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Assessing robustness of hazard ratio estimates to outcome misclassification in longitudinal panel studies with application to Alzheimer’s disease
Analyses of imperfectly assessed time to event outcomes give rise to biased hazard ratio estimates. This bias is a common challenge for studies of Alzheimer’s Disease (AD) because AD neuropathology can only be identified through brain autopsy and is therefore not available for most study participant...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Public Library of Science
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5741229/ https://www.ncbi.nlm.nih.gov/pubmed/29272296 http://dx.doi.org/10.1371/journal.pone.0190107 |
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author | Wang, Le Hubbard, Rebecca A. Walker, Rod L. Lee, Edward B. Larson, Eric B. Crane, Paul K. |
author_facet | Wang, Le Hubbard, Rebecca A. Walker, Rod L. Lee, Edward B. Larson, Eric B. Crane, Paul K. |
author_sort | Wang, Le |
collection | PubMed |
description | Analyses of imperfectly assessed time to event outcomes give rise to biased hazard ratio estimates. This bias is a common challenge for studies of Alzheimer’s Disease (AD) because AD neuropathology can only be identified through brain autopsy and is therefore not available for most study participants. Clinical AD diagnosis, although more widely available, has imperfect sensitivity and specificity relative to AD neuropathology. In this study we present a sensitivity analysis approach using a bias-adjusted discrete proportional hazards model to quantify robustness of results to misclassification of a time to event outcome and apply this method to data from a longitudinal panel study of AD. Using data on 1,955 participants from the Adult Changes in Thought study we analyzed the association between average glucose level and AD neuropathology and conducted sensitivity analyses to explore how estimated hazard ratios varied according to AD classification accuracy. Unadjusted hazard ratios were closer to the null than estimates obtained under most scenarios for misclassification investigated. Confidence interval estimates from the unadjusted model were substantially underestimated compared to adjusted estimates. This study demonstrates the importance of exploring outcome misclassification in time to event analyses and provides an approach that can be undertaken without requiring validation data. |
format | Online Article Text |
id | pubmed-5741229 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Public Library of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-57412292018-01-10 Assessing robustness of hazard ratio estimates to outcome misclassification in longitudinal panel studies with application to Alzheimer’s disease Wang, Le Hubbard, Rebecca A. Walker, Rod L. Lee, Edward B. Larson, Eric B. Crane, Paul K. PLoS One Research Article Analyses of imperfectly assessed time to event outcomes give rise to biased hazard ratio estimates. This bias is a common challenge for studies of Alzheimer’s Disease (AD) because AD neuropathology can only be identified through brain autopsy and is therefore not available for most study participants. Clinical AD diagnosis, although more widely available, has imperfect sensitivity and specificity relative to AD neuropathology. In this study we present a sensitivity analysis approach using a bias-adjusted discrete proportional hazards model to quantify robustness of results to misclassification of a time to event outcome and apply this method to data from a longitudinal panel study of AD. Using data on 1,955 participants from the Adult Changes in Thought study we analyzed the association between average glucose level and AD neuropathology and conducted sensitivity analyses to explore how estimated hazard ratios varied according to AD classification accuracy. Unadjusted hazard ratios were closer to the null than estimates obtained under most scenarios for misclassification investigated. Confidence interval estimates from the unadjusted model were substantially underestimated compared to adjusted estimates. This study demonstrates the importance of exploring outcome misclassification in time to event analyses and provides an approach that can be undertaken without requiring validation data. Public Library of Science 2017-12-22 /pmc/articles/PMC5741229/ /pubmed/29272296 http://dx.doi.org/10.1371/journal.pone.0190107 Text en © 2017 Wang 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 (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited. |
spellingShingle | Research Article Wang, Le Hubbard, Rebecca A. Walker, Rod L. Lee, Edward B. Larson, Eric B. Crane, Paul K. Assessing robustness of hazard ratio estimates to outcome misclassification in longitudinal panel studies with application to Alzheimer’s disease |
title | Assessing robustness of hazard ratio estimates to outcome misclassification in longitudinal panel studies with application to Alzheimer’s disease |
title_full | Assessing robustness of hazard ratio estimates to outcome misclassification in longitudinal panel studies with application to Alzheimer’s disease |
title_fullStr | Assessing robustness of hazard ratio estimates to outcome misclassification in longitudinal panel studies with application to Alzheimer’s disease |
title_full_unstemmed | Assessing robustness of hazard ratio estimates to outcome misclassification in longitudinal panel studies with application to Alzheimer’s disease |
title_short | Assessing robustness of hazard ratio estimates to outcome misclassification in longitudinal panel studies with application to Alzheimer’s disease |
title_sort | assessing robustness of hazard ratio estimates to outcome misclassification in longitudinal panel studies with application to alzheimer’s disease |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5741229/ https://www.ncbi.nlm.nih.gov/pubmed/29272296 http://dx.doi.org/10.1371/journal.pone.0190107 |
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