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Statistical approaches to identify subgroups in meta-analysis of individual participant data: a simulation study

BACKGROUND: Individual participant data meta-analysis (IPD-MA) is considered the gold standard for investigating subgroup effects. Frequently used regression-based approaches to detect subgroups in IPD-MA are: meta-regression, per-subgroup meta-analysis (PS-MA), meta-analysis of interaction terms (M...

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Autores principales: Belias, Michail, Rovers, Maroeska M., Reitsma, Johannes B., Debray, Thomas P. A., IntHout, Joanna
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6720416/
https://www.ncbi.nlm.nih.gov/pubmed/31477023
http://dx.doi.org/10.1186/s12874-019-0817-6
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author Belias, Michail
Rovers, Maroeska M.
Reitsma, Johannes B.
Debray, Thomas P. A.
IntHout, Joanna
author_facet Belias, Michail
Rovers, Maroeska M.
Reitsma, Johannes B.
Debray, Thomas P. A.
IntHout, Joanna
author_sort Belias, Michail
collection PubMed
description BACKGROUND: Individual participant data meta-analysis (IPD-MA) is considered the gold standard for investigating subgroup effects. Frequently used regression-based approaches to detect subgroups in IPD-MA are: meta-regression, per-subgroup meta-analysis (PS-MA), meta-analysis of interaction terms (MA-IT), naive one-stage IPD-MA (ignoring potential study-level confounding), and centred one-stage IPD-MA (accounting for potential study-level confounding). Clear guidance on the analyses is lacking and clinical researchers may use approaches with suboptimal efficiency to investigate subgroup effects in an IPD setting. Therefore, our aim is to overview and compare the aforementioned methods, and provide recommendations over which should be preferred. METHODS: We conducted a simulation study where we generated IPD of randomised trials and varied the magnitude of subgroup effect (0, 25, 50% relative reduction), between-study treatment effect heterogeneity (none, medium, large), ecological bias (none, quantitative, qualitative), sample size (50,100,200), and number of trials (5,10) for binary, continuous and time-to-event outcomes. For each scenario, we assessed the power, false positive rate (FPR) and bias of aforementioned five approaches. RESULTS: Naive and centred IPD-MA yielded the highest power, whilst preserving acceptable FPR around the nominal 5% in all scenarios. Centred IPD-MA showed slightly less biased estimates than naïve IPD-MA. Similar results were obtained for MA-IT, except when analysing binary outcomes (where it yielded less power and FPR < 5%). PS-MA showed similar power as MA-IT in non-heterogeneous scenarios, but power collapsed as heterogeneity increased, and decreased even more in the presence of ecological bias. PS-MA suffered from too high FPRs in non-heterogeneous settings and showed biased estimates in all scenarios. Meta-regression showed poor power (< 20%) in all scenarios and completely biased results in settings with qualitative ecological bias. CONCLUSIONS: Our results indicate that subgroup detection in IPD-MA requires careful modelling. Naive and centred IPD-MA performed equally well, but due to less bias of the estimates in the presence of ecological bias, we recommend the latter. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1186/s12874-019-0817-6) contains supplementary material, which is available to authorized users.
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spelling pubmed-67204162019-09-06 Statistical approaches to identify subgroups in meta-analysis of individual participant data: a simulation study Belias, Michail Rovers, Maroeska M. Reitsma, Johannes B. Debray, Thomas P. A. IntHout, Joanna BMC Med Res Methodol Research Article BACKGROUND: Individual participant data meta-analysis (IPD-MA) is considered the gold standard for investigating subgroup effects. Frequently used regression-based approaches to detect subgroups in IPD-MA are: meta-regression, per-subgroup meta-analysis (PS-MA), meta-analysis of interaction terms (MA-IT), naive one-stage IPD-MA (ignoring potential study-level confounding), and centred one-stage IPD-MA (accounting for potential study-level confounding). Clear guidance on the analyses is lacking and clinical researchers may use approaches with suboptimal efficiency to investigate subgroup effects in an IPD setting. Therefore, our aim is to overview and compare the aforementioned methods, and provide recommendations over which should be preferred. METHODS: We conducted a simulation study where we generated IPD of randomised trials and varied the magnitude of subgroup effect (0, 25, 50% relative reduction), between-study treatment effect heterogeneity (none, medium, large), ecological bias (none, quantitative, qualitative), sample size (50,100,200), and number of trials (5,10) for binary, continuous and time-to-event outcomes. For each scenario, we assessed the power, false positive rate (FPR) and bias of aforementioned five approaches. RESULTS: Naive and centred IPD-MA yielded the highest power, whilst preserving acceptable FPR around the nominal 5% in all scenarios. Centred IPD-MA showed slightly less biased estimates than naïve IPD-MA. Similar results were obtained for MA-IT, except when analysing binary outcomes (where it yielded less power and FPR < 5%). PS-MA showed similar power as MA-IT in non-heterogeneous scenarios, but power collapsed as heterogeneity increased, and decreased even more in the presence of ecological bias. PS-MA suffered from too high FPRs in non-heterogeneous settings and showed biased estimates in all scenarios. Meta-regression showed poor power (< 20%) in all scenarios and completely biased results in settings with qualitative ecological bias. CONCLUSIONS: Our results indicate that subgroup detection in IPD-MA requires careful modelling. Naive and centred IPD-MA performed equally well, but due to less bias of the estimates in the presence of ecological bias, we recommend the latter. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1186/s12874-019-0817-6) contains supplementary material, which is available to authorized users. BioMed Central 2019-09-02 /pmc/articles/PMC6720416/ /pubmed/31477023 http://dx.doi.org/10.1186/s12874-019-0817-6 Text en © The Author(s). 2019 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.
spellingShingle Research Article
Belias, Michail
Rovers, Maroeska M.
Reitsma, Johannes B.
Debray, Thomas P. A.
IntHout, Joanna
Statistical approaches to identify subgroups in meta-analysis of individual participant data: a simulation study
title Statistical approaches to identify subgroups in meta-analysis of individual participant data: a simulation study
title_full Statistical approaches to identify subgroups in meta-analysis of individual participant data: a simulation study
title_fullStr Statistical approaches to identify subgroups in meta-analysis of individual participant data: a simulation study
title_full_unstemmed Statistical approaches to identify subgroups in meta-analysis of individual participant data: a simulation study
title_short Statistical approaches to identify subgroups in meta-analysis of individual participant data: a simulation study
title_sort statistical approaches to identify subgroups in meta-analysis of individual participant data: a simulation study
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6720416/
https://www.ncbi.nlm.nih.gov/pubmed/31477023
http://dx.doi.org/10.1186/s12874-019-0817-6
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