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阿托伐他汀与钙调神经磷酸酶抑制剂联合治疗:与他克莫司无相互作用。

Combined therapy with atorvastatin and calcineurin inhibitors: no interactions with tacrolimus.

作者信息

Lemahieu W P D, Hermann M, Asberg A, Verbeke K, Holdaas H, Vanrenterghem Y, Maes B D

机构信息

Department of Medicine, Division of Nephrology and Laboratory of Gastrointestinal Research, University Hospitals Gasthuisberg, Leuven, Belgium.

出版信息

Am J Transplant. 2005 Sep;5(9):2236-43. doi: 10.1111/j.1600-6143.2005.01005.x.

DOI:10.1111/j.1600-6143.2005.01005.x
PMID:16095503
Abstract

Increased systemic exposure to statins and consequent risk for complications has been reported in patients concomitantly treated with cyclosporin A (CsA). This has been ascribed to inhibition of drug catabolism by cytochrome P450 3A4 (CYP3A4) or drug transport by P-glycoprotein (PGP) and organic anion transporting polypeptide (OATP1B1). It is not known whether the combination of statins and tacrolimus (Tac) also suffers from this drawback. Therefore, a pharmacokinetic study of atorvastatin and its metabolites was performed in 13 healthy volunteers after 4 days' treatment, and after short (12 h) concomitant exposure to CsA and Tac. A complementary assessment of overall CYP, and hepatic and intestinal CYP3A4+PGP activity was performed after each treatment episode and compared to baseline (no drugs). Systemic exposure to atorvastatin acid and its metabolites was significantly increased when administered with CsA. In contrast, intake of Tac did not have any impact on atorvastatin pharmacokinetics. Concomitantly, a profound decrease of hepatic and intestinal PGP and an increase of intestinal CYP3A4 were noted with CsA, whereas no effect was seen after atorvastatin therapy with or without Tac. Based on these findings treatment with Tac appears a safer option for patients needing a combination of statins and calcineurin inhibitors.

摘要

据报道,同时接受环孢素A(CsA)治疗的患者中,他汀类药物的全身暴露增加,并发症风险随之升高。这归因于细胞色素P450 3A4(CYP3A4)对药物分解代谢的抑制,或P-糖蛋白(PGP)和有机阴离子转运多肽(OATP1B1)对药物转运的抑制。尚不清楚他汀类药物与他克莫司(Tac)联合使用是否也存在这一缺点。因此,在13名健康志愿者接受4天治疗后,以及短期(12小时)同时暴露于CsA和Tac后,对阿托伐他汀及其代谢物进行了药代动力学研究。在每个治疗阶段后,对总体CYP以及肝脏和肠道CYP3A4+PGP活性进行了补充评估,并与基线(未用药)进行比较。与CsA联用时,阿托伐他汀酸及其代谢物的全身暴露显著增加。相比之下,摄入Tac对阿托伐他汀的药代动力学没有任何影响。同时,CsA使肝脏和肠道PGP显著降低,肠道CYP3A4增加,而阿托伐他汀单独治疗或联合Tac治疗后均未见此效应。基于这些发现,对于需要联合使用他汀类药物和钙调神经磷酸酶抑制剂的患者,Tac治疗似乎是一个更安全的选择。

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