Department of Biostatistics and Bioinformatics, Colorado School of Public Health.
Division of Infectious Diseases, School of Medicine, University of Colorado-AMC.
AIDS. 2021 Oct 1;35(12):1949-1956. doi: 10.1097/QAD.0000000000002981.
Emtricitabine triphosphate (FTC-TP) in dried blood spots (DBS), a measure of short-term antiretroviral therapy (ART) adherence, is associated with viral suppression in persons with HIV (PWH). However, its ability to predict future viremia remains unknown.
Prospective, observational cohort (up to three visits in 48 weeks).
PWH receiving TDF/FTC-based ART had DBS and HIV viral load obtained at routine clinical visits. FTC-TP in DBS was dichotomized into quantifiable vs. below the limit of quantification (BLQ). The adjusted odds ratio (aOR) of future viremia (≥20 copies/ml at next study visit) was estimated according to FTC-TP at the current visit. To assess for possible interactions, additional models adjusted for tenofovir diphosphate (TFV-DP) in DBS and 3-day self-reported adherence.
Data from 433 PWH (677 paired DBS/HIV viral load samples) were analyzed. The aOR [95% confidence interval (CI)] for future viremia for BLQ vs. quantifiable FTC-TP was 3.4 (1.8--6.5; P = 0.0002). This diminished after adjusting for TFV-DP [aOR 1.9 (0.9--4.1); P = 0.090]. Among PWH reporting 100% 3-day adherence, the odds of future viremia were 6.0 times higher [(1.8--20.3); P = 0.001] when FTC-TP was BLQ vs. quantifiable. Among participants (n = 75) reporting less than 100% adherence, BLQ FTC-TP in DBS was not predictive of future viremia [aOR 1.3 (0.4--4.6); P = 0.96].
Nonquantifiable FTC-TP in DBS predicts future viremia and is particularly informative in PWH reporting perfect adherence. As point-of-care adherence measures become available, mismatches between objective and subjective measures, such as FTC-TP in DBS and self-report, could help clinicians identify individuals at an increased risk of future viremia.
在接受替诺福韦/恩曲他滨(TDF/FTC)治疗的 HIV 感染者(PWH)中,干血斑(DBS)中的恩曲他滨三磷酸(FTC-TP)可衡量短期抗逆转录病毒治疗(ART)的依从性,与病毒抑制相关。然而,其预测未来病毒血症的能力尚不清楚。
前瞻性、观察性队列研究(48 周内最多进行 3 次访视)。
接受 TDF/FTC 为基础的 ART 的 PWH 在常规临床访视时采集 DBS 和 HIV 病毒载量。DBS 中的 FTC-TP 分为可定量与低于定量下限(BLQ)。根据当前访视时的 FTC-TP,估计未来病毒血症(下一次研究访视时≥20 拷贝/ml)的调整后比值比(aOR)。为了评估可能的相互作用,还根据 DBS 中的替诺福韦二磷酸(TFV-DP)和 3 天自我报告的依从性调整了额外的模型。
共纳入 433 例 PWH(677 对 DBS/HIV 病毒载量样本)进行分析。BLQ 与可定量 FTC-TP 相比,未来病毒血症的 aOR [95%置信区间(CI)]为 3.4(1.8--6.5;P=0.0002)。调整 TFV-DP 后,该比值降低[aOR 1.9(0.9--4.1);P=0.090]。在报告 100%3 天依从性的 PWH 中,当 FTC-TP 为 BLQ 时,未来病毒血症的几率是可定量 FTC-TP 的 6.0 倍[比值比(OR)1.8--20.3;P=0.001]。在报告依从性低于 100%的参与者(n=75)中,DBS 中 BLQ FTC-TP 不能预测未来病毒血症[OR 1.3(0.4--4.6);P=0.96]。
DBS 中不可定量的 FTC-TP 可预测未来病毒血症,在报告完全依从的 PWH 中尤其具有提示意义。随着即时检测依从性的方法出现,客观和主观指标(如 DBS 中的 FTC-TP 和自我报告)之间的不匹配可能有助于临床医生识别未来病毒血症风险增加的个体。