1. CYP2D6 Genotype Phenotype Discordance Due to Drug-Drug Interaction.
- Author
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Monte AA, West K, McDaniel KT, Flaten HK, Saben J, Shelton S, Abdelmawla F, Bushman LR, Williamson K, Abbott D, and Anderson PL
- Subjects
- Administration, Oral, Aged, Colorado, Dextromethorphan administration & dosage, Dextromethorphan pharmacokinetics, Drug Interactions, Female, Genotype, Humans, Male, Middle Aged, Models, Biological, Phenotype, Prospective Studies, Risk Assessment, Substrate Specificity, Cytochrome P-450 CYP2D6 genetics, Cytochrome P-450 CYP2D6 metabolism, Cytochrome P-450 CYP2D6 Inhibitors administration & dosage, Dextromethorphan metabolism, Pharmacogenomic Variants
- Abstract
Drug-drug interactions have been demonstrated to alter cytochrome 2D6 (CYP2D6) enzyme phenotype due to inhibitor ingestion, although it is unclear how substrate interactions affect phenotype. This was a pragmatic clinical trial examining the kinetics of a CYP2D6 enzyme probe drug with and without CYP2D6-dependent substrates. Patients were enrolled into an inpatient study unit, and orally administered a 2 mg microdose of dextromethorphan (DM) to probe enzyme activity with and without CYP2D6-dependent drug-drug interactions. Thirty-nine subjects were enrolled in this trial. Twelve subjects were on no CYP2D6-dependent drugs and 27 were on one or more CYP2D6-dependent drugs. There were 1 poor metabolizer, 5 intermediate metabolizers, 31 normal metabolizers, and 2 ultra-rapid metabolizers. Those with co-ingestion of another CYP2D6-dependent drug were 9.49 (95% confidence interval (CI): 1.54-186.41; P = 0.01) times more likely to have genotype-phenotype discordance based upon the 3 hours dextrophan/dextromethorphan (DX/DM) ratio. CYP2D6 substrate co-ingestions can cause genotype-phenotype discordance., (© 2018 American Society for Clinical Pharmacology and Therapeutics.)
- Published
- 2018
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