Literature DB >> 27101231

Relation between CYP2D6 Genotype, Phenotype and Therapeutic Drug Concentrations among Nortriptyline and Venlafaxine Users in Old Age Psychiatry.

E Berm1, R Kok2, E Hak3, B Wilffert1.   

Abstract

Objectives: To determine relations between drug concentrations and the cytochrome P450-CYP2D6 genotype or phenotype among elderly patients treated with nortriptyline or venlafaxine.
Methods: A post-hoc analysis of a clinical trial was performed. Patients were grouped into phenotypes according to the metabolite/mother compound ratio. Genotypes were assessed by the CYP2D6 *3 and *4 alleles.
Results: Data was available from 81 patients (41 nortriptyline, 40 venlafaxine) with a mean age of 72 years. No phenoconversion from poor metabolizers (PM) to extensive metabolizers (EM), or vice versa, was found. However, we did find phenoconversion from PM to intermediate metabolizers (IM), IM to EM, or vice versa in 36% of observations. Among nortriptyline users, patients with a PM or IM genotype had more supra-therapeutic blood levels, although this did not reach statistical significance. In exploratory analyses we found men were more likely (RR: 2.4; 95% CI: 1.14-5.07) to display phenoconversion from an IM genotype to EM phenotype. In addition, compared to non-PMs, PMs were found to have higher risk (RR: 1.56; 95% CI: 1.03-2.37) on non-response, although this was only significant when response was measured on the Hamilton Rating Scale for Depression and not on the Montgomery Åsberg Depression Rating Scale.
Conclusion: Patients phenoconversed, but we did not observe phenoconversion from PM to EM or vice versa. Genotype information could be used as a valuable tool, in addition to therapeutic drug monitoring, to prevent supratherapeutic drug levels of nortriptyline or venlafaxine in elderly patients with a PM genotype. © Georg Thieme Verlag KG Stuttgart · New York.

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Year:  2016        PMID: 27101231     DOI: 10.1055/s-0042-105443

Source DB:  PubMed          Journal:  Pharmacopsychiatry        ISSN: 0176-3679            Impact factor:   5.788


  5 in total

1.  Inhibition of CYP2D6 with low dose (5 mg) paroxetine in patients with high 10-hydroxynortriptyline serum levels - a review of routine practice.

Authors:  Naomi Jessurun; Eugène P van Puijenbroek; Leila S Otten; Oenone Mikes; Annemieke Vermeulen Windsant; Rob J van Marum; Koen Grootens; Hieronymus J Derijks
Journal:  Br J Clin Pharmacol       Date:  2017-01-29       Impact factor: 4.335

2.  Discontinuation and dose adjustment of metoprolol after metoprolol-paroxetine/fluoxetine co-prescription in Dutch elderly.

Authors:  Muh Akbar Bahar; Yuanyuan Wang; Jens H J Bos; Bob Wilffert; Eelko Hak
Journal:  Pharmacoepidemiol Drug Saf       Date:  2018-03-24       Impact factor: 2.890

3.  No Effect of Dose Adjustment to the CYP2D6 Genotype in Patients With Severe Mental Illness.

Authors:  Anne B Koopmans; David J Vinkers; Igmar T Poulina; Petra J A Gelan; Ron H N van Schaik; Hans W Hoek; Peter N van Harten
Journal:  Front Psychiatry       Date:  2018-08-07       Impact factor: 4.157

Review 4.  Pharmacogenomic Biomarkers and Their Applications in Psychiatry.

Authors:  Heejin Kam; Hotcherl Jeong
Journal:  Genes (Basel)       Date:  2020-11-30       Impact factor: 4.096

Review 5.  Meta-analysis of probability estimates of worldwide variation of CYP2D6 and CYP2C19.

Authors:  Anne B Koopmans; Mario H Braakman; David J Vinkers; Hans W Hoek; Peter N van Harten
Journal:  Transl Psychiatry       Date:  2021-02-24       Impact factor: 6.222

  5 in total

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