Department of Internal Medicine, College of Medicine, Institute of Kidney Disease Research, Yonsei University, Seoul, 03722, Republic of Korea.
Division of Nephrology, Soonchunhyang University Hospital, Seoul, Republic of Korea.
BMC Nephrol. 2019 Mar 25;20(1):104. doi: 10.1186/s12882-019-1292-3.
Guidelines for general hypertension treatment do not recommend the combined use of renin-angiotensin-aldosterone system (RAAS) inhibitors due to the risk of hyperkalemia. However, a recent clinical trial showed that polycystic kidney disease (PKD) patients had infrequent episodes of hyperkalemia despite receiving combined RAAS inhibitors. Because intrarenal RAAS is a main component for renal potassium handling, we further investigated the association between intrarenal RAAS activity and serum potassium level in patients with chronic kidney disease, particularly in PKD patients, and examined whether intrarenal RAAS activity has a prognostic role in patients with PKD.
A total of 1788 subjects from the KoreaN cohort study for Outcome in patients With Chronic Kidney Disease (KNOW-CKD) were enrolled in this study. Intrarenal RAAS activity was assessed by the measurement of urinary angiotensinogen (AGT). The primary outcome was the composite of all-cause mortality and renal function decline.
Patients with PKD had a significantly lower serum potassium level in chronic kidney disease stages 1 to 3b than non-PKD patients. In logistic regression analysis, after adjusting for multiple confounders, PKD patients had a significantly lower risk of hyperkalemia than non-PKD patients. In multivariable linear regression analysis, the urinary AGT/creatinine (Cr) ratio was negatively correlated with the serum potassium level (β = - 0.058, P = 0.017) and positively correlated with the transtubular potassium gradient (TTKG, β = 0.087, P = 0.001). In propensity score matching analysis, after matching factors associated with serum potassium and TTKG, PKD patients had a significantly higher TTKG (P = 0.021) despite a lower serum potassium level (P = 0.004). Additionally, the urinary AGT/Cr ratio was significantly higher in PKD patients than in non-PKD patients (P = 0.011). In 293 patients with PKD, high urinary AGT/Cr ratio was associated with increased risk of the composite outcome (hazard ratio 1.29; 95% confidence interval, 1.07-1.55; P = 0.007).
High activity of intrarenal RAAS is associated with increased urinary potassium excretion and low serum potassium level in patients with PKD. In addition, intrarenal RAAS activity can be a prognostic marker for mortality and renal function decline in these patients.
由于高钾血症的风险,一般高血压治疗指南不建议联合使用肾素-血管紧张素-醛固酮系统(RAAS)抑制剂。然而,最近的一项临床试验表明,多囊肾病(PKD)患者尽管接受了联合 RAAS 抑制剂治疗,但高钾血症的发作频率较低。由于肾内 RAAS 是肾脏钾处理的主要组成部分,因此我们进一步研究了慢性肾脏病患者,特别是 PKD 患者肾内 RAAS 活性与血清钾水平之间的关系,并检查了肾内 RAAS 活性在 PKD 患者中的预后作用。
本研究共纳入了韩国慢性肾脏病患者结局研究(KNOW-CKD)的 1788 名受试者。通过测量尿血管紧张素原(AGT)评估肾内 RAAS 活性。主要结局是全因死亡率和肾功能下降的复合结局。
在慢性肾脏病 1 至 3b 期,PKD 患者的血清钾水平明显低于非 PKD 患者。在多变量逻辑回归分析中,调整了多个混杂因素后,PKD 患者发生高钾血症的风险明显低于非 PKD 患者。在多变量线性回归分析中,尿 AGT/肌酐(Cr)比值与血清钾水平呈负相关(β=−0.058,P=0.017),与跨小管钾梯度(TTKG,β=0.087,P=0.001)呈正相关。在倾向评分匹配分析中,在匹配与血清钾和 TTKG 相关的因素后,尽管 PKD 患者的血清钾水平较低(P=0.004),但他们的 TTKG 明显较高(P=0.021)。此外,PKD 患者的尿 AGT/Cr 比值明显高于非 PKD 患者(P=0.011)。在 293 名 PKD 患者中,高尿 AGT/Cr 比值与复合结局的风险增加相关(风险比 1.29;95%置信区间,1.07-1.55;P=0.007)。
在 PKD 患者中,肾内 RAAS 活性升高与尿钾排泄增加和血清钾水平降低有关。此外,肾内 RAAS 活性可能是这些患者死亡率和肾功能下降的预后标志物。