Department of Nephrology and Transplantation Medicine, Wroclaw Medical University, 50-556 Wroclaw, Poland.
Institute of Cardiology, Wroclaw Medical University, 50-556 Wroclaw, Poland.
Int J Mol Sci. 2023 Jun 12;24(12):10036. doi: 10.3390/ijms241210036.
Volume status, congestion, endothelial activation, and injury all play roles in glomerular filtration rate (GFR) decline. In this study, we aimed to determine whether the plasma endothelial and overhydration markers could serve as independent predictors for dialysis initiation in patients with chronic kidney disease (CKD) 3b-5 (GFR < 45 mL/min/1.72 m) and preserved ejection fraction. A prospective, observational study in a single academic center was conducted from March 2019 to March 2022. Plasma levels of angiopoietin (Ang)-2, Vascular Endothelial Growth Factor-C (VEGF-C), Vascular Cell Adhesion Molecule-1 (VCAM-1), Copeptin (CPP), beta-trace protein (BTP), brain natriuretic peptide (BNP), and cardiac troponin I (cTnI) were all measured. Lung ultrasound (US) B-lines, bioimpedance, and echocardiography with global longitudinal strain (GLS) were recorded. The study outcome was the initiation of chronic dialysis (renal replacement therapy) during 24 months of follow-up. A total of 105 consecutive patients with a mean eGFR of 21.3 mL/min/1.73 m were recruited and finally analyzed. A positive correlation between Ang-2 and VCAM-1 and BTP was observed. Ang-2 correlated positively with BNP, cTnI, sCr, E/e', and the extracellular water (ECW)/intracellular water (ICW) ratio (ECW/ICW). After 24 months, a deterioration in renal function was observed in 47 patients (58%). In multivariate regression analysis, both VCAM-1 and Ang-2 showed independent influences on risk of renal replacement therapy initiation. In a Kaplan-Meier analysis, 72% of patients with Ang-2 concentrations below the median (3.15 ng/mL) survived without dialysis for two years. Such an impact was not observed for GFR, VCAM, CCP, VEGF-C, or BTP. Endothelial activation, quantified by plasma levels of Ang-2, may play a key role in GFR decline and the need for dialysis initiation in patients with CKD 3b, 4, and 5.
容量状态、充血、内皮激活和损伤都在肾小球滤过率(GFR)下降中起作用。在这项研究中,我们旨在确定血浆内皮和过度水化标志物是否可作为慢性肾脏病(CKD)3b-5(GFR<45 mL/min/1.72 m)和射血分数保留患者开始透析的独立预测因子。这是一项在单家学术中心进行的前瞻性、观察性研究,时间为 2019 年 3 月至 2022 年 3 月。测量了血管生成素(Ang)-2、血管内皮生长因子-C(VEGF-C)、血管细胞黏附分子-1(VCAM-1)、copeptin(CPP)、β-痕迹蛋白(BTP)、脑钠肽(BNP)和心脏肌钙蛋白 I(cTnI)的血浆水平。记录了肺部超声(US)B 线、生物电阻抗和整体纵向应变(GLS)的超声心动图。研究结果为 24 个月随访期间开始慢性透析(肾脏替代治疗)。共招募了 105 例平均 eGFR 为 21.3 mL/min/1.73 m 的连续患者,并最终进行了分析。观察到 Ang-2 与 VCAM-1 和 BTP 之间存在正相关。Ang-2 与 BNP、cTnI、sCr、E/e'和细胞外水(ECW)/细胞内水(ICW)比值(ECW/ICW)呈正相关。24 个月后,47 例(58%)患者肾功能恶化。在多变量回归分析中,VCAM-1 和 Ang-2 均对开始肾脏替代治疗的风险有独立影响。在 Kaplan-Meier 分析中,Ang-2 浓度低于中位数(3.15ng/mL)的 72%患者两年内无需透析即可存活。而 GFR、VCAM、CCP、VEGF-C 或 BTP 则没有这种影响。通过血浆 Ang-2 水平定量的内皮激活可能在 CKD 3b、4 和 5 患者的 GFR 下降和开始透析的需求中起关键作用。