Unreported alcohol use was common but did not impact hepatitis C cure in HIV-infected persons who use drugs.
HIV
alcohol use
hepatitis C care continuum
hepatitis C virus
substance use
Journal
Journal of viral hepatitis
ISSN: 1365-2893
Titre abrégé: J Viral Hepat
Pays: England
ID NLM: 9435672
Informations de publication
Date de publication:
05 2020
05 2020
Historique:
received:
07
10
2019
revised:
19
11
2019
accepted:
25
11
2019
pubmed:
20
12
2019
medline:
10
8
2021
entrez:
20
12
2019
Statut:
ppublish
Résumé
We investigated the prevalence and impact of heavy alcohol use on the hepatitis C virus (HCV) care continuum amongst HIV/HCV co-infected persons who use drugs. In the CHAMPS study, 144 HIV/HCV co-infected persons were randomized to contingent cash incentives, peer mentors and usual care to evaluate the impact on HCV care. Alcohol use was ascertained using the 10-item AUDIT (hazardous: male ≥8, female ≥4) and phosphatidylethanol (PEth) (heavy: ≥50 ng/mL), an alcohol biomarker. Log binomial regression was used to evaluate the association between heavy alcohol use and failure to initiate treatment and to achieve sustained virologic response (SVR). Of the 135 participants with PEth data, median age was 55 years, 59% were male, 92% were Black, 91% reported a history of drug use, and 97% were on antiretroviral therapy. Hazardous drinking was reported on AUDIT by 28% of participants, and 35% had heavy alcohol use by PEth. Of the 47 individuals with a PEth ≥50 ng/mL, 23 (49%) reported no or minimal alcohol use by AUDIT. HCV treatment was initiated in 103 of 135 participants, and SVR was achieved in 92%. PEth ≥50 ng/mL (Relative Risk [RR] 0.72, 95% CI 0.35-1.48) was not significantly associated with failure to initiate HCV treatment or failure to achieve SVR (RR 0.85, 95% CI 0.46-1.57).In conclusion, alcohol use was common and frequently not detected by self-report. However, heavy alcohol use, even when measured objectively, was not associated with failure to initiate HCV treatment or to achieve cure.
Identifiants
pubmed: 31854069
doi: 10.1111/jvh.13251
pmc: PMC7890377
mid: NIHMS1555154
doi:
Types de publication
Journal Article
Randomized Controlled Trial
Research Support, N.I.H., Extramural
Langues
eng
Sous-ensembles de citation
IM
Pagination
476-483Subventions
Organisme : NIDA NIH HHS
ID : K24 DA034621
Pays : United States
Organisme : NIH HHS
ID : K23DA041294
Pays : United States
Organisme : NIAAA NIH HHS
ID : K24AA027483
Pays : United States
Organisme : NIH HHS
ID : U24AA020801
Pays : United States
Organisme : NIDA NIH HHS
ID : U01 DA036935
Pays : United States
Organisme : National Institute of Allergy and Infectious Diseases
ID : P30AI094189
Pays : International
Organisme : NIDA NIH HHS
ID : U01DA036935
Pays : United States
Organisme : NIDA NIH HHS
ID : R37DA013806
Pays : United States
Organisme : NIDA NIH HHS
ID : K23 DA041294
Pays : United States
Organisme : NIH HHS
ID : K24AA027483
Pays : United States
Organisme : NIAAA NIH HHS
ID : U24 AA020801
Pays : United States
Organisme : NIDA NIH HHS
ID : K24DA034621
Pays : United States
Organisme : Johns Hopkins Center for AIDS Research
ID : P30AI094189
Pays : International
Organisme : NIH HHS
ID : U01DA036935
Pays : United States
Organisme : NIAAA NIH HHS
ID : U24AA020801
Pays : United States
Organisme : NIDA NIH HHS
ID : K23DA041294
Pays : United States
Organisme : NIH HHS
ID : R01DA16065
Pays : United States
Organisme : NIDA NIH HHS
ID : R37 DA013806
Pays : United States
Organisme : NIH HHS
ID : K24DA034621
Pays : United States
Organisme : NCATS NIH HHS
ID : UL1 TR001079
Pays : United States
Organisme : NCATS NIH HHS
ID : UL1TR001079
Pays : United States
Organisme : NIAID NIH HHS
ID : P30 AI094189
Pays : United States
Organisme : NIAAA NIH HHS
ID : K24 AA027483
Pays : United States
Organisme : NIH HHS
ID : R37DA013806
Pays : United States
Organisme : NIDA NIH HHS
ID : R01DA16065
Pays : United States
Organisme : NIDA NIH HHS
ID : R01 DA016065
Pays : United States
Informations de copyright
© 2019 John Wiley & Sons Ltd.
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