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A novel method based on unbiased correlations tests for covariate selection in nonlinear mixed effects models: The COSSAC approach

Building a covariate model is a crucial task in population pharmacokinetics and pharmacodynamics in order to understand the determinants of the interindividual variability. Identifying a good covariate model usually requires many runs. Several procedures have been proposed in the past to automatize...

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Autores principales: Ayral, Géraldine, Si Abdallah, Jean‐François, Magnard, Claude, Chauvin, Jonathan
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8099437/
https://www.ncbi.nlm.nih.gov/pubmed/33755345
http://dx.doi.org/10.1002/psp4.12612
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author Ayral, Géraldine
Si Abdallah, Jean‐François
Magnard, Claude
Chauvin, Jonathan
author_facet Ayral, Géraldine
Si Abdallah, Jean‐François
Magnard, Claude
Chauvin, Jonathan
author_sort Ayral, Géraldine
collection PubMed
description Building a covariate model is a crucial task in population pharmacokinetics and pharmacodynamics in order to understand the determinants of the interindividual variability. Identifying a good covariate model usually requires many runs. Several procedures have been proposed in the past to automatize this task. The most commonly used is Stepwise Covariate Modeling (SCM). Here, we present a novel stepwise method based on statistical tests between individual parameters sampled from their conditional distribution and the covariates. This strategy, called the COnditional Sampling use for Stepwise Approach based on Correlation tests (COSSAC), makes use of the information contained in the current model to choose which parameter‐covariate relationship to try next. This strategy greatly reduces the number of covariate models tested, while retaining on its search path the models improving the log‐likelihood (LL). In this article, we detail the COSSAC method and its implementation in Monolix, and evaluate its performance. The performance was assessed by comparing COSSAC to the traditional SCM method on 17 representative data sets. For the large majority of cases (15 out of 17), the final covariate model is identical (11 cases) or very similar (4 cases with LL differences less than 3.84) with both procedures. Yet, COSSAC requires between 2 to 20 times fewer runs than SCM. This represents a decisive speed up, especially for models that take long to run and would not be tractable using the SCM method.
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spelling pubmed-80994372021-05-10 A novel method based on unbiased correlations tests for covariate selection in nonlinear mixed effects models: The COSSAC approach Ayral, Géraldine Si Abdallah, Jean‐François Magnard, Claude Chauvin, Jonathan CPT Pharmacometrics Syst Pharmacol Research Building a covariate model is a crucial task in population pharmacokinetics and pharmacodynamics in order to understand the determinants of the interindividual variability. Identifying a good covariate model usually requires many runs. Several procedures have been proposed in the past to automatize this task. The most commonly used is Stepwise Covariate Modeling (SCM). Here, we present a novel stepwise method based on statistical tests between individual parameters sampled from their conditional distribution and the covariates. This strategy, called the COnditional Sampling use for Stepwise Approach based on Correlation tests (COSSAC), makes use of the information contained in the current model to choose which parameter‐covariate relationship to try next. This strategy greatly reduces the number of covariate models tested, while retaining on its search path the models improving the log‐likelihood (LL). In this article, we detail the COSSAC method and its implementation in Monolix, and evaluate its performance. The performance was assessed by comparing COSSAC to the traditional SCM method on 17 representative data sets. For the large majority of cases (15 out of 17), the final covariate model is identical (11 cases) or very similar (4 cases with LL differences less than 3.84) with both procedures. Yet, COSSAC requires between 2 to 20 times fewer runs than SCM. This represents a decisive speed up, especially for models that take long to run and would not be tractable using the SCM method. John Wiley and Sons Inc. 2021-05-05 2021-04 /pmc/articles/PMC8099437/ /pubmed/33755345 http://dx.doi.org/10.1002/psp4.12612 Text en © 2021 Lixoft. CPT: Pharmacometrics & Systems Pharmacology published by Wiley Periodicals LLC on behalf of American Society for Clinical Pharmacology and Therapeutics https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by-nc-nd/4.0/ (https://creativecommons.org/licenses/by-nc-nd/4.0/) License, which permits use and distribution in any medium, provided the original work is properly cited, the use is non‐commercial and no modifications or adaptations are made.
spellingShingle Research
Ayral, Géraldine
Si Abdallah, Jean‐François
Magnard, Claude
Chauvin, Jonathan
A novel method based on unbiased correlations tests for covariate selection in nonlinear mixed effects models: The COSSAC approach
title A novel method based on unbiased correlations tests for covariate selection in nonlinear mixed effects models: The COSSAC approach
title_full A novel method based on unbiased correlations tests for covariate selection in nonlinear mixed effects models: The COSSAC approach
title_fullStr A novel method based on unbiased correlations tests for covariate selection in nonlinear mixed effects models: The COSSAC approach
title_full_unstemmed A novel method based on unbiased correlations tests for covariate selection in nonlinear mixed effects models: The COSSAC approach
title_short A novel method based on unbiased correlations tests for covariate selection in nonlinear mixed effects models: The COSSAC approach
title_sort novel method based on unbiased correlations tests for covariate selection in nonlinear mixed effects models: the cossac approach
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8099437/
https://www.ncbi.nlm.nih.gov/pubmed/33755345
http://dx.doi.org/10.1002/psp4.12612
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