Associations of hepatitis C virus (HCV) antibody positivity with opioid, stimulant, and polysubstance injection among people who inject drugs (PWID) in rural U.S. communities.

HCV Injection drug use Opioids Polysubstance use Rural Stimulants

Journal

The International journal on drug policy
ISSN: 1873-4758
Titre abrégé: Int J Drug Policy
Pays: Netherlands
ID NLM: 9014759

Informations de publication

Date de publication:
06 Oct 2023
Historique:
received: 19 01 2023
revised: 18 09 2023
accepted: 29 09 2023
medline: 9 10 2023
pubmed: 9 10 2023
entrez: 8 10 2023
Statut: aheadofprint

Résumé

People who inject drugs (PWID) in the rural U.S. often inject stimulants, alone or with opioids. The impact of these substance use patterns may influence HCV risk behaviors. This analysis examines the associations of HCV antibody positivity with injecting only opioids, only stimulants (methamphetamine/cocaine), and opioids and stimulants together among rural PWID. The Rural Opioid Initiative (ROI) consists of eight research sites that enrolled people who use drugs in rural communities in ten U.S. states from 2018 to 2020. This cross-sectional analysis included adult participants who resided in a study area and injected any drug in the past 30 days. The primary outcome was HCV antibody positivity. The exposure of interest was injection drug use classified as only opioids, only stimulants, separate injections of opioids and stimulants, and same-syringe injection of both in the past 30 days. We used multivariable log-binomial regression with generalized linear mixed models to generate prevalence ratios (P.R.) adjusted for demographics, injection history, health insurance, and substance use treatment. Among 3,084 participants enrolled in the ROI, 1,982 met inclusion criteria. Most participants injected opioids and stimulants in the same syringe (34%) or separately (21%), followed by injecting only stimulants (26%), and injecting only opioids (19%). Half (51%) were HCV antibody positive. Compared to people who injected only stimulants, HCV antibody positivity was more prevalent among people who injected opioids alone (aPR=1.62, 95% CI:(1.29-2.03)), injected both opioids and stimulants separately (aPR=1.61, 95% CI:(1.32-1.95)), and in the same syringe (aPR=1.54, 95% CI:(1.28-1.85)). HCV antibody positivity, indicating prior exposure, was highest among those who had recently injected opioids, alone or with stimulants. Additional nucleic acid testing is necessary to confirm active infection. More research is needed to determine the underlying causes of HCV antibody positivity by injection use.

Sections du résumé

BACKGROUND BACKGROUND
People who inject drugs (PWID) in the rural U.S. often inject stimulants, alone or with opioids. The impact of these substance use patterns may influence HCV risk behaviors. This analysis examines the associations of HCV antibody positivity with injecting only opioids, only stimulants (methamphetamine/cocaine), and opioids and stimulants together among rural PWID.
METHODS METHODS
The Rural Opioid Initiative (ROI) consists of eight research sites that enrolled people who use drugs in rural communities in ten U.S. states from 2018 to 2020. This cross-sectional analysis included adult participants who resided in a study area and injected any drug in the past 30 days. The primary outcome was HCV antibody positivity. The exposure of interest was injection drug use classified as only opioids, only stimulants, separate injections of opioids and stimulants, and same-syringe injection of both in the past 30 days. We used multivariable log-binomial regression with generalized linear mixed models to generate prevalence ratios (P.R.) adjusted for demographics, injection history, health insurance, and substance use treatment.
RESULTS RESULTS
Among 3,084 participants enrolled in the ROI, 1,982 met inclusion criteria. Most participants injected opioids and stimulants in the same syringe (34%) or separately (21%), followed by injecting only stimulants (26%), and injecting only opioids (19%). Half (51%) were HCV antibody positive. Compared to people who injected only stimulants, HCV antibody positivity was more prevalent among people who injected opioids alone (aPR=1.62, 95% CI:(1.29-2.03)), injected both opioids and stimulants separately (aPR=1.61, 95% CI:(1.32-1.95)), and in the same syringe (aPR=1.54, 95% CI:(1.28-1.85)).
CONCLUSION CONCLUSIONS
HCV antibody positivity, indicating prior exposure, was highest among those who had recently injected opioids, alone or with stimulants. Additional nucleic acid testing is necessary to confirm active infection. More research is needed to determine the underlying causes of HCV antibody positivity by injection use.

