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CYP3A4*22多态性和CYP2D6多态性对精神科患者血清阿立哌唑、氟哌啶醇、匹莫齐特和利培酮浓度的影响。

The Influence of the CYP3A4*22 Polymorphism and CYP2D6 Polymorphisms on Serum Concentrations of Aripiprazole, Haloperidol, Pimozide, and Risperidone in Psychiatric Patients.

作者信息

van der Weide Karen, van der Weide Jan

机构信息

From the *Department of Clinical Chemistry, St Jansdal Hospital, Harderwijk; and †GGz Centraal, Veldwijk, Ermelo, The Netherlands.

出版信息

J Clin Psychopharmacol. 2015 Jun;35(3):228-36. doi: 10.1097/JCP.0000000000000319.

Abstract

INTRODUCTION

Cytochrome P450 3A4 (CYP3A4) is involved in the metabolism of greater than 50% of the prescribed drugs. Recently, the CYP3A422 allele was reported to be associated with lower CYP3A4 expression and activity. Quetiapine, an antipsychotic metabolized by only CYP3A4, displayed higher serum levels in CYP3A422 carriers. Aripiprazole, haloperidol, pimozide, and risperidone are antipsychotics that are metabolized by CYP3A4 and CYP2D6. We investigated to which degree the CYP3A4*22 single-nucleotide polymorphism affects serum concentrations of patients receiving these drugs and compared this with the influence of CYP2D6 polymorphisms.

METHODS

Eight hundred thirty-four adult patients were included in this study, of whom 130 used aripiprazole, 312 used haloperidol, 86 used pimozide, and 396 used risperidone. Serum levels of the drug and, if available, their active metabolites were collected as well as information on dose. Patients were genotyped for CYP3A4*22 using restriction fragment length polymorphism analysis. Genotyping for CYP2D6 was done with allele-specific polymerase chain reaction.

RESULTS

No differences were found in serum (dose-corrected) concentrations of the antipsychotics between CYP3A4*22 wild-type and carrier groups. In contrast, CYP2D6 genotype did affect dose-corrected concentrations of the antipsychotics: for example, median dose-corrected concentrations were 56%, 86%, and 400% higher in predicted poor metabolizers versus extensive metabolizers for aripiprazole (P = 0.004), haloperidol (P > 0.001), and risperidone (P < 0.001), respectively, although a multiple regression analysis showed that only 4% to 17% of the variation in these concentrations could be explained by CYP2D6 status.

CONCLUSIONS

Heterozygous presence of CYP3A4*22 does not increase serum levels of antipsychotics metabolized by both CYP3A4 and CYP2D6, whereas CYP2D6 polymorphisms do affect serum levels to a limited extent.

摘要

引言

细胞色素P450 3A4(CYP3A4)参与超过50%的处方药代谢。最近,有报道称CYP3A422等位基因与较低的CYP3A4表达和活性相关。喹硫平是一种仅由CYP3A4代谢的抗精神病药物,在CYP3A422携带者中血清水平较高。阿立哌唑、氟哌啶醇、匹莫齐特和利培酮是由CYP3A4和CYP2D6代谢的抗精神病药物。我们研究了CYP3A4*22单核苷酸多态性对接受这些药物治疗患者血清浓度的影响程度,并将其与CYP2D6多态性的影响进行比较。

方法

本研究纳入了834名成年患者,其中130人使用阿立哌唑,312人使用氟哌啶醇,86人使用匹莫齐特,396人使用利培酮。收集了药物及其活性代谢物(如可用)的血清水平以及剂量信息。使用限制性片段长度多态性分析对患者进行CYP3A4*22基因分型。使用等位基因特异性聚合酶链反应对CYP2D6进行基因分型。

结果

在CYP3A4*22野生型和携带者组之间,抗精神病药物的血清(剂量校正)浓度未发现差异。相比之下,CYP2D6基因型确实影响抗精神病药物的剂量校正浓度:例如,对于阿立哌唑(P = 0.004)、氟哌啶醇(P > 0.001)和利培酮(P < 0.001),预测的慢代谢者与快代谢者相比,剂量校正浓度中位数分别高出56%、86%和400%,尽管多元回归分析表明这些浓度变化中只有4%至17%可由CYP2D6状态解释。

结论

CYP3A4*22杂合子的存在不会增加由CYP3A4和CYP2D6共同代谢的抗精神病药物的血清水平,而CYP2D6多态性在一定程度上确实会影响血清水平。

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