Department of Medicine, Faculty of Medicine, Ramathibodi Hospital, Mahidol University, Bangkok 10400, Thailand.
Section for Translational Medicine, Research Center, Faculty of Medicine, Ramathibodi Hospital, Mahidol University, Bangkok 10400, Thailand.
Cytokine. 2018 Apr;104:1-7. doi: 10.1016/j.cyto.2018.01.015. Epub 2018 Feb 4.
The balance of several cytokines likely influences the resolution of glomerulonephritis. Monocyte chemoattractant protein-1(MCP-1) is a chemokine that promotes renal inflammation whereas epidermal growth factor (EGF) stimulates protective responses. Previously, high urine MCP-1(MCP-1) and low urine EGF (EGF) levels were found to be associated with tubulointerstitial fibrosis, but there is limited information on the value of these mediators as predictors of therapeutic responses or long term outcome in primary glomerulonephritis.
To determine the performance of urine EGF, MCP-1 or their ratio at baseline as biomarkers to predict complete remission, and the relationship of these mediators with subsequent renal function 24 months later in primary glomerulonephritis.
This is a prospective study of patients with biopsy-proven primary glomerulonephritis. Baseline urine samples were collected at biopsy before therapy. MCP-1 and EGF were analyzed by enzyme-linked immunosorbent assays and expressed as a ratio to urine creatinine (ng/mgCr) or as EGF/MCP-1 ratio (ng/ng). Proteinuria and estimated glomerular filtration rate (eGRF) were monitored after therapy. Complete remission (CR) was defined as proteinuria ≤ 0.3 g/gCr.
Median follow-up was 20 months. Of all patients (n = 74), 38 patients (51.4%) subsequently achieved CR. Baseline urine EGF and EGF/MCP-1 levels were significantly higher in CR compared to Not CR. By contrast, MCP-1 was not different. High EGF (EGF > 75 ng/mgCr) was a significant predictor (OR 2.28) for CR by multivariate analysis after adjusting for proteinuria, blood pressure, baseline eGFR. In patients who completed 24 months follow-up (n = 43), baseline EGF correlated inversely with proteinuria and positively with eGFR at 24 months.
High urine EGF level is a promising biomarker of CR. Baseline EGF levels correlated with kidney function at 2 years. EGF/MCP-1 was not superior to EGF alone. Further studies are necessary to determine the role of urine EGF as a guide to therapy in primary GN.
几种细胞因子的平衡可能会影响肾小球肾炎的缓解。单核细胞趋化蛋白-1(MCP-1)是一种趋化因子,可促进肾脏炎症,而表皮生长因子(EGF)则刺激保护性反应。先前发现,高尿 MCP-1(MCP-1)和低尿 EGF(EGF)水平与肾小管间质纤维化有关,但有关这些介质作为原发性肾小球肾炎治疗反应或长期预后预测指标的价值的信息有限。
确定基线时尿 EGF、MCP-1 或其比值作为预测完全缓解的生物标志物的性能,并确定这些介质与原发性肾小球肾炎 24 个月后随后的肾功能之间的关系。
这是一项对经活检证实的原发性肾小球肾炎患者的前瞻性研究。在治疗前的活检时收集基线尿样。通过酶联免疫吸附试验分析 MCP-1 和 EGF,并以尿肌酐(ng/mgCr)的比值或 EGF/MCP-1 比值(ng/ng)表示。治疗后监测蛋白尿和估计肾小球滤过率(eGRF)。完全缓解(CR)定义为蛋白尿≤0.3 g/gCr。
中位随访时间为 20 个月。在所有患者(n=74)中,有 38 名患者(51.4%)随后达到 CR。CR 组的基线尿 EGF 和 EGF/MCP-1 水平明显高于非 CR 组。相比之下,MCP-1 没有差异。多变量分析调整蛋白尿、血压和基线 eGFR 后,高 EGF(EGF>75ng/mgCr)是 CR 的显著预测因子(OR 2.28)。在完成 24 个月随访的患者(n=43)中,基线 EGF 与蛋白尿呈负相关,与 24 个月时的 eGFR 呈正相关。
高尿 EGF 水平是 CR 的有希望的生物标志物。基线 EGF 水平与 2 年时的肾功能相关。EGF/MCP-1 并不优于单独的 EGF。需要进一步研究确定尿 EGF 作为原发性 GN 治疗指南的作用。