"Dynamic range" of inferred phenotypic HIV drug resistance values in clinical practice.
<h4>Background</h4>'Virtual' or inferred phenotypes (vPhenotypes) are commonly used to assess resistance to antiretroviral agents in patients failing therapy. In this study, we provide a clinical context for understanding vPhenotype values.<h4>Methods</h4>All HIV-in...
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oai:doaj.org-article:3059e66ab4d6446b86b08340fd903ccc2021-11-18T06:58:18Z"Dynamic range" of inferred phenotypic HIV drug resistance values in clinical practice.1932-620310.1371/journal.pone.0017402https://doaj.org/article/3059e66ab4d6446b86b08340fd903ccc2011-02-01T00:00:00Zhttps://www.ncbi.nlm.nih.gov/pmc/articles/pmid/21390218/?tool=EBIhttps://doaj.org/toc/1932-6203<h4>Background</h4>'Virtual' or inferred phenotypes (vPhenotypes) are commonly used to assess resistance to antiretroviral agents in patients failing therapy. In this study, we provide a clinical context for understanding vPhenotype values.<h4>Methods</h4>All HIV-infected persons enrolled in the British Columbia Drug Treatment Program with a baseline plasma viral load (pVL) and follow-up genotypic resistance and pVL results were included up to October 29, 2008 (N = 5,277). Change from baseline pVL was determined as a function of Virco vPhenotype, and the "dynamic range" (defined here by the 10th and 90th percentiles for fold-change in IC₅₀ amongst all patients) was estimated from the distribution of vPhenotye fold-changes across the cohort.<h4>Results</h4>The distribution of vPhenotypes from a large cohort of HIV patients who have failed therapy are presented for all available antiretroviral agents. A maximum change in IC₅₀ of at least 13-fold was observed for all drugs. The dideoxy drugs, tenofovir and most PIs exhibited small "dynamic ranges" with values of <4-fold change observed in > 99% of samples. In contrast, zidovudine, lamivudine, emtricitabine and the non-nucleoside reverse transcriptase inihibitors (excluding etravirine) had large dynamic ranges.<h4>Conclusion</h4>We describe the populational distribution of vPhenotypes such that vPhenotype results can be interpreted relative to other patients in a drug-specific manner.Luke C SwensonGraham PollockBrian WynhovenTheresa MoWinnie DongRobert S HoggJulio S G MontanerP Richard HarriganPublic Library of Science (PLoS)articleMedicineRScienceQENPLoS ONE, Vol 6, Iss 2, p e17402 (2011) |
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Medicine R Science Q Luke C Swenson Graham Pollock Brian Wynhoven Theresa Mo Winnie Dong Robert S Hogg Julio S G Montaner P Richard Harrigan "Dynamic range" of inferred phenotypic HIV drug resistance values in clinical practice. |
description |
<h4>Background</h4>'Virtual' or inferred phenotypes (vPhenotypes) are commonly used to assess resistance to antiretroviral agents in patients failing therapy. In this study, we provide a clinical context for understanding vPhenotype values.<h4>Methods</h4>All HIV-infected persons enrolled in the British Columbia Drug Treatment Program with a baseline plasma viral load (pVL) and follow-up genotypic resistance and pVL results were included up to October 29, 2008 (N = 5,277). Change from baseline pVL was determined as a function of Virco vPhenotype, and the "dynamic range" (defined here by the 10th and 90th percentiles for fold-change in IC₅₀ amongst all patients) was estimated from the distribution of vPhenotye fold-changes across the cohort.<h4>Results</h4>The distribution of vPhenotypes from a large cohort of HIV patients who have failed therapy are presented for all available antiretroviral agents. A maximum change in IC₅₀ of at least 13-fold was observed for all drugs. The dideoxy drugs, tenofovir and most PIs exhibited small "dynamic ranges" with values of <4-fold change observed in > 99% of samples. In contrast, zidovudine, lamivudine, emtricitabine and the non-nucleoside reverse transcriptase inihibitors (excluding etravirine) had large dynamic ranges.<h4>Conclusion</h4>We describe the populational distribution of vPhenotypes such that vPhenotype results can be interpreted relative to other patients in a drug-specific manner. |
format |
article |
author |
Luke C Swenson Graham Pollock Brian Wynhoven Theresa Mo Winnie Dong Robert S Hogg Julio S G Montaner P Richard Harrigan |
author_facet |
Luke C Swenson Graham Pollock Brian Wynhoven Theresa Mo Winnie Dong Robert S Hogg Julio S G Montaner P Richard Harrigan |
author_sort |
Luke C Swenson |
title |
"Dynamic range" of inferred phenotypic HIV drug resistance values in clinical practice. |
title_short |
"Dynamic range" of inferred phenotypic HIV drug resistance values in clinical practice. |
title_full |
"Dynamic range" of inferred phenotypic HIV drug resistance values in clinical practice. |
title_fullStr |
"Dynamic range" of inferred phenotypic HIV drug resistance values in clinical practice. |
title_full_unstemmed |
"Dynamic range" of inferred phenotypic HIV drug resistance values in clinical practice. |
title_sort |
"dynamic range" of inferred phenotypic hiv drug resistance values in clinical practice. |
publisher |
Public Library of Science (PLoS) |
publishDate |
2011 |
url |
https://doaj.org/article/3059e66ab4d6446b86b08340fd903ccc |
work_keys_str_mv |
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