Publication:
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

dc.contributor.authorSasisopin Kiertiburanakulen_US
dc.contributor.authorDavid Boettigeren_US
dc.contributor.authorOon Tek Ngen_US
dc.contributor.authorNguyen Kinhen_US
dc.contributor.authorTuti Parwati Meratien_US
dc.contributor.authorAnchalee Avihingsanonen_US
dc.contributor.authorWing Wai Wongen_US
dc.contributor.authorMan Po Leeen_US
dc.contributor.authorRomanee Chaiwarithen_US
dc.contributor.authorAdeeba Kamarulzamanen_US
dc.contributor.authorPacharee Kantipongen_US
dc.contributor.authorFujie Zhangen_US
dc.contributor.authorJun Yong Choien_US
dc.contributor.authorNagalingeswaran Kumarasamyen_US
dc.contributor.authorRossana Ditangcoen_US
dc.contributor.authorDo Duy Cuongen_US
dc.contributor.authorShinichi Okaen_US
dc.contributor.authorBenedict Lim Heng Simen_US
dc.contributor.authorWinai Ratanasuwanen_US
dc.contributor.authorPenh Sun Lyen_US
dc.contributor.authorEvy Yunihastutien_US
dc.contributor.authorSanjay Pujarien_US
dc.contributor.authorJeremy L. Rossen_US
dc.contributor.authorMatthew Lawen_US
dc.contributor.authorSomnuek Sungkanuparphen_US
dc.contributor.authorV. Kholen_US
dc.contributor.authorF. J. Zhangen_US
dc.contributor.authorH. X. Zhaoen_US
dc.contributor.authorN. Hanen_US
dc.contributor.authorP. C.K. Lien_US
dc.contributor.authorW. Lamen_US
dc.contributor.authorY. T. Chanen_US
dc.contributor.authorS. Saghayamen_US
dc.contributor.authorC. Ezhilarasien_US
dc.contributor.authorK. Joshien_US
dc.contributor.authorS. Gaikwaden_US
dc.contributor.authorA. Chitalikaren_US
dc.contributor.authorD. N. Wirawanen_US
dc.contributor.authorF. Yulianaen_US
dc.contributor.authorD. Imranen_US
dc.contributor.authorA. Widhanien_US
dc.contributor.authorJ. Tanumaen_US
dc.contributor.authorT. Nishijimaen_US
dc.contributor.authorS. Naen_US
dc.contributor.authorJ. M. Kimen_US
dc.contributor.authorY. M. Ganien_US
dc.contributor.authorR. Daviden_US
dc.contributor.authorS. F. Syed Omaren_US
dc.contributor.authorS. Ponnampalavanaren_US
dc.contributor.authorI. Azwaen_US
dc.contributor.authorE. Uyen_US
dc.contributor.authorR. Bantiqueen_US
dc.contributor.authorW. W. Kuen_US
dc.contributor.authorP. C. Wuen_US
dc.contributor.authorP. L. Limen_US
dc.contributor.authorL. S. Leeen_US
dc.contributor.authorP. S. Ohnmaren_US
dc.contributor.authorS. Gatechompolen_US
dc.contributor.authorP. Phanuphaken_US
dc.contributor.authorC. Phadungphonen_US
dc.contributor.authorL. Chumlaen_US
dc.contributor.authorN. Sanmeemaen_US
dc.contributor.authorT. Sirisanthanaen_US
dc.contributor.authorW. Kotarathititumen_US
dc.contributor.authorJ. Praparattanapanen_US
dc.contributor.authorP. Kambuaen_US
dc.contributor.authorR. Sriondeeen_US
dc.contributor.authorK. V. Nguyenen_US
dc.contributor.authorH. V. Buien_US
dc.contributor.authorD. T.H. Nguyenen_US
dc.contributor.authorD. T. Nguyenen_US
dc.contributor.authorN. V. Anen_US
dc.contributor.authorN. T. Luanen_US
dc.contributor.authorA. H. Sohnen_US
dc.contributor.authorB. Petersenen_US
dc.contributor.authorD. A. Cooperen_US
dc.contributor.authorA. Jiamsakulen_US
dc.contributor.authorD. C. Boettigeren_US
dc.contributor.otherMahidol Universityen_US
dc.contributor.otherUniversity of New South Wales (UNSW) Australiaen_US
dc.contributor.otherTan Tock Seng Hospitalen_US
dc.contributor.otherNational Hospital of Tropical Diseasesen_US
dc.contributor.otherUniversitas Udayanaen_US
dc.contributor.otherThe HIV Netherlands Australia Thailand Research Collaborationen_US
dc.contributor.otherVeterans General Hospital-Taipeien_US
dc.contributor.otherQueen Elizabeth Hospital Hong Kongen_US
dc.contributor.otherResearch Institute for Health Sciencesen_US
dc.contributor.otherUniversity of Malaya Medical Centreen_US
dc.contributor.otherChiangrai Prachanukroh Hospitalen_US
dc.contributor.otherBeijing Ditan Hospitalen_US
dc.contributor.otherYonsei University College of Medicineen_US
dc.contributor.otherVHS Medical Centre Indiaen_US
dc.contributor.otherGokilaen_US
dc.contributor.otherBach Mai Hospitalen_US
dc.contributor.otherNational Center for Global Health and Medicineen_US
dc.contributor.otherHospital Sungai Bulohen_US
dc.contributor.otherUniversity of Health Sciencesen_US
dc.contributor.otherUniversity of Indonesia, RSUPN Dr. Cipto Mangunkusumoen_US
dc.contributor.otherInstitute of Infectious Diseasesen_US
dc.contributor.otherFoundation for AIDS Researchen_US
dc.contributor.otherNational Hospital for Tropical Diseasesen_US
dc.date.accessioned2018-12-21T06:49:12Z
dc.date.accessioned2019-03-14T08:02:55Z
dc.date.available2018-12-21T06:49:12Z
dc.date.available2019-03-14T08:02:55Z
dc.date.issued2017-05-05en_US
dc.description.abstract© 2017 The Author(s). 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/mm3; 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/m2 (OR 2.4 vs. <18.5 kg/m2; 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/mm3 (OR 3.9 vs. <100 cells/mm3; 95% CI 2.0-4.1, p < 0.01), total lymphocyte count >2000 cells/mm3 (OR 1.7 vs. <1000 cells/mm3; 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.en_US
dc.identifier.citationAIDS Research and Therapy. Vol.14, No.1 (2017)en_US
dc.identifier.doi10.1186/s12981-017-0151-1en_US
dc.identifier.issn17426405en_US
dc.identifier.other2-s2.0-85018734109en_US
dc.identifier.urihttps://repository.li.mahidol.ac.th/handle/123456789/41907
dc.rightsMahidol Universityen_US
dc.rights.holderSCOPUSen_US
dc.source.urihttps://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=85018734109&origin=inwarden_US
dc.subjectBiochemistry, Genetics and Molecular Biologyen_US
dc.subjectImmunology and Microbiologyen_US
dc.titleFactors 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 settingsen_US
dc.typeArticleen_US
dspace.entity.typePublication
mu.datasource.scopushttps://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=85018734109&origin=inwarden_US

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