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洛匹那韦/利托那韦对HIV感染患者中替诺福韦肾清除率的影响。

The effect of lopinavir/ritonavir on the renal clearance of tenofovir in HIV-infected patients.

作者信息

Kiser J J, Carten M L, Aquilante C L, Anderson P L, Wolfe P, King T M, Delahunty T, Bushman L R, Fletcher C V

机构信息

School of Pharmacy, University of Colorado at Denver and Health Sciences Center, Denver, Colorado, USA.

出版信息

Clin Pharmacol Ther. 2008 Feb;83(2):265-72. doi: 10.1038/sj.clpt.6100269. Epub 2007 Jun 27.

Abstract

We determined the effects of lopinavir/ritonavir on tenofovir renal clearance. Human immunodeficiency virus-infected subjects taking tenofovir disoproxil fumarate (TDF) were matched on age, race, and gender and were enrolled into one of the following two groups: group 1: subjects taking TDF plus lopinavir/ritonavir plus other nucleoside reverse transcriptase inhibitors (NRTIs); group 2: subjects taking TDF plus NRTIs and/or non-NRTIs but no protease inhibitors. Twenty-four-hour blood and urine collections were carried out in subjects for tenofovir quantification. Drug transporter genotype associations with tenofovir pharmacokinetics were examined. In 30 subjects, median (range) tenofovir apparent oral clearance, renal clearance, and fraction excreted in urine were 34.6 l/h (20.6-89.5), 11.3 l/h (6.2-22.6), and 0.33 (0.23-0.5), respectively. After adjusting for renal function, tenofovir renal clearance was 17.5% slower (P=0.04) in subjects taking lopinavir/ritonavir versus those not taking a protease inhibitor, consistent with a renal interaction between these drugs. Future studies should clarify the exact mechanism and whether there is an increased risk of nephrotoxicity.

摘要

我们确定了洛匹那韦/利托那韦对替诺福韦肾清除率的影响。将服用富马酸替诺福韦二吡呋酯(TDF)的人类免疫缺陷病毒感染受试者按年龄、种族和性别进行匹配,并纳入以下两组之一:第1组:服用TDF加洛匹那韦/利托那韦加其他核苷类逆转录酶抑制剂(NRTIs)的受试者;第2组:服用TDF加NRTIs和/或非NRTIs但未服用蛋白酶抑制剂的受试者。对受试者进行24小时血液和尿液采集以定量替诺福韦。研究了药物转运体基因型与替诺福韦药代动力学的相关性。在30名受试者中,替诺福韦的中位(范围)表观口服清除率、肾清除率和尿中排泄分数分别为34.6 l/h(20.6 - 89.5)、11.3 l/h(6.2 - 22.6)和0.33(0.23 - 0.5)。在调整肾功能后,服用洛匹那韦/利托那韦的受试者的替诺福韦肾清除率比未服用蛋白酶抑制剂的受试者慢17.5%(P = 0.04),这与这些药物之间的肾相互作用一致。未来的研究应阐明确切机制以及是否存在肾毒性风险增加的情况。

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