Severe COVID-19 Infection Associated with Endothelial Dysfunction Induces Multiple Organ Dysfunction: A Review of Therapeutic Interventions

Since December 2019, the SARS-CoV-2 (COVID-19) pandemic has transfixed the medical world. COVID-19 symptoms vary from mild to severe and underlying chronic conditions such as pulmonary/cardiovascular disease and diabetes induce excessive inflammatory responses to COVID-19 and these underlying chronic diseases are mediated by endothelial dysfunction. Acute respiratory distress syndrome (ARDS) is the most common cause of death in COVID-19 patients, but coagulation induced by excessive inflammation, thrombosis, and disseminated intravascular coagulation (DIC) also induce death by multiple-organ dysfunction syndrome. These associations imply that maintaining endothelial integrity is crucial for favorable prognoses with COVID-19 and therapeutic intervention to support this may be beneficial. Here, we summarize the extent of heart injuries, ischemic stroke and hemorrhage, acute kidney injury, and liver injury caused by immune-mediated endothelial dysfunction that result in the phenomenon of multi-organ dysfunction seen in COVID-19 patients. Moreover, the potential therapeutic effect of angiotensin receptor blockers and angiotensin-converting enzyme inhibitors that improve endothelial dysfunction as well as the bradykinin storm are discussed.


Introduction
SARS-CoV-2 (COVID-19) rapidly spread throughout the world from December 2019 and, within only three months, had spread to numerous nations, demonstrating high morbidity and mortality in patients with chronic diseases [1]. As of November 2020, an estimated 143,900 patients worldwide have succumbed to this pandemic [2]. COVID-19 symptoms may be mild to severe, depending on underlying chronic conditions such as pulmonary or cardiovascular diseases and the presence of diabetes, all of which induce excessive inflammatory responses to COVID-19 [3]. Interestingly, these underlying chronic diseases result in dysfunction of the endothelial cells that mediate vascular tone, causing excessive inflammation and coagulation. Acute respiratory distress syndrome (ARDS) is the most common cause of death in COVID-19 patients, but coagulation activation induced by excessive inflammation, thrombosis, and disseminated intravascular coagulation (DIC) also induces death by multiple-organ dysfunction syndrome [4][5][6]. These associations imply that maintenance of endothelial integrity is crucial for surviving COVID-19 and that therapeutic intervention to bolster these barrier cells may bring clinical benefits.
ET-1, a potent endogenous vasoconstrictor [27] and reported pro-inflammatory peptide in the lungs [28], has a direct role in the development of ALI and also worsens its severity by increasing pulmonary microvasculature pressure in early sepsis [29,30]. ET-1 is mainly expressed in the lungs of patients with ARDS and increases edema while reducing the oxygenation [31]. ET-1 is also related to the pathogenesis of sepsis-induced ALI and vascular failure [32] and, from this aspect, ET blockers have been reported to have a protective effect against MODS in sepsis and ALI [33][34][35][36][37]. The reports of ET blockers for ARDS patients are still limited but Guo et al. reported a patient with influenza A (H7N9)-induced ARDS that required mechanical ventilation. After bosentan administration, right ventricular function significantly improved and weaning from mechanical ventilation occurred successfully [38].
NO is also an important vasodilator and platelet aggregation factor and NO has been reported to play roles in the pathogenesis of ALI. NO regulates microvascular permeability during ALI [39,40] and various isoforms of NO synthase (NOS), such as inducible NOS (iNOS) and endothelial NOS (eNOS), synthesize NO from L-arginine. Pulmonary vascular endothelial cells constantly generate eNOS under normal conditions [41] and a previous study reported chronic eNOS overexpression may protect the ALI by inhibiting inflammatory cytokine production [42]. However, another study reported that a high bioavailability of NO from iNOS worsens ALI [43].
Ang-II pathways are related to pathologic features of ARDS and Ang-II is not only a vasoconstrictor but also interferes with adaptive immunity through the stimulation of macrophages and other immune cells [44] in addition to enhancing inflammatory cytokines such as tumor necrosis factor-alpha (TNF-α) and interleukin (IL)-6. Ang-II mediates several pro-inflammatory responses by signaling through Angiotensin II receptor type 1 (AT1R) and the recruitment of circulating inflammatory cells to the endothelium induces an inflammatory response. This response increases leukocyte recruitment through AT1R-mediated upregulation of selectins (E-selectin and P-selectin) and chemokine (CC-chemokine ligand 5 [CCL5], known as RANTES and CC-chemokine ligand 2 [CCL2], known as MCP1) expression in endothelial cells [45,46]. These immune and inflammatory responses promote thrombosis and, interestingly, also promote microvascular COVID-19 lung vessels obstructive thromboinflammatory syndrome (MicroCLOTS) [47]. A previous case study reported that acute pulmonary embolism was present in a COVID-19 pneumonia patient and this was observed by pulmonary CT angiography [48].
These findings suggest that direct damage by viral invasion and inflammatory response, coupled with subsequent cytokine storm and endothelial dysfunction-related obstructive thrombosis, is the potential underlying mechanism for ARDS in COVID-19 patients.

