Department of Medicine, Boston University School of Medicine, Boston, Massachusetts, United States of America.
Department of Biostatistics, Boston University School of Public Health, Boston, Massachusetts, United States of America.
PLoS One. 2019 Aug 22;14(8):e0219710. doi: 10.1371/journal.pone.0219710. eCollection 2019.
Biomarkers of monocyte activation (soluble CD14 [sCD14]), inflammation (interleukin-6 [IL-6]), and altered coagulation (D-dimer) are associated with increased mortality risk in people with HIV. The objective of the Russia Alcohol Research Collaboration on HIV/AIDS (ARCH) study was to evaluate the association between heavy alcohol use and inflammatory biomarkers over time.
The study sought antiretroviral therapy naive participants with HIV (n = 350) and assessed them at baseline, 12 and 24 months. Linear mixed effects models were used to determine whether heavy drinking (self-report augmented by phosphatidylethanol [PEth], an alcohol biomarker) was longitudinally associated with IL-6, sCD14 and D-dimer adjusting for potential confounders (e.g., demographics, HIV factors, comorbid conditions).
Participants' baseline characteristics were as follows: 71% male; mean age of 34 years; 87% self-reported hepatitis C; and 86% current smokers. Mean log10 (HIV RNA) was 4.3 copies/mL. Heavy alcohol use, based on National Institute of Alcohol Abuse and Alcoholism risky drinking criteria and PEth (versus non-heavy alcohol use) was associated with higher sCD14 (adjusted mean difference 125 ng/mL [95% CI: 42, 209]), IL-6 (ratio of means 1.35 [95% CI: 1.17, 1.55] pg/mL), and D-dimer (ratio of means 1.20 [95% CI: 1.06, 1.37] ug/mL) across the two-year follow-up.
Among HIV+ adults, current heavy alcohol use is associated with higher sCD14, IL-6 and D-dimer over time. Since these biomarkers are associated with mortality, interventions to mitigate effects of heavy drinking on these immune processes merit consideration.
单核细胞活化的生物标志物(可溶性 CD14 [sCD14])、炎症(白细胞介素-6 [IL-6])和凝血改变(D-二聚体)与 HIV 感染者的死亡风险增加有关。俄罗斯艾滋病研究合作组织(ARCH)的目的是评估随着时间的推移,重度饮酒与炎症生物标志物之间的关系。
该研究寻求接受抗逆转录病毒治疗的 HIV 初治参与者(n = 350),并在基线、12 个月和 24 个月进行评估。线性混合效应模型用于确定在调整潜在混杂因素(例如,人口统计学、HIV 因素、合并症)后,重度饮酒(自我报告,通过磷脂酰乙醇 [PEth] ,一种酒精生物标志物)是否与 IL-6、sCD14 和 D-二聚体呈纵向相关。
参与者的基线特征如下:71%为男性;平均年龄为 34 岁;87%自我报告患有丙型肝炎;86%为当前吸烟者。平均 log10(HIV RNA)为 4.3 拷贝/ml。根据国家酒精滥用和酒精中毒研究所的危险饮酒标准和 PEth(与非重度饮酒相比),重度饮酒与更高的 sCD14(调整后的平均差异为 125 ng/ml [95%CI:42,209])、IL-6(比值均数为 1.35 [95%CI:1.17,1.55] pg/ml)和 D-二聚体(比值均数为 1.20 [95%CI:1.06,1.37] ug/ml)相关,在两年的随访期间。
在 HIV 阳性成年人中,目前的重度饮酒与随着时间的推移 sCD14、IL-6 和 D-二聚体的升高有关。由于这些生物标志物与死亡率相关,因此需要考虑采取干预措施来减轻重度饮酒对这些免疫过程的影响。