Cilostazol in patients with heart failure and preserved ejection fraction-The CLIP-HFpEF trial.

IF 3.2 2区 医学 Q2 CARDIAC & CARDIOVASCULAR SYSTEMS ESC Heart Failure Pub Date : 2024-11-17 DOI:10.1002/ehf2.15162
Norman Aiad, Jeanne du Fay de Lavallaz, Michael J Zhang, Thanat Chaikijurajai, Bo Ye, Prabhjot S Nijjar, Julie A Lahiri, Cindy M Martin, Tamas Alexy, Markus Meyer
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Abstract

Background and aims: 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.

Methods: 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.

Results: 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).

Conclusions: 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.

Trial registration: ClinicalTrials.gov Identifier: NCT05126836.

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西洛他唑治疗射血分数保留型心力衰竭患者--CLIP-HFpEF 试验。
背景和目的:射血分数保留型心力衰竭(HFpEF)患者的静息心率和运动心率往往较低。磷酸二酯酶-3(PDE-3)抑制剂可改善射血分数保留型心衰患者的心率、血液动力学和症状。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端脑钠肽(NT-proBNP)水平和作用机制的短期影响:在一项随机安慰剂对照多重交叉试验(CLIP-HFpEF)中,对 23 名高频血友病患者的西洛他唑效果进行了评估。参与者接受安慰剂或西洛他唑治疗 1 周,然后在第 2 周、第 3 周和第 4 周进行三次交叉交替治疗。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) 总分。NT-proBNP 是次要终点。在一项探索性机理分析中,对五名植入压力监测器的参与者的肺动脉(PA)压力和心率进行了跟踪:西洛他唑将 KCCQ 评分提高了 4.8 分(95% 置信区间为 2.0-7.7,P = 0.003)。服用安慰剂时,NT-proBNP 水平为 448 (154-1056) pg/mL,服用西洛他唑时为 375 (68-974) pg/mL(P = 0.006)。在使用 PA 压力监测仪的患者中,安慰剂的舒张压为 20.5(18.7-23.0)mmHg,西洛他唑的舒张压为 18.0(17.0-20.0)mmHg,这种效应与较高的心率有关(P 结论:安慰剂和西洛他唑对舒张压的影响是相同的:与安慰剂相比,西洛他唑短期治疗可改善高房颤患者的健康状况和NT-proBNP。这些效果可能是通过心率依赖性降低心脏充盈压产生的:试验注册:ClinicalTrials.gov Identifier:试验注册:ClinicalTrials.gov Identifier:NCT05126836。
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来源期刊
ESC Heart Failure
ESC Heart Failure Medicine-Cardiology and Cardiovascular Medicine
CiteScore
7.00
自引率
7.90%
发文量
461
审稿时长
12 weeks
期刊介绍: ESC Heart Failure is the open access journal of the Heart Failure Association of the European Society of Cardiology dedicated to the advancement of knowledge in the field of heart failure. The journal aims to improve the understanding, prevention, investigation and treatment of heart failure. Molecular and cellular biology, pathology, physiology, electrophysiology, pharmacology, as well as the clinical, social and population sciences all form part of the discipline that is heart failure. Accordingly, submission of manuscripts on basic, translational, clinical and population sciences is invited. Original contributions on nursing, care of the elderly, primary care, health economics and other specialist fields related to heart failure are also welcome, as are case reports that highlight interesting aspects of heart failure care and treatment.
期刊最新文献
Two causes of COVID-19-related myocardial injury-associated cardiogenic shock: Myocarditis and microvascular thrombosis. Effects of sodium-glucose co-transporter inhibitors on individual clinical endpoints and quality of life. Machine learning-based prediction of elevated N terminal pro brain natriuretic peptide among US general population. Cilostazol in patients with heart failure and preserved ejection fraction-The CLIP-HFpEF trial. An unexpected ally in heart failure treatment: Unlocking the potential of sodium-glucose cotransporter 2 inhibitors across patient subpopulations.
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