Departments of Medicine; and.
Epidemiology and Biostatistics, University of California San Francisco, San Francisco, CA.
J Acquir Immune Defic Syndr. 2021 Sep 1;88(1):57-60. doi: 10.1097/QAI.0000000000002727.
Tenofovir alafenamide (TAF) is increasingly used in HIV treatment, with or without agents that require pharmacologic boosters such as ritonavir/cobicistat. Boosters increase TAF levels, so the TAF dose is lowered in single-pill combinations. We hypothesized that individuals on dose-adjusted boosted TAF would have similar urine tenofovir (TFV) concentrations to those on unboosted TAF.
SETTING/METHODS: We collected urine samples from patients with HIV on TAF, with evidence of virologic suppression and high self-reported adherence at 2 San Francisco clinics from June 2019 to January 2020. We measured urine TFV levels by liquid chromatography/tandem mass spectrometry and used linear regression to compare natural log-transformed urine TFV levels for patients on boosted versus unboosted TAF.
Our analysis included 30 patients on unboosted TAF (25 mg daily TAF) and 15 on boosted TAF (12 on 10 mg daily TAF and 3 on 25 mg daily TAF). Patients on unboosted vs. boosted TAF had similar baseline age, weight, sex, and creatinine. In unadjusted univariate linear regression, there were no significant differences in urine TFV levels based on presence/absence of boosting after TAF dose reduction to 10 mg (geometric mean ratio 1.07; 95% confidence interval: 0.53 to 2.16). This finding was unchanged in adjusted analysis.
No significant differences in urine TFV levels were seen for patients on unboosted vs. boosted dose-reduced TAF. These results have important implications for our forthcoming point-of-care urine immunoassay for TAF, implying that separate adherence cutoffs will not be necessary for patients on boosters and dose-reduced TAF. A single POC TAF immunoassay will, thus, support monitoring on most TAF-based antiretroviral therapy.
替诺福韦艾拉酚胺(TAF)越来越多地用于 HIV 治疗,无论是否使用需要利托那韦/考比司他等药物增效剂的药物。增效剂会增加 TAF 水平,因此在单一片剂复方制剂中降低 TAF 剂量。我们假设接受剂量调整的增效 TAF 治疗的个体的尿液替诺福韦(TFV)浓度与未接受增效 TAF 治疗的个体相似。
我们于 2019 年 6 月至 2020 年 1 月在旧金山的 2 家诊所收集了接受 TAF 治疗且病毒学抑制且自述高依从性的 HIV 患者的尿液样本。我们通过液相色谱/串联质谱法测量尿液 TFV 水平,并使用线性回归比较接受增效与未增效 TAF 治疗的患者的自然对数转换尿液 TFV 水平。
我们的分析纳入了 30 名接受未增效 TAF(每日 25mg TAF)治疗的患者和 15 名接受增效 TAF 治疗的患者(12 名每日接受 10mg TAF,3 名每日接受 25mg TAF)。接受未增效与增效 TAF 治疗的患者在基线年龄、体重、性别和肌酐方面相似。在 TAF 剂量减少至 10mg 后,未经调整的单变量线性回归分析中,根据有无增效剂,尿液 TFV 水平没有显著差异(几何均数比 1.07;95%置信区间:0.53 至 2.16)。调整分析后,这一发现没有改变。
在接受未增效与增效剂量减少的 TAF 治疗的患者中,尿液 TFV 水平没有显著差异。这些结果对我们即将推出的 TAF 点-of-care 尿液免疫分析法具有重要意义,这意味着对于接受增效剂和剂量减少的 TAF 的患者,不需要单独的依从性截止值。因此,一个单一的 POC TAF 免疫分析法将支持大多数基于 TAF 的抗逆转录病毒治疗的监测。