Hobbs F D Richard, McManus Richard J, Taylor Clare J, Jones Nicholas R, Rahman Joy K, Wolstenholme Jane, Kim Sungwook, Kwon Joseph, Jones Louise, Hirst Jennifer A, Yu Ly-Mee, Mort Sam
Nuffield Department of Primary Care Health Sciences, University of Oxford, Oxford, UK.
Department of Applied Health Sciences, University of Birmingham, Birmingham, UK.
Nat Med. 2024 Dec;30(12):3634-3645. doi: 10.1038/s41591-024-03263-5. Epub 2024 Sep 30.
Chronic kidney disease (CKD) is associated with a substantial risk of progression to end-stage renal disease and vascular events. The nonsteroidal mineralocorticoid receptor antagonist (MRA), finerenone, offers cardiorenal protection for people with CKD and diabetes, but there is uncertainty if the steroidal MRA, spironolactone, provides the same protection. In this prospective, randomized, open, blinded endpoint trial, we assessed the effectiveness of 25 mg spironolactone in addition to usual care or usual care alone for reducing cardiovascular outcomes in stage 3b CKD among an older community cohort (mean age = 74.8 years and s.d. = 8.1). We recruited 1,434 adults from English primary care, of whom 1,372 (96%) were included in the primary analysis. The primary outcome was time from randomization until the first occurrence of death, hospitalization for heart disease, stroke, heart failure, transient ischemic attack or peripheral arterial disease, or first onset of any condition listed not present at baseline. Across 3 years of follow-up, the primary endpoint occurred in 113 of 677 participants randomized to spironolactone (16.7%) and 111 of 695 participants randomized to usual care (16.0%) with no significant difference between groups (hazard ratio = 1.05, 95% confidence interval: 0.81-1.37). Two-thirds of participants randomized to spironolactone stopped treatment within 6 months, predominantly because they met prespecified safety stop criteria. The most common reason for stopping spironolactone was a decrease in the estimated glomerular filtration rate that met prespecified stop criteria (n = 239, 35.4%), followed by participants being withdrawn due to treatment side effects (n = 128, 18.9%) and hyperkalemia (n = 54, 8.0%). In conclusion, we found that spironolactone was frequently discontinued due to safety concerns, with no evidence that it reduced cardiovascular outcomes in people with stage 3b CKD. Spironolactone should not be used for people with stage 3b CKD without another explicit treatment indication. ClinicalTrials.gov registration: ISRCTN44522369 .
慢性肾脏病(CKD)与进展至终末期肾病和血管事件的重大风险相关。非甾体类盐皮质激素受体拮抗剂(MRA)非奈利酮可为患有CKD和糖尿病的患者提供心肾保护作用,但甾体类MRA螺内酯是否能提供同样的保护尚不确定。在这项前瞻性、随机、开放、盲终点试验中,我们评估了在常规治疗基础上加用25mg螺内酯或仅采用常规治疗,对老年社区队列(平均年龄 = 74.8岁,标准差 = 8.1)中3b期CKD患者降低心血管结局的有效性。我们从英国初级医疗保健机构招募了1434名成年人,其中1372人(96%)纳入了主要分析。主要结局是从随机分组到首次出现死亡、因心脏病住院、中风、心力衰竭、短暂性脑缺血发作或外周动脉疾病,或首次出现任何在基线时不存在的上述疾病的时间。在3年的随访中,随机分组接受螺内酯治疗的677名参与者中有113人(16.7%)发生了主要终点事件,随机分组接受常规治疗的695名参与者中有111人(16.0%)发生了主要终点事件,两组之间无显著差异(风险比 = 1.05,95%置信区间:0.81 - 1.37)。随机分组接受螺内酯治疗的参与者中有三分之二在6个月内停止了治疗,主要原因是他们符合预先设定的安全停药标准。停止使用螺内酯最常见的原因是估计肾小球滤过率下降达到预先设定的停药标准(n = 239,35.4%),其次是参与者因治疗副作用被撤药(n = 128,18.9%)和高钾血症(n = 54,8.0%)。总之,我们发现螺内酯常因安全问题而停药,没有证据表明它能降低3b期CKD患者的心血管结局。对于没有其他明确治疗指征的3b期CKD患者,不应使用螺内酯。ClinicalTrials.gov注册号:ISRCTN44522369 。