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卢美他定与常用抗逆转录病毒治疗药物相互作用的个体参与者数据群体药代动力学荟萃分析。

An Individual Participant Data Population Pharmacokinetic Meta-analysis of Drug-Drug Interactions between Lumefantrine and Commonly Used Antiretroviral Treatment.

机构信息

Division of Clinical Pharmacology, Department of Medicine, University of Cape Town, Cape Town, South Africa.

WorldWide Antimalarial Resistance Network (WWARN) Pharmacology/Southern African Regional Centre, University of Cape Town, Cape Town, South Africa.

出版信息

Antimicrob Agents Chemother. 2020 Apr 21;64(5). doi: 10.1128/AAC.02394-19.

Abstract

Treating malaria in HIV-coinfected individuals should consider potential drug-drug interactions. Artemether-lumefantrine is the most widely recommended treatment for uncomplicated malaria globally. Lumefantrine is metabolized by CYP3A4, an enzyme that commonly used antiretrovirals often induce or inhibit. A population pharmacokinetic meta-analysis was conducted using individual participant data from 10 studies with 6,100 lumefantrine concentrations from 793 nonpregnant adult participants (41% HIV-malaria-coinfected, 36% malaria-infected, 20% HIV-infected, and 3% healthy volunteers). Lumefantrine exposure increased 3.4-fold with coadministration of lopinavir-ritonavir-based antiretroviral therapy (ART), while it decreased by 47% with efavirenz-based ART and by 59% in the patients with rifampin-based antituberculosis treatment. Nevirapine- or dolutegravir-based ART and malaria or HIV infection were not associated with significant effects. Monte Carlo simulations showed that those on concomitant efavirenz or rifampin have 49% and 80% probability of day 7 concentrations <200 ng/ml, respectively, a threshold associated with an increased risk of treatment failure. The risk of achieving subtherapeutic concentrations increases with larger body weight. An extended 5-day and 6-day artemether-lumefantrine regimen is predicted to overcome these drug-drug interactions with efavirenz and rifampin, respectively.

摘要

治疗 HIV 合并疟疾感染者时应考虑潜在的药物相互作用。青蒿琥酯-咯萘啶是目前全球推荐用于治疗无并发症疟疾的最广泛的治疗方法。咯萘啶主要通过 CYP3A4 代谢,而这种酶常被常用于治疗艾滋病的抗逆转录病毒药物诱导或抑制。对 10 项研究的个体参与者数据进行了群体药代动力学meta 分析,这些研究共涉及 6100 个咯萘啶浓度,来自 793 名未怀孕的成年参与者(41%为 HIV-疟疾合并感染,36%为疟疾感染,20%为 HIV 感染,3%为健康志愿者)。与洛匹那韦/利托那韦为基础的抗逆转录病毒治疗(ART)同时使用时,咯萘啶的暴露量增加了 3.4 倍,而与依非韦伦为基础的 ART 同时使用时则降低了 47%,与利福平为基础的抗结核治疗同时使用时降低了 59%。奈韦拉平或多替拉韦为基础的 ART 以及疟疾或 HIV 感染与显著影响无关。蒙特卡罗模拟显示,同时使用依非韦伦或利福平的患者,第 7 天的浓度<200ng/ml 的概率分别为 49%和 80%,这一阈值与治疗失败风险增加有关。达到治疗浓度的风险随着体重的增加而增加。预测延长 5 天和 6 天的青蒿琥酯-咯萘啶方案分别可以克服与依非韦伦和利福平的药物相互作用。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7d70/7179577/8dd04f87285b/AAC.02394-19-f0001.jpg

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