Resumen
Background. Transmitted drug resistance (TDR) may compromise response to antiretroviral therapy (ART). However, there are limited data on TDR patterns and impacts among people who use illicit drugs (PWUD). Methods. Data were drawn from 2 prospective cohorts of PWUD in Vancouver, Canada. We characterized patterns of TDR among human immunodeficiency virus (HIV)-infected PWUD, and assessed its impacts on first-line ART virological outcomes. Results. Between 1996 and 2015, among 573 ART-naive PWUD (18% with recent HIV infection), the overall TDR prevalence was 9.8% (95% confidence interval [CI], 7.3%-12.2%), with an increasing trend over time, from 8.5% in 1996-1999 to 21.1% in 2010- 2015 (P = .003), mainly driven by resistance to nonnucleoside reverse transcriptase inhibitors (NNRTIs). TDR-associated mutations were more common for NNRTIs (5.4%), followed by nucleoside reverse transcriptase inhibitors (3.0%) and protease inhibitors (1.9%). TDR prevalence was lower among recently infected PWUD (adjusted odds ratio, 0.39 [95% CI, .15-.87]). Participants with TDR had higher risk of virological failure than those without TDR (log-rank P = .037) in the first year of ART. Conclusions. Between 1996 and 2015, TDR prevalence increased significantly among PWUD in Vancouver. Higher risk of virological failure among PWUD with TDR may be explained by some inappropriate ART prescribing, as well as undetected minority resistant variants in participants with chronic HIV infection. Our findings support baseline resistance testing early in the course of HIV infection to guide ART selection among PWUD in our setting.
Idioma original | English |
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Páginas (desde-hasta) | 796-802 |
Número de páginas | 7 |
Publicación | Clinical Infectious Diseases |
Volumen | 65 |
N.º | 5 |
DOI | |
Estado | Published - sep. 1 2017 |
Publicado de forma externa | Sí |
Nota bibliográfica
Funding Information:Potential conflicts of interest. The University of British Columbia has received unstructured funding from NG Biomed, Ltd, an applicant to the Canadian federal government, for a license to produce medical cannabis, to support M.-J. M.’s research. J. M. has received limited unrestricted funding, paid to his institution, from AbbVie, Bristol-Myers Squibb, Gilead Sciences, Janssen, Merck, and ViiV Healthcare. P. R. H. has received grants from, served as an ad hoc advisor to, or spoke at various events sponsored by Pfizer, GlaxoSmithKline, Abbott, Merck, Virco, and Monogram. All other authors report no potential conflicts. All authors have submitted the ICMJE Form for Disclosure of Potential Conflicts of Interest. Conflicts that the editors consider relevant to the content of the manuscript have been disclosed.
Funding Information:
Financial support. This work was supported by the US National Institute on Drug Abuse (NIDA) at the US National Institutes of Health (NIH) (grant numbers U01-DA038886 and R01-DA021525). M. E. S. is supported by a Michael Smith Foundation for Health Research (MSFHR) postdoctoral fellowship award and a Canada Addiction Medicine Research Fellowship from NIDA (R25-DA037756). M.-J. M. is supported in part by the NIH (grant number R01-DA021525), a Scholar Award from MSFHR, and a New Investigator award from the Canadian Institutes of Health Research (CIHR). P. R. H. is supported by a CIHR/GlaxoSmithKline Research Chair in clinical virology. J. M. is supported by the British Columbia Ministry of Health and through an Avant-Garde Award from NIDA at the NIH (1DP1DA026182). K. H. is supported by a CIHR New Investigator Award (MSH-141971).
Publisher Copyright:
© Author 2017. Published by Oxford University Press for the Infectious Diseases Society of America. All rights reserved.
ASJC Scopus Subject Areas
- Microbiology (medical)
- Infectious Diseases
PubMed: MeSH publication types
- Journal Article