Myocardial Injury
It is well known that influenza and SARS viruses can cause myocarditis and, like these viruses, SARS-CoV-2 is associated with numerous cardiovascular complications, especially in older populations. Previous studies have revealed that endothelial dysfunction, platelet activation, excessive inflammation, and stasis are likely to induce higher risks of venous thromboembolism and acute myocardial infarctions [49]. A previous study also reported that elevated cardiac troponin T (TnT) (10%) and N-terminal pro-brain natriuretic peptides (NT-proBNP) (27.5%) were observed in COVID-19 patients [50]. An additional report noted that 27.8% of COVID-19 patients had myocardial injuries marked by elevated TnT levels and that patients with elevated TnT levels had dramatically higher mortality than normal TnT level patients (59.6% vs. 8.9%). Moreover, NT-proBNP was significantly correlated with elevated TnT levels. Not only these biomarkers, but also mortality, suggest an association between severity of myocardial injury and severity of COVID-19. Myocardial injury mostly occurs in admitted severe or fatal cases of COVID-19 and Zhao et al. summarized a previous study [51] to reveal that even mild cases may have myocardial injury (2-4%) [51,52] and severe or fatal cases have much higher rates of myocardial injury (22.2-31%) [51,[53][54][55], but fatal COVID-19 cases had injury rates of approximately 28-89% [53,56,57]. Therefore, myocardial injury is an important prognostic factor in COVID-19 patients that is significantly associated with mortality [58].

Immune Response and Myocardial Endothelial Dysfunction
With regard to immune response effects in the myocardium, influenza virus infection increases risks of ischemic myocardial infarction (MI) and heart disease (IHD) as seen in the increase of deaths during influenza seasons [59]. Another study revealed that the number of emergency room visits was correlated with an increased number of IHD deaths among influenza-infected adults 65 years and older [60]. Increased inflammatory cytokines and cellular recruitment are thought to mediate these influenza-related cardiovascular diseases and reports of increased levels of TNFα, VEGF, GCSF, CM-CSF, basic FGF, IFNg, IL-1b, IL-1RA, IL-7, IL-8, IL-9, IL-10, IP-10, MIP-1a, MIP-1b, MCP-1, and PDGF in COVID-19 infected patients versus healthy controls bolsters this theory [51]. Interestingly, hypersensitive, TnT-related decreases in immune competency (CD4+ cells, CD8+ T cells lymphocytes, and monocytes) and increased inflammatory levels (PCT, CRP, IL-6, and neutrophils) [61] implicates an overaggressive host immune response triggering the cytokine storm that causes cardiac injury. Severely infected patients exhibit leukopenia and depleted/exhausted CD4+ and CD8+ T cells compared with moderately infected patients [62]. Indeed, several studies have reported a multi-systemic inflammatory syndrome (MIS-C), which consists of Kawasaki's disease-like features in children with COVID-19. First observed in a few cases in the United Kingdom [63,64], another study reported that 22% of children with COVID-19 [65] exhibited this phenomenon which is mediated by cytokines and dysregulated inflammatory responses in the cardiovascular system.

