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Comparing the efficacy of efavirenz and boosted lopinavir using viremia copy-years
INTRODUCTION: HIV-1 plasma viral load during treatment can be highly variable. Thus, there is the need to find a measure of cumulative viremia that can be used to assess both the short- and long-term efficacy of highly active antiretroviral therapy (HAART). Here, we validate a measure of cumulative...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
International AIDS Society
2014
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4013478/ https://www.ncbi.nlm.nih.gov/pubmed/24805184 http://dx.doi.org/10.7448/IAS.17.1.18617 |
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author | Lima, Viviane D Sierra-Madero, Juan Wu, Zunyou Singer, Joel Wood, Evan Hull, Mark W Harrigan, Paul Richard Montaner, Julio SG |
author_facet | Lima, Viviane D Sierra-Madero, Juan Wu, Zunyou Singer, Joel Wood, Evan Hull, Mark W Harrigan, Paul Richard Montaner, Julio SG |
author_sort | Lima, Viviane D |
collection | PubMed |
description | INTRODUCTION: HIV-1 plasma viral load during treatment can be highly variable. Thus, there is the need to find a measure of cumulative viremia that can be used to assess both the short- and long-term efficacy of highly active antiretroviral therapy (HAART). Here, we validate a measure of cumulative viremia to evaluate HAART efficacy. METHODS: We accessed HAART efficacy using data from a randomized clinical trial conducted in Mexico. We compared the proportion of individuals achieving a viral load <50 and <400 copies/mL at week 48, against the cumulative plasma viral load, estimated as the area under the plasma viral load curve (AUVLC). High AUVLC indicates high cumulative viremia. RESULTS AND DISCUSSION: There was a strong and significant association between the proportion of individuals achieving a viral load <50 and <400 copies/mL at week 48, with individuals suppressed having significant lower cumulative viremia. The median area was 7513 (25th–75th percentile [Q1–Q3] 6634−8180) if viral load <50 copies/mL and 7679 (Q1–Q3 6899−9373) if viral load ≥50 copies/mL (p-value 0.0284). When the analysis was stratified by study arm, individuals on efavirenz had lower cumulative viremia than those on boosted lopinavir. CONCLUSIONS: Our findings suggest that cumulative viremia should be explored further as a tool to simultaneously evaluate the individual and public health efficacy of HAART. This is particularly relevant to the implementation and evaluation of the Treatment 2.0 strategy recently proposed by UNAIDS and the WHO, as a means to maximize the individual and public health benefit of HAART. |
format | Online Article Text |
id | pubmed-4013478 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2014 |
publisher | International AIDS Society |
record_format | MEDLINE/PubMed |
spelling | pubmed-40134782014-06-18 Comparing the efficacy of efavirenz and boosted lopinavir using viremia copy-years Lima, Viviane D Sierra-Madero, Juan Wu, Zunyou Singer, Joel Wood, Evan Hull, Mark W Harrigan, Paul Richard Montaner, Julio SG J Int AIDS Soc Short Report INTRODUCTION: HIV-1 plasma viral load during treatment can be highly variable. Thus, there is the need to find a measure of cumulative viremia that can be used to assess both the short- and long-term efficacy of highly active antiretroviral therapy (HAART). Here, we validate a measure of cumulative viremia to evaluate HAART efficacy. METHODS: We accessed HAART efficacy using data from a randomized clinical trial conducted in Mexico. We compared the proportion of individuals achieving a viral load <50 and <400 copies/mL at week 48, against the cumulative plasma viral load, estimated as the area under the plasma viral load curve (AUVLC). High AUVLC indicates high cumulative viremia. RESULTS AND DISCUSSION: There was a strong and significant association between the proportion of individuals achieving a viral load <50 and <400 copies/mL at week 48, with individuals suppressed having significant lower cumulative viremia. The median area was 7513 (25th–75th percentile [Q1–Q3] 6634−8180) if viral load <50 copies/mL and 7679 (Q1–Q3 6899−9373) if viral load ≥50 copies/mL (p-value 0.0284). When the analysis was stratified by study arm, individuals on efavirenz had lower cumulative viremia than those on boosted lopinavir. CONCLUSIONS: Our findings suggest that cumulative viremia should be explored further as a tool to simultaneously evaluate the individual and public health efficacy of HAART. This is particularly relevant to the implementation and evaluation of the Treatment 2.0 strategy recently proposed by UNAIDS and the WHO, as a means to maximize the individual and public health benefit of HAART. International AIDS Society 2014-05-06 /pmc/articles/PMC4013478/ /pubmed/24805184 http://dx.doi.org/10.7448/IAS.17.1.18617 Text en © 2014 Lima VD et al; licensee International AIDS Society http://creativecommons.org/licenses/by/3.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Short Report Lima, Viviane D Sierra-Madero, Juan Wu, Zunyou Singer, Joel Wood, Evan Hull, Mark W Harrigan, Paul Richard Montaner, Julio SG Comparing the efficacy of efavirenz and boosted lopinavir using viremia copy-years |
title | Comparing the efficacy of efavirenz and boosted lopinavir using viremia copy-years |
title_full | Comparing the efficacy of efavirenz and boosted lopinavir using viremia copy-years |
title_fullStr | Comparing the efficacy of efavirenz and boosted lopinavir using viremia copy-years |
title_full_unstemmed | Comparing the efficacy of efavirenz and boosted lopinavir using viremia copy-years |
title_short | Comparing the efficacy of efavirenz and boosted lopinavir using viremia copy-years |
title_sort | comparing the efficacy of efavirenz and boosted lopinavir using viremia copy-years |
topic | Short Report |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4013478/ https://www.ncbi.nlm.nih.gov/pubmed/24805184 http://dx.doi.org/10.7448/IAS.17.1.18617 |
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