Division of Gastroenterology & Hepatology, Department of Medicine, Johns Hopkins University School of Medicine, Baltimore, MD 21205, USA.
Department of Epidemiology, Johns Hopkins University Bloomberg School of Public Health, Baltimore, MD 21205, USA.
Drug Alcohol Depend. 2022 Dec 1;241:109673. doi: 10.1016/j.drugalcdep.2022.109673. Epub 2022 Oct 22.
Direct-acting antivirals (DAA) are highly effective against hepatitis C virus (HCV) infection among persons with human immunodeficiency virus (PWH). However, alcohol use post-DAA treatment poses a continued threat to the liver. Whether the focus on liver health alone during HCV treatment can impact alcohol consumption is unclear. Therefore, we examined the change in alcohol use among HCV-coinfected PWH who received DAA therapy by non-addiction medical providers.
In our longitudinal clinical cohort study, we identified HCV-coinfected PWH who received interferon-free DAA therapy between January 2014 and June 2019 in the Centers for AIDS Research Network of Integrated Clinical Systems. The Alcohol Use Disorders Identification Test-Consumption (AUDIT-C) was the alcohol screening instrument. We used mixed-effects logistic regression models to estimate the longitudinal change in alcohol use upon DAA therapy.
Among 738 HCV-coinfected PWH, 339 (46 %) reported any alcohol use at the end of HCV treatment, including 113 (15 %) with high-risk use (i.e., AUDIT-C ≥3 for women, ≥4 for men). Concurrently, 280 (38 %) PWH noted active drug use, and 357 (48 %) were currently smoking. We observed no changes in the odds of any alcohol or high-risk alcohol use over time with DAA therapy. Findings were similar in the PWH subgroup with a history of alcohol use before DAA treatment.
For PWH with HCV, alcohol use did not change following interferon-free DAA treatment by non-addiction medical providers. Thus, clinicians should consider integrating targeted alcohol use interventions into HCV care to motivate reduced alcohol consumption and safeguard future liver health.
直接作用抗病毒药物(DAA)对人类免疫缺陷病毒(HIV)感染者的丙型肝炎病毒(HCV)感染具有高度疗效。然而,DAA 治疗后饮酒仍会持续对肝脏造成威胁。在 HCV 治疗期间仅关注肝脏健康是否会影响饮酒行为尚不清楚。因此,我们研究了由非成瘾医学提供者为 HCV 合并感染 HIV 的患者提供 DAA 治疗后,其饮酒行为的变化。
在我们的纵向临床队列研究中,我们确定了 2014 年 1 月至 2019 年 6 月期间在艾滋病研究网络综合临床系统中心接受无干扰素 DAA 治疗的 HCV 合并感染 HIV 的患者。酒精使用障碍识别测试 - 摄入量(AUDIT-C)是酒精筛查工具。我们使用混合效应逻辑回归模型来估计 DAA 治疗后饮酒行为的纵向变化。
在 738 名 HCV 合并感染 HIV 的患者中,339 名(46%)在 HCV 治疗结束时报告有任何饮酒行为,其中 113 名(15%)有高风险饮酒(即,女性 AUDIT-C≥3,男性 AUDIT-C≥4)。同时,280 名(38%)HIV 感染者报告有正在使用药物,357 名(48%)正在吸烟。我们没有观察到 DAA 治疗后任何饮酒或高风险饮酒的可能性随时间的变化。在 DAA 治疗前有饮酒史的 HIV 感染者亚组中,发现结果相似。
对于 HCV 合并感染 HIV 的患者,无干扰素 DAA 治疗后其饮酒行为没有改变。因此,临床医生应考虑将针对性的饮酒干预措施纳入 HCV 护理中,以激励减少饮酒并保护未来的肝脏健康。