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      COVID‐19, hypertension, and renin‐angiotensin‐aldosterone system inhibitors: Much ado about nothing or real problem to be solved?

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      Journal of Clinical Hypertension (Greenwich, Conn.)
      John Wiley and Sons Inc.

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          Abstract

          The pandemic of coronavirus disease 2019 (COVID‐19) caught the whole world unprepared. Tens of millions infected patients, close to a million victims and thousands of conducted and published studies in the last several months. However, there is still a large gap in the knowledge of how to fight and defeat this virus and it does not seem that it will be fulfilled in the near future. Studies recognized the important risk factors for the severity of COVID‐19 and prediction of adverse outcome in these patients. The most cited risk factors are older age, cardiovascular diseases, hypertension, diabetes, chronic obstructive disease, and chronic kidney disease. 1 , 2 Since investigations revealed that severe acute respiratory syndrome coronavirus 2 (SARS‐CoV‐2), causative agent of COVID‐19, is using angiotensin‐converting enzyme 2 (ACE2) as the receptor to infect cells and replicate, 3 immediately started speculation about the potential negative role of the renin‐angiotensin‐aldosterone system (RAAS) antagonists in COVID‐19 patients. This was supported by the study that reported higher prevalence of RAAS usage in COVID‐19 patients with myocardial injury and adverse outcome. 4 However, it was an observational study with limited number of patients and could not provide information about potential causal relationship between RAAS inhibitors and higher mortality in COVID‐19 patients, 4 but information was realized and panic spread rapidly through the world. Under the large public pressure, the majority of national and international professional societies had to publish official reassurance that RAAS inhibitors are safe in COVID‐19 patients and that they should not be excluded from chronic therapy or switched to other antihypertensive medications. 5 , 6 The largest problem is that RAAS inhibitors present the most frequently proscribed medications in patients with arterial hypertension, heart failure, coronary artery disease, diabetes, and renal disease. RAAS inhibitors represent the cornerstone of therapy in many conditions, which are at the same time the important risk factors for adverse outcome in COVID‐19 patients. Even though large studies and meta‐analyses denied any association between RAAS inhibitors and severity or adverse outcome in COVID‐19 patients, 1 , 8 , 9 , 10 , 11 the initial suspicious about RAAS inhibitors is difficult to dismiss. In the current issue of the Journal, Chen et al represented study that included 2864 COVID‐19 patients, among which 57% were hypertensive, and showed that individuals with grade 2 and 3 of hypertension experienced worse outcome than participants with normal blood pressure (BP) or grade 1 of hypertension. 12 Previous studies investigated the influence of hypertension, without separating different subgroups according to the level of BP. 1 , 8 In the current investigation, hypertensive patients were divided into 3 groups depending of BP level and according to the European guidelines. 13 Interestingly, the majority of patients with grade 1 hypertension (140/90 mm Hg ≤ BP < 160/100 mm Hg) were undiagnosed (63%) before admission for COVID‐19. Patients with grade 2 and 3 hypertension (BP ≥ 160/100 mm Hg) had significantly higher mortality, prevalence of septic shock, respiratory failure, acute respiratory distress syndrome, mechanical ventilation, and admission in intensive care unit than hypertensive patients with grade 1 hypertension. 12 However, inflammatory markers, as well as incidence of kidney and liver injuries, were more prevalent among patients with grade 2 and 3 hypertension, which might contribute to worse outcome in these patients. 12 Study demonstrated that patients who used RAAS inhibitors before hospital admission for COVID‐19 had significantly better survival than those who did not take any antihypertensive drug or used some other antihypertensive medication. 12 The same results were obtained for hypertensive patients who started taking RAAS inhibitors after admission for COVID‐19. 12 After adjustment, subjects with pre‐admission usage of RAAS inhibitors had lower risk of adverse clinical outcomes, including death, acute respiratory distress syndrome, respiratory failure, septic shock, mechanical ventilation, and intensive care unit admission. 12 Interestingly, hypertensive patients with COVID‐19 who were treated with RAAS at any point (before or during hospitalization) had significantly lower risk of adverse clinical outcomes than patients who were treated with other antihypertensive medications. 12 Recent large investigation showed high prevalence of hypertension among COVID‐19 patients (55%), but hypertension was not an independent predictor associated with mortality in these patients. 1 Findings showed that diabetes, chronic obstructive pulmonary disease, and chronic kidney disease were independent predictors. 1 Angiotensin‐converting enzyme inhibitors (ACEI) were not related with mortality in COVID‐19 patients. 1 UK study performed in 1439 COVID‐19 patients demonstrated that hypertension, together with male sex, diabetes, greater BMI and smoking, was independently associated with corona virus infection. 7 Use of RAAS inhibitors was not associated with the risk of COVID‐19 infection. 7 Italian study that included 6272 COVID‐19 patients revealed the presence of hypertension in 58% of all patients. 8 After multivariable adjustment, RAAS inhibitors did not have significant association with the risk of COVID‐19, which was also confirmed for calcium‐channel blockers, beta‐blockers, and diuretics. 