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Factors associated with pre-treatment HIV RNA: application for the use of abacavir and rilpivirine as the first-line regimen for HIV-infected patients in resource-limited settings

BACKGROUND: Abacavir and rilpivirine are alternative antiretroviral drugs for treatment-naïve HIV-infected patients. However, both drugs are only recommended for the patients who have pre-treatment HIV RNA <100,000 copies/mL. In resource-limited settings, pre-treatment HIV RNA is not routinely pe...

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Autores principales: Kiertiburanakul, Sasisopin, Boettiger, David, Ng, Oon Tek, Van Kinh, Nguyen, Merati, Tuti Parwati, Avihingsanon, Anchalee, Wong, Wing-Wai, Lee, Man Po, Chaiwarith, Romanee, Kamarulzaman, Adeeba, Kantipong, Pacharee, Zhang, Fujie, Choi, Jun Yong, Kumarasamy, Nagalingeswaran, Ditangco, Rossana, Cuong, Do Duy, Oka, Shinichi, Sim, Benedict Lim Heng, Ratanasuwan, Winai, Ly, Penh Sun, Yunihastuti, Evy, Pujari, Sanjay, Ross, Jeremy L., Law, Matthew, Sungkanuparph, Somnuek
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5420083/
https://www.ncbi.nlm.nih.gov/pubmed/28484509
http://dx.doi.org/10.1186/s12981-017-0151-1
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author Kiertiburanakul, Sasisopin
Boettiger, David
Ng, Oon Tek
Van Kinh, Nguyen
Merati, Tuti Parwati
Avihingsanon, Anchalee
Wong, Wing-Wai
Lee, Man Po
Chaiwarith, Romanee
Kamarulzaman, Adeeba
Kantipong, Pacharee
Zhang, Fujie
Choi, Jun Yong
Kumarasamy, Nagalingeswaran
Ditangco, Rossana
Cuong, Do Duy
Oka, Shinichi
Sim, Benedict Lim Heng
Ratanasuwan, Winai
Ly, Penh Sun
Yunihastuti, Evy
Pujari, Sanjay
Ross, Jeremy L.
Law, Matthew
Sungkanuparph, Somnuek
author_facet Kiertiburanakul, Sasisopin
Boettiger, David
Ng, Oon Tek
Van Kinh, Nguyen
Merati, Tuti Parwati
Avihingsanon, Anchalee
Wong, Wing-Wai
Lee, Man Po
Chaiwarith, Romanee
Kamarulzaman, Adeeba
Kantipong, Pacharee
Zhang, Fujie
Choi, Jun Yong
Kumarasamy, Nagalingeswaran
Ditangco, Rossana
Cuong, Do Duy
Oka, Shinichi
Sim, Benedict Lim Heng
Ratanasuwan, Winai
Ly, Penh Sun
Yunihastuti, Evy
Pujari, Sanjay
Ross, Jeremy L.
Law, Matthew
Sungkanuparph, Somnuek
author_sort Kiertiburanakul, Sasisopin
collection PubMed
description BACKGROUND: Abacavir and rilpivirine are alternative antiretroviral drugs for treatment-naïve HIV-infected patients. However, both drugs are only recommended for the patients who have pre-treatment HIV RNA <100,000 copies/mL. In resource-limited settings, pre-treatment HIV RNA is not routinely performed and not widely available. The aims of this study are to determine factors associated with pre-treatment HIV RNA <100,000 copies/mL and to construct a model to predict this outcome. METHODS: HIV-infected adults enrolled in the TREAT Asia HIV Observational Database were eligible if they had an HIV RNA measurement documented at the time of ART initiation. The dataset was randomly split into a derivation data set (75% of patients) and a validation data set (25%). Factors associated with pre-treatment HIV RNA <100,000 copies/mL were evaluated by logistic regression adjusted for study site. A prediction model and prediction scores were created. RESULTS: A total of 2592 patients were enrolled for the analysis. Median [interquartile range (IQR)] age was 35.8 (29.9–42.5) years; CD4 count was 147 (50–248) cells/mm(3); and pre-treatment HIV RNA was 100,000 (34,045–301,075) copies/mL. Factors associated with pre-treatment HIV RNA <100,000 copies/mL were age <30 years [OR 1.40 vs. 41–50 years; 95% confidence interval (CI) 1.10–1.80, p = 0.01], body mass index >30 kg/m(2) (OR 2.4 vs. <18.5 kg/m(2); 95% CI 1.1–5.1, p = 0.02), anemia (OR 1.70; 95% CI 1.40–2.10, p < 0.01), CD4 count >350 cells/mm(3) (OR 3.9 vs. <100 cells/mm(3); 95% CI 2.0–4.1, p < 0.01), total lymphocyte count >2000 cells/mm(3) (OR 1.7 vs. <1000 cells/mm(3); 95% CI 1.3–2.3, p < 0.01), and no prior AIDS-defining illness (OR 1.8; 95% CI 1.5–2.3, p < 0.01). Receiver-operator characteristic (ROC) analysis yielded area under the curve of 0.70 (95% CI 0.67–0.72) among derivation patients and 0.69 (95% CI 0.65–0.74) among validation patients. A cut off score >25 yielded the sensitivity of 46.7%, specificity of 79.1%, positive predictive value of 67.7%, and negative predictive value of 61.2% for prediction of pre-treatment HIV RNA <100,000 copies/mL among derivation patients. CONCLUSION: A model prediction for pre-treatment HIV RNA <100,000 copies/mL produced an area under the ROC curve of 0.70. A larger sample size for prediction model development as well as for model validation is warranted.
