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Title: | Brief Report: Validation of a Urine Tenofovir Immunoassay for Adherence Monitoring to PrEP and ART and Establishing the Cutoff for a Point-of-Care Test |
Authors: | Monica Gandhi Peter Bacchetti Matthew A. Spinelli Hideaki Okochi Jared M. Baeten Oraphan Siriprakaisil Virat Klinbuayaem Warren C. Rodrigues Guohong Wang Michael Vincent Tim R. Cressey Paul K. Drain |
Authors: | Monica Gandhi Peter Bacchetti Matthew A. Spinelli Hideaki Okochi Jared M. Baeten Oraphan Siriprakaisil Virat Klinbuayaem Warren C. Rodrigues Guohong Wang Michael Vincent Tim R. Cressey Paul K. Drain |
Keywords: | Medicine |
Issue Date: | 1-May-2019 |
Abstract: | BACKGROUND: Current pharmacologic adherence monitoring for antiretrovirals involves expensive, labor-intensive liquid chromatography/tandem mass spectrometry (LC-MS/MS)-based methods. Antibody-based assays can monitor and support adherence in real time. We developed a tenofovir (TFV)-based immunoassay and further validated it in a directly observed therapy (DOT) study. DESIGN: Pharmacologic DOT study of TFV disoproxil fumarate (TDF)/emtricitabine (FTC) administered to HIV-noninfected volunteers. METHODS: The TARGET study provided directly observed TDF 300 mg/FTC 200 mg 7 (high adherence), 4 (moderate), and 2 doses/week (low) to 30 volunteers (10/group) in Thailand, collecting a total of 637 urine samples over 6 weeks of administration and during washout. ELISA measured urine TFV levels by the immunoassay and LC-MS/MS-based concentrations served as the gold standard. A mixed-effects regression model evaluated cutoffs for a point-of-care assay. Performance characteristics of the immunoassay were compared with LC-MS/MS at a chosen cutoff. RESULTS: Median TFV levels were 12,000 ng/mL by the immunoassay 1 day after dosing; 5000 ng/mL 2 days after dosing; 1500 ng/mL 3 days after dosing; and below the lower limit of quantification thereafter (≥4 days). An immunoassay cutoff of 1500 ng/mL accurately classified 98% of patients who took a dose 24 hours ago as adherent. The specificity and sensitivity of the immunoassay compared with LC-MS/MS at the 1500 ng/mL cutoff were 99% and 94%; the correlation between TFV levels by the 2 assays was high (0.92, P < 0.00001). CONCLUSIONS: We have developed a novel TFV immunoassay that is highly specific, sensitive, and correlates strongly with LC-MS/MS measurements in a large DOT study. Adherence benchmarks from this DOT study will guide the development of a low-cost rapid point-of-care test for pre-exposure prophylaxis and antiretroviral treatment adherence monitoring and interventions. |
URI: | https://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=85064721305&origin=inward http://cmuir.cmu.ac.th/jspui/handle/6653943832/65760 |
ISSN: | 19447884 |
Appears in Collections: | CMUL: Journal Articles |
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