Possible involvement of multiple human cytochrome P450 isoforms in the liver metabolism of propofol

J Guitton, T Buronfosse, M Desage, JP Flinois… - British journal of …, 1998 - Elsevier
Previous studies of propofol (2, 6-diisopropylphenol) pharmacology have shown that this
widely used anaesthetic drug is extensively cleared from the body by conjugation of the …

Impact of CYP3A4* 1G polymorphism on metabolism of fentanyl in Chinese patients undergoing lower abdominal surgery

R Yuan, X Zhang, Q Deng, Y Wu, G Xiang - Clinica Chimica Acta, 2011 - Elsevier
PURPOSE: This study aimed to investigate the impact of CYP3A4* 1G genetic
polymorphism on metabolism of fentanyl in Chinese patients undergoing lower abdominal …

Genotype–phenotype associations for common CYP3A4 and CYP3A5 variants in the basal and induced metabolism of midazolam in European-and African-American …

MD Floyd, G Gervasini, AL Masica… - Pharmacogenetics …, 2003 - journals.lww.com
CYP3A activity in adults varies between individuals and it has been suggested that this has
a genetic basis, possibly related to variant alleles in CYP3A4 and CYP3A5 genes …

Cytochrome P450 polymorphism and postoperative cognitive dysfunction.

J Steinmetz, C Jespersgaard, K Dalhoff… - Minerva …, 2012 - europepmc.org
Background The etiology of postoperative cognitive dysfunction (POCD) remains unclear but
toxicity of anesthetic drugs and their metabolites could be important. We aimed to assess the …

CYP2C19 genotype affects diazepam pharmacokinetics and emergence from general anesthesia

S Inomata, A Nagashima, F Itagaki… - Clinical …, 2005 - Wiley Online Library
Objectives Diazepam is widely used to relieve preoperative anxiety in patients. The
objective of this study was to investigate the effects of polymorphism in CYP2C19 and the …

Dutch Pharmacogenetics Working Group (DPWG) guideline for the gene–drug interaction between CYP2D6 and opioids (codeine, tramadol and oxycodone)

M Matic, M Nijenhuis, B Soree… - European Journal of …, 2022 - nature.com
Abstract The current Dutch Pharmacogenetics Working Group (DPWG) guideline, describes
the gene–drug interaction between CYP2D6 and the opioids codeine, tramadol and …

An optimized methodology for combined phenotyping and genotyping on CYP2D6 and CYP2C19

WJ Tamminga, J Wemer, B Oosterhuis… - European journal of …, 2001 - Springer
A method for simultaneous phenotyping and genotyping for CYP2D6 and CYP2C19 was
tested. Six healthy volunteers were selected (three extensive and three poor metabolisers …

Impact of the CYP2D6 genotype on post‐operative intravenous oxycodone analgesia

ST Zwisler, TP Enggaard, S Mikkelsen… - Acta …, 2010 - Wiley Online Library
Background: Oxycodone is a semi‐synthetic opioid with a μ‐receptor agonist‐mediated
effect in several pain conditions, including post‐operative pain. Oxycodone is metabolized to …

The limited impact of CYP3A5 genotype for the pharmacokinetics of CYP3A substrates

O Burk, M Schwab - European journal of clinical pharmacology, 2007 - Springer
Cytochrome P450 enzymes of subfamily 3A account for as much as 30 and 80% of total
P450 content in liver and intestine, respectively [1, 2]. Their abundant expression, as well as …

Role of cytochrome P450 genotype in the steps toward personalized drug therapy

LH Cavallari, H Jeong, A Bress - … and personalized medicine, 2011 - Taylor & Francis
Genetic polymorphism for cytochrome 450 (P450) enzymes leads to interindividual
variability in the plasma concentrations of many drugs. In some cases, P450 genotype …