Division of HIV, ID, and Global Medicine, Department of Medicine, University of California, San Francisco.
Center for AIDS Prevention Studies, Division of Prevention Science, Department of Medicine, University of California, San Francisco.
AIDS. 2020 Sep 1;34(11):1665-1671. doi: 10.1097/QAD.0000000000002595.
We sought to examine the prospective association between internalized HIV stigma and unsuppressed viral load and to investigate whether this relationship was sequentially mediated by depressive symptoms and antiretroviral therapy (ART) adherence.
Longitudinal study in a multisite observational clinical cohort.
The Center for AIDS Research Network of Integrated Clinical Systems patient-reported outcomes survey measures internalized HIV stigma yearly using a four-item assessment (response scale 1 = strongly disagree to 5 = strongly agree). We obtained patient-reported outcome, lab, and appointment data from six center for AIDS research network of integrated clinical systems sites. We used multivariable logistic regression to examine the association between mean stigma and subsequent viremia. We then used Bayesian sequential mediation to fit a longitudinal sequential path model spanning four time points to test if depressive symptoms at T1 and ART adherence at T2 mediated the effect of stigma at T0 on viral load at T3, adjusting for baseline covariates.
Between February 2016 and November 2018, 6859 patients underwent stigma assessment and were 81% cis-men, 38% Black, 16% Latinx, 32% heterosexual-identified, and 49% at least 50 years of age. Mean stigma level was 2.00 (SD 1.08). Stigma was significantly associated with subsequent viremia (adjusted odds ratio = 1.16, 95% confidence interval: 1.05-1.28, P = 0.004), as were younger age and Black race. The chained indirect effect from stigma to unsuppressed viral load through depressive symptoms and then adherence was significant (standardized β = 0.002; SD = 0.001).
Internalized HIV stigma positively predicts subsequent viremia through depressive symptoms and ART adherence. Addressing the link between stigma and depressive symptoms could help improve viral suppression.
本研究旨在探讨内化的 HIV 耻辱感与未抑制的病毒载量之间的前瞻性关联,并调查这种关系是否通过抑郁症状和抗逆转录病毒治疗(ART)依从性的顺序中介。
多站点观察性临床队列的纵向研究。
艾滋病研究中心网络综合临床系统的患者报告结果调查每年使用四项评估(反应量表 1=强烈不同意到 5=强烈同意)来衡量内化的 HIV 耻辱感。我们从六个艾滋病研究中心网络综合临床系统站点获得了患者报告的结果、实验室和预约数据。我们使用多变量逻辑回归来检查平均耻辱感与随后的病毒血症之间的关联。然后,我们使用贝叶斯序贯中介来拟合跨越四个时间点的纵向序贯路径模型,以测试 T0 时的耻辱感是否通过 T1 时的抑郁症状和 T2 时的 ART 依从性来调节 T3 时的病毒载量,同时调整基线协变量。
在 2016 年 2 月至 2018 年 11 月期间,6859 名患者接受了耻辱感评估,其中 81%为 cis 男性,38%为黑人,16%为拉丁裔,32%为异性恋者,49%年龄至少为 50 岁。平均耻辱感水平为 2.00(SD 1.08)。耻辱感与随后的病毒血症显著相关(调整后的优势比=1.16,95%置信区间:1.05-1.28,P=0.004),年龄较小和黑人为黑人种族也是如此。从耻辱感到未抑制的病毒载量通过抑郁症状和随后的依从性的连锁间接效应是显著的(标准化β=0.002;SD=0.001)。
内化的 HIV 耻辱感通过抑郁症状和 ART 依从性正向预测随后的病毒血症。解决耻辱感和抑郁症状之间的联系可能有助于提高病毒抑制率。