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The relationship between risk of bias criteria, research outcomes, and study sponsorship in a cohort of preclinical thiazolidinedione animal studies: a meta‐analysis
INTRODUCTION: There is little evidence regarding the influence of conflicts of interest on preclinical research. This study examines whether industry sponsorship is associated with increased risks of bias and/or effect sizes of outcomes in published preclinical thiazolidinedione (TZD) studies. METHO...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2014
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4306285/ https://www.ncbi.nlm.nih.gov/pubmed/25642330 http://dx.doi.org/10.1002/ebm2.5 |
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author | Abdel‐Sattar, M. Krauth, D. Anglemyer, A. Bero, L. |
author_facet | Abdel‐Sattar, M. Krauth, D. Anglemyer, A. Bero, L. |
author_sort | Abdel‐Sattar, M. |
collection | PubMed |
description | INTRODUCTION: There is little evidence regarding the influence of conflicts of interest on preclinical research. This study examines whether industry sponsorship is associated with increased risks of bias and/or effect sizes of outcomes in published preclinical thiazolidinedione (TZD) studies. METHODS: We identified preclinical TZD studies published between January 1, 1965, and November 14, 2012. Coders independently extracted information on study design criteria aimed at reducing bias, results for all relevant outcomes, sponsorship source and investigator financial ties from the 112 studies meeting the inclusion criteria. The average standardized mean difference (SMD) across studies was calculated for plasma glucose (efficacy outcome) and weight gain (harm outcome). In subgroup analyses, TZD outcomes were assessed by sponsorship source and risk of bias criteria. RESULTS: Seven studies were funded by industry alone, 17 studies funded by both industry and non‐industry, 49 studies funded by non‐industry alone and 39 studies had no disclosures. None of the studies used sample size calculations, intention‐to‐treat analyses, blinding of investigators or concealment of allocation. Most studies reported favourable results (88 of 112) and conclusions (95 of 112) supporting TZD use. Efficacy estimates were significantly larger in six studies sponsored by industry alone (−3.41; 95% CI −5.21, −1.53; I(2) = 93%) versus 42 studies sponsored by non‐industry sources (−0.97; 95% CI −1.37, −0.56; I(2) = 81%; p‐value = 0.01). Harms estimates were significantly larger in four studies sponsored by industry alone (5.00; 95% CI 1.22, 8.77; I(2) = 93%) versus 38 studies sponsored by non‐industry sources (0.30; 95% CI −0.08, 0.68; I(2) = 79%; p‐value = 0.02). TZD efficacy and harms did not differ by disclosure of financial COIs or risks of bias. CONCLUSIONS: Industry‐sponsored TZD animal studies have exaggerated efficacy and harms outcomes compared with studies funded by non‐industry sources. There was poor reporting of COIs. |
format | Online Article Text |
id | pubmed-4306285 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2014 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-43062852015-04-01 The relationship between risk of bias criteria, research outcomes, and study sponsorship in a cohort of preclinical thiazolidinedione animal studies: a meta‐analysis Abdel‐Sattar, M. Krauth, D. Anglemyer, A. Bero, L. Evid Based Preclin Med Systematic Reviews INTRODUCTION: There is little evidence regarding the influence of conflicts of interest on preclinical research. This study examines whether industry sponsorship is associated with increased risks of bias and/or effect sizes of outcomes in published preclinical thiazolidinedione (TZD) studies. METHODS: We identified preclinical TZD studies published between January 1, 1965, and November 14, 2012. Coders independently extracted information on study design criteria aimed at reducing bias, results for all relevant outcomes, sponsorship source and investigator financial ties from the 112 studies meeting the inclusion criteria. The average standardized mean difference (SMD) across studies was calculated for plasma glucose (efficacy outcome) and weight gain (harm outcome). In subgroup analyses, TZD outcomes were assessed by sponsorship source and risk of bias criteria. RESULTS: Seven studies were funded by industry alone, 17 studies funded by both industry and non‐industry, 49 studies funded by non‐industry alone and 39 studies had no disclosures. None of the studies used sample size calculations, intention‐to‐treat analyses, blinding of investigators or concealment of allocation. Most studies reported favourable results (88 of 112) and conclusions (95 of 112) supporting TZD use. Efficacy estimates were significantly larger in six studies sponsored by industry alone (−3.41; 95% CI −5.21, −1.53; I(2) = 93%) versus 42 studies sponsored by non‐industry sources (−0.97; 95% CI −1.37, −0.56; I(2) = 81%; p‐value = 0.01). Harms estimates were significantly larger in four studies sponsored by industry alone (5.00; 95% CI 1.22, 8.77; I(2) = 93%) versus 38 studies sponsored by non‐industry sources (0.30; 95% CI −0.08, 0.68; I(2) = 79%; p‐value = 0.02). TZD efficacy and harms did not differ by disclosure of financial COIs or risks of bias. CONCLUSIONS: Industry‐sponsored TZD animal studies have exaggerated efficacy and harms outcomes compared with studies funded by non‐industry sources. There was poor reporting of COIs. John Wiley and Sons Inc. 2014-12 2015-01-20 /pmc/articles/PMC4306285/ /pubmed/25642330 http://dx.doi.org/10.1002/ebm2.5 Text en © 2015 The Authors. Evidence‐based Preclinical 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 | Systematic Reviews Abdel‐Sattar, M. Krauth, D. Anglemyer, A. Bero, L. The relationship between risk of bias criteria, research outcomes, and study sponsorship in a cohort of preclinical thiazolidinedione animal studies: a meta‐analysis |
title | The relationship between risk of bias criteria, research outcomes, and study sponsorship in a cohort of preclinical thiazolidinedione animal studies: a meta‐analysis |
title_full | The relationship between risk of bias criteria, research outcomes, and study sponsorship in a cohort of preclinical thiazolidinedione animal studies: a meta‐analysis |
title_fullStr | The relationship between risk of bias criteria, research outcomes, and study sponsorship in a cohort of preclinical thiazolidinedione animal studies: a meta‐analysis |
title_full_unstemmed | The relationship between risk of bias criteria, research outcomes, and study sponsorship in a cohort of preclinical thiazolidinedione animal studies: a meta‐analysis |
title_short | The relationship between risk of bias criteria, research outcomes, and study sponsorship in a cohort of preclinical thiazolidinedione animal studies: a meta‐analysis |
title_sort | relationship between risk of bias criteria, research outcomes, and study sponsorship in a cohort of preclinical thiazolidinedione animal studies: a meta‐analysis |
topic | Systematic Reviews |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4306285/ https://www.ncbi.nlm.nih.gov/pubmed/25642330 http://dx.doi.org/10.1002/ebm2.5 |
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