Warren Annabelle M, Cheng Allen C, Watson Kerrie, Lewin Sharon R, Hoy Jennifer F
Department of Infectious Diseases, The Alfred Hospital and Monash University, 55 Commercial Road, Melbourne, Vic. 3004, Australia.
Sex Health. 2017 Jun;14(3):238-243. doi: 10.1071/SH16165.
Progressively sensitive assays for plasma HIV RNA have led to increased detection of plasma HIV RNA between 20 and 200 copies/ml, known as low level viremia (LLV) when recurrent or persistent, in HIV-infected patients on antiretroviral therapy (ART). The aim of this study was to determine outcomes following initial detection of LLV in an Australian cohort.
A retrospective study using the HIV Service Database (Alfred Hospital) included all patients on ART who recorded plasma HIV RNA 20-200 copies/mL following prior virological suppression (viral load (VL) HIV RNA <20 copies/mL) over 2 years (2010 to 2012), with follow-up to June 2013. Factors associated with subsequent virological outcome were assessed via univariate and multivariate analysis.
Of 919 patients managed by The Alfred HIV service, 207 (22.5%) met inclusion criteria. Mean age was 48.8 years, 91.3% were male. During follow-up, 54% patients recorded no further HIV RNA 20-200 copies/mL (viral blip); 39% had recurrent or persistent VL 20-200 copies/mL (LLV); and 7% progressed to virological failure with VL >200 copies/mL. Factors associated with LLV included co-morbid type 2 diabetes, shorter prior virological suppression and lower nadir CD4 cell count. Clinician management of VL 20-200 copies/mL was generally conservative, with infrequent requests for genotypic analysis (3.3% cases) or change in ART (<1% cases).
LLV following virological suppression is common, and occurred as an isolated viral blip in half the patients. Those patients with persistent or recurrent LLV had higher rates of type 2 diabetes, shorter prior virological suppression and lower nadir CD4 cell count.
血浆HIV RNA的逐步敏感检测方法已使HIV感染患者接受抗逆转录病毒治疗(ART)期间血浆HIV RNA在20至200拷贝/毫升之间的检测增加,反复或持续出现时称为低水平病毒血症(LLV)。本研究的目的是确定澳大利亚队列中初次检测到LLV后的转归。
一项使用HIV服务数据库(阿尔弗雷德医院)的回顾性研究纳入了所有在2年(2010年至2012年)期间接受ART且在先前病毒学抑制(病毒载量(VL)HIV RNA<20拷贝/毫升)后记录血浆HIV RNA为20 - 200拷贝/毫升的患者,并随访至2013年6月。通过单因素和多因素分析评估与后续病毒学转归相关的因素。
在阿尔弗雷德HIV服务机构管理的919例患者中,207例(22.5%)符合纳入标准。平均年龄为48.8岁,91.3%为男性。随访期间,54%的患者未再记录到HIV RNA为20 - 200拷贝/毫升(病毒波动);39%有反复或持续的VL为20 - 200拷贝/毫升(LLV);7%进展为病毒学失败,VL>200拷贝/毫升。与LLV相关的因素包括合并2型糖尿病、先前病毒学抑制时间较短和最低CD4细胞计数较低。临床医生对VL为20 - 200拷贝/毫升的管理通常较为保守,很少要求进行基因分型分析(3.3%的病例)或改变ART(<1%的病例)。
病毒学抑制后的LLV很常见,半数患者表现为孤立的病毒波动。那些持续或反复出现LLV的患者2型糖尿病发病率较高、先前病毒学抑制时间较短且最低CD4细胞计数较低。