Accumulation of HIV-1 Drug Resistance Mutations and Methamphetamine Use.


Journal

Current HIV research
ISSN: 1873-4251
Titre abrégé: Curr HIV Res
Pays: Netherlands
ID NLM: 101156990

Informations de publication

Date de publication:
2021
Historique:
received: 01 02 2021
revised: 03 05 2021
accepted: 17 05 2021
pubmed: 29 6 2021
medline: 3 5 2022
entrez: 28 6 2021
Statut: ppublish

Résumé

Antiretroviral therapy (ART) non-adherence and methamphetamine use are associated with higher HIV drug resistance prevalence. How they affect drug resistance mutations accumulation is less studied. We assessed factors associated with drug resistance mutations accumulation. We evaluated HIV chronically-infected patients from a clinic-based research cohort on first-line ART regimens with genotype results within 30 days of baseline. Methamphetamine use and ART adherence were self-reported at each study visit. High ART adherence was defined as 0-5% missed doses in the last 30 days. One-hundred twenty-five patients contributed 496 study visits. At baseline, 81% of patients reported high ART adherence; 90% reported no methamphetamine use in the prior 4 months, 8% used monthly or less and 2% used daily or weekly. Methamphetamine users and non-users had similarly high ART adherence (p=0.93). Adjusted incidence rate ratio (aIRR) of drug resistance mutations accumulation was 2.04 (95% CI 0.64, 6.46) for daily/weekly users and 1.71 (95% CI 0.66, 4.42) for patients with monthly or less users, compared to non-users. aIRR was 0.71 (95% CI 0.44, 1.15) with >5-10% missed ART doses and 1.21 (95% CI 0.80, 1.83) with >10% missed doses compared to 0-5% missed doses. We found no strong evidence for the effect of methamphetamine use and ART adherence on drug resistance mutations accumulation. Research cohort patients may have been more engaged in care and treatment adherent than non-cohort patients. Our findings suggest methamphetamine use might not lead to treatment failure among HIV patients who are otherwise engaged in care.

Sections du résumé

BACKGROUND
Antiretroviral therapy (ART) non-adherence and methamphetamine use are associated with higher HIV drug resistance prevalence. How they affect drug resistance mutations accumulation is less studied.
OBJECTIVE
We assessed factors associated with drug resistance mutations accumulation.
METHODS
We evaluated HIV chronically-infected patients from a clinic-based research cohort on first-line ART regimens with genotype results within 30 days of baseline. Methamphetamine use and ART adherence were self-reported at each study visit. High ART adherence was defined as 0-5% missed doses in the last 30 days.
RESULTS
One-hundred twenty-five patients contributed 496 study visits. At baseline, 81% of patients reported high ART adherence; 90% reported no methamphetamine use in the prior 4 months, 8% used monthly or less and 2% used daily or weekly. Methamphetamine users and non-users had similarly high ART adherence (p=0.93). Adjusted incidence rate ratio (aIRR) of drug resistance mutations accumulation was 2.04 (95% CI 0.64, 6.46) for daily/weekly users and 1.71 (95% CI 0.66, 4.42) for patients with monthly or less users, compared to non-users. aIRR was 0.71 (95% CI 0.44, 1.15) with >5-10% missed ART doses and 1.21 (95% CI 0.80, 1.83) with >10% missed doses compared to 0-5% missed doses.
CONCLUSION
We found no strong evidence for the effect of methamphetamine use and ART adherence on drug resistance mutations accumulation. Research cohort patients may have been more engaged in care and treatment adherent than non-cohort patients. Our findings suggest methamphetamine use might not lead to treatment failure among HIV patients who are otherwise engaged in care.

Identifiants

pubmed: 34176462
pii: CHR-EPUB-116329
doi: 10.2174/1570162X19666210625103902
pmc: PMC10659984
mid: NIHMS1940656
doi:

Substances chimiques

Anti-HIV Agents 0
Methamphetamine 44RAL3456C

Types de publication

Journal Article Research Support, N.I.H., Extramural

Langues

eng

Sous-ensembles de citation

IM

Pagination

497-503

Subventions

Organisme : NIAID NIH HHS
ID : P30 AI027763
Pays : United States
Organisme : NIDA NIH HHS
ID : R01 DA017476
Pays : United States
Organisme : NIMH NIH HHS
ID : R01 MH096642
Pays : United States
Organisme : NIAID NIH HHS
ID : R24 AI067039
Pays : United States

Informations de copyright

Copyright© Bentham Science Publishers; For any queries, please email at epub@benthamscience.net.

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Auteurs

Hong-Ha M Truong (HM)

Department of Medicine, University of California, San Francisco, 94158, United States.

Robin Fatch (R)

Department of Medicine, University of California, San Francisco, 94158, United States.

Steven G Deeks (SG)

Department of Medicine, University of California, San Francisco, 94158, United States.

Melissa Krone (M)

Department of Medicine, University of California, San Francisco, 94158, United States.

Jeffrey N Martin (JN)

Department of Medicine, University of California, San Francisco, 94158, United States.

Peter W Hunt (PW)

Department of Medicine, University of California, San Francisco, 94158, United States.

Paula J Lum (PJ)

Department of Medicine, University of California, San Francisco, 94158, United States.

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Classifications MeSH