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CYP1A2和CYP2D6基因多态性对氯氮平治疗患者药物代谢、胰岛素及血脂升高和胰岛素抵抗的影响。

Impact of CYP1A2 and CYP2D6 polymorphisms on drug metabolism and on insulin and lipid elevations and insulin resistance in clozapine-treated patients.

作者信息

Melkersson Kristina I, Scordo M Gabriella, Gunes Arzu, Dahl Marja-Liisa

机构信息

Department of Molecular Medicine and Surgery, Karolinska Institute, Stockholm, Sweden.

出版信息

J Clin Psychiatry. 2007 May;68(5):697-704. doi: 10.4088/jcp.v68n0506.

Abstract

OBJECTIVE

Adverse metabolic effects of atypical antipsychotics have increasingly been recognized. Recently, we found that levels of insulin and triglycerides increased by increasing serum clozapine concentration in clozapine-treated patients. As these insulin and triglyceride elevations probably are drug concentration-dependent, they also would be expected to be drug metabolism-related. The genetically polymorphic cytochromes P450 CYP1A2 and CYP2D6 catalyze the metabolism of clozapine. The aim of this study was to evaluate the impact of CYP1A2 and CYP2D6 polymorphisms on serum drug and metabolite levels and on insulin and triglyceride elevations and insulin resistance in patients receiving clozapine.

METHOD

Seventeen clozapine-treated patients were genotyped for CYP1A2 and CYP2D6 by polymerase chain reaction-based methods. Serum concentrations of clozapine and its N-desmethylmetabolite, blood glucose, and serum levels of insulin, C-peptide, triglycerides, and cholesterol were analyzed, and homeostasis model assessment index for insulin resistance (HOMA-IR) was determined.

RESULTS

Clozapine and N-desmethylclozapine concentration-to-dose (C/D) ratios were significantly higher in patients carrying 2 CYP1A2 single nucleotide polymorphisms (SNPs), previously suggested to cause low enzyme activity, compared to those with no such SNPs (p < .05). In contrast, clozapine and N-desmethylclozapine C/D ratios were not related to the CYP2D6 genotype. Furthermore, patients with elevated insulin levels more frequently carried CYP1A2*1C and/or *1D alleles, had higher clozapine and N-desmethylclozapine C/D ratios, and had higher lipid levels and HOMA-IR, compared to patients with normal insulin levels (p < .05).

CONCLUSION

CYP1A2 variants *1C and *1D seem to be associated with higher serum clozapine concentrations and an increased risk of developing insulin and lipid elevations and insulin resistance on a given dose of clozapine.

摘要

目的

非典型抗精神病药物的不良代谢作用已日益受到关注。最近,我们发现氯氮平治疗的患者中,随着血清氯氮平浓度升高,胰岛素和甘油三酯水平也会升高。由于这些胰岛素和甘油三酯的升高可能与药物浓度有关,因此预计它们也与药物代谢相关。基因多态性细胞色素P450 CYP1A2和CYP2D6催化氯氮平的代谢。本研究的目的是评估CYP1A2和CYP2D6基因多态性对接受氯氮平治疗患者的血清药物和代谢物水平、胰岛素和甘油三酯升高以及胰岛素抵抗的影响。

方法

采用基于聚合酶链反应的方法对17例接受氯氮平治疗的患者进行CYP1A2和CYP2D6基因分型。分析氯氮平及其N-去甲基代谢物的血清浓度、血糖、胰岛素、C肽、甘油三酯和胆固醇的血清水平,并测定胰岛素抵抗的稳态模型评估指数(HOMA-IR)。

结果

与无此类单核苷酸多态性(SNP)的患者相比,携带2个先前提示会导致低酶活性的CYP1A2单核苷酸多态性的患者,氯氮平和N-去甲基氯氮平的浓度-剂量(C/D)比显著更高(p < 0.05)。相比之下,氯氮平和N-去甲基氯氮平的C/D比与CYP2D6基因型无关。此外,与胰岛素水平正常的患者相比,胰岛素水平升高的患者更频繁地携带CYP1A21C和/或1D等位基因,氯氮平和N-去甲基氯氮平的C/D比更高,血脂水平和HOMA-IR也更高(p < 0.05)。

结论

CYP1A2变体1C和1D似乎与较高的血清氯氮平浓度以及在给定剂量氯氮平治疗下发生胰岛素和血脂升高及胰岛素抵抗的风险增加有关。

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