Section of Infectious Diseases, Department of Medicine, Boston Medical Center, Boston, MA.
Department of Biostatistics, Boston University School of Public Health, Boston, MA.
J Acquir Immune Defic Syndr. 2023 Nov 1;94(3):244-252. doi: 10.1097/QAI.0000000000003250.
Delayed CD4 recovery after initiating antiretroviral therapy (ART) is a novel potential mechanism by which alcohol consumption leads to increased morbidity and mortality in people with HIV. We hypothesized that alcohol consumption at ART initiation is associated with slower CD4 recovery.
We retrospectively analyzed 2 pooled longitudinal alcohol/HIV cohorts (2014-2019) in St. Petersburg, Russia. Eligible participants initiated the first ART during parent studies; had alcohol consumption assessed by the blood biomarker, phosphatidylethanol (PEth), at the last research visit before ART initiation; and had ≥1 CD4 count measurement before and after initiating ART. Participants were stratified by low, moderate, and high PEth (<8, 8-80, and >80 ng/mL, respectively). We used random-effects piecewise linear regression models to estimate CD4 recovery, defined as CD4 count change per 30 days after ART initiation, by the alcohol group.
Of 60 eligible participants, median age was 34 years and 28% were female. The median pre-ART PEth in the low, moderate, and high PEth groups were <8, 23, and 232 ng/mL, respectively. After starting ART, the CD4 count increased by 13.60 cells/mm3/mo (95% CI: 0.33 to 26.87) with low PEth, 0.93 cells/mm3/mo (95% CI: -6.18 to 8.04) with moderate PEth, and 2.33 cells/mm3/mo (95% CI: -3.44 to 8.09) with high PEth.
Among Russians with HIV, we observed faster CD4 recovery after ART initiation in those with low alcohol consumption compared with those with moderate and high alcohol consumption, as assessed by PEth. This analysis provides further evidence for the possible value of alcohol reduction interventions for people with HIV who are initiating ART.
在开始抗逆转录病毒疗法 (ART) 后 CD4 恢复延迟是酒精消费导致 HIV 感染者发病率和死亡率增加的一种新的潜在机制。我们假设,在开始 ART 时饮酒与 CD4 恢复较慢有关。
我们回顾性分析了俄罗斯圣彼得堡的两个纵向酒精/ HIV 队列(2014-2019 年)。合格的参与者在父母研究中开始首次 ART;在开始 ART 前的最后一次研究访问中通过血液生物标志物血基乙基磷脂(PEth)评估酒精摄入量;并且在开始 ART 前后至少有 1 次 CD4 计数测量。参与者根据低、中、高 PEth(分别为<8、8-80 和>80ng/mL)分层。我们使用随机效应分段线性回归模型来估计 CD4 恢复,定义为 ART 后 30 天内 CD4 计数的变化,通过酒精组来表示。
在 60 名合格的参与者中,中位年龄为 34 岁,28%为女性。低、中、高 PEth 组的 ART 前中位 PEth 分别为<8、23 和 232ng/mL。开始 ART 后,低 PEth 组的 CD4 计数增加了 13.60 个细胞/mm3/月(95%CI:0.33 至 26.87),中 PEth 组增加了 0.93 个细胞/mm3/月(95%CI:-6.18 至 8.04),高 PEth 组增加了 2.33 个细胞/mm3/月(95%CI:-3.44 至 8.09)。
在俄罗斯 HIV 感染者中,我们观察到与中、高酒精摄入者相比,低酒精摄入者在开始 ART 后 CD4 恢复更快,这是通过 PEth 评估的。该分析为正在开始 ART 的 HIV 感染者减少酒精干预的可能价值提供了进一步的证据。