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调查澳大利亚艾滋病毒观察数据库中病毒学反弹、低水平病毒血症和病毒学失败的发生率和预测因素。

Investigating rates and predictors of viral blips, low-level viraemia and virological failure in the Australian HIV observational database.

机构信息

Kirby Institute, UNSW Sydney, Sydney, New South Wales, Australia.

Infectious Diseases Research Network, Sunshine Coast University Hospital, Birtinya, Queensland, Australia.

出版信息

Trop Med Int Health. 2024 Jan;29(1):42-56. doi: 10.1111/tmi.13951. Epub 2023 Nov 27.

Abstract

OBJECTIVES

Australia has made significant progress towards achieving the UNAIDS's 95-95-95 cascade targets including HIV viral suppression. To investigate the burden of HIV viraemia, we assessed viral blips, low-level viraemia (LLV) and virologic failure (VF) in an Australian cohort.

METHODS

We studied the proportion of people with viral suppression, viral blips, LLV and VF in the Australian HIV observational database (AHOD) between 2010 and 2021. The association between blips or LLV, and VF was investigated using Cox regression, and predictors of viral blips and LLV were assessed using repeated-measured logistic regression.

RESULTS

Among 2544 AHOD participants who were in follow-up and on antiretroviral therapy (ART) from 1 January 2010 (88.7% male), 444 had experienced VF (incidence rate: 2.45 [95% CI: 2.23-2.69] per 100 person-years [PY]) during 18,125 PY of follow-up (a median of 7.6 years). The proportion of people with VF decreased over time, whereas rates of blips and LLV remained stable. Participants with blips (hazard ratio, 2.89; 95% CI: 2.31-3.61) and LLV (4.46; 95% CI: 3.38-5.89) were at increased risk of VF. Hepatitis B co-infection, longer documented treatment interruption duration, younger age and lower CD4 at ART initiation, and protease inhibitors-based initial regimen were associated with an increased risk of VF. Common predictors of blips and LLV such as higher HIV-1 RNA and lower CD4 at ART initiation, longer treatment interruption, more VL testing and types of care settings (hospitals vs. sexual health services) were identified.

CONCLUSIONS

Blips and LLV predict subsequent VF development. We identified important predictors of HIV viraemia including VF among individuals on INSTI-based regimens to help direct HIV management plans.

摘要

目的

澳大利亚在实现联合国艾滋病规划署的 95-95-95 级联目标方面取得了重大进展,包括艾滋病毒病毒抑制。为了调查艾滋病毒病毒血症的负担,我们评估了澳大利亚队列中病毒爆发、低水平病毒血症(LLV)和病毒学失败(VF)的情况。

方法

我们研究了 2010 年至 2021 年期间澳大利亚艾滋病毒观察数据库(AHOD)中病毒抑制、病毒爆发、LLV 和 VF 的人群比例。使用 Cox 回归分析了爆发或 LLV 与 VF 的关联,并使用重复测量逻辑回归评估了病毒爆发和 LLV 的预测因素。

结果

在 2544 名从 2010 年 1 月 1 日开始接受抗逆转录病毒治疗(ART)并接受随访的 AHOD 参与者中,444 名(88.7%为男性)在 18125 人年(中位时间为 7.6 年)的随访中发生了 VF(发生率:2.45[95%CI:2.23-2.69]每 100 人年[PY])。随着时间的推移,VF 的比例下降,而爆发和 LLV 的比例保持稳定。爆发(危险比,2.89;95%CI:2.31-3.61)和 LLV(4.46;95%CI:3.38-5.89)的参与者发生 VF 的风险增加。乙型肝炎合并感染、更长的记录治疗中断时间、更年轻的年龄和更低的 CD4 在 ART 开始时,以及基于蛋白酶抑制剂的初始方案与 VF 风险增加相关。还确定了爆发和 LLV 的常见预测因素,如更高的 HIV-1 RNA 和 CD4 在 ART 开始时更低,治疗中断时间更长,更多的 VL 检测和护理场所类型(医院与性健康服务)。

结论

爆发和 LLV 预测随后的 VF 发展。我们确定了基于 INSTI 方案的个体中 HIV 病毒血症的重要预测因素,包括 VF,以帮助指导 HIV 管理计划。

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