Dutch Pharmacogenetics Working Group (DPWG) guideline for the gene-drug interaction between CYP2D6, CYP3A4 and CYP1A2 and antipsychotics

利培酮 阿立哌唑 奎硫平 奥氮平 药理学 CYP2D6型 医学 氯氮平 药物遗传学 吡莫唑 氟哌啶醇 精神科 内科学 精神分裂症(面向对象编程) 基因型 生物 遗传学 多巴胺 细胞色素P450 新陈代谢 基因
作者
Lianne Beunk,Marga Nijenhuis,Bianca Soree,Nienke J. de Boer‐Veger,Anne‐Marie Buunk,Henk‐Jan Guchelaar,Elisa J. F. Houwink,Arne J. Risselada,Gerard A. Rongen,Ron H. N. van Schaik,Jesse J. Swen,Daan J. Touw,Roos van Westrhenen,Vera H.M. Deneer,Jan van der Weide
出处
期刊:European Journal of Human Genetics [Springer Nature]
卷期号:32 (3): 278-285 被引量:51
标识
DOI:10.1038/s41431-023-01347-3
摘要

The Dutch Pharmacogenetics Working Group (DPWG) aims to facilitate pharmacogenetics implementation in clinical practice by developing evidence-based guidelines to optimize pharmacotherapy. A guideline describing the gene-drug interaction between the genes CYP2D6, CYP3A4 and CYP1A2 and antipsychotics is presented here. The DPWG identified gene-drug interactions that require therapy adjustments when respective genotype is known for CYP2D6 with aripiprazole, brexpiprazole, haloperidol, pimozide, risperidone and zuclopenthixol, and for CYP3A4 with quetiapine. Evidence-based dose recommendations were obtained based on a systematic review of published literature. Reduction of the normal dose is recommended for aripiprazole, brexpiprazole, haloperidol, pimozide, risperidone and zuclopenthixol for CYP2D6-predicted PMs, and for pimozide and zuclopenthixol also for CYP2D6 IMs. For CYP2D6 UMs, a dose increase or an alternative drug is recommended for haloperidol and an alternative drug or titration of the dose for risperidone. In addition, in case of no or limited clinical effect, a dose increase is recommended for zuclopenthixol for CYP2D6 UMs. Even though evidence is limited, the DPWG recommends choosing an alternative drug to treat symptoms of depression or a dose reduction for other indications for quetiapine and CYP3A4 PMs. No therapy adjustments are recommended for the other CYP2D6 and CYP3A4 predicted phenotypes. In addition, no action is required for the gene-drug combinations CYP2D6 and clozapine, flupentixol, olanzapine or quetiapine and also not for CYP1A2 and clozapine or olanzapine. For identified gene-drug interactions requiring therapy adjustments, genotyping of CYP2D6 or CYP3A4 prior to treatment should not be considered for all patients, but on an individual patient basis only.
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