Por favor, use este identificador para citar o enlazar este ítem: https://hdl.handle.net/10495/44827
Título : Frequency of CYP3A5 Genetic Polymorphisms and Tacrolimus Pharmacokinetics in Pediatric Liver Transplantation
Autor : Buendía Rodríguez, Jefferson Antonio
Halac, Esteban
Bosaleh, Andrea
García de Dávila, María Teresa
Imvertasa, Óscar César
Bramuglia, Guillermo Federico
metadata.dc.subject.*: Tacrolimus
Trasplante de Hígado
Liver Transplantation
Farmacocinética
Pharmacokinetics
Polimorfismo Genético
Polymorphism, Genetic
Citocromo P-450 CYP3A
Cytochrome P-450 CYP3A
https://id.nlm.nih.gov/mesh/D016559
https://id.nlm.nih.gov/mesh/D016031
https://id.nlm.nih.gov/mesh/D010599
https://id.nlm.nih.gov/mesh/D011110
https://id.nlm.nih.gov/mesh/D051544
Fecha de publicación : 2020
Editorial : MDPI
Citación : Buendía JA, Halac E, Bosaleh A, Garcia de Davila MT, Imvertasa O, Bramuglia G. Frequency of CYP3A5 Genetic Polymorphisms and Tacrolimus Pharmacokinetics in Pediatric Liver Transplantation. Pharmaceutics. 2020 Sep 22;12(9):898. doi: 10.3390/pharmaceutics12090898.
Resumen : ABSTRACT: The evidence available in the pediatric population is limited for making clinical decisions regarding the optimization of tacrolimus (TAC) in pharmacotherapy. The objective of this study was to estimate the frequency of CYP3A5 genetic polymorphisms and their relationship with tacrolimus requirements in the pediatric population. This was a longitudinal cohort study with a two-year follow-up of 77 patients under 18 years old who underwent a liver transplant during the period 2009–2012 at the J.P. Garrahan Pediatric Hospital. Tacrolimus levels from day five up to two years after the transplant were obtained from hospital records of routine therapeutic drug monitoring. The genotyping of CYP3A5 (CYP3A5*1/*3 or *3/*3) was performed in liver biopsies from both the donor and the recipient. The frequency of CYP3A5*1 expression for recipients was 37.1% and 32.2% for donors. Patients who received an expresser organ showed lower Co/dose, especially following 90 days after the surgery. The role of each polymorphism is di erent according to the number of days after the transplant, and it must be taken into account to optimize the benefits of TAC therapy during the post-transplant induction and maintenance phases.
metadata.dc.identifier.eissn: 1999-4923
metadata.dc.identifier.doi: 10.3390/pharmaceutics12090898
Aparece en las colecciones: Artículos de Revista en Ciencias Médicas

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