UOC Malattie Infettive, Fondazione Policlinico Universitario A. Gemelli IRCCS, Rome, Italy.
Infectious Diseases Unit, Università Vita-Salute San Raffaele, Milan, Italy.
AIDS Res Hum Retroviruses. 2024 Feb;40(2):80-89. doi: 10.1089/AID.2023.0015. Epub 2023 Jul 14.
Despite effective antiretroviral therapies (ARTs), a subset of people living with HIV (PLWH) still experience low-level viremia (LLV, i.e., 50-1,000 copies/mL). The present study compared PLWH experiencing LLV with those maintaining virological suppression (VS) and explored the potential impact of preexisting drug resistance and other factors on LLV. We conducted a retrospective, 1:1 matched case-control study within a cohort of drug-experienced VS subjects from the Italian Antiviral Response Cohort Analysis database, followed in the period 2009-2019. Cases were individuals experiencing LLV, while controls were those who maintained VS. Matching was for calendar year of first ART regimen. Preexisting drug resistance was calculated as cumulative genotypic susceptibility score (GSS) according to regimen administered at the observational period start. To explore the effect of cumulative GSS, treated as a binary variable (≥2 and <2) and other factors on LLV, we performed a logistic regression analysis. Within a main population of 3,455 PLWH, 337 cases were selected. Cases were comparable to the controls for both gender and age. However, cases showed that they had experienced a longer time since HIV diagnosis, a higher number of drugs previously administered, lower baseline CD4 T cell count and a higher zenith viral load (VL). By multivariate analysis, we found that higher zenith VL [adjusted odds ratio (aOR) (95% confidence interval [CI]) 1.30 (1.14-1.48)], a cumulative usage of both PI [aOR (95% CI): 2.03 (1.19-3.48)] and InSTI [aOR (95% CI): 2.23 (1.47-3.38)] and a cumulative GSS <2 [aOR (95% CI) 0.67 (0.46-0.98)], were associated with a higher risk in developing LLV. In current high-efficacy ART era, in drug-experienced PLWH, the predictors of increased risk of LLV were the presence of preexisting drug resistance, higher zenith VL, and previous PI, and InSTI exposure.
尽管有有效的抗逆转录病毒疗法 (ART),但仍有一部分 HIV 感染者 (PLWH) 存在低水平病毒血症 (LLV,即 50-1000 拷贝/ml)。本研究比较了 LLV 患者与维持病毒学抑制 (VS) 的 PLWH,并探讨了预先存在的耐药性和其他因素对 LLV 的潜在影响。我们在意大利抗病毒反应队列分析数据库中进行了一项回顾性、1:1 匹配的病例对照研究,研究对象为 2009-2019 年期间接受过药物治疗的 VS 患者队列。病例组为 LLV 患者,对照组为维持 VS 的患者。匹配是根据首次接受 ART 方案的年份进行的。预先存在的耐药性根据观察期开始时接受的方案计算为累积基因型耐药评分 (GSS)。为了探讨累积 GSS (作为二分类变量处理,≥2 和<2) 及其他因素对 LLV 的影响,我们进行了逻辑回归分析。在 3455 名 PLWH 主要人群中,选择了 337 名病例。病例组在性别和年龄方面与对照组相当。然而,病例组在 HIV 诊断后时间较长、以前接受的药物种类较多、基线 CD4 T 细胞计数较低、峰值病毒载量 (VL) 较高。多变量分析显示,更高的峰值 VL [调整后的优势比 (aOR) (95%置信区间 [CI]):1.30(1.14-1.48)]、累积使用 PI [aOR (95% CI):2.03(1.19-3.48)] 和 INSTI [aOR (95% CI):2.23(1.47-3.38)] 和累积 GSS<2 [aOR (95% CI)0.67(0.46-0.98)],与发展为 LLV 的风险增加相关。在当前高效 ART 时代,在有药物治疗经验的 PLWH 中,增加 LLV 风险的预测因素是预先存在的耐药性、更高的峰值 VL 和之前的 PI 和 INSTI 暴露。