医学
血管病学
胸痛
心脏病学
随机对照试验
内科学
冠状动脉疾病
压力测试(软件)
血压
冠状动脉
冠状动脉血流储备
心肌灌注成像
急性冠脉综合征
血流
磁共振成像
部分流量储备
冠状动脉循环
灌注
心肌梗塞
动脉
缺血
灌注扫描
负荷超声心动图
不利影响
血流动力学
肌钙蛋白
作者
Cho-Kiu Lo,Niki Hiu-Yee Ip,Tsun‐Hei Sin,S Y Ho,Chun-Ka Wong,Frankie Chor-Cheung Tam,Simon Cheung-Chi Lam,Kai Hang Yiu,Michael Shu-Yue Sze,Thomas Tsun-Ho Lam,Alston Conrad Ho-On Chiu,Karen Ka-Ying Li,Timothy Ka Chun Un,Esther Yee-Tak Yu,Eric Kwong-Yu Chan,Kevin Ka-Chun Lee,Shing Ching,Pok-Him Lee,Chi-yuen Wong,Hiu-Lam Chan
标识
DOI:10.1016/j.jocmr.2026.102744
摘要
BACKGROUND: Previous studies have shown that ~50% of patients with stable chest pain have no obstructive coronary artery disease (CAD), yet remain at higher risk of major adverse cardiovascular events (MACE) compared to patients without chest pain. Coronary microvascular dysfunction (CMD) is a major cause of ischaemia with no obstructive coronary arteries (INOCA). While therapies for CMD are lacking, Vericiguat, a soluble guanylate cyclase stimulator, has shown improvement in coronary microvascular circulation in animal studies. Quantitative stress cardiovascular magnetic resonance (CMR) allows the quantification of stress myocardial blood flow (MBF) and myocardial perfusion reserve (MPR). This study aims to conduct a randomized controlled trial to determine if Vericiguat improves MBF and MPR in patients with stable chest pain and INOCA caused by CMD. METHODS/DESIGN: V-COM is a single-blind, randomized controlled trial. 94 patients aged 40-80 years with recurrent stable chest pain, non-obstructive coronary arteries on recent coronary computed tomography (CT) or invasive angiography, and CMD defined by stress CMR (MPR <2.19 or stress MBF <2.19ml/g/min) will be recruited across six centres in Hong Kong. Participants will be randomised 1:1 to vericiguat plus optimal medical therapy (intervention) or optimal medical therapy alone (control). Vericiguat will be prescribed once daily for 6 months, starting at 2.5mg and titrated up to a target dose of 10mg based on systolic blood pressure and tolerability. CMR (including quantitative stress perfusion) will be performed at baseline and 6 months. The primary outcome is the between-group difference in change in stress MBF and MPR from baseline to 6 months. Secondary outcomes include change in six-minute walk distance and Seattle Angina Questionnaire-7 (SAQ-7) scores. DISCUSSION: This study will provide evidence on whether Vericiguat can improve myocardial perfusion in patients with CMD and offer insights into its potential as a novel therapy for CMD.
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