Mulder Hans, Herder Anita, Wilmink Frederik W, Tamminga Wim J, Belitser Svetlana V, Egberts Antoine C G
Department of Pharmacoepidemiology and Pharmacotherapy, Utrecht Institute for Pharmaceutical Sciences (UIPS), Utrecht University, The Netherlands.
Pharmacoepidemiol Drug Saf. 2006 Feb;15(2):107-14. doi: 10.1002/pds.1173.
This retrospective follow-up study investigates whether cytochrome P450-2D6 (CYP2D6) genotype explains variability in plasma concentrations of psychotropic drugs in daily psychiatric practice.
The study population consisted of 62 hospitalised psychiatric patients genotyped for CYP2D6. Primary endpoint was the normalised plasma concentration ratio which was defined as the [measured concentration]/[mean therapeutic concentration] allowing comparison of plasma concentrations of different substrates. Secondary endpoint was a plasma concentration above the therapeutic range. The determinant was CYP2D6 genotype classified as ultrarapid metaboliser (UM), extensive metaboliser (EM), intermediate metaboliser (IM), or poor metaboliser (PM). The relation between CYP2D6 genotype and the normalised plasma concentration ratio was assessed with a linear mixed-effects model after adjustment for the Prescribed Daily Dose (PDD). The risk of having a plasma concentration above the therapeutic range was assessed with a logistic mixed-effects model.
For antidepressants, CYP2D6 genotype PM (1.68 (95%CI: 1.01-2.28)) and IM (1.09 (95%CI: 0.77-1.29)) were associated with higher normalised plasma concentration ratios of antidepressants compared to EMs (0.56 (95%CI: 0.26-0.74)). In addition, the risk of a plasma concentration above the therapeutic range was increased for PMs (OR 33.1 (95%CI: 2.0-544.6)) and IMs (OR 8.2 (95%CI: 1.1-60.3)) relative to EMs using antidepressants. CYP2D6 genotype could not clearly explain variability in plasma concentrations of antipsychotics possibly due to a low frequency of therapeutic drug monitoring (TDM) in antipsychotics primarily metabolised by CYP2D6 in daily psychiatric practice.
CYP2D6 genotype contributes to clinically relevant variability in plasma concentrations of antidepressants but probably not antipsychotics in daily clinical practice.
这项回顾性随访研究调查了细胞色素P450-2D6(CYP2D6)基因型是否能解释日常精神科实践中精神药物血浆浓度的变异性。
研究人群包括62例接受CYP2D6基因分型的住院精神科患者。主要终点是标准化血浆浓度比,其定义为[测量浓度]/[平均治疗浓度],以便比较不同底物的血浆浓度。次要终点是血浆浓度高于治疗范围。决定因素是CYP2D6基因型,分为超快代谢者(UM)、广泛代谢者(EM)、中间代谢者(IM)或慢代谢者(PM)。在调整规定日剂量(PDD)后,使用线性混合效应模型评估CYP2D6基因型与标准化血浆浓度比之间的关系。使用逻辑混合效应模型评估血浆浓度高于治疗范围的风险。
对于抗抑郁药,与EMs(0.56(95%CI:0.26-0.74))相比,CYP2D6基因型PM(1.68(95%CI:1.01-2.28))和IM(1.09(95%CI:0.77-1.29))与更高的抗抑郁药标准化血浆浓度比相关。此外,与使用抗抑郁药的EMs相比,PMs(OR 33.1(95%CI:2.0-544.6))和IMs(OR 8.2(95%CI:1.1-60.3))血浆浓度高于治疗范围的风险增加。CYP2D6基因型无法清楚地解释抗精神病药物血浆浓度的变异性,这可能是由于在日常精神科实践中,主要由CYP2D6代谢的抗精神病药物的治疗药物监测(TDM)频率较低。
在日常临床实践中,CYP2D6基因型导致抗抑郁药血浆浓度出现临床相关的变异性,但可能不会导致抗精神病药物血浆浓度出现这种变异性。