8 However, the authors did not investigate the influence of hypertension and RAAS inhibitors on outcome. 8 Meta‐analysis that involved 3936 hypertensive COVID‐19 patients showed that RAAS inhibitors were not associated with COVID‐19 disease severity, but with lower mortality. 9 Another meta‐analysis that included 17 311 COVID‐19–infected hypertensive patients showed that RAAS inhibitors were associated with 16% reduced risk of the composite outcome (death, admission to intensive care unit, mechanical ventilation requirement or progression to severe, or critical pneumonia). 10 However, Salah et al did not show any impact of RAAS inhibitors on outcome in 16 101 COVID‐19 patients with concomitant hypertension included in this meta‐analysis. 11 The novel finding from the current study was a difference in inflammatory and cardiac biomarkers, parameters of liver, and kidney function between COVID‐19 patients with different levels of hypertension. 12 All parameters were significantly higher among patients with hypertension grade 2 and 3 than those with grade 1. 12 Interestingly, inflammatory and cardiac biomarkers (hs‐CRP and creatine kinase MB), as well as prevalence of kidney, liver, and myocardial injuries, were higher in grade 2 than in grade 3 hypertension. 12 Nevertheless, there was no difference in coagulation profiles between 3 groups of COVID‐19–infected hypertensive patients or between normotensive and hypertensive COVID‐19 patients. 12 One should consider the potential influence of these parameters on the interaction between BP and severity/outcome in COVID‐19 patients in the current study. Indeed, the multivariable regression analysis demonstrated that age, cardiac injury, acute renal injury, neutrophil, lymphocyte, hs‐CRP, chronic obstructive pulmonary disease, and hypertension ≥ grade 2 were independently associated with adverse outcome in hypertensive COVID‐19 patients. 12 The importance of laboratory parameters, and particularly inflammation, cardiac, and renal injuries, has been previously reported as important predictors of adverse outcome in the population of COVID‐19 patients. 12 The interesting point of this study was evaluation of effect of RAAS inhibitors that were used before and after admission. COVID‐19 patients who continuously used RAAS, before and after hospital admission, had the best survival and those who used other antihypertensive medications had the worst survival. 12 Furthermore, participants who started usage of RAAS inhibitors after admission had better survival than those who were switched from RAAS inhibitors to other antihypertensive medications. 12 This emphasized the importance of RAAS inhibitors in treatment of hypertension in COVID‐19 patients and confirmed the recommendations of various professional societies that RAAS inhibitors should not be excluded from antihypertensive therapy or switched to another medication because it might be related to increased risk of adverse outcome. Additionally, study underlined the importance of BP control in COVID‐19 patients because individuals with normal BP and grade 1 hypertension had significantly better outcome than patients with grade 2 and 3 hypertension. 12 This investigation revealed some limitations that deserve to be mentioned and further discussed. The large percentage of hypertensive patients was undiagnosed and untreated before admission for COVID‐19. The prevalence of undiagnosed patients gradually decreased from patients with grade 1 to grade 3 hypertension. Data regarding usage of other antihypertensive classes remained unknown, and their influence on outcome could not be investigated. The authors reported better outcome in COVID‐19 patients treated with RAAS inhibitors in comparison to patients treated with all other antihypertensive classes combined into one group. One should emphasize that majority of patients were treated with traditional Chinese medicines, which is the important part of Chinese tradition and lifestyle. Unfortunately, the influence of this therapy is difficult to estimate and this could significantly interfere the relationship between hypertension, antihypertensive medications, and COVID‐19 outcome. The authors did not include any parameter of obesity, which is significantly associated with COVID‐19 infection and mortality. 14 The lack of body mass index, as the basic parameter of obesity, is very important limitation that did not allow evaluation of overweight and obesity on outcome in hypertensive COVID‐19 patients. 12 However, one must acknowledge that obesity in Chinese population is significantly less prevalent than in Western countries. There is lack of data regarding the percentage of treated hypertension patients before admission. 12 Considering the fact that the percentage of treated hypertensive patients, as well as the distribution of antihypertensive classes, is significantly different in China from Western world, the obtained results may not be applicable to other countries with different lifestyle, diagnostic, and therapeutic approach. There are several important take‐home massages from the current research. First, hypertensive patients, particularly undiagnosed, are very prevalent among COVID‐19 subjects. Second, BP control and prompt diagnose of hypertension are necessary in all COVID‐19 patients. Third, antihypertensive therapy should include RAAS inhibitors and should be initiated as soon as hypertension is diagnosed. This investigation does not recommend the exclusion or switching RAAS inhibitors to another antihypertensive medication. Nevertheless, future longitudinal studies are necessary to investigate the effect of hypertension and its treatment on outcome in COVID‐19 patients. CONFLICT OF INTEREST The authors have nothing to disclose. AUTHOR CONTRIBUTIONS Marijana Tadic contributed to writing the article. Cesare Cuspidi contributed to detailed review with constructive remarks that substantially changed the article.

