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Estimation of Body Fat Percentage for Clinical Pharmacokinetic Studies in Children

Obesity is a prevalent childhood condition and the degree of adiposity appears likely to be an important covariate in the pharmacokinetics (PKs) of many drugs. We undertook these studies to facilitate the evaluation and, where appropriate, quantification of the covariate effect of body fat percentag...

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Autores principales: Green, Thomas P., Binns, Helen J., Wu, Huali, Ariza, Adolfo J., Perrin, Eliana M., Quadri, Maheen, Hornik, Christoph P., Cohen‐Wolkowiez, Michael
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7993323/
https://www.ncbi.nlm.nih.gov/pubmed/33142010
http://dx.doi.org/10.1111/cts.12896
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author Green, Thomas P.
Binns, Helen J.
Wu, Huali
Ariza, Adolfo J.
Perrin, Eliana M.
Quadri, Maheen
Hornik, Christoph P.
Cohen‐Wolkowiez, Michael
author_facet Green, Thomas P.
Binns, Helen J.
Wu, Huali
Ariza, Adolfo J.
Perrin, Eliana M.
Quadri, Maheen
Hornik, Christoph P.
Cohen‐Wolkowiez, Michael
author_sort Green, Thomas P.
collection PubMed
description Obesity is a prevalent childhood condition and the degree of adiposity appears likely to be an important covariate in the pharmacokinetics (PKs) of many drugs. We undertook these studies to facilitate the evaluation and, where appropriate, quantification of the covariate effect of body fat percentage (BF%) on PK parameters in children. We examined two large databases to determine the values and variabilities of BF% in children with healthy body weights and in those with obesity, comparing the accuracy and precision of BF% estimation by both clinical methods and demographically derived techniques. Additionally, we conducted simulation studies to evaluate the utility of the several methods for application in clinical trials. BF% was correlated with body mass index (BMI), but was highly variable among both children with healthy body weights and those with obesity. Bio‐impedance and several demographically derived techniques produced mean estimates of BF% that differed from dual x‐ray absorptiometry by < 1% (accuracy) and a SD of 5% or less (precision). Simulation studies confirmed that when the differences in precision among the several methods were small compared with unexplained between‐subject variability of a PK parameter, the techniques were of similar value in assessing the contribution of BF%, if any, as a covariate for that PK parameter. The combination of sex and obesity stage explained 68% of the variance of BF% with BMI. The estimation of BF% from sex and obesity stage can routinely be applied to PK clinical trials to evaluate the contribution of BF% as a potential covariate.
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spelling pubmed-79933232021-03-29 Estimation of Body Fat Percentage for Clinical Pharmacokinetic Studies in Children Green, Thomas P. Binns, Helen J. Wu, Huali Ariza, Adolfo J. Perrin, Eliana M. Quadri, Maheen Hornik, Christoph P. Cohen‐Wolkowiez, Michael Clin Transl Sci Research Obesity is a prevalent childhood condition and the degree of adiposity appears likely to be an important covariate in the pharmacokinetics (PKs) of many drugs. We undertook these studies to facilitate the evaluation and, where appropriate, quantification of the covariate effect of body fat percentage (BF%) on PK parameters in children. We examined two large databases to determine the values and variabilities of BF% in children with healthy body weights and in those with obesity, comparing the accuracy and precision of BF% estimation by both clinical methods and demographically derived techniques. Additionally, we conducted simulation studies to evaluate the utility of the several methods for application in clinical trials. BF% was correlated with body mass index (BMI), but was highly variable among both children with healthy body weights and those with obesity. Bio‐impedance and several demographically derived techniques produced mean estimates of BF% that differed from dual x‐ray absorptiometry by < 1% (accuracy) and a SD of 5% or less (precision). Simulation studies confirmed that when the differences in precision among the several methods were small compared with unexplained between‐subject variability of a PK parameter, the techniques were of similar value in assessing the contribution of BF%, if any, as a covariate for that PK parameter. The combination of sex and obesity stage explained 68% of the variance of BF% with BMI. The estimation of BF% from sex and obesity stage can routinely be applied to PK clinical trials to evaluate the contribution of BF% as a potential covariate. John Wiley and Sons Inc. 2020-11-22 2021-03 /pmc/articles/PMC7993323/ /pubmed/33142010 http://dx.doi.org/10.1111/cts.12896 Text en © 2020 The Authors. Clinical and Translational Science published by Wiley Periodicals LLC on behalf of the American Society for Clinical Pharmacology and Therapeutics. This is an open access article under the terms of the http://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
Green, Thomas P.
Binns, Helen J.
Wu, Huali
Ariza, Adolfo J.
Perrin, Eliana M.
Quadri, Maheen
Hornik, Christoph P.
Cohen‐Wolkowiez, Michael
Estimation of Body Fat Percentage for Clinical Pharmacokinetic Studies in Children
title Estimation of Body Fat Percentage for Clinical Pharmacokinetic Studies in Children
title_full Estimation of Body Fat Percentage for Clinical Pharmacokinetic Studies in Children
title_fullStr Estimation of Body Fat Percentage for Clinical Pharmacokinetic Studies in Children
title_full_unstemmed Estimation of Body Fat Percentage for Clinical Pharmacokinetic Studies in Children
title_short Estimation of Body Fat Percentage for Clinical Pharmacokinetic Studies in Children
title_sort estimation of body fat percentage for clinical pharmacokinetic studies in children
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7993323/
https://www.ncbi.nlm.nih.gov/pubmed/33142010
http://dx.doi.org/10.1111/cts.12896
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