Relationship between peripheral and intracoronary blood flow in patients with angina and nonobstructive coronary arteries.

IF 4.1 2区 医学 Q1 CARDIAC & CARDIOVASCULAR SYSTEMS
Janneke Woudstra, Sanne G J Mourmans, Caitlin E M Vink, Koen M J Marques, Elize A M de Jong, Rahma Y R Haddad, Tim P van de Hoef, Steven A J Chamuleau, Peter Damman, Marcel A M Beijk, Vanessa P M van Empel, Erik H Serné, Yolande Appelman, Etto C Eringa
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引用次数: 0

Abstract

Coronary vasomotor dysfunction, an important underlying cause of angina and nonobstructive coronary arteries (ANOCA), encompassing coronary vasospasm, coronary endothelial dysfunction, and/or coronary microvascular dysfunction, is clinically assessed by invasive coronary function testing (ICFT). As ICFT imposes a high burden on patients and carries risks, developing noninvasive alternatives is important. We evaluated whether coronary vasomotor dysfunction is a component of systemic microvascular endothelial and smooth muscle dysfunction and can be detected using laser speckle contrast analysis (LASCA). Forty-three consecutive patients with ANOCA underwent ICFT, with intracoronary acetylcholine, adenosine, and flow measurements, to assess coronary vasomotor dysfunction. Cutaneous microvascular function was assessed using LASCA in the forearm, combined with vasodilators acetylcholine, sodium nitroprusside, and insulin and using EndoPAT, by measuring the reactive hyperemia index (RHI). Of the 43 included patients with ANOCA (79% women, 59 ± 9 yr old), 38 patients had coronary vasomotor dysfunction, including 28 with coronary vasospasm, 26 with coronary endothelial dysfunction, and 18 with coronary microvascular dysfunction, with overlapping endotypes. Patients with and without coronary vasomotor dysfunction had similar peripheral flow responses to acetylcholine, insulin, and RHI. In contrast, coronary vasomotor dysfunction was associated with lower peripheral flow responses to sodium nitroprusside (P < 0.001). An absolute flow response to sodium nitroprusside of 83.95 APU resulted in 86.1% sensitivity and 80.0% specificity for coronary vasomotor dysfunction (area under the ROC curve, 0.883; P = 0.006). In conclusion, this study provides evidence of systemic vascular smooth muscle dysfunction in patients with ANOCA with coronary vasomotor dysfunction and the diagnostic value of peripheral microvascular function testing as a noninvasive tool for detecting coronary vasomotor dysfunction.NEW & NOTEWORTHY This study provides proof of concept that assessment of the peripheral vasculature, particularly vascular smooth muscle cells measured using the LASCA technology holds potential as a noninvasive tool for detecting coronary vasomotor dysfunction. This finding highlights the potential of the LASCA technology in, for example, medication studies for coronary vasomotor dysfunction, especially when investigating whether medication improves vascular function, as repeated peripheral measurements are less invasive than invasive coronary function testing, the current gold standard.

心绞痛和冠状动脉无阻塞患者的外周血流与冠状动脉内血流之间的关系。
背景:冠状动脉血管运动功能障碍是导致心绞痛和冠状动脉非阻塞性病变(ANOCA)的重要根本原因,包括冠状动脉血管痉挛、冠状动脉内皮功能障碍和/或冠状动脉微血管功能障碍。由于有创冠状动脉功能检测给患者带来了沉重的负担和风险,因此开发无创替代方法非常重要。我们评估了冠状动脉血管运动功能障碍是否是全身微血管内皮和平滑肌功能障碍的一个组成部分,是否可以通过激光斑点对比分析(LASCA)检测出来。方法连续 43 例 ANOCA 患者接受了 ICFT,并进行了冠状动脉内乙酰胆碱、腺苷和血流测量,以评估冠状动脉血管运动功能障碍。使用 LASCA 评估皮肤微血管功能,结合使用血管扩张剂乙酰胆碱、硝普钠和胰岛素,并使用 EndoPAT 测量反应性充血指数 (RHI)。结果:在纳入的 43 名 ANOCA 患者(79% 为女性,59±9 岁)中,38 名患者有冠状动脉血管运动功能障碍,其中 28 名患者有冠状动脉血管痉挛,26 名患者有冠状动脉内皮功能障碍,18 名患者有冠状动脉微血管功能障碍,且内型重叠。冠状血管运动功能障碍患者和无冠状血管运动功能障碍患者对乙酰胆碱、胰岛素和 RHI 的外周血流反应相似。相反,冠状动脉血管运动功能障碍患者对硝普钠的外周血流反应较低:本研究提供的证据表明,ANOCA 患者伴有冠状动脉血管运动功能障碍的全身血管平滑肌功能障碍,以及外周微血管功能测试作为检测冠状动脉血管运动功能障碍的无创工具的诊断价值。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
CiteScore
9.60
自引率
10.40%
发文量
202
审稿时长
2-4 weeks
期刊介绍: The American Journal of Physiology-Heart and Circulatory Physiology publishes original investigations, reviews and perspectives on the physiology of the heart, vasculature, and lymphatics. These articles include experimental and theoretical studies of cardiovascular function at all levels of organization ranging from the intact and integrative animal and organ function to the cellular, subcellular, and molecular levels. The journal embraces new descriptions of these functions and their control systems, as well as their basis in biochemistry, biophysics, genetics, and cell biology. Preference is given to research that provides significant new mechanistic physiological insights that determine the performance of the normal and abnormal heart and circulation.
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