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