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伊曲康唑对阿托伐他汀药代动力学的影响程度大于西立伐他汀或普伐他汀。

Itraconazole alters the pharmacokinetics of atorvastatin to a greater extent than either cerivastatin or pravastatin.

作者信息

Mazzu A L, Lasseter K C, Shamblen E C, Agarwal V, Lettieri J, Sundaresen P

机构信息

Bayer Corporation Pharmaceutical Division, Department of Clinical Pharmacology, West Haven, Conn 06516, USA.

出版信息

Clin Pharmacol Ther. 2000 Oct;68(4):391-400. doi: 10.1067/mcp.2000.110537.

Abstract

BACKGROUND

3-Hydroxy-3-methylglutaryl coenzyme A reductase inhibitors (statins) are metabolized by distinct pathways that may alter the extent of drug-drug interactions. Cerivastatin is metabolized by cytochrome P450 (CYP)3A4 and CYP2C8. Atorvastatin is metabolized solely by CYP3A4, and pravastatin metabolism is not well defined. Coadministration of higher doses of these statins with CYP3A4 inhibitors has the potential for eliciting adverse drug-drug interactions.

OBJECTIVE

To determine the comparative effect of itraconazole, a potent CYP3A4 inhibitor, on the pharmacokinetics of cerivastatin, atorvastatin, and pravastatin.

METHODS

In this single-site, randomized, three-way crossover, open-labeled study, healthy subjects (n = 18) received single doses of cerivastatin 0.8 mg, atorvastatin 20 mg, or pravastatin 40 mg without and with itraconazole 200 mg. Pharmacokinetic parameters [AUC(0-infinity), AUC(0-tn), peak concentration (Cmax), time to reach Cmax (tmax), and half-life (t1/2)] were determined for parent statins and major metabolites.

RESULTS

Concomitant cerivastatin/itraconazole treatment produced small elevations in the cerivastatin AUC(0-infinity), Cmax, and t1/2 (27%, 25%, and 19%, respectively; P < .05 versus cerivastatin alone). Itraconazole coadministration produced similar changes in pravastatin pharmacokinetics [AUC elevated 51% (P < .05 versus pravastatin alone), 24% (Cmax), and 23% (t1/2), respectively]. However, itraconazole dramatically increased atorvastatin AUC (150%), Cmax (38%), and t1/2 (30%) (P < .05). The elevation in atorvastatin AUC was significantly greater than that of cerivastatin (P < .005) or pravastatin (P < .005).

CONCLUSION

Itraconazole markedly elevated atorvastatin plasma levels (2.5-fold) after 20 mg dosing, suggesting that concomitant itraconazole/atorvastatin therapy be carefully considered. Itraconazole produced modest elevations in the plasma levels of cerivastatin 0.8 mg or pravastatin 40 mg (1.3-fold and 1.5-fold, respectively), indicating that combination treatment with itraconazole with cerivastatin or pravastatin may be preferable.

摘要

背景

3-羟基-3-甲基戊二酰辅酶A还原酶抑制剂(他汀类药物)通过不同途径代谢,这可能会改变药物相互作用的程度。西立伐他汀由细胞色素P450(CYP)3A4和CYP2C8代谢。阿托伐他汀仅由CYP3A4代谢,普伐他汀的代谢情况尚不明确。这些他汀类药物与CYP3A4抑制剂高剂量合用有可能引发不良药物相互作用。

目的

确定强效CYP3A4抑制剂伊曲康唑对西立伐他汀、阿托伐他汀和普伐他汀药代动力学的比较影响。

方法

在这项单中心、随机、三交叉、开放标签研究中,18名健康受试者分别接受单剂量的西立伐他汀0.8毫克、阿托伐他汀20毫克或普伐他汀40毫克,给药时不服用伊曲康唑和服用200毫克伊曲康唑。测定了母体他汀类药物及其主要代谢产物的药代动力学参数[AUC(0-∞)、AUC(0-tn)、峰浓度(Cmax)、达峰时间(tmax)和半衰期(t1/2)]。

结果

西立伐他汀与伊曲康唑联合治疗使西立伐他汀的AUC(0-∞)、Cmax和t1/2略有升高(分别升高27%、25%和19%;与单独使用西立伐他汀相比,P < 0.05)。伊曲康唑合用使普伐他汀药代动力学发生类似变化[AUC升高51%(与单独使用普伐他汀相比,P < 0.05)、Cmax升高24%、t1/2升高23%]。然而,伊曲康唑使阿托伐他汀的AUC(升高150%)、Cmax(升高38%)和t1/2(升高30%)显著增加(P < 0.05)。阿托伐他汀AUC的升高显著大于西立伐他汀(P < 0.005)或普伐他汀(P < 0.005)。

结论

服用20毫克剂量后,伊曲康唑使阿托伐他汀血浆水平显著升高(2.5倍),提示应谨慎考虑伊曲康唑与阿托伐他汀联合治疗。伊曲康唑使0.8毫克西立伐他汀或40毫克普伐他汀的血浆水平适度升高(分别为1.3倍和1.5倍),表明伊曲康唑与西立伐他汀或普伐他汀联合治疗可能更可取。

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