Low level viremia is associated with Serious Non-AIDS Events in People Living with HIV

A. Ganesan, H. Hsieh, X. Chu, R. Colombo, C. Berjohn, T. Lalani, Joseph M. Yabes, Christie A. Joya, J. Blaylock, B. Agan
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Abstract

The consequences of low-level viremia in people living with HIV are unclear. We used data from the U.S. Military HIV Natural History Study (NHS) to examine the association of low-level viremia (LLV) and serious non-AIDS events (SNAEs). Included participants initiated antiretroviral therapy (ART) after 1996, had ≥3 viral loads (VLs) measured, using an assay with a lower limit of detection of <50 copies/mL, ≥6 months after ART initiation. VLs were categorized as lower levels of LLV (51-199 copies/mL), higher level of low-level viremia (HLLV-200-999 copies/mL), and virologic failure (VF- ≥200 copies/mL on 2 or more successive determinations or a single VL ≥1000 copies/mL), and virologic suppression (VS- i.e., VL <50 copies/mL). Viral blips [i.e., VLs between 50 and 999 copies/mL that are preceded and succeeded by VL <50 copies/mL] were analyzed in the VS category. Cox Proportional Hazards models were used to examine the association of LLV and SNAEs, adjusted hazard ratios and 95% CI are presented. A total of 439 (17.4%) SNAEs were recorded among the 2528 participants (93% male, 40% Caucasian, 43% African American) followed for a median of 11 years. In 8.5% and 4.6% of the participants, respectively, LLV and HLLV were the highest recorded viremia strata. Compared with VS, SNAEs were associated with LLV (1.3, [1.2 to 1.4]), HLLV (1.6, [1.5 to 1.7]), and VF (1.7, [1.7 to 1.8]). The results of this study suggest that LLV is associated with the occurrence of SNAEs and needs further study.
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低水平病毒血症与艾滋病毒感染者的严重非艾滋病事件有关
艾滋病病毒感染者低水平病毒血症的后果尚不清楚。我们利用美国军方艾滋病自然史研究(NHS)的数据,研究了低水平病毒血症(LLV)与严重非艾滋病事件(SNAEs)之间的关系。 所纳入的参与者于 1996 年后开始接受抗逆转录病毒疗法(ART),并在开始接受抗逆转录病毒疗法≥6 个月后使用检测下限小于 50 拷贝/毫升的检测方法测量了≥3 个病毒载量(VLs)。病毒载量分为较低水平的 LLV(51-199 拷贝/毫升)、较高水平的低水平病毒血症(HLLV-200-999 拷贝/毫升)、病毒学失败(VF- 连续两次或两次以上测定结果≥200 拷贝/毫升或单次 VL ≥1000 拷贝/毫升)和病毒学抑制(VS- 即 VL <50 拷贝/毫升)。病毒突变[即 VL <50 拷贝/毫升之前和之后的 VL 在 50 至 999 拷贝/毫升之间]在 VS 类别中进行分析。采用 Cox 比例危险度模型检测 LLV 与 SNAEs 的相关性,并给出调整后的危险度比和 95% CI。 在 2528 名参与者(93% 为男性,40% 为白种人,43% 为非裔美国人)中,共记录了 439 例(17.4%)SNAE,随访时间中位数为 11 年。在分别占 8.5% 和 4.6% 的参与者中,LLV 和 HLLV 是记录到的最高病毒血症层。与 VS 相比,SNAE 与 LLV(1.3,[1.2 至 1.4])、HLLV(1.6,[1.5 至 1.7])和 VF(1.7,[1.7 至 1.8])相关。 本研究结果表明,LLV 与 SNAE 的发生有关,需要进一步研究。
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