Literature DB >> 32356625

Inhibitors of the Renin-Angiotensin-Aldosterone System and Covid-19.

John A Jarcho1, Julie R Ingelfinger1, Mary Beth Hamel1, Ralph B D'Agostino1, David P Harrington1.   

Abstract

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Year:  2020        PMID: 32356625      PMCID: PMC7224604          DOI: 10.1056/NEJMe2012924

Source DB:  PubMed          Journal:  N Engl J Med        ISSN: 0028-4793            Impact factor:   91.245


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SARS-CoV-2, the coronavirus that causes Covid-19, enters human cells by binding of its viral spike protein to the membrane-bound form of the monocarboxypeptidase angiotensin-converting enzyme 2 (ACE2).[1] From the viewpoint of human physiology, ACE2 plays an important regulatory role in the renin–angiotensin–aldosterone system (RAAS), metabolizing angiotensin II (a potent vasoconstrictor) to generate angiotensin-(1–7) (a vasodilator).[2] Studies in animals have suggested that angiotensin-converting–enzyme (ACE) inhibitors and angiotensin-receptor blockers (ARBs) may up-regulate ACE2 expression,[3] thus increasing the availability of target molecules for SARS-CoV-2. These considerations have led to speculation that ACE inhibitors and ARBs might be harmful in patients with Covid-19.[4,5] Although this is only a hypothesis, the argument has aroused potential concerns. Case series have indicated that hypertension, diabetes, and coronary artery disease — conditions for which clinicians often prescribe RAAS inhibitors — are more common in patients with severe Covid-19 than in those with milder illness.[6] Coverage of the hypothesis by the press and some websites has emphasized the theoretical risk with statements such as, “People with high blood pressure and diabetes could be at higher risk of severe or fatal coronavirus symptoms because of how their medicines work, scientists say,”[7] and, “[Reports suggest that] you are four times as likely to die from Covid-19 if you are taking one of these drugs, prior to contracting the virus.”[8] In this rapidly evolving setting, clinicians are weighing the alleged harm of continuing these medications in patients for whom ACE inhibitors and ARBs have known benefit against the harm to their cardiovascular and kidney health associated with discontinuing them. Three articles now published in the Journal provide data about whether ACE inhibitors and ARBs are indeed harmful in the context of the Covid-19 epidemic. All are observational studies with the looming possibility of confounding, but each has unique strengths, and their message is consistent — none of the three studies showed evidence of harm with continued use of ACE inhibitors and ARBs. Mehra et al.[9] conducted a database study involving patients who had been hospitalized in 11 countries on three continents. The study included 8910 patients who had received a diagnosis of Covid-19, who had been admitted to the hospital between December 20, 2019, and March 15, 2020, and who had either died in the hospital or survived to hospital discharge. In multivariate logistic-regression analysis, an age greater than 65 years, coronary artery disease, congestive heart failure, history of cardiac arrhythmia, chronic obstructive pulmonary disease, and current smoking were associated with an increased risk of in-hospital death. Female sex was associated with a decreased risk. Neither ACE inhibitors nor ARBs were associated with an increased risk of in-hospital death. A secondary analysis that was restricted to patients with hypertension (those for whom an ACE inhibitor or ARB would be indicated) also did not show harm. Mancia et al.[10] conducted a case–control study involving patients with confirmed Covid-19 in the Lombardy region of Italy, which has been severely affected by the pandemic. In this analysis, 6272 people with confirmed SARS-CoV-2 infection that had been diagnosed between February 21 and March 11, 2020, were compared with 30,759 controls who were matched according to age, sex, and municipality of residence. In a conditional logistic-regression multivariate analysis, neither ACE inhibitors nor ARBs were associated with the likelihood of SARS-CoV-2 infection. An additional analysis comparing patients with severe or fatal infections with matched controls also did not show an association between these drugs and severe Covid-19. Reynolds et al.[11] conducted a study based on data from the electronic health records of 12,594 patients in the New York University (NYU) Langone Health system who were tested for Covid-19 between March 1 and April 15, 2020. A total of 5894 patients had a positive test, among whom 1002 had severe illness (defined as admission to the intensive care unit, mechanical ventilation, or death). Propensity-score matching was performed among all tested patients and among patients with hypertension (to assess whether the likelihood of a positive test result was associated with each of several antihypertensive drug classes), as well as among Covid-19–positive patients and all such patients with hypertension (to assess whether the likelihood of severe illness among those with a positive test was associated with the same drug classes). The investigators’ Bayesian analysis showed no positive association for any of the analyzed drug classes, including ACE inhibitors and ARBs, for either a positive test result or severe illness. Taken together, these three studies do not provide evidence to support the hypothesis that ACE inhibitor or ARB use is associated with the risk of SARS-CoV-2 infection, the risk of severe Covid-19 among those infected, or the risk of in-hospital death among those with a positive test. Each of these studies has weaknesses inherent in observational data, but we find it reassuring that three studies in different populations and with different designs arrive at the consistent message that the continued use of ACE inhibitors and ARBs is unlikely to be harmful in patients with Covid-19. Several other smaller studies from China and the United Kingdom have come to the same conclusion.[12-15] We note that Mehra et al. found that use of either ACE inhibitors or statins may be associated with a lower risk of in-hospital death than nonuse, but neither of the other two studies estimated a lower risk of Covid-19 or the likelihood of a positive test among patients treated with these agents. The unexpected result in the study by Mehra et al. may be due to unmeasured confounding and, in the absence of a randomized trial, should not be regarded as evidence to prescribe these drugs in patients with Covid-19. Professional scientific societies and experts have spoken with one voice in advising that patients should not discontinue ACE inhibitor or ARB therapy out of a concern that they are at increased risk for infection, severe illness, or death during the Covid-19 pandemic.[16-18] The data from these three studies support those recommendations. Ultimately, one or more randomized trials will be needed to answer definitively the question of whether ACE inhibitors or ARBs pose a harm to patients with Covid-19.
  13 in total

