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在一组 HIV 阳性患者中,持续低水平病毒血症后的病毒学失败:12 年观察结果。

Virologic failure following persistent low-level viremia in a cohort of HIV-positive patients: results from 12 years of observation.

机构信息

Department of Social and Preventive Medicine, University of Montreal, Sainte-Justine Hospital Research Center.

出版信息

Clin Infect Dis. 2013 Nov;57(10):1489-96. doi: 10.1093/cid/cit529. Epub 2013 Aug 14.

Abstract

BACKGROUND

The current goal of antiretroviral therapy (ART) is to maintain a suppressed human immunodeficiency virus (HIV) viral load below limits of assay detection. When viral loads remain in low-level viremia (LLV), especially between 50 and 200 copies/mL, the best management and clinical consequences remain unknown. Our objective was to study the long-term impact of persistent LLV on the subsequent risk of virologic failure in a cohort of people living with HIV in Montreal, Canada.

METHODS

We compared the cumulative incidence of subsequent virologic failure (defined as an HIV RNA viral load of >1000 copies/mL) in patients receiving ART for at least 12 months by following 4 persistence categories (<50, 50-199, 200-499, and 500-999 copies/mL) for 6, 9, or 12 months, using Kaplan-Meier analysis. The association between subsequent virologic failure and persistence status were estimated using a Cox proportional hazards model.

RESULTS

The cumulative incidence of virologic failure 1 year after having maintained a LLV for 6 months was 22.7% (95% confidence interval [CI], 14.9-33.6) for 50-199 copies/mL, 24.2% (95% CI, 14.5-38.6) for 200-499 copies/mL, and 58.9% (95% CI, 43.1-75.2) for 500-999 copies/mL, compared with 6.6% (95% CI, 5.3-8.2) for an undetectable HIV RNA viral load. Even after adjustment for potential confounders, a persistent LLV of 50-199 copies/mL for 6 months doubled the risk of virologic failure (hazard ratio, 2.22; 95% CI, 1.60-3.09), compared with undetectable viral loads for the same duration. Similar results have been found for persistent LLV of 9 or 12 months.

CONCLUSIONS

In this cohort, all categories of persistent LLV between 50 and 999 copies/mL were associated with an increased risk of virologic failure. The results shed new light for the management of patients with LLV, especially with regard to LLV of 50-199 copies/mL.

摘要

背景

目前抗逆转录病毒疗法(ART)的目标是将人类免疫缺陷病毒(HIV)病毒载量抑制在低于检测极限以下。当病毒载量保持在低水平病毒血症(LLV)时,尤其是在 50 至 200 拷贝/毫升之间时,最佳的管理和临床后果仍不清楚。我们的目的是研究在加拿大蒙特利尔的 HIV 感染者队列中,持续的 LLV 对随后发生病毒学失败的长期影响。

方法

我们通过 Kaplan-Meier 分析比较了在接受至少 12 个月 ART 治疗的患者中,按照 4 个持续时间类别(<50、50-199、200-499 和 500-999 拷贝/毫升),在 6、9 或 12 个月时,随后发生病毒学失败(定义为 HIV RNA 病毒载量>1000 拷贝/毫升)的累积发生率。使用 Cox 比例风险模型估计随后的病毒学失败与持续状态之间的关联。

结果

在维持 LLV 6 个月后,1 年内发生病毒学失败的累积发生率分别为 50-199 拷贝/毫升时为 22.7%(95%置信区间[CI],14.9-33.6),200-499 拷贝/毫升时为 24.2%(95% CI,14.5-38.6),500-999 拷贝/毫升时为 58.9%(95% CI,43.1-75.2),而不可检测的 HIV RNA 病毒载量时为 6.6%(95% CI,5.3-8.2)。即使在调整了潜在的混杂因素后,持续的 LLV 为 50-199 拷贝/毫升持续 6 个月,病毒学失败的风险也增加了一倍(风险比,2.22;95% CI,1.60-3.09),而持续相同时间的不可检测病毒载量则无此风险。对于持续的 LLV 为 9 个月或 12 个月的情况,也得到了类似的结果。

结论

在本队列中,所有 50-999 拷贝/毫升的持续 LLV 类别均与病毒学失败风险增加相关。这些结果为 LLV 患者的管理提供了新的视角,特别是对于 50-199 拷贝/毫升的 LLV。

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