Publication:
HIV-1 drug resistance mutations in children after failure of first-line nonnucleoside reverse transcriptase inhibitor-based antiretroviral therapy

dc.contributor.authorT. Puthanakiten_US
dc.contributor.authorG. Jourdainen_US
dc.contributor.authorS. Hongsiriwonen_US
dc.contributor.authorP. Suntarattiwongen_US
dc.contributor.authorK. Chokephaibulkiten_US
dc.contributor.authorV. Sirisanthanaen_US
dc.contributor.authorP. Kosalaraksaen_US
dc.contributor.authorW. Petdachaien_US
dc.contributor.authorR. Hansudewechakulen_US
dc.contributor.authorU. Siangphoeen_US
dc.contributor.authorT. Suwanlerken_US
dc.contributor.authorJ. Ananworanichen_US
dc.contributor.otherThe HIV Netherlands Australia Thailand Research Collaborationen_US
dc.contributor.otherChulalongkorn Universityen_US
dc.contributor.otherChiang Mai Universityen_US
dc.contributor.otherRegional Hospitalen_US
dc.contributor.otherQueen Sirikit National Institute of Child Healthen_US
dc.contributor.otherMahidol Universityen_US
dc.contributor.otherKhon Kaen Universityen_US
dc.contributor.otherPetchburi Hospitalen_US
dc.contributor.otherChiang Rai Regional Hospitalen_US
dc.contributor.otherSouth East Asia Research Collaboration with Hawaiien_US
dc.date.accessioned2018-09-24T09:21:02Z
dc.date.available2018-09-24T09:21:02Z
dc.date.issued2010-10-01en_US
dc.description.abstractObjectives: The aim of the study was to assess the prevalence, predictors and patterns of genotypic resistance mutations in children after failure of World Health Organization-recommended initial nonnucleoside reverse transcriptase inhibitor (NNRTI)-based treatment regimens. Methods: We carried out a multicentre retrospective study of genotyping tests performed for all HIV-infected children at eight paediatric centres in Thailand who experienced failure of NNRTI therapy at a time when virological monitoring was not routinely available. Results: One hundred and twenty children were included in the study. Their median age (interquartile range) was 9.1 (6.8-11.0) years, the median duration of their NNRTI regimens was 23.7 (15.7-32.6) months, their median CD4 percentage was 12% (4-20%), and their median plasma HIV RNA at the time of genotype testing was 4.8 (4.3-5.2) log10 HIV-1 RNA copies/mL. The nucleoside reverse transcriptase inhibitor (NRTI) resistance mutations found were as follows: 85% of the children had M184V/I, 23% had at least four thymidine analogue mutations, 12% had the Q151M complex, 5% had K65R, and 1% had the 69 insertion. Ninety-eight per cent of the children had at least one NNRTI resistance mutation, and 48% had etravirine mutation-weighted scores ≥4. CD4 percentage <15% prior to switching regimens [odds ratio (OR) 5.49; 95% confidence interval (CI) 2.02-14.93] and plasma HIV RNA>5 log10 copies/mL (OR 2.46; 95% CI 1.04-5.82) were independent predictors of at least four thymidine analogue mutations, the Q151M complex or the 69 insertion. Conclusions: In settings without routine viral load monitoring, second-line antiretroviral therapy regimens should be designed assuming that clinical or immunological failure is associated with high rates of multi-NRTI resistance and NNRTI resistance, including resistance to etravirine. © 2010 British HIV Association.en_US
dc.identifier.citationHIV Medicine. Vol.11, No.9 (2010), 565-572en_US
dc.identifier.doi10.1111/j.1468-1293.2010.00828.xen_US
dc.identifier.issn14681293en_US
dc.identifier.issn14642662en_US
dc.identifier.other2-s2.0-77955610006en_US
dc.identifier.urihttps://repository.li.mahidol.ac.th/handle/20.500.14594/29527
dc.rightsMahidol Universityen_US
dc.rights.holderSCOPUSen_US
dc.source.urihttps://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=77955610006&origin=inwarden_US
dc.subjectMedicineen_US
dc.titleHIV-1 drug resistance mutations in children after failure of first-line nonnucleoside reverse transcriptase inhibitor-based antiretroviral therapyen_US
dc.typeArticleen_US
dspace.entity.typePublication
mu.datasource.scopushttps://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=77955610006&origin=inwarden_US

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