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氯氮平与细胞色素P450诱导剂之间的“拔河比赛”:一例报告

Tug of war between clozapine and CYP450 inducers: A case report.

作者信息

Taneja Gaurav, Leontieva Luba

机构信息

Department of Psychiatry, SUNY Upstate Medical University, Syracuse, NY, USA.

出版信息

SAGE Open Med Case Rep. 2024 Sep 21;12:2050313X241283262. doi: 10.1177/2050313X241283262. eCollection 2024.

Abstract

The management of schizoaffective disorder bipolar type often involves a combination of pharmacotherapy and psychotherapy. Clozapine, an effective antipsychotic for treatment-resistant schizophrenia, and oxcarbazepine, a mood stabilizer, is a commonly prescribed medication. We present a case report of a 56-year-old male with schizoaffective disorder bipolar type who experienced subtherapeutic clozapine levels despite dose adjustments, leading to deteriorating symptoms. Oxcarbazepine, a weak CYP450 inducer, likely contributed to the subtherapeutic levels. Additionally, the pharmacogenetic analysis revealed a CYP1A2 *1F/*1F genotype, indicating normal activity with a potential for decreased serum levels and adverse events in the presence of inducers. The patient was eventually stabilized on a regimen of lithium, paliperidone, and quetiapine, avoiding oxcarbazepine. This case highlights the importance of considering individual patient factors, including pharmacogenetics when managing treatment-resistant patients. Monitoring serum clozapine levels and assessing enzyme activity before initiating therapy may help optimize treatment outcomes and minimize adverse events.

摘要

双相型分裂情感性障碍的治疗通常需要药物治疗和心理治疗相结合。氯氮平是一种治疗难治性精神分裂症的有效抗精神病药物,奥卡西平是一种心境稳定剂,它们是常用的处方药。我们报告一例56岁双相型分裂情感性障碍男性患者,尽管调整了剂量,但氯氮平水平仍低于治疗剂量,导致症状恶化。奥卡西平是一种弱CYP450诱导剂,可能导致了低于治疗剂量的水平。此外,药物遗传学分析显示该患者为CYP1A2 *1F/*1F基因型,表明在有诱导剂存在的情况下,其活性正常,但血清水平可能降低并可能出现不良事件。该患者最终通过锂盐、帕利哌酮和喹硫平的联合治疗方案病情稳定,避免使用奥卡西平。该病例强调了在治疗难治性患者时考虑个体患者因素(包括药物遗传学)的重要性。在开始治疗前监测血清氯氮平水平并评估酶活性,可能有助于优化治疗效果并将不良事件降至最低。

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