Rivera-Martinez Juan Carlos, Sabina Michael, Khanani Aqeel, Lurie Andrew, Rigdon Amanda, Abusnina Waiel, Lugo Rosado Luis Daniel, Bizanti Anas, Paul Timir K
Department of Internal Medicine, Lakeland Regional Health Medical Center, Lakeland, FL, USA.
Department of Cardiology, MedStar Georgetown University Hospital, Washington, DC, USA.
Cardiovasc Drugs Ther. 2025 Jan 4. doi: 10.1007/s10557-024-07666-x.
Heart failure (HF) management is well-defined for reduced ejection fraction (HFrEF) but less so for mildly reduced (HFmrEF) or preserved ejection fraction (HFpEF). This meta-analysis evaluates the impact of Finerenone, a nonsteroidal mineralocorticoid receptor antagonist, on cardiovascular and renal outcomes in these patient populations.
A systematic search in PubMed and Embase identified randomized controlled trials (RCTs) on Finerenone's cardiovascular and renal effects. Three RCTs were included-FIDELIO-DKD, FIGARO-DKD, and FINEARTS-HF-encompassing 19,027 participants. Primary outcomes included cardiovascular death, HF hospitalization, and renal failure. Secondary outcomes focused on safety and adverse events like acute kidney injury and hyperkalemia. Meta-analyses were performed using hazard ratios (HR), confidence intervals (CI), and Relative Risk (RR).
Finerenone was associated with a 20% reduction in HF hospitalization risk (HR 0.80, 95% CI: 0.72-0.90) and a 14% reduction in all-cause mortality (RR 0.86, 95% CI: 0.77-0.97). Finerenone did not significantly reduce cardiovascular death (HR 0.91, 95% CI: 0.82-1.01, p = 0.06). Renal failure rates were similar between Finerenone and placebo (RR 1.05, 95% CI: 0.65-1.68). Hyperkalemia incidence was significantly higher with Finerenone, with a RR of 2.31 (95% CI: 1.98-2.69).
This meta-analysis shows that Finerenone significantly reduces HF hospitalizations and all-cause mortality in patients with chronic kidney disease and heart failure. Further studies are needed to clarify its effects on cardiovascular death and renal failure.
心力衰竭(HF)管理对于射血分数降低(HFrEF)的情况已有明确界定,但对于轻度降低(HFmrEF)或射血分数保留(HFpEF)的情况则界定较少。本荟萃分析评估非甾体类盐皮质激素受体拮抗剂非奈利酮对这些患者群体心血管和肾脏结局的影响。
在PubMed和Embase中进行系统检索,以确定关于非奈利酮心血管和肾脏作用的随机对照试验(RCT)。纳入了三项RCT——FIDELIO-DKD、FIGARO-DKD和FINEARTS-HF,共19,027名参与者。主要结局包括心血管死亡、心力衰竭住院和肾衰竭。次要结局集中在安全性和不良事件,如急性肾损伤和高钾血症。使用风险比(HR)、置信区间(CI)和相对风险(RR)进行荟萃分析。
非奈利酮使心力衰竭住院风险降低20%(HR 0.80,95% CI:0.72 - 0.90),全因死亡率降低14%(RR 0.86,95% CI:0.77 - 0.97)。非奈利酮未显著降低心血管死亡(HR 0.91,95% CI:0.82 - 1.01,p = 0.06)。非奈利酮组和安慰剂组的肾衰竭发生率相似(RR 1.05,95% CI:0.65 - 1.68)。非奈利酮组高钾血症发生率显著更高,RR为2.31(95% CI:1.98 - 2.69)。
本荟萃分析表明,非奈利酮可显著降低慢性肾脏病和心力衰竭患者的心力衰竭住院率和全因死亡率。需要进一步研究以阐明其对心血管死亡和肾衰竭的影响。