meta‐analyses are preferable to examine interactions utilizing individual‐level information. However, one‐stage IPD models are often wrongly specified, such that interactions are based on amalgamating within‐ and across‐trial information. We compare, through simulations and an applied example, fixed‐effect and random‐effects models for a one‐stage IPD meta‐analysis of time‐to‐event data where the goal is to estimate a treatment‐covariate interaction. We show that it is crucial to centre patient‐level covariates by their mean value in each trial, in order to separate out within‐trial and across‐trial information. Otherwise, bias and coverage of interaction estimates may be adversely affected, leading to potentially erroneous conclusions driven by ecological bias. We revisit an IPD meta‐analysis of five epilepsy trials and examine age as a treatment effect modifier. The interaction is −0.011 (95% CI: −0.019 to −0.003; p = 0.004), and thus highly significant, when amalgamating within‐trial and across‐trial information. However, when separating within‐trial from across‐trial information, the interaction is −0.007 (95% CI: −0.019 to 0.005; p = 0.22), and thus its magnitude and statistical significance are greatly reduced. We recommend that meta‐analysts should only use within‐trial information to examine individual predictors of treatment effect and that one‐stage IPD models should separate within‐trial from across‐trial information to avoid ecological bias. © 2016 The Authors. Statistics in Medicine published by John Wiley & Sons Ltd. John Wiley and Sons Inc. 2016-12-01 2017-02-28 /pmc/articles/PMC5299543/ /pubmed/27910122 http://dx.doi.org/10.1002/sim.7171 Text en © 2016 The Authors. Statistics in Medicine published by John Wiley & Sons Ltd. This is an open access article under the terms of the Creative Commons Attribution (http://creativecommons.org/licenses/by/4.0/) License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Research Articles Hua, Hairui Burke, Danielle L. Crowther, Michael J. Ensor, Joie Tudur Smith, Catrin Riley, Richard D. One‐stage individual participant data meta‐analysis models: estimation of treatment‐covariate interactions must avoid ecological bias by separating out within‐trial and across‐trial information |
title | One‐stage individual participant data meta‐analysis models: estimation of treatment‐covariate interactions must avoid ecological bias by separating out within‐trial and across‐trial information |
title_full | One‐stage individual participant data meta‐analysis models: estimation of treatment‐covariate interactions must avoid ecological bias by separating out within‐trial and across‐trial information |
title_fullStr | One‐stage individual participant data meta‐analysis models: estimation of treatment‐covariate interactions must avoid ecological bias by separating out within‐trial and across‐trial information |
title_full_unstemmed | One‐stage individual participant data meta‐analysis models: estimation of treatment‐covariate interactions must avoid ecological bias by separating out within‐trial and across‐trial information |
title_short | One‐stage individual participant data meta‐analysis models: estimation of treatment‐covariate interactions must avoid ecological bias by separating out within‐trial and across‐trial information |
title_sort | one‐stage individual participant data meta‐analysis models: estimation of treatment‐covariate interactions must avoid ecological bias by separating out within‐trial and across‐trial information |
topic | Research Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5299543/ https://www.ncbi.nlm.nih.gov/pubmed/27910122 http://dx.doi.org/10.1002/sim.7171 |
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