Impact of Abstinence and of Reducing Illicit Drug Use Without Abstinence on Human Immunodeficiency Virus Viral Load.


Journal

Clinical infectious diseases : an official publication of the Infectious Diseases Society of America
ISSN: 1537-6591
Titre abrégé: Clin Infect Dis
Pays: United States
ID NLM: 9203213

Informations de publication

Date de publication:
14 02 2020
Historique:
received: 22 10 2018
accepted: 11 04 2019
pubmed: 18 4 2019
medline: 7 1 2021
entrez: 18 4 2019
Statut: ppublish

Résumé

Substance use is common among people living with human immunodeficiency virus (PLWH) and a barrier to achieving viral suppression. Among PLWH who report illicit drug use, we evaluated associations between HIV viral load (VL) and reduced use of illicit opioids, methamphetamine/crystal, cocaine/crack, and marijuana, regardless of whether or not abstinence was achieved. This was a longitudinal cohort study of PLWH from 7 HIV clinics or 4 clinical studies. We used joint longitudinal and survival models to examine the impact of decreasing drug use and of abstinence for each drug on viral suppression. We repeated analyses using linear mixed models to examine associations between change in frequency of drug use and VL. The number of PLWH who were using each drug at baseline ranged from n = 568 (illicit opioids) to n = 4272 (marijuana). Abstinence was associated with higher odds of viral suppression (odds ratio [OR], 1.4-2.2) and lower relative VL (ranging from 21% to 42% by drug) for all 4 drug categories. Reducing frequency of illicit opioid or methamphetamine/crystal use without abstinence was associated with VL suppression (OR, 2.2, 1.6, respectively). Reducing frequency of illicit opioid or methamphetamine/crystal use without abstinence was associated with lower relative VL (47%, 38%, respectively). Abstinence was associated with viral suppression. In addition, reducing use of illicit opioids or methamphetamine/crystal, even without abstinence, was also associated with viral suppression. Our findings highlight the impact of reducing substance use, even when abstinence is not achieved, and the potential benefits of medications, behavioral interventions, and harm-reduction interventions.

Sections du résumé

BACKGROUND
Substance use is common among people living with human immunodeficiency virus (PLWH) and a barrier to achieving viral suppression. Among PLWH who report illicit drug use, we evaluated associations between HIV viral load (VL) and reduced use of illicit opioids, methamphetamine/crystal, cocaine/crack, and marijuana, regardless of whether or not abstinence was achieved.
METHODS
This was a longitudinal cohort study of PLWH from 7 HIV clinics or 4 clinical studies. We used joint longitudinal and survival models to examine the impact of decreasing drug use and of abstinence for each drug on viral suppression. We repeated analyses using linear mixed models to examine associations between change in frequency of drug use and VL.
RESULTS
The number of PLWH who were using each drug at baseline ranged from n = 568 (illicit opioids) to n = 4272 (marijuana). Abstinence was associated with higher odds of viral suppression (odds ratio [OR], 1.4-2.2) and lower relative VL (ranging from 21% to 42% by drug) for all 4 drug categories. Reducing frequency of illicit opioid or methamphetamine/crystal use without abstinence was associated with VL suppression (OR, 2.2, 1.6, respectively). Reducing frequency of illicit opioid or methamphetamine/crystal use without abstinence was associated with lower relative VL (47%, 38%, respectively).
CONCLUSIONS
Abstinence was associated with viral suppression. In addition, reducing use of illicit opioids or methamphetamine/crystal, even without abstinence, was also associated with viral suppression. Our findings highlight the impact of reducing substance use, even when abstinence is not achieved, and the potential benefits of medications, behavioral interventions, and harm-reduction interventions.

Identifiants

pubmed: 30994900
pii: 5474820
doi: 10.1093/cid/ciz299
pmc: PMC7319266
doi:

