Li Zihan, Li Tingting, Liu Tingxun, Liu Yuanqiao, Si Daoyuan, He Yuquan, Yang Ping
Department of Cardiology, Engineering Laboratory for Endothelial Function, China-Japan Union Hospital of Jilin University, Changchun, Jilin, China.
Front Cardiovasc Med. 2025 Mar 4;12:1465700. doi: 10.3389/fcvm.2025.1465700. eCollection 2025.
Vericiguat-a novel oral soluble guanylate cyclase stimulator-was developed for the treatment of chronic heart failure (HF). Although the value of vericiguat therapy in chronic HF has been gradually recognized, its safety and efficacy in the acute phase of HF remain elusive.
100 patients with acute HF receiving vericiguat therapy at the China-Japan Union Hospital of Jilin University between September 2022 and June 2023 were retrospectively analyzed. An external control was built from real-world data of acute HF subjects contemporaneously hospitalized in the same hospital using a propensity score matching (PSM) method.
After a median follow-up of 68 days, 80 patients completed at least one outpatient follow-up or had an endpoint event and cardiovascular death occurred in 6 patients. We matched 75 external control patients for this purpose. In single-arm study, overall, although systolic blood pressure (SBP) decreased significantly before and after treatment, there was little change in SBP in the SBP low group (baseline SBP less than 120mmHg) (from 109 mmHg to 105 mmHg, = 0.109). Estimated glomerular filtration rate (eGFR) and serum potassium did not change significantly ( = 0.521 and 0.070, respectively). However, compared with the renal function normal group, eGFR showed a slower downward trend in the renal insufficiency group ( = 0.025). After using the PSM method, significant improvements in left ventricular ejection fraction and N-terminal pro-B-type natriuretic peptide were seen in both groups before and after treatment. There was no significant difference between the two groups. However, the downward trend in eGFR was even less significant in the vericiguat group, with significant differences between the two groups ( = 0.024).
Vericiguat is feasible in acute HF, even in patients with hypotension and renal dysfunction. At the same time, vericiguat may have a potential renoprotective effect, which warrants further exploration.
维立西呱——一种新型口服可溶性鸟苷酸环化酶刺激剂——被开发用于治疗慢性心力衰竭(HF)。尽管维立西呱治疗慢性HF的价值已逐渐得到认可,但其在HF急性期的安全性和疗效仍不明确。
回顾性分析2022年9月至2023年6月在吉林大学中日联谊医院接受维立西呱治疗的100例急性HF患者。使用倾向评分匹配(PSM)方法,从同期在同一医院住院的急性HF受试者的真实世界数据中建立外部对照组。
中位随访68天后,80例患者完成了至少一次门诊随访或发生终点事件,6例患者发生心血管死亡。为此我们匹配了75例外部对照患者。在单臂研究中,总体而言,尽管治疗前后收缩压(SBP)显著下降,但SBP低组(基线SBP低于120mmHg)的SBP变化不大(从109mmHg降至105mmHg,P = 0.109)。估算肾小球滤过率(eGFR)和血清钾无显著变化(分别为P = 0.521和0.070)。然而,与肾功能正常组相比,肾功能不全组的eGFR下降趋势较慢(P = 0.025)。使用PSM方法后,两组治疗前后左心室射血分数和N末端B型利钠肽原均有显著改善。两组之间无显著差异。然而,维立西呱组eGFR的下降趋势更不明显,两组之间存在显著差异(P = 0.024)。
维立西呱在急性HF中是可行的,即使在低血压和肾功能不全的患者中也是如此。同时,维立西呱可能具有潜在的肾脏保护作用,值得进一步探索。