Damborská Alena, Hanáková Lenka, Pindurová Eva, Horská Kateřina
Department of Psychiatry, University Hospital Brno and Faculty of Medicine, Masaryk University, Brno, Czechia.
CEITEC - Central European Institute of Technology, Masaryk University, Brno, Czechia.
Front Pharmacol. 2024 Sep 4;15:1444857. doi: 10.3389/fphar.2024.1444857. eCollection 2024.
The cytochrome P450 2D6 (CYP2D6) is an enzyme involved in the oxidative biotransformation of various widely used drugs, including paroxetine, a substrate and strong inhibitor of the enzyme. The aim is to report on a case of protracted intoxication with paroxetine after a single overdose in a genotype-predicted intermediate CYP2D6 metabolizer.
A 49-year-old man was receiving chronic treatment for more than 6 years with paroxetine 60 mg/day for an indication of agoraphobia. The patient ingested fifty 20 mg tablets of paroxetine in a suicide attempt. The toxic plasma level, accompanied by delirium, persisted for approximately 1 month after the overdose. According to the genotype profile, the patient was evaluated as an intermediate metabolizer with reduced CYP2D6 enzyme activity.
As a consequence of the suicide attempt with overdose and the chronic paroxetine treatment that preceded it, phenoconversion to a poor metabolizer with very low CYP2D6 enzyme activity is suggested as contributing to an extremely long intoxication accompanied by delirium. Prolonged monitoring over a standard 24 h of both physical symptoms and drug plasma levels, together with a genetic profile assessment and phenoconversion consideration, is recommended after a single overdose in patients chronically treated with paroxetine.
细胞色素P450 2D6(CYP2D6)是一种参与多种广泛使用药物氧化生物转化的酶,这些药物包括帕罗西汀,它是该酶的底物和强效抑制剂。本文旨在报告1例基因型预测为CYP2D6中间代谢型的患者单次过量服用帕罗西汀后发生的迁延性中毒病例。
一名49岁男性因广场恐惧症接受帕罗西汀60mg/天的长期治疗超过6年。该患者为自杀企图服用了50片20mg的帕罗西汀。过量服药后,伴有谵妄的中毒血浆水平持续了约1个月。根据基因型分析,该患者被评估为CYP2D6酶活性降低的中间代谢型。
由于过量服药自杀企图以及之前的帕罗西汀长期治疗,提示表型转化为CYP2D6酶活性极低的慢代谢型是导致伴有谵妄的极长时间中毒的原因。对于长期接受帕罗西汀治疗的患者单次过量服药后,建议对身体症状和药物血浆水平进行超过标准24小时的长期监测,并进行基因分析评估和表型转化考量。