1.  Are patients with hypertension and diabetes mellitus at increased risk for COVID-19 infection?

Authors:  Lei Fang; George Karakiulakis; Michael Roth
Journal:  Lancet Respir Med       Date:  2020-03-11       Impact factor: 30.700

2.  Renin-Angiotensin-Aldosterone System Inhibitors and Risk of Covid-19.

Authors:  Harmony R Reynolds; Samrachana Adhikari; Claudia Pulgarin; Andrea B Troxel; Eduardo Iturrate; Stephen B Johnson; Anaïs Hausvater; Jonathan D Newman; Jeffrey S Berger; Sripal Bangalore; Stuart D Katz; Glenn I Fishman; Dennis Kunichoff; Yu Chen; Gbenga Ogedegbe; Judith S Hochman
Journal:  N Engl J Med       Date:  2020-05-01       Impact factor: 91.245

3.  Renin-Angiotensin-Aldosterone System Blockers and the Risk of Covid-19.

Authors:  Giuseppe Mancia; Federico Rea; Monica Ludergnani; Giovanni Apolone; Giovanni Corrao
Journal:  N Engl J Med       Date:  2020-05-01       Impact factor: 91.245

4.  Cardiovascular Disease, Drug Therapy, and Mortality in Covid-19.

Authors:  Mandeep R Mehra; Sapan S Desai; SreyRam Kuy; Timothy D Henry; Amit N Patel
Journal:  N Engl J Med       Date:  2020-05-01       Impact factor: 91.245

5.  Clinical Characteristics of Coronavirus Disease 2019 in China.

Authors:  Wei-Jie Guan; Zheng-Yi Ni; Yu Hu; Wen-Hua Liang; Chun-Quan Ou; Jian-Xing He; Lei Liu; Hong Shan; Chun-Liang Lei; David S C Hui; Bin Du; Lan-Juan Li; Guang Zeng; Kwok-Yung Yuen; Ru-Chong Chen; Chun-Li Tang; Tao Wang; Ping-Yan Chen; Jie Xiang; Shi-Yue Li; Jin-Lin Wang; Zi-Jing Liang; Yi-Xiang Peng; Li Wei; Yong Liu; Ya-Hua Hu; Peng Peng; Jian-Ming Wang; Ji-Yang Liu; Zhong Chen; Gang Li; Zhi-Jian Zheng; Shao-Qin Qiu; Jie Luo; Chang-Jiang Ye; Shao-Yong Zhu; Nan-Shan Zhong
Journal:  N Engl J Med       Date:  2020-02-28       Impact factor: 91.245

Review 6.  ACE2: angiotensin II/angiotensin-(1-7) balance in cardiac and renal injury.

