High levels of pretreatment and acquired HIV drug resistance in Nicaragua: results from the first nationally representative survey, 2016.
HIV
Nicaragua
World Health Organization
antiretroviral therapy
drug resistance
surveillance
treatment failure
Journal
Journal of the International AIDS Society
ISSN: 1758-2652
Titre abrégé: J Int AIDS Soc
Pays: Switzerland
ID NLM: 101478566
Informations de publication
Date de publication:
12 2019
12 2019
Historique:
received:
22
02
2019
revised:
04
11
2019
accepted:
20
11
2019
entrez:
21
12
2019
pubmed:
21
12
2019
medline:
5
6
2020
Statut:
ppublish
Résumé
A nationally representative HIV drug resistance (HIVDR) survey in Nicaragua was conducted to estimate the prevalence of pretreatment HIVDR (PDR) among antiretroviral therapy (ART) initiators and acquired HIVDR among people living with HIV (PLHIV) who had received ART for 12 ± 3 months (ADR12) and ≥48 months (ADR48). A nationwide cross-sectional survey with a two-stage cluster sampling was conducted from March to November 2016. Nineteen of 45 total ART clinics representing >90% of the national cohort of adults on ART were included. ART initiators were defined as PLHIV initiating or reinitiating first-line ART. HIVDR was assessed for protease, reverse transcriptase and integrase Sanger sequences using the Stanford HIVdb algorithm. Viral load (VL) suppression was defined as <1000 copies/mL. Results were weighted according to the survey design. A total of 638 participants were enrolled (PDR: 171; ADR12: 114; ADR48: 353). The proportion of ART initiators with prior exposure to antiretrovirals (ARVs) was 12.3% (95% CI: 5.8% to 24.3%). PDR prevalence to any drug was 23.4% (95% CI: 14.4% to 35.6%), and 19.3% (95% CI: 12.2% to 29.1%) to non-nucleoside reverse transcriptase inhibitors (NNRTI). NNRTI PDR was higher in ART initiators with previous ARV exposure compared with those with no exposure (76.2% vs. 11.0%, p < 0.001). Protease inhibitors (PI) and integrase strand transfer inhibitors PDR was not observed. VL suppression rate was 77.8% (95% CI: 67.1% to 85.8%) in ADR12 and 70.3% (95% CI: 66.7% to 73.8%) in ADR48. ADR12 prevalence to any drug among PLHIV without VL suppression was 85.1% (95% CI: 66.1% to 94.4%), 82.4% to NNRTI and 70.2% to nucleoside reverse transcriptase inhibitors (NRTI). ADR48 prevalence to any drug among PLHIV without VL suppression was 75.5% (95% CI: 63.5% to 84.5 %), 70.7% to NNRTI, 59.4% to NRTI and 4.6% to PI. Despite implementation challenges yielding low-precision HIVDR estimates, high rates of NNRTI PDR were observed in Nicaragua, suggesting consideration of non-NNRTI-based first-line regimens for ART initiators. Strengthened HIVDR monitoring, systematic VL testing, and improved ART adherence support are also warranted.
Identifiants
pubmed: 31860167
doi: 10.1002/jia2.25429
pmc: PMC6924533
doi:
Substances chimiques
Anti-HIV Agents
0
Types de publication
Journal Article
Research Support, Non-U.S. Gov't
Research Support, U.S. Gov't, P.H.S.
Langues
eng
Sous-ensembles de citation
IM
Pagination
e25429Subventions
Organisme : PEPFAR
Pays : United States
Informations de copyright
© 2019 The Authors. Journal of the International AIDS Society published by John Wiley & Sons Ltd on behalf of the International AIDS Society.
Références
J Infect Dis. 2017 Dec 1;216(suppl_9):S801-S804
pubmed: 29040686
J Int AIDS Soc. 2019 Dec;22(12):e25429
pubmed: 31860167
PLoS One. 2016 Oct 13;11(10):e0164156
pubmed: 27736898
J Virol Methods. 2008 Nov;153(2):176-81
pubmed: 18706932
J Antimicrob Chemother. 2017 Nov 01;72(11):3149-3158
pubmed: 28961972
J Infect Dis. 2017 Dec 1;216(suppl_9):S798-S800
pubmed: 28973412
Lancet Infect Dis. 2018 Mar;18(3):346-355
pubmed: 29198909
J Clin Microbiol. 2012 Jun;50(6):1936-42
pubmed: 22403431
PLoS One. 2015 Nov 11;10(11):e0142604
pubmed: 26558396
Rev Chilena Infectol. 2013 Dec;30(6):630-7
pubmed: 24522307
J Antimicrob Chemother. 2019 Apr 1;74(4):1044-1055
pubmed: 30597094
Nucleic Acids Res. 2003 Jan 1;31(1):298-303
pubmed: 12520007
J Acquir Immune Defic Syndr. 2013 Sep 1;64(1):74-8
pubmed: 23774877
Infect Genet Evol. 2013 Oct;19:337-48
pubmed: 23660484