Literature DB >> 23486447

Clinical Pharmacogenetics Implementation Consortium guideline for CYP2D6 and CYP2C19 genotypes and dosing of tricyclic antidepressants.

J K Hicks1, J J Swen, C F Thorn, K Sangkuhl, E D Kharasch, V L Ellingrod, T C Skaar, D J Müller, A Gaedigk, J C Stingl.   

Abstract

Polymorphisms in CYP2D6 and CYP2C19 affect the efficacy and safety of tricyclics, with some drugs being affected by CYP2D6 only, and others by both polymorphic enzymes. Amitriptyline, clomipramine, doxepin, imipramine, and trimipramine are demethylated by CYP2C19 to pharmacologically active metabolites. These drugs and their metabolites, along with desipramine and nortriptyline, undergo hydroxylation by CYP2D6 to less active metabolites. Evidence from published literature is presented for CYP2D6 and CYP2C19 genotype-directed dosing of tricyclic antidepressants.

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Year:  2013        PMID: 23486447      PMCID: PMC3689226          DOI: 10.1038/clpt.2013.2

Source DB:  PubMed          Journal:  Clin Pharmacol Ther        ISSN: 0009-9236            Impact factor:   6.875


  39 in total

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Journal:  Clin Pharmacol Ther       Date:  2009-11-11       Impact factor: 6.875

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Authors:  L Bertilsson; B Mellström; F Sjökvist; B Mårtenson; M Asberg
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8.  The CYP2D6 polymorphism in relation to the metabolism of amitriptyline and nortriptyline in the Faroese population.

Authors:  Jónrit Halling; Pál Weihe; Kim Brosen
Journal:  Br J Clin Pharmacol       Date:  2007-08-31       Impact factor: 4.335

9.  The nonlinear kinetics of desipramine and 2-hydroxydesipramine in plasma.

Authors:  R G Cooke; J J Warsh; H C Stancer; K L Reed; E Persad
Journal:  Clin Pharmacol Ther       Date:  1984-09       Impact factor: 6.875

10.  Single-dose kinetics predict steady-state concentrations on imipramine and desipramine.

Authors:  W Z Potter; A P Zavadil; I J Kopin; F K Goodwin
Journal:  Arch Gen Psychiatry       Date:  1980-03
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9.  Personalized sequencing and the future of medicine: discovery, diagnosis and defeat of disease.

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