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Quantifying Selective Reporting and the Proteus Phenomenon for Multiple Datasets with Similar Bias

Meta-analyses play an important role in synthesizing evidence from diverse studies and datasets that address similar questions. A major obstacle for meta-analyses arises from biases in reporting. In particular, it is speculated that findings which do not achieve formal statistical significance are l...

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Detalles Bibliográficos
Autores principales: Pfeiffer, Thomas, Bertram, Lars, Ioannidis, John P. A.
Formato: Texto
Lenguaje:English
Publicado: Public Library of Science 2011
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3066227/
https://www.ncbi.nlm.nih.gov/pubmed/21479240
http://dx.doi.org/10.1371/journal.pone.0018362
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author Pfeiffer, Thomas
Bertram, Lars
Ioannidis, John P. A.
author_facet Pfeiffer, Thomas
Bertram, Lars
Ioannidis, John P. A.
author_sort Pfeiffer, Thomas
collection PubMed
description Meta-analyses play an important role in synthesizing evidence from diverse studies and datasets that address similar questions. A major obstacle for meta-analyses arises from biases in reporting. In particular, it is speculated that findings which do not achieve formal statistical significance are less likely reported than statistically significant findings. Moreover, the patterns of bias can be complex and may also depend on the timing of the research results and their relationship with previously published work. In this paper, we present an approach that is specifically designed to analyze large-scale datasets on published results. Such datasets are currently emerging in diverse research fields, particularly in molecular medicine. We use our approach to investigate a dataset on Alzheimer's disease (AD) that covers 1167 results from case-control studies on 102 genetic markers. We observe that initial studies on a genetic marker tend to be substantially more biased than subsequent replications. The chances for initial, statistically non-significant results to be published are estimated to be about 44% (95% CI, 32% to 63%) relative to statistically significant results, while statistically non-significant replications have almost the same chance to be published as statistically significant replications (84%; 95% CI, 66% to 107%). Early replications tend to be biased against initial findings, an observation previously termed Proteus phenomenon: The chances for non-significant studies going in the same direction as the initial result are estimated to be lower than the chances for non-significant studies opposing the initial result (73%; 95% CI, 55% to 96%). Such dynamic patters in bias are difficult to capture by conventional methods, where typically simple publication bias is assumed to operate. Our approach captures and corrects for complex dynamic patterns of bias, and thereby helps generating conclusions from published results that are more robust against the presence of different coexisting types of selective reporting.
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spelling pubmed-30662272011-04-08 Quantifying Selective Reporting and the Proteus Phenomenon for Multiple Datasets with Similar Bias Pfeiffer, Thomas Bertram, Lars Ioannidis, John P. A. PLoS One Research Article Meta-analyses play an important role in synthesizing evidence from diverse studies and datasets that address similar questions. A major obstacle for meta-analyses arises from biases in reporting. In particular, it is speculated that findings which do not achieve formal statistical significance are less likely reported than statistically significant findings. Moreover, the patterns of bias can be complex and may also depend on the timing of the research results and their relationship with previously published work. In this paper, we present an approach that is specifically designed to analyze large-scale datasets on published results. Such datasets are currently emerging in diverse research fields, particularly in molecular medicine. We use our approach to investigate a dataset on Alzheimer's disease (AD) that covers 1167 results from case-control studies on 102 genetic markers. We observe that initial studies on a genetic marker tend to be substantially more biased than subsequent replications. The chances for initial, statistically non-significant results to be published are estimated to be about 44% (95% CI, 32% to 63%) relative to statistically significant results, while statistically non-significant replications have almost the same chance to be published as statistically significant replications (84%; 95% CI, 66% to 107%). Early replications tend to be biased against initial findings, an observation previously termed Proteus phenomenon: The chances for non-significant studies going in the same direction as the initial result are estimated to be lower than the chances for non-significant studies opposing the initial result (73%; 95% CI, 55% to 96%). Such dynamic patters in bias are difficult to capture by conventional methods, where typically simple publication bias is assumed to operate. Our approach captures and corrects for complex dynamic patterns of bias, and thereby helps generating conclusions from published results that are more robust against the presence of different coexisting types of selective reporting. Public Library of Science 2011-03-29 /pmc/articles/PMC3066227/ /pubmed/21479240 http://dx.doi.org/10.1371/journal.pone.0018362 Text en Pfeiffer et al. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited.
spellingShingle Research Article
Pfeiffer, Thomas
Bertram, Lars
Ioannidis, John P. A.
Quantifying Selective Reporting and the Proteus Phenomenon for Multiple Datasets with Similar Bias
title Quantifying Selective Reporting and the Proteus Phenomenon for Multiple Datasets with Similar Bias
title_full Quantifying Selective Reporting and the Proteus Phenomenon for Multiple Datasets with Similar Bias
title_fullStr Quantifying Selective Reporting and the Proteus Phenomenon for Multiple Datasets with Similar Bias
title_full_unstemmed Quantifying Selective Reporting and the Proteus Phenomenon for Multiple Datasets with Similar Bias
title_short Quantifying Selective Reporting and the Proteus Phenomenon for Multiple Datasets with Similar Bias
title_sort quantifying selective reporting and the proteus phenomenon for multiple datasets with similar bias
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3066227/
https://www.ncbi.nlm.nih.gov/pubmed/21479240
http://dx.doi.org/10.1371/journal.pone.0018362
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