Authors:  Jasmina Varagic; Sarfaraz Ahmad; Sayaka Nagata; Carlos M Ferrario
Journal:  Curr Hypertens Rep       Date:  2014-03       Impact factor: 5.369

7.  Renin-Angiotensin-Aldosterone System Inhibitors in Patients with Covid-19.

Authors:  Muthiah Vaduganathan; Orly Vardeny; Thomas Michel; John J V McMurray; Marc A Pfeffer; Scott D Solomon
Journal:  N Engl J Med       Date:  2020-03-30       Impact factor: 91.245

8.  Renin-angiotensin system inhibitors improve the clinical outcomes of COVID-19 patients with hypertension.

Authors:  Juan Meng; Guohui Xiao; Juanjuan Zhang; Xing He; Min Ou; Jing Bi; Rongqing Yang; Wencheng Di; Zhaoqin Wang; Zigang Li; Hong Gao; Lei Liu; Guoliang Zhang
Journal:  Emerg Microbes Infect       Date:  2020-12       Impact factor: 7.163

9.  SARS-CoV-2 Cell Entry Depends on ACE2 and TMPRSS2 and Is Blocked by a Clinically Proven Protease Inhibitor.

Authors:  Markus Hoffmann; Hannah Kleine-Weber; Simon Schroeder; Nadine Krüger; Tanja Herrler; Sandra Erichsen; Tobias S Schiergens; Georg Herrler; Nai-Huei Wu; Andreas Nitsche; Marcel A Müller; Christian Drosten; Stefan Pöhlmann
Journal:  Cell       Date:  2020-03-05       Impact factor: 41.582

Review 10.  Pharmacologic modulation of ACE2 expression.

Authors:  María José Soler; Clara Barrios; Raymond Oliva; Daniel Batlle
Journal:  Curr Hypertens Rep       Date:  2008-10       Impact factor: 5.369

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1.  Hypertension delays viral clearance and exacerbates airway hyperinflammation in patients with COVID-19.

Authors:  Saskia Trump; Soeren Lukassen; Markus S Anker; Robert Lorenz Chua; Johannes Liebig; Loreen Thürmann; Victor Max Corman; Marco Binder; Jennifer Loske; Christina Klasa; Teresa Krieger; Bianca P Hennig; Marey Messingschlager; Fabian Pott; Julia Kazmierski; Sven Twardziok; Jan Philipp Albrecht; Jürgen Eils; Sara Hadzibegovic; Alessia Lena; Bettina Heidecker; Thore Bürgel; Jakob Steinfeldt; Christine Goffinet; Florian Kurth; Martin Witzenrath; Maria Theresa Völker; Sarah Dorothea Müller; Uwe Gerd Liebert; Naveed Ishaque; Lars Kaderali; Leif-Erik Sander; Christian Drosten; Sven Laudi; Roland Eils; Christian Conrad; Ulf Landmesser; Irina Lehmann
Journal:  Nat Biotechnol       Date:  2020-12-24       Impact factor: 54.908

2.  Effect of Discontinuing vs Continuing Angiotensin-Converting Enzyme Inhibitors and Angiotensin II Receptor Blockers on Days Alive and Out of the Hospital in Patients Admitted With COVID-19: A Randomized Clinical Trial.

Authors:  Renato D Lopes; Ariane V S Macedo; Pedro G M de Barros E Silva; Renata J Moll-Bernardes; Tiago M Dos Santos; Lilian Mazza; André Feldman; Guilherme D'Andréa Saba Arruda; Denílson C de Albuquerque; Angelina S Camiletti; Andréa S de Sousa; Thiago C de Paula; Karla G D Giusti; Rafael A M Domiciano; Márcia M Noya-Rabelo; Alan M Hamilton; Vitor A Loures; Rodrigo M Dionísio; Thyago A B Furquim; Fábio A De Luca; Ítalo B Dos Santos Sousa; Bruno S Bandeira; Cleverson N Zukowski; Ricardo G G de Oliveira; Noara B Ribeiro; Jeffer L de Moraes; João L F Petriz; Adriana M Pimentel; Jacqueline S Miranda; Bárbara E de Jesus Abufaiad; C Michael Gibson; Christopher B Granger; John H Alexander; Olga F de Souza
Journal:  JAMA       Date:  2021-01-19       Impact factor: 56.272

Review 3.  The Disease-Modifying Role of Taurine and Its Therapeutic Potential in Coronavirus Disease 2019 (COVID-19).