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          Cardiovascular Implications of Fatal Outcomes of Patients With Coronavirus Disease 2019 (COVID-19)

          This case series study evaluates the association of underlying cardiovascular disease and myocardial injury on fatal outcomes in patients with coronavirus disease 2019 (COVID-19).
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            Is Open Access

            Angiotensin-converting enzyme 2 (ACE2) as a SARS-CoV-2 receptor: molecular mechanisms and potential therapeutic target

            A novel infectious disease, caused by severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2), was detected in Wuhan, China, in December 2019. The disease (COVID-19) spread rapidly, reaching epidemic proportions in China, and has been found in 27 other countries. As of February 27, 2020, over 82,000 cases of COVID-19 were reported, with > 2800 deaths. No specific therapeutics are available, and current management includes travel restrictions, patient isolation, and supportive medical care. There are a number of pharmaceuticals already being tested [1, 2], but a better understanding of the underlying pathobiology is required. In this context, this article will briefly review the rationale for angiotensin-converting enzyme 2 (ACE2) receptor as a specific target. SARS-CoV-2 and severe acute respiratory syndrome coronavirus (SARS-CoV) use ACE2 receptor to facilitate viral entry into target cells SARS-CoV-2 has been sequenced [3]. A phylogenetic analysis [3, 4] found a bat origin for the SARS-CoV-2. There is a diversity of possible intermediate hosts for SARS-CoV-2, including pangolins, but not mice and rats [5]. There are many similarities of SARS-CoV-2 with the original SARS-CoV. Using computer modeling, Xu et al. [6] found that the spike proteins of SARS-CoV-2 and SARS-CoV have almost identical 3-D structures in the receptor-binding domain that maintains van der Waals forces. SARS-CoV spike protein has a strong binding affinity to human ACE2, based on biochemical interaction studies and crystal structure analysis [7]. SARS-CoV-2 and SARS-CoV spike proteins share 76.5% identity in amino acid sequences [6] and, importantly, the SARS-CoV-2 and SARS-CoV spike proteins have a high degree of homology [6, 7]. Wan et al. [4] reported that residue 394 (glutamine) in the SARS-CoV-2 receptor-binding domain (RBD), corresponding to residue 479 in SARS-CoV, can be recognized by the critical lysine 31 on the human ACE2 receptor [8]. Further analysis even suggested that SARS-CoV-2 recognizes human ACE2 more efficiently than SARS-CoV increasing the ability of SARS-CoV-2 to transmit from person to person [4]. Thus, the SARS-CoV-2 spike protein was predicted to also have a strong binding affinity to human ACE2. This similarity with SARS-CoV is critical because ACE2 is a functional SARS-CoV receptor in vitro [9] and in vivo [10]. It is required for host cell entry and subsequent viral replication. Overexpression of human ACE2 enhanced disease severity in a mouse model of SARS-CoV infection, demonstrating that viral entry into cells is a critical step [11]; injecting SARS-CoV spike into mice worsened lung injury. Critically, this injury was attenuated by blocking the renin-angiotensin pathway and depended on ACE2 expression [12]. Thus, for SARS-CoV pathogenesis, ACE2 is not only the entry receptor of the virus but also protects from lung injury. We therefore previously suggested that in contrast to most other coronaviruses, SARS-CoV became highly lethal because the virus deregulates a lung protective pathway [10, 12]. Zhou et al. [13] demonstrated that overexpressing ACE2 from different species in HeLa cells with human ACE2, pig ACE2, civet ACE2 (but not mouse ACE2) allowed SARS-CoV-2 infection and replication, thereby directly showing that SARS-CoV-2 uses ACE2 as a cellular entry receptor. They further demonstrated that SARS-CoV-2 does not use other coronavirus receptors such as aminopeptidase N and dipeptidyl peptidase 4 [13]. In summary, the SARS-CoV-2 spike protein directly binds with the host cell surface ACE2 receptor facilitating virus entry and replication. Enrichment distribution of ACE2 receptor in human alveolar epithelial cells (AEC) A key question is why the lung appears to be the most vulnerable target organ. One reason is that the vast surface area of the lung makes the lung highly susceptible to inhaled viruses, but there is also a biological factor. Using normal lung tissue from eight adult donors, Zhao et al. [14] demonstrated that 83% of ACE2-expressing cells were alveolar epithelial type II cells (AECII), suggesting that these cells can serve as a reservoir for viral invasion. In addition, gene ontology enrichment analysis showed that the ACE2-expressing AECII have high levels of multiple viral process-related genes, including regulatory genes for viral processes, viral life cycle, viral assembly, and viral genome replication [14], suggesting that the ACE2-expressing AECII facilitate coronaviral