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Prevalence and trends in transmitted and acquired antiretroviral drug resistance, Washington, DC, 1999–2014
BACKGROUND: Drug resistance limits options for antiretroviral therapy (ART) and results in poorer health outcomes among HIV-infected persons. We sought to characterize resistance patterns and to identify predictors of resistance in Washington, DC. METHODS: We analyzed resistance in the DC Cohort, a...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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BioMed Central
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5594524/ https://www.ncbi.nlm.nih.gov/pubmed/28893321 http://dx.doi.org/10.1186/s13104-017-2764-9 |
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author | Aldous, Annette M. Castel, Amanda D. Parenti, David M. |
author_facet | Aldous, Annette M. Castel, Amanda D. Parenti, David M. |
author_sort | Aldous, Annette M. |
collection | PubMed |
description | BACKGROUND: Drug resistance limits options for antiretroviral therapy (ART) and results in poorer health outcomes among HIV-infected persons. We sought to characterize resistance patterns and to identify predictors of resistance in Washington, DC. METHODS: We analyzed resistance in the DC Cohort, a longitudinal study of HIV-infected persons in care in Washington, DC. We measured cumulative drug resistance (CDR) among participants with any genotype between 1999 and 2014 (n = 3411), transmitted drug resistance (TDR) in ART-naïve persons (n = 1503), and acquired drug resistance (ADR) in persons with genotypes before and after ART initiation (n = 309). Using logistic regression, we assessed associations between patient characteristics and transmitted resistance to any antiretroviral. RESULTS: Prevalence of TDR was 20.5%, of ADR 40.5%, and of CDR 45.1% in the respective analysis groups. From 2004 to 2013, TDR prevalence decreased for nucleoside and nucleotide analogue reverse transcriptase inhibitors (15.0 to 5.5%; p = 0.0003) and increased for integrase strand transfer inhibitors (INSTIs) (0.0–1.4%; p = 0.04). In multivariable analysis, TDR was not associated with age, race/ethnicity, HIV risk group, or years from HIV diagnosis. CONCLUSIONS: In this urban cohort of HIV-infected persons, almost half of participants tested had evidence of CDR; and resistance to INSTIs was increasing. If this trend continues, inclusion of the integrase-encoding region in baseline genotype testing should be strongly considered. |
format | Online Article Text |
id | pubmed-5594524 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-55945242017-09-14 Prevalence and trends in transmitted and acquired antiretroviral drug resistance, Washington, DC, 1999–2014 Aldous, Annette M. Castel, Amanda D. Parenti, David M. BMC Res Notes Research Article BACKGROUND: Drug resistance limits options for antiretroviral therapy (ART) and results in poorer health outcomes among HIV-infected persons. We sought to characterize resistance patterns and to identify predictors of resistance in Washington, DC. METHODS: We analyzed resistance in the DC Cohort, a longitudinal study of HIV-infected persons in care in Washington, DC. We measured cumulative drug resistance (CDR) among participants with any genotype between 1999 and 2014 (n = 3411), transmitted drug resistance (TDR) in ART-naïve persons (n = 1503), and acquired drug resistance (ADR) in persons with genotypes before and after ART initiation (n = 309). Using logistic regression, we assessed associations between patient characteristics and transmitted resistance to any antiretroviral. RESULTS: Prevalence of TDR was 20.5%, of ADR 40.5%, and of CDR 45.1% in the respective analysis groups. From 2004 to 2013, TDR prevalence decreased for nucleoside and nucleotide analogue reverse transcriptase inhibitors (15.0 to 5.5%; p = 0.0003) and increased for integrase strand transfer inhibitors (INSTIs) (0.0–1.4%; p = 0.04). In multivariable analysis, TDR was not associated with age, race/ethnicity, HIV risk group, or years from HIV diagnosis. CONCLUSIONS: In this urban cohort of HIV-infected persons, almost half of participants tested had evidence of CDR; and resistance to INSTIs was increasing. If this trend continues, inclusion of the integrase-encoding region in baseline genotype testing should be strongly considered. BioMed Central 2017-09-11 /pmc/articles/PMC5594524/ /pubmed/28893321 http://dx.doi.org/10.1186/s13104-017-2764-9 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 Article Aldous, Annette M. Castel, Amanda D. Parenti, David M. Prevalence and trends in transmitted and acquired antiretroviral drug resistance, Washington, DC, 1999–2014 |
title | Prevalence and trends in transmitted and acquired antiretroviral drug resistance, Washington, DC, 1999–2014 |
title_full | Prevalence and trends in transmitted and acquired antiretroviral drug resistance, Washington, DC, 1999–2014 |
title_fullStr | Prevalence and trends in transmitted and acquired antiretroviral drug resistance, Washington, DC, 1999–2014 |
title_full_unstemmed | Prevalence and trends in transmitted and acquired antiretroviral drug resistance, Washington, DC, 1999–2014 |
title_short | Prevalence and trends in transmitted and acquired antiretroviral drug resistance, Washington, DC, 1999–2014 |
title_sort | prevalence and trends in transmitted and acquired antiretroviral drug resistance, washington, dc, 1999–2014 |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5594524/ https://www.ncbi.nlm.nih.gov/pubmed/28893321 http://dx.doi.org/10.1186/s13104-017-2764-9 |
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