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Virological suppression in children and adolescents is not influenced by genotyping, but depends on optimal adherence to antiretroviral therapy
OBJECTIVE: To evaluate the virological outcomes in children and adolescents infected with HIV-1 in Salvador, Bahia according to genotyping results. METHODS: We retrospectively evaluated the rates of virological suppression of children and adolescents submitted to HIV-1 genotyping test from January/2...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Elsevier
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9427598/ https://www.ncbi.nlm.nih.gov/pubmed/28253476 http://dx.doi.org/10.1016/j.bjid.2017.02.001 |
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author | Abreu, Juliana Costa de Vaz, Sara Nunes Netto, Eduardo Martins Brites, Carlos |
author_facet | Abreu, Juliana Costa de Vaz, Sara Nunes Netto, Eduardo Martins Brites, Carlos |
author_sort | Abreu, Juliana Costa de |
collection | PubMed |
description | OBJECTIVE: To evaluate the virological outcomes in children and adolescents infected with HIV-1 in Salvador, Bahia according to genotyping results. METHODS: We retrospectively evaluated the rates of virological suppression of children and adolescents submitted to HIV-1 genotyping test from January/2008 to December/2012. The participants were followed in the two referral centers for pediatric AIDS care, in Salvador, Brazil. Resistance mutations, drug sensitivity profiles, and viral subtypes were analyzed using the Stanford HIV-1 Drug Resistance Database. Adherence was estimated by drugs withdrawal at pharmacies of the two sites. RESULTS: 101 subjects were included: 35 (34.6%) were drug-naïve, and the remaining 66 were failing ART. In drug-naïve group, 3 (8.6%), presented with NNRTIs resistance mutations, along with polymorphic mutations to PIs in most (82.8%) of them. Among the failing therapy group, we detected a high frequency (89.4%) of resistance mutations to PIs, NRTI (84.8%), and NNRTI (59.1%). Virological suppression after introduction/modification of genotyping-guided ART was achieved only for patients (53.1%) with drug withdrawal over 95%. Main detected HIV-1 subtypes were B (67.3%), F (7.9), C (1.9%), and recombinant forms (22.9%). CONCLUSIONS: Despite the use of genotyping tests in guidance of a more effective antiretroviral regimen, poor adherence to ART seems to be the main determinant of low virological suppression rate for children and adolescents, in Salvador, Brazil. |
format | Online Article Text |
id | pubmed-9427598 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Elsevier |
record_format | MEDLINE/PubMed |
spelling | pubmed-94275982022-09-01 Virological suppression in children and adolescents is not influenced by genotyping, but depends on optimal adherence to antiretroviral therapy Abreu, Juliana Costa de Vaz, Sara Nunes Netto, Eduardo Martins Brites, Carlos Braz J Infect Dis Original Article OBJECTIVE: To evaluate the virological outcomes in children and adolescents infected with HIV-1 in Salvador, Bahia according to genotyping results. METHODS: We retrospectively evaluated the rates of virological suppression of children and adolescents submitted to HIV-1 genotyping test from January/2008 to December/2012. The participants were followed in the two referral centers for pediatric AIDS care, in Salvador, Brazil. Resistance mutations, drug sensitivity profiles, and viral subtypes were analyzed using the Stanford HIV-1 Drug Resistance Database. Adherence was estimated by drugs withdrawal at pharmacies of the two sites. RESULTS: 101 subjects were included: 35 (34.6%) were drug-naïve, and the remaining 66 were failing ART. In drug-naïve group, 3 (8.6%), presented with NNRTIs resistance mutations, along with polymorphic mutations to PIs in most (82.8%) of them. Among the failing therapy group, we detected a high frequency (89.4%) of resistance mutations to PIs, NRTI (84.8%), and NNRTI (59.1%). Virological suppression after introduction/modification of genotyping-guided ART was achieved only for patients (53.1%) with drug withdrawal over 95%. Main detected HIV-1 subtypes were B (67.3%), F (7.9), C (1.9%), and recombinant forms (22.9%). CONCLUSIONS: Despite the use of genotyping tests in guidance of a more effective antiretroviral regimen, poor adherence to ART seems to be the main determinant of low virological suppression rate for children and adolescents, in Salvador, Brazil. Elsevier 2017-02-27 /pmc/articles/PMC9427598/ /pubmed/28253476 http://dx.doi.org/10.1016/j.bjid.2017.02.001 Text en © 2017 Sociedade Brasileira de Infectologia. Published by Elsevier Editora Ltda. https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/). |
spellingShingle | Original Article Abreu, Juliana Costa de Vaz, Sara Nunes Netto, Eduardo Martins Brites, Carlos Virological suppression in children and adolescents is not influenced by genotyping, but depends on optimal adherence to antiretroviral therapy |
title | Virological suppression in children and adolescents is not influenced by genotyping, but depends on optimal adherence to antiretroviral therapy |
title_full | Virological suppression in children and adolescents is not influenced by genotyping, but depends on optimal adherence to antiretroviral therapy |
title_fullStr | Virological suppression in children and adolescents is not influenced by genotyping, but depends on optimal adherence to antiretroviral therapy |
title_full_unstemmed | Virological suppression in children and adolescents is not influenced by genotyping, but depends on optimal adherence to antiretroviral therapy |
title_short | Virological suppression in children and adolescents is not influenced by genotyping, but depends on optimal adherence to antiretroviral therapy |
title_sort | virological suppression in children and adolescents is not influenced by genotyping, but depends on optimal adherence to antiretroviral therapy |
topic | Original Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9427598/ https://www.ncbi.nlm.nih.gov/pubmed/28253476 http://dx.doi.org/10.1016/j.bjid.2017.02.001 |
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