Yoon Soo-Young, Kim Jin Sug, Jung Su Woong, Kim Yang Gyun, Moon Ju-Young, Lee Sang-Ho, Yim Sung-Vin, Hwang Hyeon Seok, Jeong Kyunghwan
Division of Nephrology, Department of Internal Medicine, Kyung Hee University College of Medicine, Kyung Hee University Hospital, Seoul, Republic of Korea.
Division of Nephrology, Department of Internal Medicine, Kyung Hee University College of Medicine, Kyung Hee University Hospital at Gangdong, Seoul, Republic of Korea.
BMC Nephrol. 2024 Apr 22;25(1):142. doi: 10.1186/s12882-024-03574-2.
IgA nephropathy (IgAN) is the most common type of primary glomerulonephritis, although the definitive markers are unknown. We aimed to investigate the clinical significance of urinary cytokines in patients with IgAN.
From 2009 to 2018, the patients were divided into three groups: IgAN (n = 191), disease control (n = 53), and normal control (n = 76). We used a multiplex enzyme-linked immunosorbent assay to measure 16 selected urinary inflammatory cytokines, evaluated the correlation between clinical and pathological features following regression analysis on progression.
The IgAN group exhibited significantly different levels of urinary cytokines compared to the normal control and disease control groups. Urinary levels of B-cell-activating factor, vascular endothelial growth factor receptor-2, monocyte chemoattractant protein-1, C-X-C motif chemokine 10, C-X-C motif ligand 16, epidermal growth factor (EGF), endocan, endostatin, growth/differentiation factor-15 (GDF-15), interleukin-6 (IL-6), mannose-binding lectin, transferrin receptor, and kidney injury molecule-1 were significantly correlated with both the estimated glomerular filtration rate and urine protein-creatinine ratio. In a multivariate Cox regression analysis, urinary EGF (hazard ratio [HR] 0.40, 95% confidence interval [CI] 0.17-0.95, P = 0.04), GDF-15 (HR 2.45, 95% CI 1.01-5.94, P = 0.048), and IL-6 (HR 3.02, 95% CI 1.05-8.64, P = 0.04) were associated with progression in IgAN.
Urinary inflammatory biomarkers may serve as alternative predictive biomarkers in patients with IgAN. Further studies are needed to elucidate the physiological mechanisms and confirm the results.
IgA肾病(IgAN)是原发性肾小球肾炎最常见的类型,但其确切标志物尚不清楚。我们旨在研究IgAN患者尿细胞因子的临床意义。
2009年至2018年,将患者分为三组:IgAN组(n = 191)、疾病对照组(n = 53)和正常对照组(n = 76)。我们使用多重酶联免疫吸附测定法测量16种选定的尿炎性细胞因子,在对进展进行回归分析后评估临床和病理特征之间的相关性。
与正常对照组和疾病对照组相比,IgAN组尿细胞因子水平存在显著差异。尿B细胞活化因子、血管内皮生长因子受体2、单核细胞趋化蛋白1、C-X-C基序趋化因子10、C-X-C基序配体16、表皮生长因子(EGF)、内皮糖蛋白、内皮抑素、生长/分化因子-15(GDF-15)、白细胞介素-6(IL-6)、甘露糖结合凝集素、转铁蛋白受体和肾损伤分子-1的水平与估计肾小球滤过率和尿蛋白肌酐比值均显著相关。在多变量Cox回归分析中,尿EGF(风险比[HR] 0.40,95%置信区间[CI] 0.17 - 0.95,P = 0.04)、GDF-15(HR 2.45,95% CI 1.01 - 5.94,P = 0.048)和IL-6(HR 3.02,95% CI 1.05 - 8.64,P = 0.04)与IgAN的进展相关。
尿炎性生物标志物可能作为IgAN患者的替代预测生物标志物。需要进一步研究以阐明其生理机制并证实结果。