Laboratory Branch, Division of HIV/AIDS Prevention, Centers for Disease Control and Prevention, Atlanta, GA.
Public Health Leader Fellowship Program, Morehouse College Public Health Sciences Institute, Atlanta, GA.
J Acquir Immune Defic Syndr. 2019 Nov 1;82(3):252-256. doi: 10.1097/QAI.0000000000002133.
Urine provides a minimally invasive specimen that may allow for development of rapid tests to detect antiretroviral drugs and provide opportunities to improve individual adherence. This study sought to determine whether urine could provide a biomarker of adherence for currently approved pre-exposure prophylaxis and HIV treatment regimens.
Urine and blood were collected from 34 HIV-negative men who have sex with men aged 18-49 years, enrolled in a clinical trial comparing 2 antiretroviral regimens. Specimens were collected 4 and 24 hours after a single oral dose of tenofovir disoproxil fumarate (TDF)/emtricitabine (FTC) (n = 10) or tenofovir alafenamide (TAF)/FTC/cobicistat (COBI)/elvitegravir (EVG) (n = 8), or after 4 and 10 days of daily oral TDF/FTC (n = 9) or TAF/FTC/COBI/EVG (n = 7). Tenofovir (TFV), FTC, and EVG were measured by high-performance liquid chromatography-mass spectrometry.
Median urine FTC concentrations at 4 and 24 hours were similar between men receiving TDF/FTC (4 hours 147 µg/mL; 24 hours 10 µg/mL) and men receiving TAF/FTC/COBI/EVG (4 hours 333 µg/mL, P = 0.173; 24 hours 13 µg/mL, P = 0.681). Median urine TFV concentrations were lower among men receiving TAF/FTC/COBI/EVG (4 hours 1.2 µg/mL; 24 hours 0.8 µg/mL) compared with men receiving TDF/FTC (4 hours 17 µg/mL, P < 0.001; 24 hours 7 µg/mL, P = 0.001). Urine TFV concentrations remained reduced among men receiving TAF/FTC/COBI/EVG compared with men receiving TDF/FTC after daily dosing. EVG was not consistently measurable in urine.
High urine FTC and TFV concentrations could provide an indication of adherence to daily oral dosing with TDF or TAF-based regimens used for treatment and prevention.
尿液是一种微创样本,可用于开发快速检测抗逆转录病毒药物的方法,并为提高个体的服药依从性提供机会。本研究旨在确定尿液是否可以为目前批准的暴露前预防和 HIV 治疗方案提供依从性的生物标志物。
从 34 名年龄在 18-49 岁的男男性行为者中收集了尿液和血液,这些人参加了一项比较两种抗逆转录病毒方案的临床试验。采集了单次口服替诺福韦二吡呋酯(TDF)/恩曲他滨(FTC)(n = 10)或替诺福韦艾拉酚胺(TAF)/FTC/考比司他(COBI)/依维韦仑(EVG)(n = 8)后 4 小时和 24 小时,或每天口服 TDF/FTC(n = 9)或 TAF/FTC/COBI/EVG(n = 7)后 4 天和 10 天的尿液样本。采用高效液相色谱-质谱法测定替诺福韦(TFV)、FTC 和 EVG。
接受 TDF/FTC 治疗的男性(4 小时 147 µg/mL;24 小时 10 µg/mL)和接受 TAF/FTC/COBI/EVG 治疗的男性(4 小时 333 µg/mL,P = 0.173;24 小时 13 µg/mL,P = 0.681),4 小时和 24 小时时尿液 FTC 浓度中位数相似。接受 TAF/FTC/COBI/EVG 治疗的男性(4 小时 1.2 µg/mL;24 小时 0.8 µg/mL)尿液 TFV 浓度中位数低于接受 TDF/FTC 治疗的男性(4 小时 17 µg/mL,P < 0.001;24 小时 7 µg/mL,P = 0.001)。与接受 TDF/FTC 治疗的男性相比,接受 TAF/FTC/COBI/EVG 治疗的男性在每日治疗后尿液 TFV 浓度仍较低。尿液中未一致检测到 EVG。
高尿液 FTC 和 TFV 浓度可能表明接受 TDF 或 TAF 为基础的方案每日口服治疗和预防时的服药依从性。