Division of Nephrology, Kaohsiung Medical University Hospital, Kaohsiung Medical University, Kaohsiung, Taiwan.
PLoS One. 2013 Jul 2;8(7):e67140. doi: 10.1371/journal.pone.0067140. Print 2013.
In the chronic kidney disease (CKD) population, the impact of serum potassium (sK) on renal outcomes has been controversial. Moreover, the reasons for the potential prognostic value of hypokalemia have not been elucidated.
DESIGN PARTICIPANTS & MEASUREMENTS: 2500 participants with CKD stage 1-4 in the Integrated CKD care program Kaohsiung for delaying Dialysis (ICKD) prospective observational study were analyzed and followed up for 2.7 years. Generalized additive model was fitted to determine the cutpoints and the U-shape association between sK and end-stage renal disease (ESRD). sK was classified into five groups with the cutpoints of 3.5, 4, 4.5 and 5 mEq/L. Cox proportional hazard regression models predicting the outcomes were used.
The mean age was 62.4 years, mean sK level was 4.2±0.5 mEq/L and average eGFR was 40.6 ml/min per 1.73 m(2). Female vs male, diuretic use vs. non-use, hypertension, higher eGFR, bicarbonate, CRP and hemoglobin levels significantly correlated with hypokalemia. In patients with lower sK, nephrotic range proteinuria, and hypoalbuminemia were more prevalent but the use of RAS (renin-angiotensin system) inhibitors was less frequent. Hypokalemia was significantly associated with ESRD with hazard ratios (HRs) of 1.82 (95% CI, 1.03-3.22) in sK <3.5mEq/L and 1.67 (95% CI,1.19-2.35) in sK = 3.5-4 mEq/L, respectively, compared with sK = 4.5-5 mEq/L. Hyperkalemia defined as sK >5 mEq/L conferred 1.6-fold (95% CI,1.09-2.34) increased risk of ESRD compared with sK = 4.5-5 mEq/L. Hypokalemia was also associated with rapid decline of renal function defined as eGFR slope below 20% of the distribution range.
In conclusion, both hypokalemia and hyperkalemia are associated with increased risk of ESRD in CKD population. Hypokalemia is related to increased use of diuretics, decreased use of RAS blockade and malnutrition, all of which may impose additive deleterious effects on renal outcomes.
在慢性肾脏病(CKD)患者中,血清钾(sK)对肾脏结局的影响一直存在争议。此外,低钾血症潜在预后价值的原因尚未阐明。
设计、参与者及测量:对 Integrated CKD care program Kaohsiung for delaying Dialysis(ICKD)前瞻性观察研究中的 2500 名 CKD 1-4 期患者进行分析,并随访 2.7 年。采用广义加性模型确定 sK 与终末期肾脏疾病(ESRD)之间的切点和 U 形关联。将 sK 分为 5 组,切点为 3.5、4、4.5 和 5 mEq/L。使用 Cox 比例风险回归模型预测结局。
平均年龄为 62.4 岁,平均 sK 水平为 4.2±0.5 mEq/L,平均 eGFR 为 40.6 ml/min per 1.73 m2。与低钾血症相关的因素包括女性、利尿剂使用与非使用、高血压、更高的 eGFR、碳酸氢盐、CRP 和血红蛋白水平。在 sK 较低的患者中,肾病范围蛋白尿和低白蛋白血症更为常见,但 RAS(肾素-血管紧张素系统)抑制剂的使用率较低。与 sK=4.5-5 mEq/L 相比,sK<3.5 mEq/L(HRs 为 1.82,95%CI,1.03-3.22)和 sK=3.5-4 mEq/L(HRs 为 1.67,95%CI,1.19-2.35)与 ESRD 显著相关。与 sK=4.5-5 mEq/L 相比,高钾血症定义为 sK>5 mEq/L 与 ESRD 风险增加 1.6 倍(95%CI,1.09-2.34)。低钾血症也与肾功能快速下降相关,定义为 eGFR 斜率低于分布范围的 20%。
总之,CKD 人群中低钾血症和高钾血症均与 ESRD 风险增加相关。低钾血症与利尿剂使用增加、RAS 阻断剂使用减少和营养不良有关,所有这些因素可能对肾脏结局产生累加性有害影响。