Evidence map›Paper›PMID 34525378›Full record

ArticleStem cell reports2021

Antihypertensive drug treatment and susceptibility to SARS-CoV-2 infection in human PSC-derived cardiomyocytes and primary endothelial cells.

Jessika Iwanski, Sobhi G Kazmouz, Shuaizhi Li, Ben Stansfield, Tori T Salem, Samantha Perez-Miller, Toshinobu Kazui, Lipsa Jena, Jennifer L Uhrlaub, Scott Lick and 6 more

Open access · goldAbstract read
In one paragraph

Article in Stem cell reports, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
9citing papers in PubMed, 1 pooled it
1.2field-weighted citation impact, top 18% 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

9 citing papers in PubMed, 1 synthesis or guideline pooled it, 18 citations in OpenAlex.

  1. Pooled it
  2. Article
  3. Review
  4. Article
  5. Carbon dioxide and MAPK signalling: towards therapy for inflammation.Cell communication and signaling : CCS · 2023
    Review
  6. Article
  7. Review
  8. Review
  9. Article
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

16 authors at 1 institution in 1 country.

Jessika IwanskiDepartment of Cellular and Molecular Medicine and Sarver Heart Center Molecular Cardiovascular Research Program, The University of Arizona, Tucson, AZ, USA.
Sobhi G KazmouzDepartment of Cellular and Molecular Medicine and Sarver Heart Center Molecular Cardiovascular Research Program, The University of Arizona, Tucson, AZ, USA.
Shuaizhi LiDepartment of Immunobiology and the University of Arizona Center on Aging, The University of Arizona, Tucson, AZ, USA.
Ben StansfieldDepartment of Cellular and Molecular Medicine and Sarver Heart Center Molecular Cardiovascular Research Program, The University of Arizona, Tucson, AZ, USA; Department of Physiology, The University of Arizona, Tucson, AZ, USA.
Tori T SalemDepartment of Cellular and Molecular Medicine and Sarver Heart Center Molecular Cardiovascular Research Program, The University of Arizona, Tucson, AZ, USA; Department of Physiology, The University of Arizona, Tucson, AZ, USA.
Samantha Perez-MillerDepartment of Pharmacology, College of Medicine, University of Arizona, Tucson, AZ, USA.
Toshinobu KazuiDivision of Cardiothoracic Surgery, University of Arizona, Tucson, AZ, USA.
Lipsa JenaDepartment of Pharmacology, College of Medicine, University of Arizona, Tucson, AZ, USA.
Jennifer L UhrlaubDepartment of Immunobiology and the University of Arizona Center on Aging, The University of Arizona, Tucson, AZ, USA.
Scott LickDivision of Cardiothoracic Surgery, University of Arizona, Tucson, AZ, USA.
Janko Nikolich-ŽugichDepartment of Immunobiology and the University of Arizona Center on Aging, The University of Arizona, Tucson, AZ, USA; BIO5 Institute, The University of Arizona, Tucson, AZ, USA.
John P KonhilasDepartment of Physiology, The University of Arizona, Tucson, AZ, USA.
Carol C GregorioDepartment of Cellular and Molecular Medicine and Sarver Heart Center Molecular Cardiovascular Research Program, The University of Arizona, Tucson, AZ, USA.
May KhannaDepartment of Pharmacology, College of Medicine, University of Arizona, Tucson, AZ, USA.
Samuel K CamposDepartment of Immunobiology and the University of Arizona Center on Aging, The University of Arizona, Tucson, AZ, USA; Department of Molecular & Cellular Biology, The University of Arizona, Tucson, AZ, USA; Cancer Biology Graduate Interdisciplinary Program, The University of Arizona, Tucson, AZ, USA; BIO5 Institute, The University of Arizona, Tucson, AZ, USA.
Jared M ChurkoDepartment of Cellular and Molecular Medicine and Sarver Heart Center Molecular Cardiovascular Research Program, The University of Arizona, Tucson, AZ, USA; Department of Physiology, The University of Arizona, Tucson, AZ, USA; BIO5 Institute, The University of Arizona, Tucson, AZ, USA. Electronic address: jchurko@arizona.edu.
University of Arizona · US

Funding

PHYSIOLOGYT32HL007249 · NHLBI · UNIVERSITY OF ARIZONA · PI Brett A Colson, JOHN P KONHILAS · 1985 to 2026
$12.5M
Deciphering the role of Lmod2 in thin filament length regulation and dilated cardiomyopathyR01HL123078 · NHLBI · UNIVERSITY OF ARIZONA · PI Carol C Gregorio, Shashank Shekhar · 2015 to 2026
$5.6M
Notch signaling in cardiomyocyte transcriptome signaturesR00HL128906 · NHLBI · UNIVERSITY OF ARIZONA · PI CHURKO, JARED · 2018 to 2020
$704k
Investigating Lmod2 cardiomyopathy using human iPSC-derived cardiomyocytesF30HL151139 · NHLBI · UNIVERSITY OF ARIZONA · PI IWANSKI, JESSIKA · 2020 to 2022
$150k
NHLBI NIH HHS F30 HL151139NHLBI NIH HHS R00 HL128906NHLBI NIH HHS R01 HL123078NHLBI NIH HHS T32 HL007249
6 · The paper itself

Abstract

The pathogenicity of severe acute respiratory syndrome coronavirus-2 (SARS-CoV-2) has been attributed to its ability to enter through the membrane-bound angiotensin-converting enzyme 2 (ACE2) receptor. Therefore, it has been heavily speculated that angiotensin-converting enzyme inhibitor (ACEI) or angiotensin receptor blocker (ARB) therapy may modulate SARS-CoV-2 infection. In this study, exposure of human pluripotent stem cell-derived cardiomyocytes (hPSC-CMs) and human endothelial cells (hECs) to SARS-CoV-2 identified significant differences in protein coding genes involved in immunity, viral response, and cardiomyocyte/endothelial structure. Specifically, transcriptome changes were identified in the tumor necrosis factor (TNF), interferon α/β, and mitogen-activated protein kinase (MAPK) (hPSC-CMs) as well as nuclear factor kappa-B (NF-κB) (hECs) signaling pathways. However, pre-treatment of hPSC-CMs or hECs with two widely prescribed antihypertensive medications, losartan and lisinopril, did not affect the susceptibility of either cell type to SARS-CoV-2 infection. These findings demonstrate the toxic effects of SARS-CoV-2 in hPSC-CMs/hECs and, taken together with newly emerging multicenter trials, suggest that antihypertensive drug treatment alone does not alter SARS-CoV-2 infection.

Indexed as

COVID-19 Drug TreatmentAntihypertensive AgentsCells, CulturedCOVID-19Disease SusceptibilityEndothelial CellsHost-Pathogen InteractionsHumansLisinoprilLosartanMyocytes, CardiacSARS-CoV-2TranscriptomeAntihypertensive AgentsLisinoprilLosartanantihypertensive medicationCOVID-19endothelial cellshearthPSC-derived cardiomyocytesLisinoprillosartanRNA sequencingSARS-CoV-2stem cells

Identifiers

PMID34525378
PMCPMC8407952
OpenAlexW3198360165

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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.