Kohler Maurus, Brown Jennifer A, Tschumi Nadine, Lerotholi Malebanye, Motaboli Lipontso, Mokete Moliehi, Chammartin Frédérique, Labhardt Niklaus D
Division of Clinical Epidemiology, Department of Clinical Research, University Hospital Basel, Basel, Switzerland.
Ministry of Health Lesotho, Maseru, Lesotho.
Open Forum Infect Dis. 2024 Jan 8;11(2):ofae013. doi: 10.1093/ofid/ofae013. eCollection 2024 Feb.
Human immunodeficiency virus low-level viremia (LLV) is associated with subsequent treatment failure at least with non nucleoside reverse transcriptase inhibitor (NNRTI)-containing antiretroviral therapy. Data on implications of LLV occurring under dolutegravir, which has largely replaced NNRTIs in Africa, are scarce, however.
We included adults with human immunodeficiency virus in Lesotho who had ≥2 viral loads (VLs) taken after ≥6 months of NNRTI- or dolutegravir-based antiretroviral therapy. Within VL pairs, we assessed the association of viral suppression (<50copies/mL) and low- and high-range LLV (50-199 and 200-999copies/mL, respectively) with virological failure (≥1000copies/mL) using a mixed-effects regression model. Participants could contribute VLs to the NNRTI and the dolutegravir group.
Among 18 550 participants, 12 216 (65.9%) were female and median age at first VL included was 41.2 years (interquartile range, 33.4-51.5). In both groups, compared with a suppressed VL, odds of subsequent virological failure were higher for low-range LLV (NNRTI: adjusted odds ratio; 95% confidence interval: 1.9; 1.4-2.4 and dolutegravir: 2.1; 1.3-3.6) and high-range LLV (adjusted odds ratio; 95% confidence interval, 4.2; 3.1-5.7 and 4.4; 2.4-7.9).
In the dolutegravir era, LLV remains associated with virological failure, endorsing the need for close clinical and laboratory monitoring of those with a VL ≥50 copies/mL.
人类免疫缺陷病毒低水平病毒血症(LLV)至少与含非核苷类逆转录酶抑制剂(NNRTI)的抗逆转录病毒疗法后续治疗失败相关。然而,在非洲已基本取代NNRTIs的多替拉韦治疗下出现LLV的影响数据却很匮乏。
我们纳入了莱索托的成年人类免疫缺陷病毒感染者,这些患者在接受基于NNRTI或多替拉韦的抗逆转录病毒治疗≥6个月后进行了≥2次病毒载量(VL)检测。在VL配对中,我们使用混合效应回归模型评估病毒抑制(<50拷贝/毫升)以及低范围和高范围LLV(分别为50 - 199和200 - 999拷贝/毫升)与病毒学失败(≥1000拷贝/毫升)之间的关联。参与者的VL检测结果可同时纳入NNRTI组和多替拉韦组。
在18550名参与者中,12216名(65.9%)为女性,首次纳入VL检测时的中位年龄为41.2岁(四分位间距为33.4 - 51.5岁)。在两组中,与病毒抑制的VL相比,低范围LLV(NNRTI组:调整后的优势比;95%置信区间:1.9;1.4 - 2.4;多替拉韦组:2.1;1.3 - 3.6)和高范围LLV(调整后的优势比;95%置信区间:4.2;3.1 - 5.7和4.4;2.4 - 7.9)后续发生病毒学失败的几率更高。
在多替拉韦时代,LLV仍然与病毒学失败相关,这支持了对VL≥50拷贝/毫升的患者进行密切临床和实验室监测的必要性。