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Population Pharmacokinetics of Sertraline in Psychiatric and Substance Use Disorders.
Castillo, Cinthya Eloisa Chávez; Garibay, Susanna Edith Medellín; Segovia, Rosa Del Carmen Milán; Guzmán, Sergio Zarazúa; Cook, Helgi Jung; Contreras, Marisol Orocio; Moreno, Silvia Romano.
Afiliação
  • Castillo CEC; Pharmacy Department, Faculty of Chemical Sciences, Autonomous University of San Luis Potosi, San Luis Potosí, Mexico.
  • Garibay SEM; Pharmacy Department, Faculty of Chemical Sciences, Autonomous University of San Luis Potosi, San Luis Potosí, Mexico.
  • Segovia RDCM; Pharmacy Department, Faculty of Chemical Sciences, Autonomous University of San Luis Potosi, San Luis Potosí, Mexico.
  • Guzmán SZ; Pharmacy Department, Faculty of Chemical Sciences, Autonomous University of San Luis Potosi, San Luis Potosí, Mexico.
  • Cook HJ; Pharmacy Department, Faculty of Chemistry, National Autonomous University of Mexico, Mexico City, Mexico.
  • Contreras MO; Neuropsychopharmacology Department, National Institute of Neurology and Neurosurgery, Mexico City, Mexico.
  • Moreno SR; Centros de Integración Juvenil A.C., San Luis Potosi, Mexico.
J Clin Pharmacol ; 2024 May 08.
Article em En | MEDLINE | ID: mdl-38720595
ABSTRACT
This study aimed to characterize the population pharmacokinetics of sertraline in Mexican patients with psychiatric and substance use disorders. Fifty-nine patients (13 to 76 years old) treated with doses of sertraline between 12.5 and 100 mg/day were included. Plasma sertraline concentrations were determined in blood samples and five of the main substances of abuse were determined by rapid tests in urine samples. Demographic, clinical, and pharmacogenetic factors were also evaluated. Population pharmacokinetic analysis was performed using NONMEM software with first-order conditional estimation method. A one-compartment model with proportional residual error adequately described the sertraline concentrations versus time. CYP2D6*2 polymorphism and CYP2C19 phenotypes significantly influenced sertraline clearance, which had a population mean value of 66 L/h in the final model. The absorption constant and volume of distribution were fixed at 0.855 1/h and 20.2 L/kg, respectively. The model explained 11.3% of the interindividual variability in sertraline clearance. The presence of the CYP2D6*2 polymorphism caused a 23.1% decrease in sertraline clearance, whereas patients with intermediate and poor phenotype of CYP2C19 showed 19.06% and 48.26% decreases in sertraline clearance, respectively. The model was internally validated by bootstrap and visual predictive check. Finally, stochastic simulations were performed to propose dosing regimens to achieve therapeutic levels that contribute to improving treatment response.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Revista: J Clin Pharmacol Ano de publicação: 2024 Tipo de documento: Article País de afiliação: México País de publicação: Reino Unido

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Revista: J Clin Pharmacol Ano de publicação: 2024 Tipo de documento: Article País de afiliação: México País de publicação: Reino Unido