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The Use of ROC Analysis for the Qualitative Prediction of Human Oral Bioavailability from Animal Data

PURPOSE: To develop and evaluate a tool for the qualitative prediction of human oral bioavailability (F(human)) from animal oral bioavailability (F(animal)) data employing ROC analysis and to identify the optimal thresholds for such predictions. METHODS: A dataset of 184 compounds with known F(human...

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Autores principales: Olivares-Morales, Andrés, Hatley, Oliver J. D., Turner, David, Galetin, Aleksandra, Aarons, Leon, Rostami-Hodjegan, Amin
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer US 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4250569/
https://www.ncbi.nlm.nih.gov/pubmed/24072264
http://dx.doi.org/10.1007/s11095-013-1193-2
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author Olivares-Morales, Andrés
Hatley, Oliver J. D.
Turner, David
Galetin, Aleksandra
Aarons, Leon
Rostami-Hodjegan, Amin
author_facet Olivares-Morales, Andrés
Hatley, Oliver J. D.
Turner, David
Galetin, Aleksandra
Aarons, Leon
Rostami-Hodjegan, Amin
author_sort Olivares-Morales, Andrés
collection PubMed
description PURPOSE: To develop and evaluate a tool for the qualitative prediction of human oral bioavailability (F(human)) from animal oral bioavailability (F(animal)) data employing ROC analysis and to identify the optimal thresholds for such predictions. METHODS: A dataset of 184 compounds with known F(human) and F(animal) in at least one species (mouse, rat, dog and non-human primates (NHP)) was employed. A binary classification model for F(human) was built by setting a threshold for high/low F(human) at 50%. The thresholds for high/low F(animal) were varied from 0 to 100 to generate the ROC curves. Optimal thresholds were derived from ‘cost analysis’ and the outcomes with respect to false negative and false positive predictions were analyzed against the BDDCS class distributions. RESULTS: We successfully built ROC curves for the combined dataset and per individual species. Optimal F(animal) thresholds were found to be 67% (mouse), 22% (rat), 58% (dog), 35% (NHP) and 47% (combined dataset). No significant trends were observed when sub-categorizing the outcomes by the BDDCS. CONCLUSIONS: F(animal) can predict high/low F(human) with adequate sensitivity and specificity. This methodology and associated thresholds can be employed as part of decisions related to planning necessary studies during development of new drug candidates and lead selection. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1007/s11095-013-1193-2) contains supplementary material, which is available to authorized users.
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spelling pubmed-42505692014-12-04 The Use of ROC Analysis for the Qualitative Prediction of Human Oral Bioavailability from Animal Data Olivares-Morales, Andrés Hatley, Oliver J. D. Turner, David Galetin, Aleksandra Aarons, Leon Rostami-Hodjegan, Amin Pharm Res Research Paper PURPOSE: To develop and evaluate a tool for the qualitative prediction of human oral bioavailability (F(human)) from animal oral bioavailability (F(animal)) data employing ROC analysis and to identify the optimal thresholds for such predictions. METHODS: A dataset of 184 compounds with known F(human) and F(animal) in at least one species (mouse, rat, dog and non-human primates (NHP)) was employed. A binary classification model for F(human) was built by setting a threshold for high/low F(human) at 50%. The thresholds for high/low F(animal) were varied from 0 to 100 to generate the ROC curves. Optimal thresholds were derived from ‘cost analysis’ and the outcomes with respect to false negative and false positive predictions were analyzed against the BDDCS class distributions. RESULTS: We successfully built ROC curves for the combined dataset and per individual species. Optimal F(animal) thresholds were found to be 67% (mouse), 22% (rat), 58% (dog), 35% (NHP) and 47% (combined dataset). No significant trends were observed when sub-categorizing the outcomes by the BDDCS. CONCLUSIONS: F(animal) can predict high/low F(human) with adequate sensitivity and specificity. This methodology and associated thresholds can be employed as part of decisions related to planning necessary studies during development of new drug candidates and lead selection. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1007/s11095-013-1193-2) contains supplementary material, which is available to authorized users. Springer US 2013-09-27 2014 /pmc/articles/PMC4250569/ /pubmed/24072264 http://dx.doi.org/10.1007/s11095-013-1193-2 Text en © Springer Science+Business Media New York 2013
spellingShingle Research Paper
Olivares-Morales, Andrés
Hatley, Oliver J. D.
Turner, David
Galetin, Aleksandra
Aarons, Leon
Rostami-Hodjegan, Amin
The Use of ROC Analysis for the Qualitative Prediction of Human Oral Bioavailability from Animal Data
title The Use of ROC Analysis for the Qualitative Prediction of Human Oral Bioavailability from Animal Data
title_full The Use of ROC Analysis for the Qualitative Prediction of Human Oral Bioavailability from Animal Data
title_fullStr The Use of ROC Analysis for the Qualitative Prediction of Human Oral Bioavailability from Animal Data
title_full_unstemmed The Use of ROC Analysis for the Qualitative Prediction of Human Oral Bioavailability from Animal Data
title_short The Use of ROC Analysis for the Qualitative Prediction of Human Oral Bioavailability from Animal Data
title_sort use of roc analysis for the qualitative prediction of human oral bioavailability from animal data
topic Research Paper
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4250569/
https://www.ncbi.nlm.nih.gov/pubmed/24072264
http://dx.doi.org/10.1007/s11095-013-1193-2
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