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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...

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Autores principales: Teixeira-da-Silva, Paulo, Pérez-Blanco, Jonás Samuel, Santos-Buelga, Dolores, Otero, María José, García, María José
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2022
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.
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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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