Impact of CYP2D6 on venlafaxine metabolism in Trinidadian patients with major depressive disorder

Author:

Montané Jaime Lazara Karelia1,Paul Jeffrey2,Lalla Anthony3,Legall George1,Gaedigk Andrea4

Affiliation:

1. Pharmacology Unit, Department of Paraclinical Sciences, Faculty of Medical Sciences, The University of The West Indies, St Augustine, Trinidad & Tobago

2. JPharm Consulting, Evanston, IL 60201, USA

3. Health Science Technologies Department, College of Science, Technology & Applied Arts of Trinidad & Tobago, El Dorado Campus, Corner College & St. Cecelia Roads, El Dorado, Trinidad & Tobago

4. Division of Clinical Pharmacology, Toxicology & Therapeutic Innovation, Children's Mercy Kansas City & Department of Pediatrics, School of Medicine, University of Missouri-Kansas City, Kansas City, MO 64108, USA

Abstract

Aim: This study aimed to assess the impact of CYP2D6 and CYP2C19 variation on venlafaxine (VEN) at steady state in patients from Trinidad and Tobago of Indian and African descent with major depressive disorder. Patients & methods: Patients were phenotyped with dextromethorphan, genotyped for CYP2D6 and CYP2C19, and metabolic ratios for VEN obtained at 2-week intervals. Results: Of 61 patients, 55 were genotyped and phenotyped and 47 completed 8 weeks of VEN treatment. The majority of patients had metabolic ratios for VEN that were consistent with those for dextromethorphan and genotype-predicted phenotype using activity scores. One subject presented with a novel no-function allele, CYP2D6*99. No correlations were observed with CYP2C19 genotype. Conclusion: CYP2D6 genotype analysis provides valuable information to individualize drug therapy with VEN.

Publisher

Future Medicine Ltd

Subject

Pharmacology,Genetics,Molecular Medicine

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