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Physiologically-based pharmacokinetic modeling of pantoprazole to evaluate the role of CYP2C19 genetic variation and obesity in the pediatric population.
Thompson, Elizabeth J; Jeong, Angela; Helfer, Victória E; Shakhnovich, Valentina; Edginton, Andrea; Balevic, Stephen J; James, Laura P; Collier, David N; Anand, Ravinder; Gonzalez, Daniel.
Afiliación
  • Thompson EJ; Division of Pharmacotherapy and Experimental Therapeutics, UNC Eshelman School of Pharmacy, The University of North Carolina at Chapel Hill, Chapel Hill, North Carolina, USA.
  • Jeong A; Department of Pediatrics, Duke University Medical Center, Durham, North Carolina, USA.
  • Helfer VE; Duke Clinical Research Institute, Durham, North Carolina, USA.
  • Shakhnovich V; Division of Pharmacotherapy and Experimental Therapeutics, UNC Eshelman School of Pharmacy, The University of North Carolina at Chapel Hill, Chapel Hill, North Carolina, USA.
  • Edginton A; Division of Pharmacotherapy and Experimental Therapeutics, UNC Eshelman School of Pharmacy, The University of North Carolina at Chapel Hill, Chapel Hill, North Carolina, USA.
  • Balevic SJ; University of Missouri-Kansas City School of Medicine, Kansas City, Missouri, USA.
  • James LP; Divisions of Gastroenterology, Hepatology and Nutrition & Clinical Pharmacology, Toxicology and Therapeutic Innovation, Children's Mercy Kansas City, Kansas City, Missouri, USA.
  • Collier DN; Ironwood Pharmaceuticals, Boston, Massachusetts, USA.
  • Anand R; School of Pharmacy, University of Waterloo, Waterloo, Ontario, Canada.
  • Gonzalez D; Department of Pediatrics, Duke University Medical Center, Durham, North Carolina, USA.
CPT Pharmacometrics Syst Pharmacol ; 13(8): 1394-1408, 2024 Aug.
Article en En | MEDLINE | ID: mdl-38837864
ABSTRACT
Pantoprazole is a proton pump inhibitor indicated for the treatment of gastroesophageal reflux disease, a condition that disproportionately affects children with obesity. Appropriately dosing pantoprazole in children with obesity requires understanding the body size metric that best guides dosing, but pharmacokinetic (PK) trials using traditional techniques are limited by the need for larger sample sizes and frequent blood sampling. Physiologically-based PK (PBPK) models are an attractive alternative that can account for physiologic-, genetic-, and drug-specific changes without the need for extensive clinical trial data. In this study, we explored the effect of obesity on pantoprazole PK and evaluated label-suggested dosing in this population. An adult PBPK model for pantoprazole was developed using data from the literature and accounting for genetic variation in CYP2C19. The adult PBPK model was scaled to children without obesity using age-associated changes in anatomical and physiological parameters. Lastly, the pediatric PBPK model was expanded to children with obesity. Three pantoprazole dosing strategies were evaluated 1 mg/kg total body weight, 1.2 mg/kg lean body weight, and US Food and Drug Administration-recommended weight-tiered dosing. Simulated concentration-time profiles from our model were compared with data from a prospective cohort study (PAN01; NCT02186652). Weight-tiered dosing resulted in the most (>90%) children with pantoprazole exposures in the reference range, regardless of obesity status or CYP2C19 phenotype, confirming results from previously published population PK models. PBPK models may allow for the efficient study of physiologic and developmental effects of obesity on PK in special populations where clinical trial data may be limited.
Asunto(s)

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Inhibidores de la Bomba de Protones / Obesidad Infantil / Citocromo P-450 CYP2C19 / Pantoprazol Límite: Adolescent / Child / Child, preschool / Female / Humans / Male Idioma: En Revista: CPT Pharmacometrics Syst Pharmacol Año: 2024 Tipo del documento: Article País de afiliación: Estados Unidos Pais de publicación: Estados Unidos

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Inhibidores de la Bomba de Protones / Obesidad Infantil / Citocromo P-450 CYP2C19 / Pantoprazol Límite: Adolescent / Child / Child, preschool / Female / Humans / Male Idioma: En Revista: CPT Pharmacometrics Syst Pharmacol Año: 2024 Tipo del documento: Article País de afiliación: Estados Unidos Pais de publicación: Estados Unidos