The Routes for Covid-19 Brain Infection
Although COVID-19 has an affinity for the ACE2 receptor present in endothelial cells [66], ACE2 is also expressed in glial cells and neurons, presenting a neurotropic target for the virus [67]. Two major pathways are suspected for COVID-19 to enter the central nervous system (CNS) but the most probable is the hematogenous route. The triple-layered blood-brain barrier (BBB) prevents large molecules entering the CNS due to a highly selective structure that also excludes circulating virions. However, COVID-19 potentially infects these epithelial cells directly and the subsequent inflammation compromises the barrier function of the BBB via permeabilization, allowing infection of the CNS. A previous study observed virus-like particles in the brain capillary endothelium and active budding across endothelial cells [68].
A second pathway may be nasal as many COVID-19 patients suffer from olfactory dysfunction and this phenomenon suggests retrograde axonal transport via the olfactory bulb. The olfactory sensory neurons have a bipolar neuronal structure that connects the nasal epithelium to CNS regions and, outside of airway protection from hair and mucous membranes, is exposed to the external environment. COVID-19 rapidly penetrates into the brain via the olfactory sensory neurons and causes anosmia [69][70][71]. A recent postmortem study conducted by brain MRI revealed that COVID-19 olfactory impairment is likely to be restricted to olfactory bulbs [72] and another study found local inflammation and cytokine release as causative for injury to the olfactory sensory neurons [73].

A Potential Ischemic and/or Hemorrhagic Stroke Mechanism
It has been reported that 36.4% of patients with COVID-19 at hospitals in Wuhan, China experienced neurological manifestations and acute cerebrovascular disease more frequently observed in severe COVID-19 patients [74]. An additional study showed that 4.6% of patients with COVID-19 developed acute ischemic stroke, with half of those incidents classified as large vessel occlusions [75], while a UK report found that all instances of COVID-19-mediated acute ischemic stroke were large vessel occlusions [76], a phenomenon verified by a U.S. study [77]. Taken together, these global reports indicate that large vessel occlusions are the most frequent complication of acute ischemic stroke in COVID-19 patients.
Generally, ischemic stroke is caused by cardioembolism and this is in line with reports of arrhythmia during COVID-19 infection. A current study reported that 16.7% of admitted COVID-19 patients had arrhythmia [52] while another study reported that 5.9% of COVID-19 patients had either ventricular fibrillation (VF) or ventricular tachycardia (VT) [78]. This type of arrhythmia and excessive micro thrombosis induced by endothelial dysfunction could explain the subsequent increase in stroke risk seen in severe COVID-19 cases.
There are relatively few reports, but hemorrhagic stroke has also occurred. Recent studies indicate that COVID-19 affects both the CNS and peripheral nervous systems (PNS) [79,80] with a phenomenon newly dubbed "Neuro-COVID". The European Neurocritical Care Society (NCS) and Academy of Neurology (EAN) has endorsed the Global Consortium Studies of Neurological Dysfunction in COVID-19 (GCS-Neuro-COVID) and thus has established a formal collaboration [81] for consensus and harmonization of data. Planned and current studies will continue to shed light on COVID-related neurological dysfunction of all kinds and possibly highlight interventional strategies for dealing with COVID-specific neurological sequelae.

COVID-19 Related Kidney Injury
Several studies have already reported associations between COVID-19 and acute kidney injury (AKI) [3,82,83] where factors of kidney involvement on tests such as urea nitrogen, serum creatinine, and/or proteinuria, as well as other evidence of AKI, were independently associated with hospital death [3]. COVID-19 induced kidney dysfunction usually manifests as increased urea nitrogen levels and blood creatinine [84,85] resulting from tubular damage and impaired glomerular filtration. High ACE2 expression is found in the proximal tubular epithelial cells whereas weak to moderate signals are located in Henle's loop, collecting ducts, glomeruli, and the distal tubules thought to be a potential target for kidney injury [86][87][88][89][90][91][92]. Cellular transmembrane serine proteases (TMPRSSs) and ACE2 are co-expressed in proximal straight tubule cells and podocytes, indicating that the kidney cells are vulnerable to COVID-19 infection [93]. Pathological changes may also be observed and severe acute tubular necrosis was visible upon pathological light microscopic examination during autopsies of six patients who had died from COVID-19 in Wuhan [94].
Importantly, 32 out of 33 COVID-19 patients who developed AKI did not survive [95] and this significant association indicates that AKI is an important prognostic factor in COVID-19 that progresses to mortality. The prevalence of AKI is not consistently reported but a previous systematic review and a meta-analysis based on 21,531 patients found an AKI prevalence of 12.3% and 5.4%, respectively, in COVID-19 patients taking renal replacement therapy (RRT), but regionality may be a factor as AKI incidence was lower in Asia (6.9%) compared to Europe (22.9%) and North America (34.6%). Moreover, ICU admission reflected very high rates of AKI (39.0%) and RRT use (16.3%) [84]. Another study reported that AKI incidence in critically ill COVID-19 patients in the ICU was 29% [53], while patients with kidney insufficiencies marked by abnormal urea nitrogen, serum creatinine, and proteinuria were at increased risk of hospital death [3]. Another study of 5700 patients revealed 81 patients needed renal replacement therapy after admission and patients with diabetes were more likely to suffer from AKI [96].
Continuous renal replacement therapy (CRRT) might block the cytokine storm and improve the prognosis of COVID-19 patients. However, a previous study already reported that CRRT filters quickly clog due to coagulopathy and therefore adequate anticoagula-tion therapy will be needed for COVID-19 patients, especially severe cases, but specific knowledge of best practices in these cases is still limited [25].

