Aiad Norman, du Fay de Lavallaz Jeanne, Zhang Michael J, Chaikijurajai Thanat, Ye Bo, Nijjar Prabhjot S, Lahiri Julie A, Martin Cindy M, Alexy Tamas, Meyer Markus
Department of Medicine, Cardiology, University of Minnesota, Minneapolis, Minnesota, USA.
Lillehei Heart Institute, University of Minnesota, Minneapolis, Minnesota, USA.
ESC Heart Fail. 2025 Apr;12(2):1437-1446. doi: 10.1002/ehf2.15162. Epub 2024 Nov 17.
Patients with heart failure with preserved ejection fraction (HFpEF) tend to have low resting and exercise heart rates. Phosphodiesterase-3 (PDE-3) inhibitors improve heart rates, haemodynamics and symptoms in patients with HFpEF. Cilostazol is an oral PDE-3 inhibitor used in peripheral artery disease. This study thought to evaluate the short-term effects of cilostazol on health status, N-terminal brain natriuretic peptide (NT-proBNP) levels and mechanisms of action.
The effect of cilostazol was evaluated in 23 patients with HFpEF in a randomized placebo controlled multiple crossover trial (CLIP-HFpEF). Participants received placebo or cilostazol for 1 week followed by three crossovers to the alternate assignment at weeks 2, 3 and 4. The primary endpoint was the Kansas City Cardiomyopathy Questionnaire (KCCQ-12) overall summary score obtained at the end of each treatment period. NT-proBNP was the secondary endpoint. In an exploratory mechanistic analysis, pulmonary artery (PA) pressures and heart rates were followed amongst the five participants with implanted pressure monitors.
Cilostazol improved the KCCQ score by 4.8 points (95% confidence interval, 2.0-7.7, P = 0.003). NT-proBNP levels were 448 (154-1056) pg/mL on placebo and 375 (68-974) pg/mL on cilostazol (P = 0.006). In patients with PA pressure monitors, diastolic pressure was 20.5 (18.7-23.0) mmHg on placebo and 18.0 (17.0-20.0) mmHg on cilostazol, an effect linked to higher heart rates (P < 0.001).
Amongst patients with HFpEF, short-term treatment with cilostazol leads to improvements in health status and NT-proBNP when compared with placebo. These effects are likely conveyed by a heart rate-dependent reduction in cardiac filling pressures.
ClinicalTrials.gov Identifier: NCT05126836.
射血分数保留的心力衰竭(HFpEF)患者往往静息心率和运动心率较低。磷酸二酯酶-3(PDE-3)抑制剂可提高HFpEF患者的心率、改善血流动力学并缓解症状。西洛他唑是一种用于外周动脉疾病的口服PDE-3抑制剂。本研究旨在评估西洛他唑对健康状况、N末端脑钠肽(NT-proBNP)水平及作用机制的短期影响。
在一项随机、安慰剂对照、多次交叉试验(CLIP-HFpEF)中,对23例HFpEF患者评估西洛他唑的疗效。参与者接受安慰剂或西洛他唑治疗1周,随后在第2、3和4周进行三次交叉,改为交替治疗。主要终点是每个治疗期结束时获得的堪萨斯城心肌病问卷(KCCQ-12)总体总结评分。NT-proBNP是次要终点。在一项探索性机制分析中,对五名植入压力监测器的参与者监测肺动脉(PA)压力和心率。
西洛他唑使KCCQ评分提高了4.8分(95%置信区间,2.0-7.7,P = 0.003)。安慰剂组NT-proBNP水平为448(154-1056)pg/mL,西洛他唑组为375(68-974)pg/mL(P = 0.006)。在植入PA压力监测器的患者中,安慰剂组舒张压为20.5(18.7-23.0)mmHg,西洛他唑组为18.0(17.0-20.0)mmHg,这一效应与较高的心率有关(P < 0.001)。
在HFpEF患者中,与安慰剂相比,短期使用西洛他唑可改善健康状况和NT-proBNP水平。这些效应可能是通过心率依赖性降低心脏充盈压来实现的。
ClinicalTrials.gov标识符:NCT05126836。