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Journal:  Adv Exp Med Biol       Date:  2022       Impact factor: 3.650

4.  A network medicine approach to investigation and population-based validation of disease manifestations and drug repurposing for COVID-19.

Authors:  Yadi Zhou; Yuan Hou; Jiayu Shen; Reena Mehra; Asha Kallianpur; Daniel A Culver; Michaela U Gack; Samar Farha; Joe Zein; Suzy Comhair; Claudio Fiocchi; Thaddeus Stappenbeck; Timothy Chan; Charis Eng; Jae U Jung; Lara Jehi; Serpil Erzurum; Feixiong Cheng
Journal:  PLoS Biol       Date:  2020-11-06       Impact factor: 8.029

5.  Platelet Activation and Plasma Levels of Furin Are Associated With Prognosis of Patients With Coronary Artery Disease and COVID-19.

Authors:  Carolin Langnau; Anne-Katrin Rohlfing; Sarah Gekeler; Manina Günter; Simone Pöschel; Álvaro Petersen-Uribe; Philippa Jaeger; Alban Avdiu; Tobias Harm; Klaus-Peter Kreisselmeier; Tatsiana Castor; Tamam Bakchoul; Dominik Rath; Meinrad Paul Gawaz; Stella E Autenrieth; Karin Anne Lydia Mueller
Journal:  Arterioscler Thromb Vasc Biol       Date:  2021-04-29       Impact factor: 8.311

6.  Would ACEIs/ARBs be beneficial for COVID-19 patients without hypertension?

Authors:  Ying Huang; Changming Xie; Xiaoke Chen; Qianhui Hong; Hui Huang
Journal:  Pharmacol Res       Date:  2020-06-04       Impact factor: 7.658

7.  High prevalence of COVID-19-associated diabetic ketoacidosis in UK secondary care.

Authors:  Nina Goldman; Douglas Fink; James Cai; Yun-Ni Lee; Zoe Davies
Journal:  Diabetes Res Clin Pract       Date:  2020-06-29       Impact factor: 5.602

8.  Discontinuation versus continuation of renin-angiotensin-system inhibitors in COVID-19 (ACEI-COVID): a prospective, parallel group, randomised, controlled, open-label trial.

Authors:  Axel Bauer; Michael Schreinlechner; Nikolay Sappler; Theresa Dolejsi; Herbert Tilg; Benedikt A Aulinger; Günter Weiss; Rosa Bellmann-Weiler; Christian Adolf; Dominik Wolf; Markus Pirklbauer; Ivo Graziadei; Hannes Gänzer; Christian von Bary; Andreas E May; Ewald Wöll; Wolfgang von Scheidt; Tienush Rassaf; Daniel Duerschmied; Christoph Brenner; Stefan Kääb; Bernhard Metzler; Michael Joannidis; Hans-Ulrich Kain; Norbert Kaiser; Robert Schwinger; Bernhard Witzenbichler; Hannes Alber; Florian Straube; Niels Hartmann; Stephan Achenbach; Michael von Bergwelt-Baildon; Lukas von Stülpnagel; Sebastian Schoenherr; Lukas Forer; Sabine Embacher-Aichhorn; Ulrich Mansmann; Konstantinos D Rizas; Steffen Massberg
Journal:  Lancet Respir Med       Date:  2021-06-11       Impact factor: 30.700

9.  Use of distinct anti-hypertensive drugs and risk for COVID-19 among hypertensive people: A population-based cohort study in Southern Catalonia, Spain.

Authors:  Angel Vila-Corcoles; Eva Satue-Gracia; Olga Ochoa-Gondar; Cristina Torrente-Fraga; Frederic Gomez-Bertomeu; Angel Vila-Rovira; Imma Hospital-Guardiola; Cinta de Diego-Cabanes; Ferran Bejarano-Romero; Dolors Rovira-Veciana; Josep Basora-Gallisa
Journal:  J Clin Hypertens (Greenwich)       Date:  2020-07-25       Impact factor: 3.738

10.  Attacking COVID-19 Progression Using Multi-Drug Therapy for Synergetic Target Engagement.

Authors:  Mathew A Coban; Juliet Morrison; Sushila Maharjan; David Hyram Hernandez Medina; Wanlu Li; Yu Shrike Zhang; William D Freeman; Evette S Radisky; Karine G Le Roch; Carla M Weisend; Hideki Ebihara; Thomas R Caulfield
Journal:  Biomolecules       Date:  2021-05-23
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