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dc.contributor.authorMonica Gandhien_US
dc.contributor.authorPeter Bacchettien_US
dc.contributor.authorMatthew A. Spinellien_US
dc.contributor.authorHideaki Okochien_US
dc.contributor.authorJared M. Baetenen_US
dc.contributor.authorOraphan Siriprakaisilen_US
dc.contributor.authorVirat Klinbuayaemen_US
dc.contributor.authorWarren C. Rodriguesen_US
dc.contributor.authorGuohong Wangen_US
dc.contributor.authorMichael Vincenten_US
dc.contributor.authorTim R. Cresseyen_US
dc.contributor.authorPaul K. Drainen_US
dc.date.accessioned2019-08-05T04:40:35Z-
dc.date.available2019-08-05T04:40:35Z-
dc.date.issued2019-05-01en_US
dc.identifier.issn19447884en_US
dc.identifier.other2-s2.0-85064721305en_US
dc.identifier.other10.1097/QAI.0000000000001971en_US
dc.identifier.urihttps://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=85064721305&origin=inwarden_US
dc.identifier.urihttp://cmuir.cmu.ac.th/jspui/handle/6653943832/65760-
dc.description.abstractBACKGROUND: 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.en_US
dc.subjectMedicineen_US
dc.titleBrief Report: Validation of a Urine Tenofovir Immunoassay for Adherence Monitoring to PrEP and ART and Establishing the Cutoff for a Point-of-Care Testen_US
dc.typeJournalen_US
article.title.sourcetitleJournal of acquired immune deficiency syndromes (1999)en_US
article.volume81en_US
article.stream.affiliationsHarvard School of Public Healthen_US
article.stream.affiliationsUniversity of California, San Franciscoen_US
article.stream.affiliationsUniversity of Liverpoolen_US
article.stream.affiliationsUniversity of Washington, Seattleen_US
article.stream.affiliationsChiang Mai Universityen_US
article.stream.affiliationsSanpatong Hospitalen_US
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