U.S. Military HIV Research Program, Walter Reed Army Institute of Research, Silver Spring, Maryland, USA.
Henry M. Jackson Foundation for the Advancement of Military Medicine, Bethesda, Maryland, USA.
J Int AIDS Soc. 2024 Aug;27(8):e26316. doi: 10.1002/jia2.26316.
People living with HIV (PLWH) have higher rates of non-infectious comorbid diseases (NCDs) than individuals without HIV. We characterized the risk of NCDs among PLWH with undetectable viral load and persistent low-level viraemia (pLLV) in the African Cohort Study (AFRICOS). We secondarily quantified the role of immune activation in the association between LLV and NCDs.
AFRICOS enrols participants in 12 clinics in Uganda, Kenya, Tanzania and Nigeria. Participants on antiretroviral therapy ≥ 6 months without an NCD at enrolment were included. PLLV was defined as at least two consecutive visits with a detectable viral load <1000 copies/ml. We examined elevated blood pressure, hypercholesterolemia, hyperglycaemia, renal insufficiency and a composite variable of any NCD. Hazard ratios (HRs) and 95% confidence intervals (CIs) were estimated using Cox proportional hazard modelling. Among a subset of participants with biomarker data, we assessed the interaction between viral load and 13 biomarkers in the association with any NCD.
From 23 January 2013 to 1 December 2022, 1755 participants met the inclusion criteria for these analyses. At the first eligible visit, the majority of participants had an undetectable viral load (n = 1375, 78.35%). Participants with pLLV had an increased rate of developing any NCD (aHR: 1.22, 95% CI: 1.02-1.47) compared to participants with an undetectable viral load. There was a statistically significant interaction between LLV and TNF-α, CCL2/MCP-1 and TNF-RII in the association with any NCD.
PLLV was significantly associated with NCDs and immune inflammation in this population. Aggressive management of LLV may positively impact NCDs in PLWH.
与未感染 HIV 的个体相比,HIV 感染者(PLWH)患有非传染性合并症(NCD)的比例更高。我们在非洲队列研究(AFRICOS)中描述了病毒载量不可检测且持续低水平病毒血症(pLLV)的 PLWH 发生 NCD 的风险。我们还定量评估了免疫激活在低水平病毒血症与 NCD 之间的关联中的作用。
AFRICOS 在乌干达、肯尼亚、坦桑尼亚和尼日利亚的 12 个诊所招募参与者。招募时无 NCD 且已接受抗逆转录病毒治疗(ART)≥6 个月的参与者被纳入研究。pLLV 定义为至少两次连续就诊时病毒载量可检测但<1000 拷贝/ml。我们检查了高血压、高胆固醇血症、高血糖、肾功能不全和任何 NCD 的复合变量。使用 Cox 比例风险模型估计危险比(HR)和 95%置信区间(CI)。在具有生物标志物数据的参与者亚组中,我们评估了病毒载量与任何 NCD 关联中 13 种生物标志物之间的相互作用。
从 2013 年 1 月 23 日至 2022 年 12 月 1 日,有 1755 名参与者符合这些分析的纳入标准。在第一次符合条件的就诊时,大多数参与者的病毒载量不可检测(n=1375,78.35%)。与病毒载量不可检测的参与者相比,pLLV 患者发生任何 NCD 的风险更高(调整 HR:1.22,95%CI:1.02-1.47)。在任何 NCD 的关联中,低水平病毒血症与 TNF-α、CCL2/MCP-1 和 TNF-RII 之间存在统计学显著的相互作用。
在该人群中,pLLV 与 NCD 和免疫炎症显著相关。积极管理低水平病毒血症可能会对 PLWH 的 NCD 产生积极影响。