HIV-1 low-level viremia predicts viral failure in participants on antiretroviral therapy in the Swiss HIV Cohort Study.

IF 8.2 1区 医学 Q1 IMMUNOLOGY
Caroline Lanz, Jan Meier, Marcel Stöckle, Hansjakob Furrer, Alexandra Calmy, Matthias Cavassini, Enos Bernasconi, Patrick Schmid, Dominique L Braun, Roger D Kouyos, Tom Loosli, Katharina Kusejko, Huldrych F Günthard
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Abstract

Background: Most individuals on combination antiretroviral therapy (ART) have HIV plasma viral loads below the limit of detection. However, episodes of low-level viremia (LLV) are observed in subsets of individuals, risk factors and clinical significance of which remain debated.

Methods: We included participants enrolled in the Swiss HIV Cohort Study, starting ART between July 1999 and April 2023, with HIV RNA <200 copies/ml six months post ART initiation. Using longitudinally collected data, we applied a time-updated Cox proportional hazards model to determine the association of LLV with the risk of subsequent viral failure, defined as ≥200 copies/ml. LLV was quantified by the time-updated area under the curve (AUC) of HIV RNA values, segmented into categories undetectable, and based on AUC tertiles into low, intermediate, and high.

Results: We included 8'132 participants with a total of 49'579 person-years of follow-up. Median follow-up time was 4.7 years, and median number of HIV RNA measurements was 16. Participants had a median age of 38 years, 75.9% were male, 74.4% had white ethnicity, and 45.9% had HIV-1 subtype B. LLV was associated with an increased risk for subsequent viral failure, with the highest LLV category showing the strongest association (hazard ratio = 3.3 compared to undetectable viral load) among all included variables including ethnicity, age, and ART.

Conclusions: LLV was strongly associated with the risk for subsequent viral failure, even after adjusting for demographic and clinical characteristics, including adherence and treatment regimen. The detection of LLV should prompt appropriate measures to decrease the risk of subsequent viral failure.

瑞士艾滋病毒队列研究中,HIV-1 低水平病毒血症可预测接受抗逆转录病毒疗法者的病毒失败。
背景:大多数接受抗逆转录病毒联合疗法(ART)治疗的人的 HIV 血浆病毒载量低于检测限。然而,低水平病毒血症(LLV)会在部分人群中出现,其风险因素和临床意义仍存在争议:我们纳入了 1999 年 7 月至 2023 年 4 月期间开始接受抗逆转录病毒疗法的瑞士 HIV 队列研究参与者,他们的 HIV RNA 结果如下我们纳入了 8132 名参与者,共随访了 49579 人年。随访时间中位数为 4.7 年,HIV RNA 检测次数中位数为 16 次。LLV 与后续病毒失败的风险增加有关,在包括种族、年龄和抗逆转录病毒疗法在内的所有变量中,最高 LLV 类别显示出最强的相关性(与检测不到病毒载量相比,危险比 = 3.3):结论:即使在调整了包括依从性和治疗方案在内的人口统计学和临床特征后,LLV 仍与后续病毒失败的风险密切相关。检测出 LLV 后,应立即采取适当措施,降低后续病毒失败的风险。
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来源期刊
Clinical Infectious Diseases
Clinical Infectious Diseases 医学-传染病学
CiteScore
25.00
自引率
2.50%
发文量
900
审稿时长
3 months
期刊介绍: Clinical Infectious Diseases (CID) is dedicated to publishing original research, reviews, guidelines, and perspectives with the potential to reshape clinical practice, providing clinicians with valuable insights for patient care. CID comprehensively addresses the clinical presentation, diagnosis, treatment, and prevention of a wide spectrum of infectious diseases. The journal places a high priority on the assessment of current and innovative treatments, microbiology, immunology, and policies, ensuring relevance to patient care in its commitment to advancing the field of infectious diseases.
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