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spelling pubmed-54200832017-05-08 Factors associated with pre-treatment HIV RNA: application for the use of abacavir and rilpivirine as the first-line regimen for HIV-infected patients in resource-limited settings Kiertiburanakul, Sasisopin Boettiger, David Ng, Oon Tek Van Kinh, Nguyen Merati, Tuti Parwati Avihingsanon, Anchalee Wong, Wing-Wai Lee, Man Po Chaiwarith, Romanee Kamarulzaman, Adeeba Kantipong, Pacharee Zhang, Fujie Choi, Jun Yong Kumarasamy, Nagalingeswaran Ditangco, Rossana Cuong, Do Duy Oka, Shinichi Sim, Benedict Lim Heng Ratanasuwan, Winai Ly, Penh Sun Yunihastuti, Evy Pujari, Sanjay Ross, Jeremy L. Law, Matthew Sungkanuparph, Somnuek AIDS Res Ther Research BACKGROUND: Abacavir and rilpivirine are alternative antiretroviral drugs for treatment-naïve HIV-infected patients. However, both drugs are only recommended for the patients who have pre-treatment HIV RNA <100,000 copies/mL. In resource-limited settings, pre-treatment HIV RNA is not routinely performed and not widely available. The aims of this study are to determine factors associated with pre-treatment HIV RNA <100,000 copies/mL and to construct a model to predict this outcome. METHODS: HIV-infected adults enrolled in the TREAT Asia HIV Observational Database were eligible if they had an HIV RNA measurement documented at the time of ART initiation. The dataset was randomly split into a derivation data set (75% of patients) and a validation data set (25%). Factors associated with pre-treatment HIV RNA <100,000 copies/mL were evaluated by logistic regression adjusted for study site. A prediction model and prediction scores were created. RESULTS: A total of 2592 patients were enrolled for the analysis. Median [interquartile range (IQR)] age was 35.8 (29.9–42.5) years; CD4 count was 147 (50–248) cells/mm(3); and pre-treatment HIV RNA was 100,000 (34,045–301,075) copies/mL. Factors associated with pre-treatment HIV RNA <100,000 copies/mL were age <30 years [OR 1.40 vs. 41–50 years; 95% confidence interval (CI) 1.10–1.80, p = 0.01], body mass index >30 kg/m(2) (OR 2.4 vs. <18.5 kg/m(2); 95% CI 1.1–5.1, p = 0.02), anemia (OR 1.70; 95% CI 1.40–2.10, p < 0.01), CD4 count >350 cells/mm(3) (OR 3.9 vs. <100 cells/mm(3); 95% CI 2.0–4.1, p < 0.01), total lymphocyte count >2000 cells/mm(3) (OR 1.7 vs. <1000 cells/mm(3); 95% CI 1.3–2.3, p < 0.01), and no prior AIDS-defining illness (OR 1.8; 95% CI 1.5–2.3, p < 0.01). Receiver-operator characteristic (ROC) analysis yielded area under the curve of 0.70 (95% CI 0.67–0.72) among derivation patients and 0.69 (95% CI 0.65–0.74) among validation patients. A cut off score >25 yielded the sensitivity of 46.7%, specificity of 79.1%, positive predictive value of 67.7%, and negative predictive value of 61.2% for prediction of pre-treatment HIV RNA <100,000 copies/mL among derivation patients. CONCLUSION: A model prediction for pre-treatment HIV RNA <100,000 copies/mL produced an area under the ROC curve of 0.70. A larger sample size for prediction model development as well as for model validation is warranted. BioMed Central 2017-05-05 /pmc/articles/PMC5420083/ /pubmed/28484509 http://dx.doi.org/10.1186/s12981-017-0151-1 Text en © The Author(s) 2017 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.
spellingShingle Research
Kiertiburanakul, Sasisopin
Boettiger, David
Ng, Oon Tek
Van Kinh, Nguyen
Merati, Tuti Parwati
Avihingsanon, Anchalee
Wong, Wing-Wai
Lee, Man Po
Chaiwarith, Romanee
Kamarulzaman, Adeeba
Kantipong, Pacharee
Zhang, Fujie
Choi, Jun Yong
Kumarasamy, Nagalingeswaran
Ditangco, Rossana
Cuong, Do Duy
Oka, Shinichi
Sim, Benedict Lim Heng
Ratanasuwan, Winai
Ly, Penh Sun
Yunihastuti, Evy
Pujari, Sanjay
Ross, Jeremy L.
Law, Matthew
Sungkanuparph, Somnuek
Factors associated with pre-treatment HIV RNA: application for the use of abacavir and rilpivirine as the first-line regimen for HIV-infected patients in resource-limited settings
title Factors associated with pre-treatment HIV RNA: application for the use of abacavir and rilpivirine as the first-line regimen for HIV-infected patients in resource-limited settings
title_full Factors associated with pre-treatment HIV RNA: application for the use of abacavir and rilpivirine as the first-line regimen for HIV-infected patients in resource-limited settings
title_fullStr Factors associated with pre-treatment HIV RNA: application for the use of abacavir and rilpivirine as the first-line regimen for HIV-infected patients in resource-limited settings
title_full_unstemmed Factors associated with pre-treatment HIV RNA: application for the use of abacavir and rilpivirine as the first-line regimen for HIV-infected patients in resource-limited settings
title_short Factors associated with pre-treatment HIV RNA: application for the use of abacavir and rilpivirine as the first-line regimen for HIV-infected patients in resource-limited settings
title_sort factors associated with pre-treatment hiv rna: application for the use of abacavir and rilpivirine as the first-line regimen for hiv-infected patients in resource-limited settings
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5420083/
https://www.ncbi.nlm.nih.gov/pubmed/28484509
http://dx.doi.org/10.1186/s12981-017-0151-1
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