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Population Pharmacokinetics of Valproic Acid in Pediatric and Adult Caucasian Patients
(1) Background: The aim of this study was to explore the valproic acid (VPA) pharmacokinetic characteristics in a large population of pediatric and adult Caucasian patients and to establish a robust population pharmacokinetic (PopPK) model. (2) Methods: A total of 2527 serum VPA samples collected fr...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9031051/ https://www.ncbi.nlm.nih.gov/pubmed/35456645 http://dx.doi.org/10.3390/pharmaceutics14040811 |
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author | Teixeira-da-Silva, Paulo Pérez-Blanco, Jonás Samuel Santos-Buelga, Dolores Otero, María José García, María José |
author_facet | Teixeira-da-Silva, Paulo Pérez-Blanco, Jonás Samuel Santos-Buelga, Dolores Otero, María José García, María José |
author_sort | Teixeira-da-Silva, Paulo |
collection | PubMed |
description | (1) Background: The aim of this study was to explore the valproic acid (VPA) pharmacokinetic characteristics in a large population of pediatric and adult Caucasian patients and to establish a robust population pharmacokinetic (PopPK) model. (2) Methods: A total of 2527 serum VPA samples collected from 1204 patients included in a therapeutic drug monitoring program were retrospectively analyzed. Patients were randomly assigned to either a model development group or an external evaluation group. PopPK analysis was performed on 1751 samples from 776 patients with NONMEM using a nonlinear mixed-effect modelling approach. The influence of demographic, anthropometric, treatment and comedication variables on the apparent clearance (CL/F) of VPA was studied. The bootstrap method was used to evaluate the final model internally. External evaluation was carried out using 776 VPA serum samples from 368 patients. (3) Results: A one-compartment model with first-order absorption and elimination successfully described the data. The final model included total body weight, age and comedication with phenytoin, phenobarbital and carbamazepine with a significant impact on VPA elimination. Internal and external evaluations demonstrated the good predictability of the model. (4) Conclusions: A PopPK model of VPA in Caucasian patients was successfully established, which will be helpful for model-informed precision dosing approaches in clinical patient care. |
format | Online Article Text |
id | pubmed-9031051 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-90310512022-04-23 Population Pharmacokinetics of Valproic Acid in Pediatric and Adult Caucasian Patients Teixeira-da-Silva, Paulo Pérez-Blanco, Jonás Samuel Santos-Buelga, Dolores Otero, María José García, María José Pharmaceutics Article (1) Background: The aim of this study was to explore the valproic acid (VPA) pharmacokinetic characteristics in a large population of pediatric and adult Caucasian patients and to establish a robust population pharmacokinetic (PopPK) model. (2) Methods: A total of 2527 serum VPA samples collected from 1204 patients included in a therapeutic drug monitoring program were retrospectively analyzed. Patients were randomly assigned to either a model development group or an external evaluation group. PopPK analysis was performed on 1751 samples from 776 patients with NONMEM using a nonlinear mixed-effect modelling approach. The influence of demographic, anthropometric, treatment and comedication variables on the apparent clearance (CL/F) of VPA was studied. The bootstrap method was used to evaluate the final model internally. External evaluation was carried out using 776 VPA serum samples from 368 patients. (3) Results: A one-compartment model with first-order absorption and elimination successfully described the data. The final model included total body weight, age and comedication with phenytoin, phenobarbital and carbamazepine with a significant impact on VPA elimination. Internal and external evaluations demonstrated the good predictability of the model. (4) Conclusions: A PopPK model of VPA in Caucasian patients was successfully established, which will be helpful for model-informed precision dosing approaches in clinical patient care. MDPI 2022-04-07 /pmc/articles/PMC9031051/ /pubmed/35456645 http://dx.doi.org/10.3390/pharmaceutics14040811 Text en © 2022 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Article Teixeira-da-Silva, Paulo Pérez-Blanco, Jonás Samuel Santos-Buelga, Dolores Otero, María José García, María José Population Pharmacokinetics of Valproic Acid in Pediatric and Adult Caucasian Patients |
title | Population Pharmacokinetics of Valproic Acid in Pediatric and Adult Caucasian Patients |
title_full | Population Pharmacokinetics of Valproic Acid in Pediatric and Adult Caucasian Patients |
title_fullStr | Population Pharmacokinetics of Valproic Acid in Pediatric and Adult Caucasian Patients |
title_full_unstemmed | Population Pharmacokinetics of Valproic Acid in Pediatric and Adult Caucasian Patients |
title_short | Population Pharmacokinetics of Valproic Acid in Pediatric and Adult Caucasian Patients |
title_sort | population pharmacokinetics of valproic acid in pediatric and adult caucasian patients |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9031051/ https://www.ncbi.nlm.nih.gov/pubmed/35456645 http://dx.doi.org/10.3390/pharmaceutics14040811 |
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