Amitriptyline or Not, That Is the Question: Pharmacogenetic Testing of CYP2D6 and CYP2C19 Identifies Patients with Low or High Risk for Side Effects in Amitriptyline Therapy
- 1 February 2005
- journal article
- clinical trial
- Published by Oxford University Press (OUP) in Clinical Chemistry
- Vol. 51 (2) , 376-385
- https://doi.org/10.1373/clinchem.2004.041327
Abstract
Background: Amitriptyline has been replaced in many countries by alternative and more expensive drugs based on claims of improved tolerability and toxicity and despite slightly reduced efficacy. Preliminary studies indicate that adverse effects could be linked to polymorphisms of drug-metabolizing enzymes, but information on their clinical impact remains scanty and includes mainly case reports. We conducted a prospective blinded two-center study seeking correlations between CYP2C19 and CYP2D6 genotypes, drug concentrations, adverse events, and therapy response.Keywords
This publication has 43 references indexed in Scilit:
- Pharmacogenetics of Antidepressant Medication IntoleranceAmerican Journal of Psychiatry, 2003
- Comparison of Two CYP2D6 Genotyping Methods and Assessment of Genotype-Phenotype RelationshipsClinical Chemistry, 2003
- Molecular genetics of CYP2D6: Clinical relevance with focus on psychotropic drugsBritish Journal of Clinical Pharmacology, 2002
- Comprehensive analysis of the genetic factors determining expression and function of hepatic CYP2D6Pharmacogenetics, 2001
- Extension of a Pilot Study: Impact From the Cytochrome P450 2D6 Polymorphism on Outcome and Costs Associated With Severe Mental IllnessJournal of Clinical Psychopharmacology, 2000
- Advances in Understanding Drug Metabolism and Its Contribution to Variability in Patient ResponseTherapeutic Drug Monitoring, 2000
- The global burden of mental disorders.American Journal of Public Health, 1999
- The Texas Medication Algorithm ProjectThe Journal of Clinical Psychiatry, 1999
- Five Distinct Human Cytochromes Mediate Amitriptyline N‐Demethylation In Vitro: Dominance of CYP 2C19 and 3A4The Journal of Clinical Pharmacology, 1998
- Tricyclic Antidepressant Concentrations in PlasmaJournal of Clinical Psychopharmacology, 1994