COVID-19-Related Liver Injury
Clinical details of liver injury specifics associated with COVID-19 have yet to be reported. However, a generally overactive immune response induced by COVID-19 infection and subsequent dysregulated inflammatory cellular responses (cytokine storm) may lead to liver injury [97]. A previous study has already reported liver enzyme abnormalities, elevated serum alanine aminotransferase (ALT), and aspartate aminotransferase (AST) in 43.4% of surveyed COVID-19 patients [3], an effect also reported in a systematic review and a meta-analysis of severe and fatal COVID-19 cases where elevated serum AST levels were found. This association implies that severe COVID-19 patients are at risk of liver injury, which may accelerate the risk of developing vascular thrombosis [98], coagulopathy, and subsequent clotting issues in multiple organ systems. Patients with comorbid fatty liver or other hepatic diseases may thus be at risk of developing severe or fatal COVID-19 infections and should be monitored closely for signs of liver damage. We summarized the commodity of multi-organ dysfunction by endothelial dysfunction in COVID-19 patients in Figure 1.

Treatment of COVID-19-Associated Endothelial Dysfunction
There are several studies that have investigated the therapeutic effect of renin angiotensin system (RAS) inhibitors and statins. Angiotensin II (Ang II), an endogenous peptide hormone, is the main effector of the RAS for homeostatic adjustment of pressure in the cardiovascular system. Gencer et al. shed light on the significant role of RAS in COVID-19 in a review [99]; however, using ARB and ACE-inhibitors itself is controversial within the literature [51,[100][101][102][103][104][105][106].
Two viewpoints exist, the first being that ARB and ACE inhibitors upregulate ACE2 expression, which makes it easy for SARS-CoV-2 virions to enter target cells. As angiotensinconverting enzyme 2 (ACE2), originally discovered in 2000 by two researchers [107,108], is ubiquitous throughout the heart and kidneys, increased ACE2 expression by these regulators may increase the infective load of SARS-CoV-2 in the cardiovascular system. Therefore, it is hypothesized that increasing ACE2 via ARB and ACE inhibitors is contraindicated for COVID-19 patients [109].
The second viewpoint is that ARB and ACE inhibitors enhance vasodilation and antiinflammatory effects for COVID-19 patients, which is of importance due to associations between Ang II and reactive oxygen species (ROS). Previous studies have hypothesized that Ang II enhances ROS generation in mitochondria via the "ROS-induced ROS release" (RIRR) mechanism [110,111] and the NAD(P)H oxidase-derived ROS stimulated by Ang II may lead to a mitochondrial ROS burst that precipitates cellular death on a multicellular scale [112]. Several systematic reviews and meta-analyses revealed that ACE inhibitors, in addition to angiotensin receptor blockers (ARBs), have been shown to improve endothelial dysfunction by flow-mediated vasodilatation (FMD), a widely-used method for evaluate endothelial function [113,114]. This viewpoint thus asserts that the generation of ROS, which has both primary (tissue damage) and secondary (signaling) is an important component of the vascular damage seen in COVID-19 and that ARB and ACE inhibitors, although freeing up ACE2, dampen ROS that causes microcapillary and intimal damage within the vascular system.
However, for the pulmonary system, Imai et al. evaluated the role of ACE2 and Ang II in lung injury by using a septic mouse model. As the ACE2-knockout mice had more severe forms of lung injury, the conclusion was that ACE2 is overall protective in sepsis [115]. This data indicate that ACE2, although vital for COVID-19 penetration into somatic and neural cells, may provide a measure of protection by mediating ROS levels in the vascular and pulmonary systems. More studies will need to be conducted that examine the mechanistic interplay and how ARB and ACE inhibitors disrupt that balance.

