Programa de Pós-Graduação em Pesquisa Clínica em Doenças Infecciosas, Instituto Nacional de Infectologia Evandro Chagas, Fundação Oswaldo Cruz, Rio de Janeiro, Brazil.
Instituto Gonçalo Moniz, Fundação Oswaldo Cruz, Salvador, Brazil.
Front Immunol. 2020 Sep 24;11:588405. doi: 10.3389/fimmu.2020.588405. eCollection 2020.
Tuberculosis (TB) is associated with systemic inflammation and anemia, which are aggravated in persons living with HIV (PLWH). Here, we characterized the dynamics of hemoglobin levels in PLWH coinfected with TB undergoing antitubercular therapy (ATT). We also examined the relationships between anemia and systemic inflammatory disturbance as well as the association between persistent anemia and unfavorable clinical outcomes. Data on several blood biochemical parameters and on blood cell counts were retrospectively analyzed in a cohort of 256 TB/HIV patients from Brazil during 180 days of ATT. Multidimensional statistical analyses were employed to profile systemic inflammation of patients stratified by anemia status (hemoglobin levels <12 g/dL for female and <13.5 g/dL for male individuals) prior to treatment and to perform prediction of unfavorable outcomes, such as treatment failure, loss to follow up and death. We found that 101 (63.63%) of patients with anemia at pre-ATT persisted with such condition until day 180. Such individuals exhibited heightened degree of inflammatory perturbation (DIP), which in turn was inversely correlated with hemoglobin levels. Recovery from anemia was associated with increased pre-ATT albumin levels whereas persistent anemia was related to higher total protein levels in serum. Multivariable regression analysis revealed that lower baseline hemoglobin levels was the major determinant of the unfavorable outcomes. Our findings demonstrate that persistent anemia in PLWH during the course of ATT is closely related with chronic inflammatory perturbation. Early intervention to promote recovery from anemia may improve ATT outcomes.
结核病(TB)与全身炎症和贫血有关,而 HIV 感染者(PLWH)的情况更为严重。在这里,我们描述了接受抗结核治疗(ATT)的 TB/HIV 合并感染患者的血红蛋白水平动态变化。我们还研究了贫血与全身炎症紊乱之间的关系,以及持续性贫血与不良临床结局之间的关联。我们回顾性分析了来自巴西的 256 名 TB/HIV 患者在 ATT 期间 180 天内的多个血液生化参数和血细胞计数数据。多维统计分析用于对治疗前按贫血状态分层的患者进行全身炎症分析(女性血红蛋白水平<12 g/dL,男性<13.5 g/dL),并预测不良结局,如治疗失败、失访和死亡。我们发现,101 名(63.63%)ATT 前贫血患者在第 180 天仍处于贫血状态。这些患者的炎症紊乱程度更高(DIP),而 DIP 又与血红蛋白水平呈负相关。贫血的恢复与 ATT 前白蛋白水平升高有关,而持续性贫血与血清总蛋白水平升高有关。多变量回归分析显示,较低的基线血红蛋白水平是不良结局的主要决定因素。我们的研究结果表明,ATT 期间 PLWH 的持续性贫血与慢性炎症紊乱密切相关。早期干预以促进贫血恢复可能会改善 ATT 结局。