Lebherz-Eichinger Diana, Tudor Bianca, Ankersmit Hendrik J, Reiter Thomas, Haas Martin, Einwallner Elisa, Roth-Walter Franziska, Krenn Claus G, Roth Georg A
Department of Anesthesiology, General Intensive Care and Pain Medicine, Medical University of Vienna, Vienna, Austria.
Christian Doppler Laboratory for Cardiac and Thoracic Diagnosis and Regeneration, Medical University of Vienna, Vienna, Austria.
PLoS One. 2017 Mar 29;12(3):e0174551. doi: 10.1371/journal.pone.0174551. eCollection 2017.
In chronically damaged tissue, trefoil factor family (TFF) peptides ensure epithelial protection and restitution. In chronic kidney disease (CKD), TFF1 and TFF2 are reported to be upregulated. Especially in the early phase, CKD is associated with silently ongoing renal damage and inflammation. Moreover, many patients are diagnosed late during disease progression. We therefore sought to investigate the potential of TFF2 as biomarker for CKD. We followed 118 patients suffering from predialysis CKD and 23 healthy volunteers. TFF2 concentrations were measured using ELISA. Our results showed, that median TFF2 serum levels were significantly higher in patients with later CKD stages as compared to healthy controls (p < 0.001) or early stages (p < 0.001). In patients with mid CKD stages TFF2 serum levels were significantly higher than in healthy controls (p = 0.002). Patients with early or mid CKD stages had significantly higher TFF2 urine concentrations than later CKD stages (p < 0.001 and p = 0.009, respectively). Fractional TFF2 excretion differed significantly between early CKD stages and healthy controls (p = 0.01). ROC curve showed that TFF2 levels can predict different CKD stages (AUC > 0.75). In conclusion, urine and serum TFF2 levels of CKD patients show a different profile dependent on CKD stages. Whereas TFF2 urine levels continuously decreased with disease progression, TFF2 serum concentrations progressively increased from the early to later CKD stages, indicating changes in renal function and offering the potential to examine the course of CKD.
在慢性损伤组织中,三叶因子家族(TFF)肽可确保上皮细胞的保护和修复。据报道,在慢性肾脏病(CKD)中,TFF1和TFF2会上调。尤其是在早期阶段,CKD与隐匿性进行性肾损伤和炎症相关。此外,许多患者在疾病进展过程中被诊断较晚。因此,我们试图研究TFF2作为CKD生物标志物的潜力。我们跟踪了118例透析前CKD患者和23名健康志愿者。使用酶联免疫吸附测定法(ELISA)测量TFF2浓度。我们的结果显示,与健康对照组(p < 0.001)或早期阶段(p < 0.001)相比,CKD晚期患者的TFF2血清水平中位数显著更高。在CKD中期患者中,TFF2血清水平显著高于健康对照组(p = 0.002)。CKD早期或中期患者的TFF2尿浓度显著高于晚期CKD阶段(分别为p < 0.001和p = 0.009)。早期CKD阶段与健康对照组之间的TFF2排泄分数差异显著(p = 0.01)。ROC曲线显示,TFF2水平可预测不同的CKD阶段(曲线下面积> 0.75)。总之,CKD患者的尿液和血清TFF2水平根据CKD阶段呈现出不同的特征。随着疾病进展,TFF2尿液水平持续下降,而TFF2血清浓度从CKD早期到晚期逐渐升高,这表明肾功能发生了变化,并为检查CKD的病程提供了可能性。