Botswana Harvard Health Partnership, Gaborone 0000, Botswana.
Department of Medical Sciences, Faculty of Allied Health Professions, University of Botswana, Gaborone 0022, Botswana.
Viruses. 2024 May 1;16(5):720. doi: 10.3390/v16050720.
We evaluated subsequent virologic outcomes in individuals experiencing low-level virem ia (LLV) on dolutegravir (DTG)-based first-line antiretroviral therapy (ART) in Botswana. We used a national dataset from 50,742 adults who initiated on DTG-based first-line ART from June 2016-December 2022. Individuals with at least two viral load (VL) measurements post three months on DTG-based first-line ART were evaluated for first and subsequent episodes of LLV (VL:51-999 copies/mL). LLV was sub-categorized as low-LLV (51-200 copies/mL), medium-LLV (201-400 copies/mL) and high-LLV (401-999 copies/mL). The study outcome was virologic failure (VF) (VL ≥ 1000 copies/mL): virologic non-suppression defined as single-VF and confirmed-VF defined as two-consecutive VF measurements after an initial VL < 1000 copies/mL. Cox regression analysis identified predictive factors of subsequent VF. The prevalence of LLV was only statistically different at timepoints >6-12 (2.8%) and >12-24 (3.9%) (-value < 0.01). LLV was strongly associated with both virologic non-suppression (adjusted hazards ratio [aHR] = 2.6; 95% CI: 2.2-3.3, -value ≤ 0.001) and confirmed VF (aHR = 2.5; 95% CI: 2.4-2.7, -value ≤ 0.001) compared to initially virally suppressed PLWH. High-LLV (HR = 3.3; 95% CI: 2.9-3.6) and persistent-LLV (HR = 6.6; 95% CI: 4.9-8.9) were associated with an increased hazard for virologic non-suppression than low-LLV and a single-LLV episode, respectively. In a national cohort of PLWH on DTG-based first-line ART, LLV > 400 copies/mL and persistent-LLV had a stronger association with VF. Frequent VL testing and adherence support are warranted for individuals with VL > 50 copies/mL.
我们评估了博茨瓦纳接受基于多替拉韦(DTG)的一线抗逆转录病毒治疗(ART)的个体中出现低水平病毒血症(LLV)的后续病毒学结果。我们使用了 2016 年 6 月至 2022 年 12 月期间至少有两次基于 DTG 的一线 ART 三个月后病毒载量(VL)测量的 50742 名成年人的全国性数据集。对至少有两次基于 DTG 的一线 ART 三个月后 VL 测量的个体进行首次和随后 LLV(VL:51-999 拷贝/mL)发作的评估。将 LLV 进一步分为低 LLV(51-200 拷贝/mL)、中 LLV(201-400 拷贝/mL)和高 LLV(401-999 拷贝/mL)。研究结果是病毒学失败(VF)(VL≥1000 拷贝/mL):病毒学未抑制定义为单次 VF,确认 VF 定义为初始 VL<1000 拷贝/mL 后两次连续 VF 测量。Cox 回归分析确定了随后 VF 的预测因素。仅在时间点>6-12(2.8%)和>12-24(3.9%)时 LLV 的患病率具有统计学差异(-值<0.01)。与最初病毒抑制的 PLWH 相比,LLV 与病毒学未抑制(调整后的危害比[aHR]=2.6;95%CI:2.2-3.3,-值≤0.001)和确认 VF(aHR=2.5;95%CI:2.4-2.7,-值≤0.001)强烈相关。与低 LLV 和单次 LLV 发作相比,高 LLV(HR=3.3;95%CI:2.9-3.6)和持续 LLV(HR=6.6;95%CI:4.9-8.9)与病毒学未抑制的风险增加相关。在接受基于 DTG 的一线 ART 的 PLWH 全国队列中,>400 拷贝/mL 的 LLV 和持续 LLV 与 VF 的相关性更强。对于 VL>50 拷贝/mL 的个体,需要进行更频繁的 VL 检测和坚持支持治疗。