British Heart Foundation Cardiovascular Research Centre, University of Glasgow, Glasgow, UK.
University of Groningen, Department of Cardiology, University Medical Center Groningen, Groningen, The Netherlands.
Eur J Heart Fail. 2016 Dec;18(12):1508-1517. doi: 10.1002/ejhf.609. Epub 2016 Jul 18.
We investigated the association between worsening renal function (WRF) that occurs during renin-angiotensin-aldosterone system inhibition initation and outcome in heart failure (HF) patients with preserved ejection fraction (HFPEF) and compared this with HF patients with reduced ejection fraction (HFREF).
We examined changes in estimated glomerular filtration rate (GFR) and the relationship between WRF (defined as ≥26.5 µmol/L and ≥25% increase in serum creatinine from baseline to 6 weeks) and outcome, according to randomized treatment, in patients with HFREF (EF <45%; n = 1569) and HFPEF (EF ≥45%; n = 836) in the CHARM programme. The primary outcome was cardiovascular death or HF hospitalization. Estimated GFR decreased 9.0 ± 21 vs. 4.0 ± 21 mL/min/1.73 m with candesartan and placebo, respectively, and this was similar in HFREF and HFPEF. WRF developed more frequently with candesartan, 16% vs. 7%, P < 0.001, with similar findings in patients with HFREF and HFPEF. WRF was associated with a higher risk of the primary outcome: multivariable hazard ratio (HR) 1.26, 95% confidence interval 1.03-1.54, P = 0.022, in both treatment groups, and in both HFREF and HFPEF (P for interaction 0.98). In HFREF, WRF was mostly related to HF hospitalization, while in HFPEF, WRF seemed more associated with mortality.
GFR decreased more and WRF was more common with candesartan compared with placebo, and this was similar in HFREF and HFPEF. WRF was associated with worse outcomes in HFREF and HFPEF. Although no formal interaction was present, the association between candesartan treatment, WRF, and type of clinical outcome was slightly different between HFREF and HFPEF.
我们研究了血管紧张素-肾素-醛固酮系统抑制剂起始时肾功能恶化(WRF)与射血分数保留型心力衰竭(HFPEF)和射血分数降低型心力衰竭(HFREF)患者结局之间的关系,并将其与 HFREF 患者进行了比较。
我们在 CHARM 研究中检查了 HFREF(EF <45%;n = 1569)和 HFPEF(EF ≥45%;n = 836)患者中,根据随机治疗,WRF(定义为 6 周内血清肌酐较基线增加≥26.5 μmol/L 和≥25%)和结局之间的变化。主要结局为心血管死亡或 HF 住院。与安慰剂相比,坎地沙坦分别使估算肾小球滤过率(GFR)下降 9.0 ± 21 和 4.0 ± 21 mL/min/1.73 m2,HFREF 和 HFPEF 中结果相似。坎地沙坦组 WRF 的发生率更高,为 16%,安慰剂组为 7%,P < 0.001,HFREF 和 HFPEF 中也有类似发现。WRF 与主要结局风险增加相关:多变量危险比(HR)为 1.26,95%置信区间为 1.03-1.54,P = 0.022,在两组和 HFREF 和 HFPEF 中(P 交互作用 0.98)。在 HFREF 中,WRF 主要与 HF 住院有关,而在 HFPEF 中,WRF 似乎与死亡率更相关。
与安慰剂相比,坎地沙坦使 GFR 下降更多,WRF 更常见,HFREF 和 HFPEF 中结果相似。WRF 与 HFREF 和 HFPEF 的不良结局相关。尽管没有正式的交互作用,但坎地沙坦治疗、WRF 和临床结局类型之间的关联在 HFREF 和 HFPEF 之间略有不同。