Low-level viremia and virologic failure in persons with HIV infection treated with antiretroviral therapy

被引:77
作者
Fleming, Julia [1 ]
Mathews, W. Christopher [2 ]
Rutstein, Richard M. [3 ]
Aberg, Judith [4 ]
Somboonwit, Charurut [5 ]
Cheever, Laura W. [6 ]
Berry, Stephen A. [1 ]
Gebo, Kelly A. [1 ]
Moore, Richard D. [1 ]
机构
[1] Johns Hopkins Univ, Sch Med, Baltimore, MD 21205 USA
[2] Univ Calif San Diego, San Diego, CA 92103 USA
[3] Childrens Hosp Philadelphia, Philadelphia, PA 19104 USA
[4] Icahn Sch Med Mt Sinai, New York, NY 10029 USA
[5] Univ S Florida, Tampa, FL 33620 USA
[6] Hlth Resources & Serv Adm, Rockville, MD USA
基金
美国医疗保健研究与质量局;
关键词
blips; low-level viremia; virologic failure; DRUG-RESISTANCE MUTATIONS; HIV-1-INFECTED PATIENTS; VIRAL LOAD; BLIPS; INTERMITTENT; ADHERENCE; SUPPRESSION; PREVALENCE; COHORT; RNA;
D O I
10.1097/QAD.0000000000002306
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Background: The clinical management of low-level viremia (LLV) remains unclear. The objective of this study was to investigate the association of blips and LLV with virologic failure. Methods: We enlisted patients who newly enrolled into the HIV Research Network between 2005 and 2015, had HIV-1 RNA more than 200 copies/ml, and were either antiretroviral therapy (ART)-naive or ART-experienced and not on ART. Patients were included who achieved virologic suppression (<= 50 on two consecutive viral loads) and had at least two viral loads following suppression. Blips and LLV (>= 2 consecutive >51 copies/ml) were categorized separately into three categories: no blips/LLV, 51-200, 201-500. Cox proportional hazards regression was used to assess association between rates of blips/LLV and virologic failure (two consecutive >500). Results: The 2795 patients were mostly male (75.4%), black (50.3%), and MSM (52.9%). Median age was 38 years old (interquartile range 29-48). Most patients (88.8%) were ART-naive at study entry. Overall, 283 (10.1%) patients experienced virologic failure. A total of 152 (5.4%) patients experienced LLV to 51-200 and 110 (3.9%) patients experienced LLV to 201-500. Both LLV 51-200 [adjusted hazard ratio (aHR) 1.83 (1.10,3.04)] and LLV 201-500 [aHR 4.26 (2.65,6.86)] were associated with virologic failure. In sensitivity analysis excluding ART-experienced patients, the association between LLV 51 and 200 and virologic failure was not statistically significant. Conclusion: LLV between 201 and 500 was associated with virologic failure, as was LLV between 51 and 200, particularly among ART-experienced patients. Patients with LLV below the current Department of Health and Human Services threshold for virologic failure (persistent viremia >= 200) may require more intensive monitoring because of increased risk for virologic failure.
引用
收藏
页码:2005 / 2012
页数:8
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