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荷兰药物基因组学工作组(DPWG)关于CYP2D6、CYP3A4和CYP1A2与抗精神病药物之间基因-药物相互作用的指南。

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

作者信息

Beunk Lianne, Nijenhuis Marga, Soree Bianca, de Boer-Veger Nienke J, Buunk Anne-Marie, Guchelaar Henk Jan, Houwink Elisa J F, Risselada Arne, Rongen Gerard A P J M, van Schaik Ron H N, Swen Jesse J, Touw Daan, van Westrhenen Roos, Deneer Vera H M, van der Weide Jan

机构信息

Department of Clinical Chemistry, St Jansdal Hospital, Harderwijk, the Netherlands.

Royal Dutch Pharmacists Association (KNMP), The Hague, the Netherlands.

出版信息

Eur J Hum Genet. 2024 Mar;32(3):278-285. doi: 10.1038/s41431-023-01347-3. Epub 2023 Mar 31.

Abstract

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.

摘要

荷兰药物基因组学工作组(DPWG)旨在通过制定循证指南以优化药物治疗,促进药物基因组学在临床实践中的应用。本文介绍了一份描述细胞色素P450 2D6(CYP2D6)、细胞色素P450 3A4(CYP3A4)和细胞色素P450 1A2(CYP1A2)基因与抗精神病药物之间基因-药物相互作用的指南。DPWG确定了已知CYP2D6基因型时,阿立哌唑、布瑞哌唑、氟哌啶醇、匹莫齐特、利培酮和珠氯噻醇,以及已知CYP3A4基因型时与喹硫平之间需要调整治疗方案的基因-药物相互作用。基于对已发表文献的系统综述得出了循证剂量建议。对于CYP2D6预测的慢代谢者(PMs),建议降低阿立哌唑、布瑞哌唑、氟哌啶醇、匹莫齐特、利培酮和珠氯噻醇的常规剂量;对于匹莫齐特和珠氯噻醇,CYP2D6中间代谢者(IMs)也建议降低剂量。对于CYP2D6超快代谢者(UMs),建议增加氟哌啶醇的剂量或更换药物,对于利培酮则建议更换药物或调整剂量。此外,对于CYP2D6 UMs,如果珠氯噻醇没有临床效果或临床效果有限,建议增加剂量。尽管证据有限,但DPWG建议选择其他药物治疗抑郁症症状,或降低喹硫平和CYP3A4 PMs其他适应症的剂量。对于其他CYP2D6和CYP3A4预测表型,不建议调整治疗方案。此外,对于CYP2D6与氯氮平、氟哌噻吨、奥氮平或喹硫平的基因-药物组合,以及CYP1A2与氯氮平或奥氮平的基因-药物组合,无需采取任何措施。对于已确定需要调整治疗方案的基因-药物相互作用,不应考虑对所有患者在治疗前进行CYP2D6或CYP3A4基因分型,而应仅基于个体患者情况进行考虑。

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