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The normality assumption on between-study random effects was questionable in a considerable number of Cochrane meta-analyses

BACKGROUND: Studies included in a meta-analysis are often heterogeneous. The traditional random-effects models assume their true effects to follow a normal distribution, while it is unclear if this critical assumption is practical. Violations of this between-study normality assumption could lead to...

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Autores principales: Liu, Ziyu, Al Amer, Fahad M., Xiao, Mengli, Xu, Chang, Furuya-Kanamori, Luis, Hong, Hwanhee, Siegel, Lianne, Lin, Lifeng
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10053115/
https://www.ncbi.nlm.nih.gov/pubmed/36978059
http://dx.doi.org/10.1186/s12916-023-02823-9
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author Liu, Ziyu
Al Amer, Fahad M.
Xiao, Mengli
Xu, Chang
Furuya-Kanamori, Luis
Hong, Hwanhee
Siegel, Lianne
Lin, Lifeng
author_facet Liu, Ziyu
Al Amer, Fahad M.
Xiao, Mengli
Xu, Chang
Furuya-Kanamori, Luis
Hong, Hwanhee
Siegel, Lianne
Lin, Lifeng
author_sort Liu, Ziyu
collection PubMed
description BACKGROUND: Studies included in a meta-analysis are often heterogeneous. The traditional random-effects models assume their true effects to follow a normal distribution, while it is unclear if this critical assumption is practical. Violations of this between-study normality assumption could lead to problematic meta-analytical conclusions. We aimed to empirically examine if this assumption is valid in published meta-analyses. METHODS: In this cross-sectional study, we collected meta-analyses available in the Cochrane Library with at least 10 studies and with between-study variance estimates > 0. For each extracted meta-analysis, we performed the Shapiro–Wilk (SW) test to quantitatively assess the between-study normality assumption. For binary outcomes, we assessed between-study normality for odds ratios (ORs), relative risks (RRs), and risk differences (RDs). Subgroup analyses based on sample sizes and event rates were used to rule out the potential confounders. In addition, we obtained the quantile–quantile (Q–Q) plot of study-specific standardized residuals for visually assessing between-study normality. RESULTS: Based on 4234 eligible meta-analyses with binary outcomes and 3433 with non-binary outcomes, the proportion of meta-analyses that had statistically significant non-normality varied from 15.1 to 26.2%. RDs and non-binary outcomes led to more frequent non-normality issues than ORs and RRs. For binary outcomes, the between-study non-normality was more frequently found in meta-analyses with larger sample sizes and event rates away from 0 and 100%. The agreements of assessing the normality between two independent researchers based on Q–Q plots were fair or moderate. CONCLUSIONS: The between-study normality assumption is commonly violated in Cochrane meta-analyses. This assumption should be routinely assessed when performing a meta-analysis. When it may not hold, alternative meta-analysis methods that do not make this assumption should be considered. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s12916-023-02823-9.
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spelling pubmed-100531152023-03-30 The normality assumption on between-study random effects was questionable in a considerable number of Cochrane meta-analyses Liu, Ziyu Al Amer, Fahad M. Xiao, Mengli Xu, Chang Furuya-Kanamori, Luis Hong, Hwanhee Siegel, Lianne Lin, Lifeng BMC Med Research Article BACKGROUND: Studies included in a meta-analysis are often heterogeneous. The traditional random-effects models assume their true effects to follow a normal distribution, while it is unclear if this critical assumption is practical. Violations of this between-study normality assumption could lead to problematic meta-analytical conclusions. We aimed to empirically examine if this assumption is valid in published meta-analyses. METHODS: In this cross-sectional study, we collected meta-analyses available in the Cochrane Library with at least 10 studies and with between-study variance estimates > 0. For each extracted meta-analysis, we performed the Shapiro–Wilk (SW) test to quantitatively assess the between-study normality assumption. For binary outcomes, we assessed between-study normality for odds ratios (ORs), relative risks (RRs), and risk differences (RDs). Subgroup analyses based on sample sizes and event rates were used to rule out the potential confounders. In addition, we obtained the quantile–quantile (Q–Q) plot of study-specific standardized residuals for visually assessing between-study normality. RESULTS: Based on 4234 eligible meta-analyses with binary outcomes and 3433 with non-binary outcomes, the proportion of meta-analyses that had statistically significant non-normality varied from 15.1 to 26.2%. RDs and non-binary outcomes led to more frequent non-normality issues than ORs and RRs. For binary outcomes, the between-study non-normality was more frequently found in meta-analyses with larger sample sizes and event rates away from 0 and 100%. The agreements of assessing the normality between two independent researchers based on Q–Q plots were fair or moderate. CONCLUSIONS: The between-study normality assumption is commonly violated in Cochrane meta-analyses. This assumption should be routinely assessed when performing a meta-analysis. When it may not hold, alternative meta-analysis methods that do not make this assumption should be considered. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s12916-023-02823-9. BioMed Central 2023-03-29 /pmc/articles/PMC10053115/ /pubmed/36978059 http://dx.doi.org/10.1186/s12916-023-02823-9 Text en © The Author(s) 2023 https://creativecommons.org/licenses/by/4.0/Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/ (https://creativecommons.org/publicdomain/zero/1.0/) ) applies to the data made available in this article, unless otherwise stated in a credit line to the data.
spellingShingle Research Article
Liu, Ziyu
Al Amer, Fahad M.
Xiao, Mengli
Xu, Chang
Furuya-Kanamori, Luis
Hong, Hwanhee
Siegel, Lianne
Lin, Lifeng
The normality assumption on between-study random effects was questionable in a considerable number of Cochrane meta-analyses
title The normality assumption on between-study random effects was questionable in a considerable number of Cochrane meta-analyses
title_full The normality assumption on between-study random effects was questionable in a considerable number of Cochrane meta-analyses
title_fullStr The normality assumption on between-study random effects was questionable in a considerable number of Cochrane meta-analyses
title_full_unstemmed The normality assumption on between-study random effects was questionable in a considerable number of Cochrane meta-analyses
title_short The normality assumption on between-study random effects was questionable in a considerable number of Cochrane meta-analyses
title_sort normality assumption on between-study random effects was questionable in a considerable number of cochrane meta-analyses
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10053115/
https://www.ncbi.nlm.nih.gov/pubmed/36978059
http://dx.doi.org/10.1186/s12916-023-02823-9
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