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

Authors :
Hicks JK
Swen JJ
Thorn CF
Sangkuhl K
Kharasch ED
Ellingrod VL
Skaar TC
Müller DJ
Gaedigk A
Stingl JC
Source :
Clinical pharmacology and therapeutics [Clin Pharmacol Ther] 2013 May; Vol. 93 (5), pp. 402-8. Date of Electronic Publication: 2013 Jan 16.
Publication Year :
2013

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.

Details

Language :
English
ISSN :
1532-6535
Volume :
93
Issue :
5
Database :
MEDLINE
Journal :
Clinical pharmacology and therapeutics
Publication Type :
Academic Journal
Accession number :
23486447
Full Text :
https://doi.org/10.1038/clpt.2013.2