replication in the lung. Expression of the ACE2 receptor is also found in many extrapulmonary tissues including heart, kidney, endothelium, and intestine [15–19]. Importantly, ACE2 is highly expressed on the luminal surface of intestinal epithelial cells, functioning as a co-receptor for nutrient uptake, in particular for amino acid resorption from food [20]. We therefore predict that the intestine might also be a major entry site for SARS-CoV-2 and that the infection might have been initiated by eating food from the Wuhan market, the putative site of the outbreak. Whether SARS-CoV-2 can indeed infect the human gut epithelium has important implications for fecal–oral transmission and containment of viral spread. ACE2 tissue distribution in other organs could explain the multi-organ dysfunction observed in patients [21–23]. Of note, however, according to the Centers for Disease Control and Prevention [24], whether a person can get COVID-19 by touching surfaces or objects that have virus on them and then touching mucus membranes is yet to be confirmed. Potential approaches to address ACE2-mediated COVID-19 There are several potential therapeutic approaches (Fig. 1). Spike protein-based vaccine. Development of a spike1 subunit protein-based vaccine may rely on the fact that ACE2 is the SARS-CoV-2 receptor. Cell lines that facilitate viral replication in the presence of ACE2 may be most efficient in large-scale vaccine production. Inhibition of transmembrane protease serine 2 (TMPRSS2) activity. Hoffman et al. [25] recently demonstrated that initial spike protein priming by transmembrane protease serine 2 (TMPRSS2) is essential for entry and viral spread of SARS-CoV-2 through interaction with the ACE2 receptor [26, 27]. The serine protease inhibitor camostat mesylate, approved in Japan to treat unrelated diseases, has been shown to block TMPRSS2 activity [28, 29] and is thus an interesting candidate. Blocking ACE2 receptor. The interaction sites between ACE2 and SARS-CoV have been identified at the atomic level and from studies to date should also hold true for interactions between ACE2 and SARS-CoV-2. Thus, one could target this interaction site with antibodies or small molecules. Delivering excessive soluble form of ACE2. Kuba et al. [10] demonstrated in mice that SARS-CoV downregulates ACE2 protein (but not ACE) by binding its spike protein, contributing to severe lung injury. This suggests that excessive ACE2 may competitively bind with SARS-CoV-2 not only to neutralize the virus but also rescue cellular ACE2 activity which negatively regulates the renin-angiotensin system (RAS) to protect the lung from injury [12, 30]. Indeed, enhanced ACE activity and decreased ACE2 availability contribute to lung injury during acid- and ventilator-induced lung injury [12, 31, 32]. Thus, treatment with a soluble form of ACE2 itself may exert dual functions: (1) slow viral entry into cells and hence viral spread [7, 9] and (2) protect the lung from injury [10, 12, 31, 32]. Notably, a recombinant human ACE2 (rhACE2; APN01, GSK2586881) has been found to be safe, with no negative hemodynamic effects in healthy volunteers and in a small cohort of patients with ARDS [33–35]. The administration of APN01 rapidly decreased levels of its proteolytic target peptide angiotensin II, with a trend to lower plasma IL-6 concentrations. Our previous work on SARS-CoV pathogenesis makes ACE2 a rational and scientifically validated therapeutic target for the current COVID-19 pandemic. The availability of recombinant ACE2 was the impetus to assemble a multinational team of intensivists, scientists, and biotech to rapidly initiate a pilot trial of rhACE2 in patients with severe COVID-19 (Clinicaltrials.gov #NCT04287686). Fig. 1 Potential approaches to address ACE2-mediated COVID-19 following SARS-CoV-2 infection. The finding that SARS-CoV-2 and SARS-CoV use the ACE2 receptor for cell entry has important implications for understanding SARS-CoV-2 transmissibility and pathogenesis. SARS-CoV and likely SARS-CoV-2 lead to downregulation of the ACE2 receptor, but not ACE, through binding of the spike protein with ACE2. This leads to viral entry and replication, as well as severe lung injury. Potential therapeutic approaches include a SARS-CoV-2 spike protein-based vaccine; a transmembrane protease serine 2 (TMPRSS2) inhibitor to block the priming of the spike protein; blocking the surface ACE2 receptor by using anti-ACE2 antibody or peptides; and a soluble form of ACE2 which should slow viral entry into cells through competitively binding with SARS-CoV-2 and hence decrease viral spread as well as protecting the lung from injury through its unique enzymatic function. MasR—mitochondrial assembly receptor, AT1R—Ang II type 1 receptor
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              2018 ESC/ESH Guidelines for the management of arterial hypertension: The Task Force for the management of arterial hypertension of the European Society of Cardiology and the European Society of Hypertension

