Evidence map›Paper›PMID 33036546›Full record

ReviewAmerican journal of physiology. Heart and circulatory physiology2020

Role of angiotensin-converting enzyme 2 and pericytes in cardiac complications of COVID-19 infection.

Fulton A Robinson, Ryan P Mihealsick, Brant M Wagener, Peter Hanna, Megan D Poston, Igor R Efimov, Kalyanam Shivkumar, Donald B Hoover

Open access · hybridAbstract readReview
In one paragraph

Review in American journal of physiology. Heart and circulatory physiology, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 34 papers.

0numbers the graph read from it
0cells of the map it votes in
34citing papers in PubMed
1.2field-weighted citation impact, top 11% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

34 citing papers in PubMed, 56 citations in OpenAlex.

  1. Review
  2. Review
  3. Article
  4. Article
  5. Article
  6. Article
  7. Review
  8. Review
  9. Article
  10. Article
  11. Human Cardiac Pericytes Are Susceptible to SARS-CoV-2 Infection.JACC. Basic to translational science · 2023
    Article
  12. Article
  13. Article
  14. Review
  15. Mechanisms of COVID-19 pathogenesis in diabetes.American journal of physiology. Heart and circulatory physiology · 2022
    Review
  16. Article
  17. Review
  18. Article
  19. Article
  20. Review
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

8 authors at 4 institutions in 1 country.

Fulton A RobinsonDepartment of Biomedical Sciences, James H. Quillen College of Medicine, East Tennessee State University, Johnson City, Tennessee.
Ryan P MihealsickDepartment of Biomedical Sciences, James H. Quillen College of Medicine, East Tennessee State University, Johnson City, Tennessee.
Brant M WagenerDepartment of Anesthesiology and Perioperative Medicine, School of Medicine, University of Alabama at Birmingham, Birmingham, Alabama.ORCID 0000-0001-7889-1526
Peter HannaCardiac Arrhythmia Center and Neurocardiology Research Program of Excellence, Department of Medicine, University of California, Los Angeles, California.ORCID 0000-0003-3092-5090
Megan D PostonDepartment of Biomedical Sciences, James H. Quillen College of Medicine, East Tennessee State University, Johnson City, Tennessee.
Igor R EfimovDepartment of Biomedical Engineering, George Washington University, Washington, District of Columbia.
Kalyanam ShivkumarCardiac Arrhythmia Center and Neurocardiology Research Program of Excellence, Department of Medicine, University of California, Los Angeles, California.
Donald B HooverDepartment of Biomedical Sciences, James H. Quillen College of Medicine, East Tennessee State University, Johnson City, Tennessee.ORCID 0000-0002-0845-2488
East Tennessee State University · USUniversity of California, Los Angeles · USGeorge Washington University · USUniversity of Alabama at Birmingham · US

Funding

Comprehensive Structural and Functional Mapping of the Mammalian Cardiac Nervous SystemOT2OD023848 · OD · UNIVERSITY OF CALIFORNIA LOS ANGELES · PI EFIMOV, IGOR R, FOWLKES, CHARLESS · 2016 to 2021
$21.4M
The Role of Sex Dimorphism in Post-TBI Bacterial PneumoniaR01GM127584 · NIGMS · UNIVERSITY OF ALABAMA AT BIRMINGHAM · PI WAGENER, BRANT M · 2018 to 2022
$1.9M
The First Step toward a Neuronal Pacemaker of the HeartF32HL152609 · NHLBI · UNIVERSITY OF CALIFORNIA LOS ANGELES · PI HANNA, PETER · 2020 to 2020
$80k
RENOVATION OF SHM BWING, 3RD FLOORC06RR013551 · NCRR · YALE UNIVERSITY · PI KACZMAREK, LEONARD K · 1998 to 1998
–
Fondation LeducqHHS | National Institutes of Health (NIH) GM127584HHS | National Institutes of Health (NIH) HL152609NCRR NIH HHS C06 RR013551NHLBI NIH HHS F32 HL152609NIGMS NIH HHS R01 GM127584NIH HHS OT2 OD023848ODCDC CDC HHS OT2 OD023848
6 · The paper itself

Abstract

The prevalence of severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) quickly reached pandemic proportions, and knowledge about this virus and coronavirus disease 2019 (COVID-19) has expanded rapidly. This review focuses primarily on mechanisms that contribute to acute cardiac injury and dysfunction, which are common in patients with severe disease. The etiology of cardiac injury is multifactorial, and the extent is likely enhanced by preexisting cardiovascular disease. Disruption of homeostatic mechanisms secondary to pulmonary pathology ranks high on the list, and there is growing evidence that direct infection of cardiac cells can occur. Angiotensin-converting enzyme 2 (ACE2) plays a central role in COVID-19 and is a necessary receptor for viral entry into human cells. ACE2 normally not only eliminates angiotensin II (Ang II) by converting it to Ang-(1-7) but also elicits a beneficial response profile counteracting that of Ang II. Molecular analyses of single nuclei from human hearts have shown that ACE2 is most highly expressed by pericytes. Given the important roles that pericytes have in the microvasculature, infection of these cells could compromise myocardial supply to meet metabolic demand. Furthermore, ACE2 activity is crucial for opposing adverse effects of locally generated Ang II, so virus-mediated internalization of ACE2 could exacerbate pathology by this mechanism. While the role of cardiac pericytes in acute heart injury by SARS-CoV-2 requires investigation, expression of ACE2 by these cells has broader implications for cardiac pathophysiology.

Indexed as

Virus InternalizationAngiotensin-Converting Enzyme 2AnimalsBetacoronavirusCoronavirus InfectionsCOVID-19Heart DiseasesHost-Pathogen InteractionsHumansPandemicsPeptidyl-Dipeptidase APericytesPneumonia, ViralSARS-CoV-2ACE2 protein, humanAngiotensin-Converting Enzyme 2Peptidyl-Dipeptidase AACE2cardiac dysfunctionpericyterenin-angiotensin-aldosterone systemSARS-CoV-2

Identifiers

PMID33036546
PMCPMC7789968
OpenAlexW3092642339

What OpenQuestion holds

Textmetadata
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.