Martínez-Sánchez Carlos, Azar-Manzur Francisco, González-Pacheco Héctor, Amezcua-Guerra Luis M, Massó Felipe, Márquez-Velasco Ricardo, Bojalil Rafael, Carvajal-Juárez Isabel, Alexanderson-Rosas Erick, Hernández Salvador, Paez-Arenas Araceli, López-Mora Enrique, Venegas-Román Alejandra, Brianza-Padilla Malinalli, Gopar-Nieto Rodrigo, Sandoval Julio
Coronary Care Unit, Instituto Nacional de Cardiología Ignacio Chávez, Mexico City, Mexico.
Immunology Department, Instituto Nacional de Cardiología Ignacio Chávez, Mexico City, Mexico.
Am J Cardiol. 2021 Apr 1;144:26-32. doi: 10.1016/j.amjcard.2020.12.065. Epub 2020 Dec 29.
Extracorporeal shockwave myocardial revascularization (ESMR) is a therapy for refractory angina pectoris. Our aim was to assess the efficacy and safety of ESMR in the management of patients with stable coronary artery disease (CAD) and heart failure as well as its effects on inflammation and angiogenesis. In this single-arm prospective trial, we included 48 patients with CAD, myocardial ischemia assessed by radionuclide imaging, echocardiographic evidence of left ventricular systolic dysfunction and without revascularization options. Changes in angina grading score, myocardial perfusion, left ventricular ejection fraction, and six-minute walk test after ESMR therapy were used for efficacy assessment. Changes of inflammation and angiogenesis biomarkers were also evaluated. ESMR therapy was performed using a commercially available cardiac shockwave generator system (Cardiospec; Medispec). After 9 weeks of ESMR therapy, a significant improvement was found regarding the initial angina class, severity of ischemia, left ventricular ejection fraction, and six-minute walk test in most patients. No deleterious side effects after treatment were detected. Regarding biomarkers, endothelial progenitor cells and angiopoietin-3 were significantly increased whereas IL-18 and TGF-β were significantly decreased after ESMR in the total group. Notably, VEGF, IL-1ß, and lipoxin A4 levels were significantly increased only in patients with myocardial ischemia improvement. In conclusion, ESMR therapy is safe and effective in most but not all patients with CAD and heart failure. ESMR is associated with increased markers of angiogenesis and decreased markers of inflammation. Myocardial ischemia improvement after ESMR is associated with increased markers of angiogenesis and pro-resolving mediators.
体外冲击波心肌血运重建术(ESMR)是一种用于治疗顽固性心绞痛的疗法。我们的目的是评估ESMR在治疗稳定型冠状动脉疾病(CAD)和心力衰竭患者中的疗效和安全性,以及其对炎症和血管生成的影响。在这项单臂前瞻性试验中,我们纳入了48例CAD患者,这些患者通过放射性核素成像评估有心肌缺血,有左心室收缩功能障碍的超声心动图证据且没有血运重建选择。ESMR治疗后心绞痛分级评分、心肌灌注、左心室射血分数和六分钟步行试验的变化用于疗效评估。还评估了炎症和血管生成生物标志物的变化。ESMR治疗使用市售的心脏冲击波发生器系统(Cardiospec;Medispec)进行。经过9周的ESMR治疗,大多数患者在初始心绞痛分级、缺血严重程度、左心室射血分数和六分钟步行试验方面有显著改善。治疗后未检测到有害副作用。关于生物标志物,在整个组中,ESMR治疗后内皮祖细胞和血管生成素-3显著增加,而IL-18和转化生长因子-β显著降低。值得注意的是,仅在心肌缺血改善的患者中,VEGF、IL-1β和脂氧素A4水平显著增加。总之,ESMR治疗对大多数但并非所有CAD和心力衰竭患者是安全有效的。ESMR与血管生成标志物增加和炎症标志物减少有关。ESMR治疗后心肌缺血改善与血管生成标志物和促消退介质增加有关。