Department of Epidemiology, University of Florida, Gainesville, Florida.
School of Integrated Science and Humanity, Florida International University, Miami, Florida.
Alcohol Clin Exp Res. 2019 Aug;43(8):1790-1800. doi: 10.1111/acer.14130. Epub 2019 Jul 10.
Alcohol consumption is associated with poor health outcomes in women living with HIV (WLWH), but whether medication can help to reduce drinking in non-treatment-seeking women or whether reduction in drinking improves HIV outcomes is unclear. We conducted a randomized clinical trial (RCT) of daily oral naltrexone (50 mg) versus placebo in WLWH who met criteria for current unhealthy alcohol use.
WLWH with current unhealthy alcohol use (>7 drinks/wk or >3 drinks/occasion) were randomly assigned to daily oral naltrexone 50 mg (n = 96) or placebo (n = 98) for 4 months. Drinking outcomes, including the proportion of women who reduced (<unhealthy use criteria) or quit drinking, were assessed at baseline, 2 months, 4 months (end of treatment), and 7 months. In a secondary analysis, HIV viral suppression and changes in CD4 counts were compared in women who did or did not reduce/quit drinking, regardless of intervention assignment.
The participants' mean age was 48 years, 86% were African American, and 94% were receiving HIV antiretroviral therapy. Among all participants, 89% and 85% completed the 4-month and 7-month follow-ups, respectively. Participants in both groups substantially reduced drinking over time. At 1 and 3 months, naltrexone was associated with a greater reduction in drinking (p < 0.05), but the proportion who reduced/quit drinking at 4 months (52% vs. 45%, p = 0.36) or 7 months (64% in both groups) was not different. HIV viral suppression at follow-up was significantly better in participants who reduced/quit drinking versus those continuing unhealthy alcohol use at 4 months (72% vs. 53%, p = 0.02) and 7 months (74% vs. 54%, p = 0.02).
Participating in an RCT to reduce drinking was associated with significant drinking reduction regardless of medication assignment, suggesting that nonmedication aspects of research study participation (e.g., repeated assessments and support from research staff) could be important interventions to help reduce drinking outside of research studies. Drinking reduction was associated with improved HIV viral suppression, providing evidence to support recommendations to avoid unhealthy alcohol use among WLWH.
饮酒与 HIV 感染者(PLWH)的不良健康结局有关,但尚不清楚药物是否有助于减少非治疗寻求的女性的饮酒量,或者减少饮酒是否会改善 HIV 结局。我们进行了一项随机临床试验(RCT),比较了每日口服纳曲酮(50mg)与安慰剂在符合当前非健康饮酒标准的 PLWH 中的作用。
目前有非健康饮酒行为的 PLWH(>7 次/周或>3 次/次)被随机分配至每日口服纳曲酮 50mg(n=96)或安慰剂(n=98),持续 4 个月。在基线、2 个月、4 个月(治疗结束时)和 7 个月时评估饮酒结局,包括减少(<非健康使用标准)或戒酒的女性比例。在二次分析中,比较了无论干预分配如何,减少/戒酒的女性与未减少/戒酒的女性的 HIV 病毒抑制和 CD4 计数变化。
参与者的平均年龄为 48 岁,86%为非裔美国人,94%正在接受 HIV 抗逆转录病毒治疗。所有参与者中,89%和 85%分别完成了 4 个月和 7 个月的随访。两组参与者的饮酒量都随着时间的推移而大幅减少。在 1 个月和 3 个月时,纳曲酮与饮酒量的减少更相关(p<0.05),但在 4 个月时减少/戒酒的比例(52% vs. 45%,p=0.36)或 7 个月时(两组均为 64%)并无差异。与持续非健康饮酒的参与者相比,在 4 个月(72% vs. 53%,p=0.02)和 7 个月(74% vs. 54%,p=0.02)时,减少/戒酒的参与者的 HIV 病毒抑制显著更好。
参与降低饮酒量的 RCT 与显著的饮酒量减少有关,无论药物分配如何,这表明研究参与的非药物方面(例如,反复评估和研究人员的支持)可能是帮助在研究之外减少饮酒的重要干预措施。减少饮酒与改善 HIV 病毒抑制有关,为避免 PLWH 非健康饮酒提供了证据支持。