Substances chimiques

Illicit Drugs 0

Types de publication

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

Langues

eng

Sous-ensembles de citation

IM

Pagination

867-874

Subventions

Organisme : NIDA NIH HHS
ID : R01 DA030776
Pays : United States
Organisme : NIDA NIH HHS
ID : R01 DA030771
Pays : United States
Organisme : NIDA NIH HHS
ID : R01 DA032061
Pays : United States
Organisme : NIDA NIH HHS
ID : R34 DA035728
Pays : United States
Organisme : NIDA NIH HHS
ID : R01 DA030762
Pays : United States
Organisme : NIDA NIH HHS
ID : R01 DA032082
Pays : United States
Organisme : NIDA NIH HHS
ID : R01 DA032098
Pays : United States
Organisme : NIDA NIH HHS
ID : R01 DA030778
Pays : United States
Organisme : NIAAA NIH HHS
ID : U01 AA020802
Pays : United States
Organisme : NIDA NIH HHS
ID : R01 DA032059
Pays : United States
Organisme : NIDA NIH HHS
ID : R01 DA030793
Pays : United States
Organisme : NIDA NIH HHS
ID : U01 DA037702
Pays : United States
Organisme : NIDA NIH HHS
ID : R01 DA030766
Pays : United States
Organisme : NIDA NIH HHS
ID : U01 DA036935
Pays : United States
Organisme : NIAID NIH HHS
ID : P30 AI027767
Pays : United States
Organisme : NIDA NIH HHS
ID : R01 DA032100
Pays : United States
Organisme : NIMH NIH HHS
ID : R01 MH094090
Pays : United States
Organisme : NIDA NIH HHS
ID : R01 DA032083
Pays : United States
Organisme : NIDA NIH HHS
ID : R01 DA032057
Pays : United States
Organisme : NIDA NIH HHS
ID : R01 DA032106
Pays : United States
Organisme : NIDA NIH HHS
ID : R01 DA030781
Pays : United States
Organisme : NIDA NIH HHS
ID : R01 DA032110
Pays : United States
Organisme : NIDA NIH HHS
ID : R01 DA030770
Pays : United States
Organisme : NIAAA NIH HHS
ID : U24 AA020801
Pays : United States
Organisme : NHLBI NIH HHS
ID : R01 HL126538
Pays : United States
Organisme : NIAID NIH HHS
ID : P30 AI027757
Pays : United States
Organisme : NIDA NIH HHS
ID : R01 DA030768
Pays : United States
Organisme : NIDA NIH HHS
ID : R01 DA047045
Pays : United States
Organisme : NIAAA NIH HHS
ID : U01 AA020793
Pays : United States
Organisme : NIAID NIH HHS
ID : P30 AI094189
Pays : United States
Organisme : NIDA NIH HHS
ID : R01 DA032080
Pays : United States
Organisme : NIDA NIH HHS
ID : R01 DA030747
Pays : United States
Organisme : NIAID NIH HHS
ID : R24 AI067039
Pays : United States
Organisme : NIAID NIH HHS
ID : P30 AI050410
Pays : United States

Informations de copyright

© The Author(s) 2019. Published by Oxford University Press for the Infectious Diseases Society of America. All rights reserved. For permissions, e-mail: journals.permissions@oup.com.

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Auteurs

Robin M Nance (RM)

Department of Biostatistics, University of Washington, Collaborative Health Studies Coordinating Center, Seattle.

Maria Esther Perez Trejo (MEP)

Department of Biostatistics, University of Washington, Collaborative Health Studies Coordinating Center, Seattle.

Bridget M Whitney (BM)

Department of Biostatistics, University of Washington, Collaborative Health Studies Coordinating Center, Seattle.

Joseph A C Delaney (JAC)

Department of Biostatistics, University of Washington, Collaborative Health Studies Coordinating Center, Seattle.

Fredrick L Altice (FL)

Department of Medicine, Yale University School of Medicine, New Haven, Connecticut.

Curt G Beckwith (CG)

Department of Medicine, Alpert Medical School of Brown University, Providence, Rhode Island.

Geetanjali Chander (G)

Division of General Internal Medicine, Johns Hopkins University, Baltimore, Maryland.

Redonna Chandler (R)

National Institute on Drug Abuse, Bethesda, Maryland.

Katerina Christopoulous (K)

Department of Medicine, University of California-San Francisco.

Chinazo Cunningham (C)

Department of Medicine, Albert Einstein College of Medicine/Montefiore Medical Center, Bronx, New York.

William E Cunningham (WE)

Department of Medicine, University of California-Los Angeles.

Carlos Del Rio (C)

Department of Global Health, Emory University, Atlanta, Georgia.

Dennis Donovan (D)

Department of Psychiatry, University of Washington, Seattle.

Joseph J Eron (JJ)

Department of Medicine, University of North Carolina, Chapel Hill.

Rob J Fredericksen (RJ)

Department of Medicine, University of Washington, Seattle.

Shoshana Kahana (S)

National Institute on Drug Abuse, Bethesda, Maryland.

Mari M Kitahata (MM)

Department of Medicine, University of Washington, Seattle.

Richard Kronmal (R)

Department of Biostatistics, University of Washington, Collaborative Health Studies Coordinating Center, Seattle.

Irene Kuo (I)

Department of Epidemiology, George Washington University, Washington, DC.

Ann Kurth (A)

School of Nursing, Yale University School of Medicine, New Haven, Connecticut.

W Chris Mathews (WC)

Department of Medicine, University of California-San Diego, UCSD Medical Center.

Kenneth H Mayer (KH)

Harvard Medical School, Fenway Institute, Boston, Maryland.

Richard D Moore (RD)

Department of Medicine, Johns Hopkins University, Baltimore, Maryland.

Michael J Mugavero (MJ)

Department of Medicine, University of Alabama-Birmingham.

Lawrence J Ouellet (LJ)

University of Illinois-Chicago.

Vu M Quan (VM)

Centers for Disease Control and Prevention, Atlanta, Georgia.

Michael S Saag (MS)

Department of Medicine, University of Alabama-Birmingham.

Jane M Simoni (JM)

Department of Psychology, University of Washington, Seattle.

Sandra Springer (S)

Department of Medicine, Yale University School of Medicine, New Haven, Connecticut.

Lauren Strand (L)

Department of Biostatistics, University of Washington, Collaborative Health Studies Coordinating Center, Seattle.

Faye Taxman (F)

Department of Criminology, George Mason University, Fairfax, Virginia.

Jeremy D Young (JD)

University of Illinois-Chicago.

Heidi M Crane (HM)

Department of Medicine, University of Washington, Seattle.

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