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Expert Rev Anti Infect Ther . COVID-19 and cardiovascular complications: an update from the underlying mechanism to consequences and possible clini

tetano

Editor, Senior Moderator
Expert Rev Anti Infect Ther


. 2021 Feb 23.
doi: 10.1080/14787210.2021.1893692. Online ahead of print.
COVID-19 and cardiovascular complications: an update from the underlying mechanism to consequences and possible clinical intervention


Ashif Iqubal[SUP] 1 [/SUP], Mohammad Kashif Iqubal[SUP] 2 [/SUP], Farazul Hoda[SUP] 1 [/SUP], Abul Kalam Najmi[SUP] 1 [/SUP], Syed Ehtaishamul Haque[SUP] 1 [/SUP]



Affiliations

Abstract

Introduction: The novel coronavirus has caused significant mortality worldwide and is primarily associated with severe acute respiratory distress syndrome (ARDS). Apart from ARDS, clinical reports have shown noticeable cardiovascular complications among the patients of COVID-19. Infection from virus, stimulation of cytokine storm, altered immune response and damage to myocardial tissue are some of the proposed mechanism of cardiovascular complications in COVID-19.
Areas covered: Based on the clinical reports of CVDs among COVID-19 patients, we have discussed the molecular mechanisms involved in cardiovascular pathogenesis, its prevalence and association with COVID-19, and various available therapeutic modality for the treatment.
Expert opinion: Seeing the cardiovascular complications in COVID-19 patients and its association with the existing drug, risk-benefit ratio of treatment paradigm as well as the level of cardiac injury biomarkers must be monitored regularly. Additionally, a well-designed clinical trial should be conducted where head to head comparison can be made with anti-COVID-19 drugs and cardioprotective anti-inflammatory drugs. Nevertheless, vaccines are the best-suited approach, but until then, sanitization, social distancing and active lifestyle are the best ways to beat this global pandemic situation.

Keywords: COVID-19; Cardiac Troponin T and ACE-2 receptor; Cardiac toxicity; Cytokine storm; Immunopathology; NLRP3 inflammasome; Pneumocytes.
 
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