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Validity and Power of Missing Data Imputation for Extreme Sampling and Terminal Measures Designs in Mediation Analysis
Several authors have acknowledged that testing mediational hypotheses between treatments, genes, physiological measures, and behaviors may substantially advance our understanding of how these associations operate. In psychiatric research, the costs of measuring the putative mediator or the outcome c...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Frontiers Research Foundation
2011
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3268628/ https://www.ncbi.nlm.nih.gov/pubmed/22303370 http://dx.doi.org/10.3389/fgene.2011.00075 |
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author | Makowsky, Robert Beasley, T. Mark Gadbury, Gary L. Albert, Jeffrey M. Kennedy, Richard E. Allison, David B. |
author_facet | Makowsky, Robert Beasley, T. Mark Gadbury, Gary L. Albert, Jeffrey M. Kennedy, Richard E. Allison, David B. |
author_sort | Makowsky, Robert |
collection | PubMed |
description | Several authors have acknowledged that testing mediational hypotheses between treatments, genes, physiological measures, and behaviors may substantially advance our understanding of how these associations operate. In psychiatric research, the costs of measuring the putative mediator or the outcome can be prohibitive. Extreme sampling designs have been validated as methods for reducing study costs by increasing power per subject measured on the more expensive variable when assessing bivariate relationships. However, there exist concerns about how missing data can potentially bias the results. Additionally, most mediation analysis techniques presuppose the joint measurement of mediators and outcomes for all subjects. There have been limited methodological developments for techniques that can evaluate putative mediators in studies that have employed extreme sampling, resulting in missing data. We demonstrate that extreme (selective) sampling strategies can be beneficial in the context of mediation analyses. Handling the missing data with maximum likelihood (ML) resulted in minimal power loss and unbiased parameter estimates. We must be cautious, though, in recommending the ML approach for extreme sampling designs because it yielded inflated Type 1 error rates under some null conditions. Yet, the use of extreme sampling designs and methods to handle the resultant missing data presents a viable research strategy. |
format | Online Article Text |
id | pubmed-3268628 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2011 |
publisher | Frontiers Research Foundation |
record_format | MEDLINE/PubMed |
spelling | pubmed-32686282012-02-02 Validity and Power of Missing Data Imputation for Extreme Sampling and Terminal Measures Designs in Mediation Analysis Makowsky, Robert Beasley, T. Mark Gadbury, Gary L. Albert, Jeffrey M. Kennedy, Richard E. Allison, David B. Front Genet Genetics Several authors have acknowledged that testing mediational hypotheses between treatments, genes, physiological measures, and behaviors may substantially advance our understanding of how these associations operate. In psychiatric research, the costs of measuring the putative mediator or the outcome can be prohibitive. Extreme sampling designs have been validated as methods for reducing study costs by increasing power per subject measured on the more expensive variable when assessing bivariate relationships. However, there exist concerns about how missing data can potentially bias the results. Additionally, most mediation analysis techniques presuppose the joint measurement of mediators and outcomes for all subjects. There have been limited methodological developments for techniques that can evaluate putative mediators in studies that have employed extreme sampling, resulting in missing data. We demonstrate that extreme (selective) sampling strategies can be beneficial in the context of mediation analyses. Handling the missing data with maximum likelihood (ML) resulted in minimal power loss and unbiased parameter estimates. We must be cautious, though, in recommending the ML approach for extreme sampling designs because it yielded inflated Type 1 error rates under some null conditions. Yet, the use of extreme sampling designs and methods to handle the resultant missing data presents a viable research strategy. Frontiers Research Foundation 2011-10-31 /pmc/articles/PMC3268628/ /pubmed/22303370 http://dx.doi.org/10.3389/fgene.2011.00075 Text en Copyright © 2011 Makowsky, Beasley, Gadbury, Albert, Kennedy and Allison. http://www.frontiersin.org/licenseagreement This is an open-access article subject to a non-exclusive license between the authors and Frontiers Media SA, which permits use, distribution and reproduction in other forums, provided the original authors and source are credited and other Frontiers conditions are complied with. |
spellingShingle | Genetics Makowsky, Robert Beasley, T. Mark Gadbury, Gary L. Albert, Jeffrey M. Kennedy, Richard E. Allison, David B. Validity and Power of Missing Data Imputation for Extreme Sampling and Terminal Measures Designs in Mediation Analysis |
title | Validity and Power of Missing Data Imputation for Extreme Sampling and Terminal Measures Designs in Mediation Analysis |
title_full | Validity and Power of Missing Data Imputation for Extreme Sampling and Terminal Measures Designs in Mediation Analysis |
title_fullStr | Validity and Power of Missing Data Imputation for Extreme Sampling and Terminal Measures Designs in Mediation Analysis |
title_full_unstemmed | Validity and Power of Missing Data Imputation for Extreme Sampling and Terminal Measures Designs in Mediation Analysis |
title_short | Validity and Power of Missing Data Imputation for Extreme Sampling and Terminal Measures Designs in Mediation Analysis |
title_sort | validity and power of missing data imputation for extreme sampling and terminal measures designs in mediation analysis |
topic | Genetics |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3268628/ https://www.ncbi.nlm.nih.gov/pubmed/22303370 http://dx.doi.org/10.3389/fgene.2011.00075 |
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