Chen Tz-Heng, Ou Shuo-Ming, Lin Kuan-Hsun, Ho Yang, Tseng Wei-Cheng, Chu Yuan-Chia, Tarng Der-Cherng
Division of Nephrology, Department of Medicine, Taipei Veterans General Hospital, Taipei, Taiwan.
School of Medicine, National Yang Ming Chiao Tung University, Taipei, Taiwan.
Clin Kidney J. 2025 Aug 6;18(9):sfaf247. doi: 10.1093/ckj/sfaf247. eCollection 2025 Sep.
Steroidal mineralocorticoid receptor antagonists (MRAs), including spironolactone, effectively treat resistant hypertension, reduce proteinuria and lower mortality in heart failure with reduced ejection fraction. However, their long-term effects in chronic kidney disease (CKD) remain unclear. This study investigated spironolactone's impact on end-stage renal disease (ESRD), major adverse cardiovascular events (MACE), hyperkalemia and mortality in CKD patients.
This retrospective hospital-based cohort study enrolled patients with CKD stage 3-5 between 1 January 2011 and 30 June 2023. The patients were classified as spironolactone users or nonusers, with each user matched to two nonusers by propensity scores. The outcomes of interest included ESRD, MACE, all-cause mortality and severe hyperkalemia. MACE include nonfatal stroke, nonfatal myocardial infarction and cardiovascular death.
After propensity score matching, 2711 spironolactone users and 5422 nonusers were included in this analysis. Spironolactone users exhibited higher risks of all-cause mortality [adjusted hazard ratio (aHR) 1.23; 95% confidence interval (CI) 1.11-1.37] and severe hyperkalemia (aHR 1.44; 95% CI 1.24-1.68) than nonusers. However, there was a lower risk of MACE (aHR 0.90; 95% CI 0.82-0.99), primarily due to a significant reduction in stroke risk (aHR 0.79; 95% CI 0.71-0.88). The risk of ESRD was similar between the two groups (aHR 1.09; 95% CI 0.85-1.38).
In patients with CKD, spironolactone use was associated with a decreased risk of stroke but increased risks of severe hyperkalemia and all-cause mortality, while the risk of ESRD remained unchanged. Individualized clinical decision-making and appropriate dose adjustment are important to balance the potential benefits and risks associated with spironolactone therapy.
甾体类盐皮质激素受体拮抗剂(MRAs),包括螺内酯,可有效治疗顽固性高血压、减少蛋白尿并降低射血分数降低的心力衰竭患者的死亡率。然而,它们在慢性肾脏病(CKD)中的长期影响仍不明确。本研究调查了螺内酯对CKD患者终末期肾病(ESRD)、主要不良心血管事件(MACE)、高钾血症和死亡率的影响。
这项基于医院的回顾性队列研究纳入了2011年1月1日至2023年6月30日期间的3-5期CKD患者。患者被分为螺内酯使用者和非使用者,每个使用者通过倾向评分与两名非使用者匹配。感兴趣的结局包括ESRD、MACE、全因死亡率和严重高钾血症。MACE包括非致命性卒中、非致命性心肌梗死和心血管死亡。
倾向评分匹配后,本分析纳入了2711名螺内酯使用者和5422名非使用者。螺内酯使用者的全因死亡率(调整后风险比[aHR]1.23;95%置信区间[CI]1.11-1.37)和严重高钾血症(aHR 1.44;95%CI 1.24-1.68)风险高于非使用者。然而,MACE风险较低(aHR 0.90;95%CI 0.82-0.99),主要是由于卒中风险显著降低(aHR 0.79;95%CI 0.71-0.88)。两组间ESRD风险相似(aHR 1.09;95%CI 0.85-1.38)。
在CKD患者中,使用螺内酯与卒中风险降低相关,但与严重高钾血症和全因死亡率风险增加相关,而ESRD风险保持不变。个体化临床决策和适当的剂量调整对于平衡螺内酯治疗相关的潜在益处和风险很重要。