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DC Field | Value | Language |
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dc.contributor.author | Monica Gandhi | en_US |
dc.contributor.author | Peter Bacchetti | en_US |
dc.contributor.author | Matthew A. Spinelli | en_US |
dc.contributor.author | Hideaki Okochi | en_US |
dc.contributor.author | Jared M. Baeten | en_US |
dc.contributor.author | Oraphan Siriprakaisil | en_US |
dc.contributor.author | Virat Klinbuayaem | en_US |
dc.contributor.author | Warren C. Rodrigues | en_US |
dc.contributor.author | Guohong Wang | en_US |
dc.contributor.author | Michael Vincent | en_US |
dc.contributor.author | Tim R. Cressey | en_US |
dc.contributor.author | Paul K. Drain | en_US |
dc.date.accessioned | 2019-08-05T04:40:35Z | - |
dc.date.available | 2019-08-05T04:40:35Z | - |
dc.date.issued | 2019-05-01 | en_US |
dc.identifier.issn | 19447884 | en_US |
dc.identifier.other | 2-s2.0-85064721305 | en_US |
dc.identifier.other | 10.1097/QAI.0000000000001971 | en_US |
dc.identifier.uri | https://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=85064721305&origin=inward | en_US |
dc.identifier.uri | http://cmuir.cmu.ac.th/jspui/handle/6653943832/65760 | - |
dc.description.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. | en_US |
dc.subject | Medicine | en_US |
dc.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 | en_US |
dc.type | Journal | en_US |
article.title.sourcetitle | Journal of acquired immune deficiency syndromes (1999) | en_US |
article.volume | 81 | en_US |
article.stream.affiliations | Harvard School of Public Health | en_US |
article.stream.affiliations | University of California, San Francisco | en_US |
article.stream.affiliations | University of Liverpool | en_US |
article.stream.affiliations | University of Washington, Seattle | en_US |
article.stream.affiliations | Chiang Mai University | en_US |
article.stream.affiliations | Sanpatong Hospital | en_US |
Appears in Collections: | CMUL: Journal Articles |
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