Richterman Aaron, Sinha Pranay, Ivers Louise C, Gross Robert, Rantleru Tumelo, Tamuhla Neo, Bisson Gregory P
Department of Medicine (Infectious Diseases), University of Pennsylvania, Philadelphia, PA.
Department of Medicine (Infectious Diseases), Boston University Chobanian and Avedisian School of Medicine, Boston, MA.
J Acquir Immune Defic Syndr. 2024 Apr 15;95(5):494-504. doi: 10.1097/QAI.0000000000003386.
Food insecurity and undernutrition are related but distinct concepts contributing to poor HIV and tuberculosis outcomes. Pathways linking them with immunologic profile, which may relate to clinical outcomes, remain understudied.
We analyzed data from a cohort study of 165 antiretroviral therapy (ART)-naïve adults with advanced HIV and newly diagnosed tuberculosis in Botswana from 2009 to 2013. Twenty-nine plasma biomarkers were measured pre-ART and 4 weeks post-ART initiation. We used principal components analysis (PCA) and multivariable linear regression models to assess relationships between immunological profiles and food insecurity (based on the Household Food Insecurity Access Scale), undernutrition (body mass index <18.5 kg/m 2 ), and clinical outcomes.
PCA identified 5 principal components with eigenvalues >1. After adjustment, food insecurity was associated with PC3 pre-ART (0.19 per increased category of severity, 95% CI: 0.02 to 0.36) and post-ART (0.24, 95% CI: 0.07 to 0.41). PC3 was driven by higher levels of IFN-α, IFN-γ, interleukin (IL)-12p40, vascular endothelial growth factor, IL-1α, and IL-8 and decreased concentrations of IL-3. Undernutrition was associated with PC5 post-ART (0.49, 95% CI: 0.16 to 0.82). PC5 was driven by higher levels of IL-8, MIP-1α, IL-6, and IL-10 and decreased concentrations in IP-10 and IFN-α. Post-ART PC3 (4.3 percentage point increased risk per increased score of 1, 95% CI: 0.3 to 8.9) and post-ART PC5 (4.8, 95% CI: 0.6 to 8.9) were associated with death in adjusted models.
We identified 2 distinct immunologic profiles associated with food insecurity, undernutrition, and clinical outcomes in patients with advanced HIV and tuberculosis. Different pathophysiologic processes may link food insecurity and undernutrition with poor outcomes in this vulnerable patient population. Future studies should assess the impact of improving food access and intake on immune function and clinical outcomes.
粮食不安全与营养不良是相关但不同的概念,它们都会导致艾滋病毒和结核病的不良预后。将它们与可能与临床结果相关的免疫状况联系起来的途径仍未得到充分研究。
我们分析了2009年至2013年在博茨瓦纳进行的一项队列研究的数据,该研究涉及165名未接受过抗逆转录病毒治疗(ART)的晚期艾滋病毒感染者和新诊断的结核病患者。在开始ART前和开始ART后4周测量了29种血浆生物标志物。我们使用主成分分析(PCA)和多变量线性回归模型来评估免疫状况与粮食不安全(基于家庭粮食不安全获取量表)、营养不良(体重指数<18.5kg/m²)和临床结果之间的关系。
PCA确定了5个特征值>1的主成分。调整后,粮食不安全与ART前的PC3相关(严重程度每增加一级为0.19,95%CI:0.02至0.36)以及ART后的PC3相关(0.24,95%CI:0.07至0.41)。PC3由较高水平的IFN-α、IFN-γ、白细胞介素(IL)-12p40、血管内皮生长因子、IL-1α和IL-8以及较低浓度的IL-3驱动。营养不良与ART后的PC5相关(0.49,95%CI:0.16至0.82)。PC5由较高水平的IL-8、MIP-1α、IL-6和IL-10以及IP-10和IFN-α的较低浓度驱动。在调整后的模型中,ART后的PC3(每增加1分风险增加4.