Is the Endothelium the Missing Link in the Pathophysiology and Treatment of COVID-19 Complications?
Pedro CastroMarta PalomoAna Belen Moreno-CastañoSara FernándezSergi Torramadé-MoixGeorgina PascualJulia Martinez-SanchezEdward RichardsonAdrián TéllezJosep M NicolasEnric CarrerasPaul G RichardsonJuan José BadimonGines EscolarMaribel Díaz-RicartPublished in: Cardiovascular drugs and therapy (2021)
Patients with COVID-19 present a wide spectrum of disease severity, from asymptomatic cases in the majority to serious disease leading to critical care and even death. Clinically, four different scenarios occur within the typical disease timeline: first, an incubation and asymptomatic period; second, a stage with mild symptoms due mainly to the virus itself; third, in up to 20% of the patients, a stage with severe symptoms where a hyperinflammatory response with a cytokine storm driven by host immunity induces acute respiratory distress syndrome; and finally, a post-acute sequelae (PASC) phase, which present symptoms that can range from mild or annoying to actually quite incapacitating. Although the most common manifestation is acute respiratory failure of the lungs, other organs are also frequently involved. The clinical manifestations of the COVID-19 infection support a key role for endothelial dysfunction in the pathobiology of this condition. The virus enters into the organism via its interaction with angiotensin-converting enzyme 2-receptor that is present prominently in the alveoli, but also in endothelial cells, which can be directly infected by the virus. Cytokine release syndrome can also drive endothelial damage independently. Consequently, a distinctive feature of SARS-CoV-2 infection is vascular harm, with severe endothelial injury, widespread thrombosis, microangiopathy, and neo-angiogenesis in response to endothelial damage. Therefore, endothelial dysfunction seems to be the pathophysiological substrate for severe COVID-19 complications. Biomarkers of endothelial injury could constitute strong indicators of disease progression and severity. In addition, the endothelium could represent a very attractive target to both prevent and treat these complications. To establish an adequate therapy, the underlying pathophysiology and corresponding clinical stage should be clearly identified. In this review, the clinical features of COVID-19, the central role of the endothelium in COVID-19 and in other pathologies, and the potential of specific therapies aimed at protecting the endothelium in COVID-19 patients are addressed.
Keyphrases
- risk factors
- endothelial cells
- respiratory failure
- sars cov
- coronavirus disease
- acute respiratory distress syndrome
- extracorporeal membrane oxygenation
- mechanical ventilation
- nitric oxide
- respiratory syndrome coronavirus
- drug induced
- liver failure
- angiotensin converting enzyme
- high glucose
- early onset
- end stage renal disease
- oxidative stress
- ejection fraction
- pulmonary embolism
- vascular endothelial growth factor
- chronic kidney disease
- sleep quality
- machine learning
- angiotensin ii
- aortic dissection
- stem cells
- intensive care unit
- case report
- physical activity
- depressive symptoms
- risk assessment
- binding protein
- patient reported