Division of Cardiology, Department of Medicine, Karolinska Institutet, Stockholm, Sweden.
Heart, Vascular and Neuro Theme, Karolinska University Hospital, Stockholm, Sweden.
Eur J Heart Fail. 2023 Dec;25(12):2164-2173. doi: 10.1002/ejhf.3049. Epub 2023 Oct 18.
Mineralocorticoid receptor antagonists (MRAs) improve outcomes in heart failure with reduced ejection fraction (HFrEF) but remain underused and are often discontinued especially in patients with chronic kidney disease (CKD) due to concerns on renal safety. Therefore, in a real-world HFrEF population we investigated the safety of MRA use, in terms of risk of renal events, any mortality and any hospitalization, across the estimated glomerular filtration rate (eGFR) spectrum including severe CKD.
We analysed patients with HFrEF (ejection fraction <40%), not on dialysis, from the Swedish Heart Failure Registry. We performed multivariable logistic regression models to investigate patient characteristics independently associated with MRA use, and univariable and multivariable Cox regression models to assess the associations between MRA use and outcomes. Of 33 942 patients, 17 489 (51%) received MRA, 32%, 45%, 54%, 54% with eGFR <30, 30-44, 45-59 or ≥60 ml/min/1.73 m , respectively. An eGFR ≥60 ml/min/1.73 m and patient characteristics linked with more severe HF were independently associated with more likely MRA use. In multivariable analyses, MRA use was consistently not associated with a higher risk of renal events (i.e. composite of dialysis/renal death/hospitalization for renal failure or hyperkalaemia) (hazard ratio [HR] 1.04, 95% confidence interval [CI] 0.98-1.10), all-cause death (HR 1.02, 95% CI 0.97-1.08) as well as of all-cause hospitalization (HR 0.99, 95% CI 0.95-1.02) across the eGFR spectrum including also severe CKD.
The use of MRAs in patients with HFrEF decreased with worse renal function; however their safety profile was demonstrated to be consistent across the entire eGFR spectrum.
醛固酮受体拮抗剂(MRA)可改善射血分数降低的心力衰竭(HFrEF)患者的预后,但仍未被充分应用,并且由于对肾脏安全性的担忧,在合并慢性肾脏病(CKD)的患者中常被停药。因此,在真实世界的 HFrEF 人群中,我们研究了 MRA 应用的安全性,评估了肾小球滤过率(eGFR)谱中包括严重 CKD 患者在内的各个肾功能阶段发生肾脏不良事件、全因死亡和全因住院的风险。
我们分析了来自瑞典心力衰竭注册登记研究的射血分数<40%、未接受透析的 HFrEF 患者。我们采用多变量逻辑回归模型研究了与 MRA 应用独立相关的患者特征,并采用单变量和多变量 Cox 回归模型评估了 MRA 应用与结局之间的相关性。在 33942 例患者中,17489 例(51%)接受了 MRA 治疗,eGFR<30、30-44、45-59 和≥60ml/min/1.73m2 患者的比例分别为 32%、45%、54%和 54%。eGFR≥60ml/min/1.73m2 和与更严重 HF 相关的患者特征与更可能使用 MRA 独立相关。在多变量分析中,MRA 应用与肾脏不良事件(包括透析/肾脏死亡/因肾衰竭或高钾血症住院的复合终点)(风险比[HR]1.04,95%置信区间[CI]0.98-1.10)、全因死亡(HR 1.02,95%CI 0.97-1.08)以及全因住院(HR 0.99,95%CI 0.95-1.02)风险均无相关性,在 eGFR 谱中包括严重 CKD 患者时也是如此。
在 HFrEF 患者中,随着肾功能恶化,MRA 的应用减少;然而,其安全性在整个 eGFR 谱中保持一致。