              : Document reviewers: Guy De Backer (ESC Review Co-ordinator) (Belgium), Anthony M. Heagerty (ESH Review Co-ordinator) (UK), Stefan Agewall (Norway), Murielle Bochud (Switzerland), Claudio Borghi (Italy), Pierre Boutouyrie (France), Jana Brguljan (Slovenia), Héctor Bueno (Spain), Enrico G. Caiani (Italy), Bo Carlberg (Sweden), Neil Chapman (UK), Renata Cifkova (Czech Republic), John G. F. Cleland (UK), Jean-Philippe Collet (France), Ioan Mircea Coman (Romania), Peter W. de Leeuw (The Netherlands), Victoria Delgado (The Netherlands), Paul Dendale (Belgium), Hans-Christoph Diener (Germany), Maria Dorobantu (Romania), Robert Fagard (Belgium), Csaba Farsang (Hungary), Marc Ferrini (France), Ian M. Graham (Ireland), Guido Grassi (Italy), Hermann Haller (Germany), F. D. Richard Hobbs (UK), Bojan Jelakovic (Croatia), Catriona Jennings (UK), Hugo A. Katus (Germany), Abraham A. Kroon (The Netherlands), Christophe Leclercq (France), Dragan Lovic (Serbia), Empar Lurbe (Spain), Athanasios J. Manolis (Greece), Theresa A. McDonagh (UK), Franz Messerli (Switzerland), Maria Lorenza Muiesan (Italy), Uwe Nixdorff (Germany), Michael Hecht Olsen (Denmark), Gianfranco Parati (Italy), Joep Perk (Sweden), Massimo Francesco Piepoli (Italy), Jorge Polonia (Portugal), Piotr Ponikowski (Poland), Dimitrios J. Richter (Greece), Stefano F. Rimoldi (Switzerland), Marco Roffi (Switzerland), Naveed Sattar (UK), Petar M. Seferovic (Serbia), Iain A. Simpson (UK), Miguel Sousa-Uva (Portugal), Alice V. Stanton (Ireland), Philippe van de Borne (Belgium), Panos Vardas (Greece), Massimo Volpe (Italy), Sven Wassmann (Germany), Stephan Windecker (Switzerland), Jose Luis Zamorano (Spain).The disclosure forms of all experts involved in the development of these Guidelines are available on the ESC website www.escardio.org/guidelines.
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                Author and article information

