"When," "Where," and "How" of SARS-CoV-2 Infection Affects the Human Cardiovascular System: A Narrative Review.

IF 1.9 4区 医学 Q2 MEDICINE, GENERAL & INTERNAL Balkan Medical Journal Pub Date : 2024-01-03 DOI:10.4274/balkanmedj.galenos.2023.2023-10-25
Nicholas G Kounis, Christos Gogos, Cesare de Gregorio, Ming-Yow Hung, Sophia N Kounis, Efthymios P Tsounis, Stelios F Assimakopoulos, Soheila Pourmasumi, Virginia Mplani, George Servos, Periklis Dousdampanis, Panagiotis Plotas, Marina A Michalaki, Grigorios Tsigkas, Gerasimos Grammatikopoulos, Dimitrios Velissaris, Ioanna Koniar
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Abstract

Coronavirus disease 2019 (COVID-19) is caused by the novel severe acute respiratory coronavirus-2 (SARS-CoV-2). Several explanations for the development of cardiovascular complications during and after acute COVID-19 infection have been hypothesized. The COVID-19 pandemic, caused by SARS-CoV-2, has emerged as one of the deadliest pandemics in modern history. The myocardial injury in COVID-19 patients has been associated with coronary spasm, microthrombi formation, plaque rupture, hypoxic injury, or cytokine storm, which have the same pathophysiology as the three clinical variants of Kounis syndrome. The angiotensin-converting enzyme 2 (ACE2), reninaldosterone system (RAAS), and kinin-kallikrein system are the main proposed mechanisms contributing to cardiovascular complications with the COVID-19 infection. ACE receptors can be found in the heart, blood vessels, endothelium, lungs, intestines, testes, neurons, and other human body parts. SARS-CoV-2 directly invades the endothelial cells with ACE2 receptors and constitutes the main pathway through which the virus enters the endothelial cells. This causes angiotensin II accumulation downregulation of the ACE2 receptors, resulting in prothrombotic effects, such as hemostatic imbalance via activation of the coagulation cascade, impaired fibrinolysis, thrombin generation, vasoconstriction, endothelial and platelet activation, and pro-inflammatory cytokine release. The KKS system typically causes vasodilation and regulates tissue repair, inflammation, cell proliferation, and platelet aggregation, but SARS-CoV-2 infection impairs such counterbalancing effects. This cascade results in cardiac arrhythmias, cardiac arrest, cardiomyopathy, cytokine storm, heart failure, ischemic myocardial injuries, microvascular disease, Kounis syndrome, prolonged COVID, myocardial fibrosis, myocarditis, new-onset hypertension, pericarditis, postural orthostatic tachycardia syndrome, pulmonary hypertension, stroke, Takotsubo syndrome, venous thromboembolism, and thrombocytopenia. In this narrative review, we describe and elucidate when, where, and how COVID-19 affects the human cardiovascular system in various parts of the human body that are vulnerable in every patient category, including children and athletes.

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SARS-CoV-2 感染 "何时"、"何地"、"如何 "影响人类心血管系统:叙述性综述。
冠状病毒病 2019(COVID-19)是由新型严重急性呼吸道冠状病毒-2(SARS-CoV-2)引起的。人们对 COVID-19 急性感染期间和感染后心血管并发症的发生提出了几种解释。由 SARS-CoV-2 引起的 COVID-19 大流行已成为现代史上最致命的大流行病之一。COVID-19 患者的心肌损伤与冠状动脉痉挛、微血栓形成、斑块破裂、缺氧性损伤或细胞因子风暴有关,其病理生理与库尼斯综合征的三种临床变异型相同。血管紧张素转换酶 2(ACE2)、肾醛固酮系统(RAAS)和激肽-allikrein 系统是导致 COVID-19 感染引发心血管并发症的主要机制。ACE 受体存在于心脏、血管、内皮、肺、肠、睾丸、神经元等人体部位。SARS-CoV-2 通过 ACE2 受体直接侵入内皮细胞,成为病毒进入内皮细胞的主要途径。这导致血管紧张素 II 积聚下调 ACE2 受体,从而产生促血栓形成效应,如通过激活凝血级联、纤维蛋白溶解受损、凝血酶生成、血管收缩、内皮细胞和血小板活化以及促炎细胞因子释放等造成止血失衡。KKS 系统通常会导致血管扩张并调节组织修复、炎症、细胞增殖和血小板聚集,但 SARS-CoV-2 感染会损害这种平衡作用。这种级联反应会导致心律失常、心脏骤停、心肌病、细胞因子风暴、心力衰竭、缺血性心肌损伤、微血管疾病、库尼斯综合征、COVID 延长、心肌纤维化、心肌梗死、心力衰竭、心肌纤维化、心肌炎、新发高血压、心包炎、体位性正位性心动过速综合征、肺动脉高压、中风、Takotsubo 综合征、静脉血栓栓塞和血小板减少。在这篇叙述性综述中,我们描述并阐明了 COVID-19 在何时、何地以及如何影响人体心血管系统的各个部位,这些部位在各类患者(包括儿童和运动员)中都很脆弱。
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来源期刊
Balkan Medical Journal
Balkan Medical Journal MEDICINE, GENERAL & INTERNAL-
CiteScore
4.10
自引率
6.70%
发文量
76
审稿时长
6-12 weeks
期刊介绍: The Balkan Medical Journal (Balkan Med J) is a peer-reviewed open-access international journal that publishes interesting clinical and experimental research conducted in all fields of medicine, interesting case reports and clinical images, invited reviews, editorials, letters, comments and letters to the Editor including reports on publication and research ethics. The journal is the official scientific publication of the Trakya University Faculty of Medicine, Edirne, Turkey and is printed six times a year, in January, March, May, July, September and November. The language of the journal is English. The journal is based on independent and unbiased double-blinded peer-reviewed principles. Only unpublished papers that are not under review for publication elsewhere can be submitted. Balkan Medical Journal does not accept multiple submission and duplicate submission even though the previous one was published in a different language. The authors are responsible for the scientific content of the material to be published. The Balkan Medical Journal reserves the right to request any research materials on which the paper is based. The Balkan Medical Journal encourages and enables academicians, researchers, specialists and primary care physicians of Balkan countries to publish their valuable research in all branches of medicine. The primary aim of the journal is to publish original articles with high scientific and ethical quality and serve as a good example of medical publications in the Balkans as well as in the World.
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