Department of Tuberculosis, The first affiliated Hospital of Xinxiang Medical University, No.88, Jiankang road, Weihui, Xinxiang, 453100, China.
Respir Res. 2019 Mar 6;20(1):50. doi: 10.1186/s12931-019-1004-3.
Macrophage migration inhibitory factor (MIF) makes chemokine-like functions and plays critical roles in various inflammatory diseases. This study was designed to explore the significance of MIF serum levels in predicting the prognosis of pulmonary tuberculosis (PTB) following anti-TB treatment.
Patients diagnosed with culture-confirmed PTB without treatment were included and the serum was collected. Levels of MIF in serum were quantified with immunoassay, and the levels of established biomarkers were also determined, including C-reactive protein (CRP) and Interleukin 6 (IL-6). The outcome was estimated with all-cause mortality, with the mortality in 12 months as the primary outcome and the mortality in 3, 6, 9 months as other outcomes. The prognostic value of MIF and other factors in PTB were tested.
Two hundred eighty-seven PTB patients were included. The median MIF levels in patients with advanced disease, disseminated and drug-resistant TB were significantly higher than that observed in mild -to- moderate disease, non-disseminated and drug-sensitive TB. MIF levels in patients with the outcome of death were higher than those survived [28.0 ng/ml (Inter-quartile range [IQR]: 24.2-33.1) vs. 22.3 ng/ml (IQR: 18.7-26.5); P < 0.001]. Multivariate model analysis was performed for comparing the highest quartiles to the lowest quartile of MIF levels. MIF levels were related to the mortality, with an elevated mortality risk of 236% [Odds ratio (OR) = 3.36; 95% Confidence interval (CI): 1.21-15.14; P = 0.012]. The model was re-analysis after combing MIF with currently established risk indicators. The obtained Area Under the Receiver Operating Characteristic Curve (±standard error) was elevated from 0.81 (±0.035) to 0.84 (±0.031), with a significant difference before and after adding the MIF (difference, 0.03[0.004]; P = 0.03).
Serum level of MIF was a better biomarker than CRP or IL-6 for predicting death in HIV-negative PTB patients, and increased MIF serum levels were related to higher mortality.
巨噬细胞移动抑制因子(MIF)具有趋化因子样功能,在各种炎症性疾病中发挥关键作用。本研究旨在探讨 MIF 血清水平在预测抗结核治疗后肺结核(PTB)预后中的意义。
纳入未经治疗的培养确诊的 PTB 患者,并采集血清。采用免疫分析法定量检测血清 MIF 水平,并测定 C 反应蛋白(CRP)和白细胞介素 6(IL-6)等已建立的生物标志物水平。以全因死亡率作为结局,12 个月的死亡率为主要结局,3、6、9 个月的死亡率为其他结局。检测 MIF 和其他因素在 PTB 中的预后价值。
纳入 287 例 PTB 患者。晚期疾病、播散性和耐药性结核患者的中位 MIF 水平明显高于轻度至中度疾病、非播散性和敏感性结核患者。死亡患者的 MIF 水平高于存活患者[28.0ng/ml(四分位距 [IQR]:24.2-33.1)比 22.3ng/ml(IQR:18.7-26.5);P<0.001]。对最高四分位数与最低四分位数的 MIF 水平进行多变量模型分析。MIF 水平与死亡率相关,死亡率风险升高 236%[比值比(OR)=3.36;95%置信区间(CI):1.21-15.14;P=0.012]。在结合 MIF 与目前已建立的风险指标后,重新分析该模型。获得的接收者操作特征曲线下面积(±标准误差)从 0.81(±0.035)升高至 0.84(±0.031),在添加 MIF 前后有显著差异(差异,0.03[0.004];P=0.03)。
与 CRP 或 IL-6 相比,血清 MIF 水平是预测 HIV 阴性 PTB 患者死亡的更好生物标志物,且 MIF 血清水平升高与死亡率升高相关。