Amsterdam Institute for Global Health and Development, and Department of Global Health, Amsterdam UMC, University of Amsterdam, Amsterdam, The Netherlands.
Joint Clinical Research Centre, Kampala, Uganda.
Sci Rep. 2018 Oct 25;8(1):15751. doi: 10.1038/s41598-018-33538-0.
In ART programs in sub-Saharan Africa, a growing proportion of HIV-infected persons initiating first-line antiretroviral therapy (ART) have a history of prior antiretroviral drug use (PAU). We assessed the effect of PAU on the risk of pre-treatment drug resistance (PDR) and virological failure (VF) in a multicountry cohort of HIV-infected adults initiated on a standard non-nucleoside reverse transcriptase inhibitor (NNRTI)-based first-line ART. Multivariate logistic regression was used to assess the associations between PAU, PDR and VF (defined as viral load ≥400 cps/mL). Causal mediation analysis was used to assess the proportion of the effect of PAU on VF that could be eliminated by intervening on PDR. Of 2737 participants, 122 (4.5%) had a history of PAU. Participants with PAU had a 7.2-fold (95% CI 4.4-11.7) risk of carrying PDR and a 3.1-fold (95% CI 1.6-6.1) increased risk of VF, compared to antiretroviral-naïve participants. Controlling for PDR would eliminate nearly half the effect of PAU on the risk of VF. Patients with a history of PAU are at increased risk of ART failure, which is to a large extent attributable to PDR. These findings support the recent WHO recommendations for use of differentiated, non-NNRTI-based empiric first-line therapy in patients with PAU.
在撒哈拉以南非洲地区的艾滋病治疗项目中,越来越多的艾滋病毒感染者在开始一线抗逆转录病毒治疗(ART)前有过抗逆转录病毒药物使用史(PAU)。我们评估了 PAU 对接受标准非核苷类逆转录酶抑制剂(NNRTI)为基础的一线 ART 的多国队列中艾滋病毒感染成年人的治疗前耐药(PDR)和病毒学失败(VF)风险的影响。多变量逻辑回归用于评估 PAU、PDR 和 VF(定义为病毒载量≥400cps/ml)之间的关联。因果中介分析用于评估 PAU 对 VF 的影响中,通过干预 PDR 可以消除的比例。在 2737 名参与者中,有 122 名(4.5%)有 PAU 病史。与未接受过抗逆转录病毒治疗的参与者相比,有 PAU 病史的参与者携带 PDR 的风险增加了 7.2 倍(95%CI 4.4-11.7),VF 的风险增加了 3.1 倍(95%CI 1.6-6.1)。控制 PDR 可消除 PAU 对 VF 风险影响的近一半。有 PAU 病史的患者发生 ART 失败的风险增加,这在很大程度上归因于 PDR。这些发现支持了最近世界卫生组织关于对有 PAU 病史的患者使用差异化、非 NNRTI 为基础的经验性一线治疗的建议。