                Contributors
                marijana_tadic@hotmail.com
                Journal
                J Clin Hypertens (Greenwich)
                J Clin Hypertens (Greenwich)
                10.1111/(ISSN)1751-7176
                JCH
                Journal of Clinical Hypertension (Greenwich, Conn.)
                John Wiley and Sons Inc. (Hoboken )
                1524-6175
                1751-7176
                20 September 2020
                : 10.1111/jch.14045
                Affiliations
                [ 1 ] University Hospital “Dr. Dragisa Misovic ‐ Dedinje” Department of Cardiology Belgrade Serbia
                [ 2 ] University of Milan‐Bicocca Milan Italy
                [ 3 ] Istituto Auxologico Italiano IRCCS Italy
                Author notes
                [*] [* ] Correspondence

                Marijana Tadic, University Hospital “Dr. Dragisa Misovic ‐ Dedinje”, Department of Cardiology, Heroja Milana Tepica 1, 11000 Belgrade, Serbia.

                Email: marijana_tadic@ 123456hotmail.com

                Author information
                https://orcid.org/0000-0002-6235-5152
                https://orcid.org/0000-0002-7689-478X
                Article
                JCH14045
                10.1111/jch.14045
                7537010
                32951351
                6624e7c4-5c1a-47b3-87f0-cdbc0ae78009
                © 2020 Wiley Periodicals LLC

                This article is being made freely available through PubMed Central as part of the COVID-19 public health emergency response. It can be used for unrestricted research re-use and analysis in any form or by any means with acknowledgement of the original source, for the duration of the public health emergency.

                History
                : 16 August 2020
                : 20 August 2020
                : 24 August 2020
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