Treatment of COVID-19-Associated Endothelial Dysfunction
There are several studies that have investigated the therapeutic effect of renin angiotensin system (RAS) inhibitors and statins. Angiotensin II (Ang II), an endogenous peptide hormone, is the main effector of the RAS for homeostatic adjustment of pressure in the cardiovascular system. Gencer et al. shed light on the significant role of RAS in COVID-

Other Potential Drug Therapies for Treatment of COVID-19
Although the effectiveness is controversial, there are several drug therapies currently under examination for COVID-19. Hydroxychloroquine (HCQ) and chloroquine (CQ), used in the treatment of uncomplicated malaria, were first reported from France in June 2020 and that study administered hydroxychloroquine and azithromycin (HCQ-AZ) for 26 patients with COVID-19, resulting in 20 patients showing a significant reduction of viral loads [116]. Since that study had a small sample size, another study carried out in the USA analyzed the therapeutic effect of hydroxychloroquine in 1446 consecutive patients and could not reveal any significant therapeutic effects of hydroxychloroquine [116]. However, another French study confirmed the therapeutic effect of HCQ-AZ by analyzing 3737 patients with COVID-19, including 3119 (83.5%) treated with HCQ-AZ [117]. Other retrospective observational studies [118,119] and a prospective observational study [120], as well as RCTs [121,122], confirmed the therapeutic effect of HCQ and CQ.
Based on these studies [118][119][120][121][122], the U.S. Food and Drug Administration (FDA) approved emergency use authorization (EUA) of HCQ and CQ for COVID-19 in March 2020 but revoked it in June 2020 because of perceived limited effectiveness [123]. Additionally, side effects of these drugs have been reported, especially increased risk for Long QT Syndrome (LQTS), and several studies have confirmed this phenomenon [124,125].
Anti-inflammation therapy has also been reported as an effective treatment for COVID-19. Colchicine, an anti-inflammatory and immunomodulatory agent, was suggested to prevent some complications of COVID-19 by inhibiting IL-1 production. Several RCTs have since demonstrated this efficacy such as the GRECCO-19 (the Greek Study in the Effects of Colchicine in COVID-19 Complications Prevention) trial that evaluated a total of 105 patients and reported significantly improved clinical outcomes [126]. The ongoing COLCOVID (The ECLA PHRI COLCOVID Trial: Effects of Colchicine on Moderate/Highrisk Hospitalized COVID-19 Patients) trial (ClinicalTrials.gov: NCT04328480) has recruited 2500 patients, but the COLCORONA (Colchicine Coronavirus SARS-CoV2) multi-center RCT to evaluate the efficacy of colchicine in high-risk adult patients with COVID-19 (ClinicalTrials.gov: NCT04322682) was recently finished and briefly reported that colchicine reduced hospitalizations by 25%, the need for mechanical ventilation by 50%, and deaths by 44% [127].
Dexamethasone, a synthetic corticosteroid, has also been suggested for decreasing COVID-19 mortality as corticosteroids have been extensively used for severe lung conditions such as Acute Respiratory Distress Syndrome (ARDS) and previous outbreaks of SARS and Middle East respiratory syndrome (MERS) [128,129]. The RECOVERY (Randomized Evaluation of COVid-19 thERapY) trial revealed that the use of dexamethasone reduced 28-day mortality for oxygen therapy in mechanical ventilation patients [130] and also initially attempted to judge the efficacy of HCQ but suspended recruiting for this purpose after no significant benefits were observed [131].

