Pharmacokinetics of abacavir and lamivudine in infants living with HIV with and without rifampicin co-treatment.

IF 4.1 2区 医学 Q1 INFECTIOUS DISEASES
Laize Sílvia Dos Anjos Botas Beca, Vivian Mumbiro, Mutsa Bwakura, Hilda A Mujuru, Shepherd Mudzingwa, Alfredo Tagarro, Sara Domínguez-Rodríguez, Victor Musiime, Damalie Nalwanga, W Chris Buck, Jahit Sacarlal, Chishala Chabala, Bwendo Nduna Chansa, Pablo Rojo, David M Burger, Cinta Moraleda, Tom G Jacobs
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引用次数: 0

Abstract

Background: Lamivudine and abacavir are key components of first-line paediatric antiretroviral therapy (ART). Rifampicin is part of drug-sensitive TB treatment in children. Rifampicin induces UDP-glucuronosyltransferases and renal transporters and inhibits gastrointestinal transporters involved in the pharmacokinetics of abacavir and lamivudine, but pharmacokinetic data on this potential interaction in infants are scarce.

Objective: To evaluate the effect of rifampicin on the pharmacokinetics of abacavir and lamivudine in infants aged 28-365 days and weighing >3 kg.

Methods: This pharmacokinetic sub-study was nested within the EMPIRICAL trial (NCT03915366). Eighteen infants from Mozambique, Uganda, Zambia and Zimbabwe received once-daily fixed-dose abacavir/lamivudine with dolutegravir according to WHO guidelines. Five infants received ART alone and 13 received ART plus rifampicin-based tuberculosis treatment. Abacavir/lamivudine dosing was unchanged during rifampicin co-treatment. Six plasma concentrations were measured over 24 h and analysed using non-compartmental pharmacokinetic analysis.

Results: Median (IQR) age and weight were 6.8 (5.2-10.2) months and 6.0 (5.3-6.8) kg, respectively, and were comparable between groups. Abacavir exposure was comparable with and without rifampicin (AUC0-24h: 21.9 versus 21.0 h mg/L; Cmax: 6.2 versus 6.3 mg/L, respectively). Lamivudine exposure was also comparable (AUC0-24h: 12.6 versus 12.4 h mg/LL, respectively). The slightly higher Cmax (2.4 versus 1.9 mg/L) in the rifampicin group is probably due to interindividual variability or increased absorption from rifampicin's inhibition of gastrointestinal drug transporters, and considered not clinically relevant.

Conclusions: Rifampicin co-treatment had minimal impact on abacavir and lamivudine pharmacokinetics in infants. Dose adjustment of abacavir/lamivudine is not required during rifampicin-containing tuberculosis treatment.

阿巴卡韦和拉米夫定在接受和不接受利福平联合治疗的艾滋病毒婴儿中的药代动力学。
背景:拉米夫定和阿巴卡韦是一线儿科抗逆转录病毒治疗(ART)的关键成分。利福平是儿童药物敏感型结核病治疗的一部分。利福平诱导udp -葡萄糖醛基转移酶和肾脏转运蛋白,并抑制参与阿巴卡韦和拉米夫定药代动力学的胃肠道转运蛋白,但婴儿中这种潜在相互作用的药代动力学数据很少。目的:探讨利福平对28 ~ 365日龄、体重50 ~ 3kg婴儿阿巴卡韦和拉米夫定药动学的影响。方法:将药代动力学亚研究嵌套在实证试验(NCT03915366)中。根据世卫组织指南,来自莫桑比克、乌干达、赞比亚和津巴布韦的18名婴儿每天接受一次固定剂量的阿巴卡韦/拉米夫定和多替格拉韦。5名婴儿单独接受抗逆转录病毒治疗,13名接受抗逆转录病毒治疗加以利福平为基础的结核病治疗。在利福平联合治疗期间,阿巴卡韦/拉米夫定的剂量不变。在24小时内测量6种血浆浓度,并使用非室室药代动力学分析进行分析。结果:中位(IQR)年龄和体重分别为6.8(5.2-10.2)个月和6.0 (5.3-6.8)kg,组间具有可比性。阿巴卡韦暴露与利福平和不含利福平相当(AUC0-24h: 21.9和21.0 h mg/L; Cmax分别:6.2和6.3 mg/L)。拉米夫定暴露也具有可比性(AUC0-24h:分别为12.6和12.4 h mg/LL)。利福平组Cmax略高(2.4 vs 1.9 mg/L)可能是由于个体间差异或利福平抑制胃肠道药物转运体导致吸收增加,被认为与临床无关。结论:利福平联合治疗对婴儿阿巴卡韦和拉米夫定的药代动力学影响最小。在含利福平的结核病治疗期间,不需要调整阿巴卡韦/拉米夫定的剂量。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
CiteScore
9.20
自引率
5.80%
发文量
423
审稿时长
2-4 weeks
期刊介绍: The Journal publishes articles that further knowledge and advance the science and application of antimicrobial chemotherapy with antibiotics and antifungal, antiviral and antiprotozoal agents. The Journal publishes primarily in human medicine, and articles in veterinary medicine likely to have an impact on global health.
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