Nifedipine May Be an Inhibitor of Clozapine Metabolism as Seen in 5 Patients: 2 From a US Double-Blind Study and 3 From a German Therapeutic Drug Monitoring Study.

IF 2.8 4区 医学 Q2 MEDICAL LABORATORY TECHNOLOGY
Therapeutic Drug Monitoring Pub Date : 2025-06-01 Epub Date: 2024-11-14 DOI:10.1097/FTD.0000000000001277
Georgios Schoretsanitis, Ekkehard Haen, Hélène Verdoux, Michael Paulzen, Jose de Leon
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引用次数: 0

Abstract

Background: Clozapine is the only licensed antipsychotic for treatment-refractory schizophrenia. Therapeutic drug monitoring (TDM) refers to the measurement of clozapine concentration. Clozapine TDM can be used to optimize treatment, particularly by identifying pharmacokinetic interactions between clozapine and comedications.

Methods: We identified 5 cases of patients with available clozapine concentrations who were concomitantly receiving nifedipine and clozapine. These cases were drawn from 2 independent datasets: 2 from a double-blind, randomized clinical trial in the United States and 3 from a German TDM naturalistic database. As an index of clozapine clearance, we used the trough-level concentration-to-dose (C/D) ratios to estimate the minimum therapeutic doses. To estimate dose-correction factors for nifedipine treatment, we included only clozapine concentrations at steady state. We divided the clozapine minimum therapeutic doses (MTD) from the on-condition by the off-nifedipine condition.

Results: In 4 patients, the ratio of on/off nifedipine for MTD ranged between 0.58 and 0.82. Another patient had no data and had to be compared with published control data (female smoker of African ancestry), providing a correction factor of 0.52 after eliminating 5 concentrations contaminated by the development of obesity.

Conclusions: In the absence of access to TDM, when prescribing nifedipine to clozapine-treated patients, we recommend reducing the daily dose of clozapine by one-third because of the weak inhibition of clozapine metabolism. With access to TDM, TDM should guide dosing as unusual patients may need larger dose reductions, as it is possible that in some patients, nifedipine may be a moderate inhibitor requiring halving clozapine dose. Further prospective studies are warranted.

硝苯地平可能是5例患者氯氮平代谢抑制剂:2例来自美国双盲研究,3例来自德国治疗药物监测研究。
背景:氯氮平是唯一被批准用于治疗难治性精神分裂症的抗精神病药物。治疗药物监测(TDM)是指氯氮平浓度的测量。氯氮平TDM可用于优化治疗,特别是通过确定氯氮平和药物之间的药代动力学相互作用。方法:选择5例氯氮平可用浓度的患者同时服用硝苯地平和氯氮平。这些病例来自2个独立的数据集:2个来自美国的双盲随机临床试验,3个来自德国TDM自然数据库。作为氯氮平清除率的指标,我们使用谷浓度剂量比(C/D)来估计最小治疗剂量。为了估计硝苯地平治疗的剂量校正因子,我们只纳入稳定状态下的氯氮平浓度。我们将氯氮平最小治疗剂量(MTD)与硝苯地平状态分开。结果:4例MTD患者硝苯地平开/关比在0.58 ~ 0.82之间。另一名患者没有数据,必须与已发表的对照数据(非洲血统的女性吸烟者)进行比较,在消除了由肥胖发展污染的5种浓度后,提供了0.52的校正因子。结论:在无法获得TDM的情况下,由于对氯氮平代谢的抑制作用较弱,在给氯氮平治疗的患者开硝苯地平处方时,我们建议将氯氮平的日剂量减少三分之一。有了TDM, TDM应该指导给药,因为不寻常的患者可能需要更大的剂量减少,因为在一些患者中,硝苯地平可能是一种中等抑制剂,需要氯氮平剂量减半。进一步的前瞻性研究是必要的。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Therapeutic Drug Monitoring
Therapeutic Drug Monitoring 医学-毒理学
CiteScore
5.00
自引率
8.00%
发文量
213
审稿时长
4-8 weeks
期刊介绍: Therapeutic Drug Monitoring is a peer-reviewed, multidisciplinary journal directed to an audience of pharmacologists, clinical chemists, laboratorians, pharmacists, drug researchers and toxicologists. It fosters the exchange of knowledge among the various disciplines–clinical pharmacology, pathology, toxicology, analytical chemistry–that share a common interest in Therapeutic Drug Monitoring. The journal presents studies detailing the various factors that affect the rate and extent drugs are absorbed, metabolized, and excreted. Regular features include review articles on specific classes of drugs, original articles, case reports, technical notes, and continuing education articles.
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