Department of Medicine III, University Hospital RWTH Aachen, Aachen, Germany.
J Crit Care. 2013 Oct;28(5):882.e1-11. doi: 10.1016/j.jcrc.2012.11.007. Epub 2013 Jan 20.
Inflammatory and autoimmune diseases have been associated with the tumor necrosis factor superfamily member "A PRoliferation Inducing Ligand" (APRIL). However, up to now, APRIL has not been investigated in critical illness or sepsis. We therefore analyzed APRIL serum concentrations in a large cohort of well-characterized intensive care unit patients.
Serum concentrations of APRIL were measured in 246 critically ill patients, of which 157 fulfilled sepsis criteria in comparison with 81 healthy controls. Clinical data were recorded and correlated with APRIL serum levels.
We detected strongly elevated serum levels of APRIL in critically ill patients compared with healthy controls. Levels of APRIL were further elevated in sepsis and significantly correlated with classical markers of inflammation, bacterial infection, or multiorgan failure. Consequently, high APRIL levels were associated with an unfavorable prognosis and predicted mortality with higher diagnostic accuracy than established prognostic scoring systems such as the Acute Physiology and Chronic Health Evaluation II score.
Serum levels of APRIL were significantly elevated in intensive care unit patients, with the highest concentrations in septic patients, and associated with unfavorable outcome. Besides being used as a single marker, APRIL may be implemented into established scoring systems to further improve their sensitivity and specificity in predicting patient's prognosis.
炎症性和自身免疫性疾病与肿瘤坏死因子超家族成员“增殖诱导配体”(APRIL)有关。然而,到目前为止,APRIL 在危重病或脓毒症中尚未得到研究。因此,我们分析了大量特征明确的重症监护病房患者的 APRIL 血清浓度。
在 246 名危重病患者中测量 APRIL 的血清浓度,其中 157 名符合脓毒症标准,81 名健康对照。记录临床数据并与 APRIL 血清水平相关联。
与健康对照组相比,我们在危重病患者中检测到 APRIL 血清水平明显升高。在脓毒症患者中,APRIL 水平进一步升高,并与炎症、细菌感染或多器官衰竭的经典标志物显著相关。因此,高 APRIL 水平与不良预后相关,并具有比急性生理学和慢性健康评估 II 评分等既定预后评分系统更高的诊断准确性预测死亡率。
APRIL 的血清水平在重症监护病房患者中明显升高,脓毒症患者的浓度最高,与不良结局相关。除了作为单一标志物使用外,APRIL 还可以纳入既定的评分系统,以进一步提高其预测患者预后的敏感性和特异性。