Institute of Pathophysiology, Faculty of Medicine, Comenius University, Bratislava, Slovak Republic.
Cardiovascular Medicine Section, Boston University School of Medicine, Boston, MA, USA.
Curr Pharm Des. 2022;28(19):1581-1588. doi: 10.2174/1381612828666220328114236.
Besides acute respiratory distress syndrome, acute cardiac injury is a major complication in severe coronavirus disease 2019 (COVID-19) and is associated with a poor clinical outcome. Acute cardiac injury with COVID-19 can be of various etiologies, including myocardial ischemia or infarction and myocarditis, and may compromise cardiac function, resulting in acute heart failure or cardiogenic shock. Systemic inflammatory response increases heart rate (HR), which disrupts the myocardial oxygen supply/demand balance and worsens cardiac energy efficiency, thus further deteriorating the cardiac performance of the injured myocardium. In fact, the combination of elevated resting HR and markers of inflammation synergistically predicts adverse cardiovascular prognosis. Thus, targeted HR reduction may potentially be of benefit in cardiovascular pathologies associated with COVID-19. Ivabradine is a drug that selectively reduces HR via If current inhibition in the sinoatrial node without a negative effect on inotropy. Besides selective HR reduction, ivabradine was found to exert various beneficial pleiotropic effects, either HR-dependent or HR-independent, including anti-inflammatory, anti-atherosclerotic, anti-oxidant and antiproliferative actions and the attenuation of endothelial dysfunction and neurohumoral activation. Cardioprotection by ivabradine has already been indicated in cardiovascular pathologies that are prevalent with COVID-19, including myocarditis, acute coronary syndrome, cardiogenic shock or cardiac dysautonomia. Here, we suggest that ivabradine may be beneficial in the management of COVID-19- related cardiovascular complications.
除急性呼吸窘迫综合征外,急性心脏损伤也是严重 2019 冠状病毒病(COVID-19)的主要并发症,与不良临床结局相关。COVID-19 相关的急性心脏损伤可有多种病因,包括心肌缺血或梗死和心肌炎,可能导致心功能受损,引起急性心力衰竭或心源性休克。全身炎症反应会增加心率(HR),破坏心肌氧供需平衡,降低心肌能量效率,从而进一步恶化受损心肌的心脏功能。事实上,静息心率升高和炎症标志物的组合协同预测不良心血管预后。因此,有针对性地降低心率可能对与 COVID-19 相关的心血管疾病有益。伊伐布雷定是一种通过抑制窦房结 If 电流而选择性降低 HR 的药物,对心肌收缩力无影响。除了选择性降低心率外,伊伐布雷定还具有多种有益的多效作用,包括 HR 依赖性和 HR 非依赖性作用,如抗炎、抗动脉粥样硬化、抗氧化和抗增殖作用,以及减轻内皮功能障碍和神经体液激活。伊伐布雷定的心脏保护作用已在 COVID-19 常见的心血管疾病中得到证实,包括心肌炎、急性冠状动脉综合征、心源性休克或心脏自主神经功能障碍。在此,我们建议伊伐布雷定可能有益于 COVID-19 相关心血管并发症的管理。