Identifiants

pubmed: 37806839
pii: S0955-3959(23)00269-4
doi: 10.1016/j.drugpo.2023.104222
pii:
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

104222

Subventions

Organisme : NIDA NIH HHS
ID : UG3 DA044825
Pays : United States
Organisme : NIDA NIH HHS
ID : UH3 DA044798
Pays : United States
Organisme : NIDA NIH HHS
ID : UG3 DA044826
Pays : United States
Organisme : NIDA NIH HHS
ID : R01 DA052214
Pays : United States
Organisme : NIDA NIH HHS
ID : UG3 DA044798
Pays : United States
Organisme : NIDA NIH HHS
ID : UH3 DA044826
Pays : United States
Organisme : NIDA NIH HHS
ID : R01 DA047334
Pays : United States
Organisme : NCATS NIH HHS
ID : U01 TR002631
Pays : United States

Informations de copyright

Copyright © 2023. Published by Elsevier B.V.

Déclaration de conflit d'intérêts

Declaration of Competing Interest The authors declare that they have no known competing financial interests or personal relationships that could have appeared to influence the work reported in this paper.

Auteurs

Angela T Estadt (AT)

Ohio State University, College of Public Health, Division of Epidemiology, United States. Electronic address: estadt.24@osu.edu.

William C Miller (WC)

Ohio State University, College of Public Health, Division of Epidemiology, United States; Department of Epidemiology, University of North Carolina at Chapel Hill, Gillings School of Global Public Health, Chapel Hill, North Carolina, United States of America.

David Kline (D)

Wake Forest University School of Medicine, Division of Public Health Sciences, Department of Biostatistics and Data Science, United States.

Bridget M Whitney (BM)

University of Washington, Department of Medicine, United States.

April M Young (AM)

University of Kentucky, Department of Epidemiology and Environmental Health, Center on Drug and Alcohol Research, United States.

P Todd Korthuis (P)

Oregon Health & Science University, Department of Medicine, Section of Addiction Medicine, United States.

Thomas J Stopka (TJ)

Department of Public Health and Community Medicine, Tufts University School of Medicine, United States.

Judith Feinberg (J)

West Virginia University School of Medicine, Departments of Behavioral Medicine and Psychiatry and Medicine/Infectious Diseases, United States.

William A Zule (WA)

RTI International, Research Triangle Park, NC, United States.

Mai T Pho (MT)

University of Chicago, Department of Medicine, United States.

Peter D Friedmann (PD)

University of Massachusetts Medical School-Baystate and Baystate Health, United States.

Ryan P Westergaard (RP)

University of Wisconsin School of Medicine and Public Health, Department of Medicine, Division of Infectious Diseases, United States.

Kellene V Eagen (KV)

University of Wisconsin - Madison, School of Medicine and Public Health, Department of Family Medicine and Community Health, United States.

Andrew Seaman (A)

Oregon Health & Science University, School of Medicine, United States.

Jimmy Ma (J)

University of Washington, Department of Medicine, Division of Allergy and Infectious Diseases, United States.

Vivian F Go (VF)

University of North Carolina at Chapel Hill, Gillings School of Global Public Health, Department of Health Behavior, United States.

Kathryn E Lancaster (KE)

Ohio State University, College of Public Health, Division of Epidemiology, United States; Division of Public Health Sciences, Department of Implementation Science, Wake Forest University School of Medicine, Winston-Salem, North Carolina, United States of America.

Classifications MeSH