Bradykinin as a Potential Target Protein for COVID-19
Recently, Garvin et al. reported an in silico analysis of the potential relationship between severity of COVID-19 and bradykinin [132]. Generally, ACE2 is the main receptor for COVID-19 and is not highly expressed in lungs. However, as gene expression analysis of bronchial lavage samples showed the dramatic upregulation of ACE2 (199-fold), AGTR1 (430-fold), and AGTR2 (177-fold) receptors with downregulation of ACE (8-fold), compared to controls, this phenomenon indicates a shift in the RAS system to produce Ang1-9. Genetic pathway analysis also detected the two networks extensively involved in vasoconstriction and contained, among others, ACE, AGTR1, Bradykinin Receptor 2 (BDKR2), NOS1, and NOS2. Additionally and extensively involved in vasodilation, increased vascular permeabilization, and altered fluid balance, were ACE2, AGTR2, and the Vitamin D Receptor (VDR). Vitamin D, already known to reduce acute lung injury by blocking the Ang-2-Tie-2-myosin light chain (MLC) kinase cascade and the renin-angiotensin system [133], mediates the expression of ACE2 [134]. As the SARS-CoV-2-enhanced ex-pression of ACE2 could theoretically increase viral entry into cells, vitamin D may seem counterintuitive but Murai et al. did significant work to evaluate the therapeutic effect of vitamin D for COVID-19. Random administration of vitamin D (200,000 IU) or placebo for 240 hospitalized patients with moderate to severe COVID-19 (non-ventilator status) [135] showed a trend for a therapeutic effect of vitamin D for COVID-19 but this was not significant. However, the editorial mentioned the importance of remaining open-minded to emerging results from rigorously conducted studies of vitamin D [136].
Bradykinin is responsible for the vasodilation and permeability of the pulmonary vascular system. The kinin-kallikrein system is a zymogen system that, after activation, leads to the release of bradykinin. Binding bradykinin to BDKR2 increases vascular permeability and subsequent pulmonary edema [137]. Imai et al. reported that ACE2 plays an important role for preventing ALI [115] but, unusually, they also reported no differences in hydrostatic pressure compared with ACE2 knockout and controls, concluding that severe lung edema in ACE2 knockout mice does not seem to be secondary to systemic hemodynamic alterations [115]. Unlike the RASS system, bradykinin controls permeability and vasodilatation without vasoconstriction. Thus, this phenomenon can be explained by the kinin-kallikrein system. Bradykinin is only a substrate for ACE, not a substrate for ACE2 [138,139]. Therefore, ACE2 does not inactivate bradykinin but ACE2 and bradykinin do cross talk through potent ligands of BDKR1 in the lung, namely des-Arg9-BK and Lys des-Arg9-BK [138].
There are still limited clinical reports describing the associations between bradykinin and ARDS since these patients demonstrate markedly elevated levels of bradykinin in the bronchoalveolar lavage fluid (BALF) samples compared with healthy controls [140].
From these data, blocking bradykinin B1 receptors (BKB1R) and bradykinin B2 receptors (BKB2R) may be a potential therapeutic target. However, there is no licensed BKB1R drug to date [141] and the BKB2R drug icatibant (Firazyr) is only available in the U.S. and Europe. There are already reports on the use of icatibant for COVID-19 patients as van de Veerdonk et al. included 10 patients for treatment with three doses of 30 mg of icatibant by subcutaneous injection at 6-h intervals and evaluated the therapeutic effect by matched-pair analysis [142]. All nine patients prescribed icatibant experienced a marked decrease in oxygen supplementation and four patients (44%) were weaned from oxygen within 10-35 h after three doses of icatibant. Additionally, eight out of nine patients (89%) treated with icatibant confirmed a reduction in oxygen use of 3 L/min or greater after 24 h. After matched-pair analysis (nine patients using icatibant vs. 18 control patients), only three out of 18 patients (17%) without icatibant showed a reduction in oxygen use of 3 L/min or greater after 24 h. From these results, the authors revealed an association between the use of icatibant and improvements in lung injury. Interestingly, three out of 10 patients (30%) using icatibant did need to go back on oxygen again, which may be due to icatibant's short-acting effect (half-life of 2 h) [143]. Recently, an RCT to evaluate the efficacy and safety of icatibant, a C1 esterase/kallikrein inhibitor, in severe COVID-19 has been launched [144] and this study may lead to a more rigorous association between COVID-19 infection and bradykinin systems.

