CYP2D6基因型与米氮平、勉色林血清浓度的关系

IF 2.7 4区 医学 Q2 PHARMACOLOGY & PHARMACY
Kristine Hole, Espen Molden
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引用次数: 0

摘要

本研究的目的是探讨CYP2D6基因型对米氮平和米安色林血清浓度的影响。患者回顾性纳入治疗药物监测服务。采用多元线性回归分析CYP2D6基因型、年龄和性别对米氮平和米安色林浓度剂量比(C/D)的影响。该研究包括2315名米氮平患者和474名米安色林患者,他们被分配到CYP2D6不良代谢(pm)、中间代谢(IMs)、正常代谢(NMs)和超快速代谢(UMs)的基因型预测表型组。多元线性回归分析显示,CYP2D6患者中米氮平C/D比值分别比NMs高18%和14% (p≤0.004)。对于米安色林,与NMs相比,pm组和IMs组的C/D比率分别高出80%和45% (p < 0.001)。两种药物的C/D比值均无差异(p≥0.3)。综上所述,CYP2D6基因型仅与米氮平血清浓度的微小变化相关。CYP2D6基因型与米安色林血清浓度的相关性更大,CYP2D6 pm的米安色林C/D比值比NMs高80%。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Association Between CYP2D6 Genotypes and Serum Concentrations of Mirtazapine and Mianserin

The aim of the present study was to investigate the effect of CYP2D6 genotypes on mirtazapine and mianserin serum concentrations. Patients were included retrospectively from a therapeutic drug monitoring service. Multiple linear regression analysis was used to investigate the effect of CYP2D6 genotype, age and sex on mirtazapine and mianserin concentration-to-dose (C/D) ratio. The study included 2315 mirtazapine patients and 474 mianserin patients who were assigned to the genotype-predicted phenotype groups of CYP2D6 poor metabolizers (PMs), intermediate metabolizers (IMs), normal metabolizers (NMs) and ultrarapid metabolizers (UMs). Multiple linear regression analysis revealed 18% and 14% higher mirtazapine C/D ratio in CYP2D6 PMs and IMs, respectively, compared with NMs (p ≤ 0.004). For mianserin, the C/D ratio was 80% and 45% higher in PMs and IMs, respectively, compared with NMs (p < 0.001). The C/D ratio in UMs did not differ from NMs for either drug (p ≥ 0.3). In conclusion, CYP2D6 genotype was only associated with a minor change in mirtazapine serum concentration. The association between CYP2D6 genotype and mianserin serum concentration was greater, with 80% higher mianserin C/D ratio in CYP2D6 PMs compared with NMs.

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来源期刊
CiteScore
5.60
自引率
6.50%
发文量
126
审稿时长
1 months
期刊介绍: Basic & Clinical Pharmacology and Toxicology is an independent journal, publishing original scientific research in all fields of toxicology, basic and clinical pharmacology. This includes experimental animal pharmacology and toxicology and molecular (-genetic), biochemical and cellular pharmacology and toxicology. It also includes all aspects of clinical pharmacology: pharmacokinetics, pharmacodynamics, therapeutic drug monitoring, drug/drug interactions, pharmacogenetics/-genomics, pharmacoepidemiology, pharmacovigilance, pharmacoeconomics, randomized controlled clinical trials and rational pharmacotherapy. For all compounds used in the studies, the chemical constitution and composition should be known, also for natural compounds.
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