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Tailoring the Implementation of New Biomarkers Based on Their Added Predictive Value in Subgroups of Individuals
BACKGROUND: The value of new biomarkers or imaging tests, when added to a prediction model, is currently evaluated using reclassification measures, such as the net reclassification improvement (NRI). However, these measures only provide an estimate of improved reclassification at population level. W...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Public Library of Science
2015
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4306488/ https://www.ncbi.nlm.nih.gov/pubmed/25622035 http://dx.doi.org/10.1371/journal.pone.0114020 |
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author | van Giessen, A. Moons, K. G. M. de Wit, G. A. Verschuren, W. M. M. Boer, J. M. A. Koffijberg, H. |
author_facet | van Giessen, A. Moons, K. G. M. de Wit, G. A. Verschuren, W. M. M. Boer, J. M. A. Koffijberg, H. |
author_sort | van Giessen, A. |
collection | PubMed |
description | BACKGROUND: The value of new biomarkers or imaging tests, when added to a prediction model, is currently evaluated using reclassification measures, such as the net reclassification improvement (NRI). However, these measures only provide an estimate of improved reclassification at population level. We present a straightforward approach to characterize subgroups of reclassified individuals in order to tailor implementation of a new prediction model to individuals expected to benefit from it. METHODS: In a large Dutch population cohort (n = 21,992) we classified individuals to low (<5%) and high (≥5%) fatal cardiovascular disease risk by the Framingham risk score (FRS) and reclassified them based on the systematic coronary risk evaluation (SCORE). Subsequently, we characterized the reclassified individuals and, in case of heterogeneity, applied cluster analysis to identify and characterize subgroups. These characterizations were used to select individuals expected to benefit from implementation of SCORE. RESULTS: Reclassification after applying SCORE in all individuals resulted in an NRI of 5.00% (95% CI [-0.53%; 11.50%]) within the events, 0.06% (95% CI [-0.08%; 0.22%]) within the nonevents, and a total NRI of 0.051 (95% CI [-0.004; 0.116]). Among the correctly downward reclassified individuals cluster analysis identified three subgroups. Using the characterizations of the typically correctly reclassified individuals, implementing SCORE only in individuals expected to benefit (n = 2,707,12.3%) improved the NRI to 5.32% (95% CI [-0.13%; 12.06%]) within the events, 0.24% (95% CI [0.10%; 0.36%]) within the nonevents, and a total NRI of 0.055 (95% CI [0.001; 0.123]). Overall, the risk levels for individuals reclassified by tailored implementation of SCORE were more accurate. DISCUSSION: In our empirical example the presented approach successfully characterized subgroups of reclassified individuals that could be used to improve reclassification and reduce implementation burden. In particular when newly added biomarkers or imaging tests are costly or burdensome such a tailored implementation strategy may save resources and improve (cost-)effectiveness. |
format | Online Article Text |
id | pubmed-4306488 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2015 |
publisher | Public Library of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-43064882015-01-30 Tailoring the Implementation of New Biomarkers Based on Their Added Predictive Value in Subgroups of Individuals van Giessen, A. Moons, K. G. M. de Wit, G. A. Verschuren, W. M. M. Boer, J. M. A. Koffijberg, H. PLoS One Research Article BACKGROUND: The value of new biomarkers or imaging tests, when added to a prediction model, is currently evaluated using reclassification measures, such as the net reclassification improvement (NRI). However, these measures only provide an estimate of improved reclassification at population level. We present a straightforward approach to characterize subgroups of reclassified individuals in order to tailor implementation of a new prediction model to individuals expected to benefit from it. METHODS: In a large Dutch population cohort (n = 21,992) we classified individuals to low (<5%) and high (≥5%) fatal cardiovascular disease risk by the Framingham risk score (FRS) and reclassified them based on the systematic coronary risk evaluation (SCORE). Subsequently, we characterized the reclassified individuals and, in case of heterogeneity, applied cluster analysis to identify and characterize subgroups. These characterizations were used to select individuals expected to benefit from implementation of SCORE. RESULTS: Reclassification after applying SCORE in all individuals resulted in an NRI of 5.00% (95% CI [-0.53%; 11.50%]) within the events, 0.06% (95% CI [-0.08%; 0.22%]) within the nonevents, and a total NRI of 0.051 (95% CI [-0.004; 0.116]). Among the correctly downward reclassified individuals cluster analysis identified three subgroups. Using the characterizations of the typically correctly reclassified individuals, implementing SCORE only in individuals expected to benefit (n = 2,707,12.3%) improved the NRI to 5.32% (95% CI [-0.13%; 12.06%]) within the events, 0.24% (95% CI [0.10%; 0.36%]) within the nonevents, and a total NRI of 0.055 (95% CI [0.001; 0.123]). Overall, the risk levels for individuals reclassified by tailored implementation of SCORE were more accurate. DISCUSSION: In our empirical example the presented approach successfully characterized subgroups of reclassified individuals that could be used to improve reclassification and reduce implementation burden. In particular when newly added biomarkers or imaging tests are costly or burdensome such a tailored implementation strategy may save resources and improve (cost-)effectiveness. Public Library of Science 2015-01-26 /pmc/articles/PMC4306488/ /pubmed/25622035 http://dx.doi.org/10.1371/journal.pone.0114020 Text en © 2015 van Giessen 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 van Giessen, A. Moons, K. G. M. de Wit, G. A. Verschuren, W. M. M. Boer, J. M. A. Koffijberg, H. Tailoring the Implementation of New Biomarkers Based on Their Added Predictive Value in Subgroups of Individuals |
title | Tailoring the Implementation of New Biomarkers Based on Their Added Predictive Value in Subgroups of Individuals |
title_full | Tailoring the Implementation of New Biomarkers Based on Their Added Predictive Value in Subgroups of Individuals |
title_fullStr | Tailoring the Implementation of New Biomarkers Based on Their Added Predictive Value in Subgroups of Individuals |
title_full_unstemmed | Tailoring the Implementation of New Biomarkers Based on Their Added Predictive Value in Subgroups of Individuals |
title_short | Tailoring the Implementation of New Biomarkers Based on Their Added Predictive Value in Subgroups of Individuals |
title_sort | tailoring the implementation of new biomarkers based on their added predictive value in subgroups of individuals |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4306488/ https://www.ncbi.nlm.nih.gov/pubmed/25622035 http://dx.doi.org/10.1371/journal.pone.0114020 |
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