Future Direction
ARB and ACE-I usage in COVID-19 is still controversial as observational studies cannot eliminate bias and confounding factors. Recent reviews stated that underlying diseases such as hypertension are not the sole independent risk factor and ARB and/or ACE-I are also not risk factors [145]. However, a previous review noted a therapeutic effect of ARB for endothelial dysfunction during viral infection and subsequent sepsis [145] while a recent review on COVID-19 treatment also confirmed the therapeutic effect of ARB for endothelial dysfunction [146]. Such conflicting reports currently complicate the removal of bias in results, but Donald B. Rubin has suggested expanding the method of causal inference to reveal any rigorous associations between factors and results in observational studies [147].
Currently, several randomized clinical trials (RCTs) are ongoing to confirm the therapeutic effect of ARB and ACE-I for COVID-19 as shown in Table 1. Diverse studies of various sizes in adults plus one study in the elderly are awaiting study completion and publication. The COVID-RASi Trial (COVID-19) focuses exclusively on elderly patients with hypertension (HT), diabetes mellitus (DM), coronary artery disease (CAD), history of myocardial infarction (MI), heart failure (HF) ischemic stroke, or renal dysfunction. This RCT compares the mortality of relatively high-risk patients after ACE-I/ARB treatment and standard care. Meanwhile, the REPLACE COVID (Randomized Elimination and Prolongation of ACE inhibitors and ARBs in coronavirus 2019) trial, the Randomized ACORES-2 Study (ACE Inhibitors or ARBs Discontinuation for Clinical Outcome Risk Reduction in Patients Hospitalized for the Endemic Severe Acute Respiratory Syndrome Coronavirus SARS-CoV-2 Infection), the ACEI-COVID (Stopping ACE-inhibitors in COVID-19) trial, the BRACE CORONA trial (Continuing versus suspending angiotensin-converting enzyme inhibitors and angiotensin receptor blockers: Impact on adverse outcomes in hospitalized patients with severe acute respiratory syndrome coronavirus 2 SARS-CoV-2), and RASCOVID-19 trial (Effects of Discontinuing Renin-angiotensin System Inhibitors in Patients With COVID-19) are being conducted to compare outcomes from continuing or discontinuing use of ARB or ACE-I treatment.
On the other hand, CAPTOCOVID (Efficacy of Captopril in Covid-19 Patients With Severe Acute Respiratory Syndrome (SARS) CoV-2 Pneumonia), CLARITY (Controlled evaLuation of Angiotensin Receptor Blockers for COVID-19 respIraTorY Disease), and STAR-COVID (Telmisartan in Respiratory Failure Due to COVID-19) trials are currently comparing the outcomes of using or foregoing ARB or ACE-I treatments. Additionally, angiotensin 1-7 is being investigated as a therapeutic treatment for COVID-19 in two RCTs (ClinicalTrials.gov Identifier: NCT04332666: NCT04605887).
Moreover, a living network meta-analysis through the Cochrane Library is now active to rate interventions for the treatment of COVID-19 [148]. These living network metaanalyses have recently been suggested as the new paradigm in comparative effectiveness research [149,150] as they can reach robust conclusions on the relative effectiveness of treatments earlier than sequential meta-analyses, reducing research waste, and offering timely recommendations [149][150][151]. Moreover, even though the idea of the bradykinin storm is now gaining attention, no RCTs have been done or are being done to confirm the therapeutic effect. As supercomputers were able to detect the potential relationship between the bradykinin storm and COVID-19, both in silico and living network metaanalyses may synergistically and systematically detect targets. As recent third waves of infection have been announced, time is of the essence and these rapid data sorting and evaluation methods may be invaluable for determining best practice in treating both severe and "long-haul" cases of COVID-19 that feature cardiovascular, neurological, and multi-organ sequelae.

Conclusions
Based on current evidence, COVID-19 infections cause frequent multi-organ damage, mainly via endothelial dysfunction in the heart, brain, kidney, and liver. Usage of ARB and ACE-I, potential tools to ameliorate this endothelial dysfunction, have competing theories and current RCTs will be the ultimate judge of their usefulness in both severe and chronic cases of COVID-19. While several studies have implicated that bradykinin is a promising target protein for COVID-19, the results of the various clinical trials for ARB, ACE I, and bradykinin blockers must be tabulated and analyzed for rigorous associations. Further studies, especially well constructed RCTs, will bring clear evidence for definitive COVID-19 treatment guidelines.