Evidence map›Paper›PMID 33200140›Full record

ArticlemedRxiv : the preprint server for health sciences2020

Physiology of cardiomyocyte injury in COVID-19.

Mustafa M Siddiq, Angel T Chan, Lisa Miorin, Arjun S Yadaw, Kristin G Beaumont, Thomas Kehrer, Kris M White, Anastasija Cupic, Rosa E Tolentino, Bin Hu and 20 more

Open access · greenAbstract readPreprint
In one paragraph

Article in medRxiv : the preprint server for health sciences, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
–field-weighted citation impact
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

1 citing paper in PubMed, 10 citations in OpenAlex.

  1. Article
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

30 authors at 3 institutions in 1 country.

Mustafa M SiddiqDepartment of Pharmacological Sciences, and Institute for Systems Biomedicine, Icahn School of Medicine at Mount Sinai, New York NY 10029.
Angel T ChanDepartment of Pharmacological Sciences, and Institute for Systems Biomedicine, Icahn School of Medicine at Mount Sinai, New York NY 10029.
Lisa MiorinDepartment of Microbiology and Global Health and Emerging Pathogens Institute, Icahn School of Medicine at Mount Sinai, New York NY 10029.
Arjun S YadawDepartment of Pharmacological Sciences, and Institute for Systems Biomedicine, Icahn School of Medicine at Mount Sinai, New York NY 10029.
Kristin G BeaumontDepartment of Genetics and Genomic Sciences, Icahn School of Medicine at Mount Sinai, New York NY 10029.
Thomas KehrerDepartment of Microbiology and Global Health and Emerging Pathogens Institute, Icahn School of Medicine at Mount Sinai, New York NY 10029.
Kris M WhiteDepartment of Microbiology and Global Health and Emerging Pathogens Institute, Icahn School of Medicine at Mount Sinai, New York NY 10029.
Anastasija CupicDepartment of Microbiology and Global Health and Emerging Pathogens Institute, Icahn School of Medicine at Mount Sinai, New York NY 10029.
Rosa E TolentinoDepartment of Pharmacological Sciences, and Institute for Systems Biomedicine, Icahn School of Medicine at Mount Sinai, New York NY 10029.
Bin HuDepartment of Pharmacological Sciences, and Institute for Systems Biomedicine, Icahn School of Medicine at Mount Sinai, New York NY 10029.
Alan D SternDepartment of Pharmacological Sciences, and Institute for Systems Biomedicine, Icahn School of Medicine at Mount Sinai, New York NY 10029.
Iman TavassolyDepartment of Pharmacological Sciences, and Institute for Systems Biomedicine, Icahn School of Medicine at Mount Sinai, New York NY 10029.
Jens HansenDepartment of Pharmacological Sciences, and Institute for Systems Biomedicine, Icahn School of Medicine at Mount Sinai, New York NY 10029.
Pedro MartinezDepartment of Pharmacological Sciences, and Institute for Systems Biomedicine, Icahn School of Medicine at Mount Sinai, New York NY 10029.
Nicole DuboisDepartment of Cell Developmental and Regenerative Biology and Black Family Stem Cell Center, Icahn School of Medicine at Mount Sinai, New York NY 10029.
Christoph SchanielDivision of Hematology & Oncology Department of Medicine and Black Family Stem Cell Center, Icahn School of Medicine at Mount Sinai, New York NY 10029.
Rupa Iyengar-KapugantiDivision of Cardiology, Department of Medicine, Icahn School of Medicine at Mount Sinai, New York NY 10029.
Nina KukarDivision of Cardiology, Department of Medicine, Icahn School of Medicine at Mount Sinai, New York NY 10029.
Gennaro GiustinoDivision of Hematology & Oncology Department of Medicine and Black Family Stem Cell Center, Icahn School of Medicine at Mount Sinai, New York NY 10029.
Karan SudDivision of Cardiology, Department of Medicine, Icahn School of Medicine at Mount Sinai, New York NY 10029.
Sharon NirenbergDepartment of Scientific Computing and Data Science, Icahn School of Medicine at Mount Sinai, New York NY 10029.
Patricia KovatchDepartment of Genetics and Genomic Sciences, Icahn School of Medicine at Mount Sinai, New York NY 10029.
Joseph GoldfarbDepartment of Pharmacological Sciences, and Institute for Systems Biomedicine, Icahn School of Medicine at Mount Sinai, New York NY 10029.
Lori CroftDivision of Cardiology, Department of Medicine, Icahn School of Medicine at Mount Sinai, New York NY 10029.
Maryann A McLaughlinDivision of Cardiology, Department of Medicine, Icahn School of Medicine at Mount Sinai, New York NY 10029.
Edgar ArgulianDivision of Cardiology, Department of Medicine, Icahn School of Medicine at Mount Sinai, New York NY 10029.
Stamatios LerakisDivision of Cardiology, Department of Medicine, Icahn School of Medicine at Mount Sinai, New York NY 10029.
Jagat NarulaDivision of Cardiology, Department of Medicine, Icahn School of Medicine at Mount Sinai, New York NY 10029.
Adolfo García-SastreDepartment of Microbiology and Global Health and Emerging Pathogens Institute, Icahn School of Medicine at Mount Sinai, New York NY 10029.
Ravi IyengarDepartment of Pharmacological Sciences, and Institute for Systems Biomedicine, Icahn School of Medicine at Mount Sinai, New York NY 10029.
Icahn School of Medicine at Mount Sinai · USMemorial Sloan Kettering Cancer Center · USTisch Hospital · US

Funding

X-RAY CRYSTALLOGRAPHYP30CA008748 · NCI · SLOAN-KETTERING INSTITUTE FOR CANCER RES · PI Hongbiao Carl Lekaye · 1985 to 2026
$347.4M
Drug Combination Signatures for Prediction and Mitigation of ToxicityU54HG008098 · NHGRI · ICAHN SCHOOL OF MEDICINE AT MOUNT SINAI · PI BIRTWISTLE, MARC R., SOBIE, ERIC A · 2014 to 2019
$11.8M
Vulnerability of SARS- CoV-2 Infection in Lung Cancer Based on Serological Antibody AnalysesU54CA260560 · NCI · ICAHN SCHOOL OF MEDICINE AT MOUNT SINAI · PI GARCIA-SASTRE, ADOLFO, HIRSCH, FRED R · 2020 to 2024
$10.0M
NCI NIH HHS P30 CA008748NCI NIH HHS U54 CA260560NHGRI NIH HHS U54 HG008098NIAID NIH HHS HHSN272201400008C
6 · The paper itself

Abstract

COVID-19 affects multiple organs. Clinical data from the Mount Sinai Health System shows that substantial numbers of COVID-19 patients without prior heart disease develop cardiac dysfunction. How COVID-19 patients develop cardiac disease is not known. We integrate cell biological and physiological analyses of human cardiomyocytes differentiated from human induced pluripotent stem cells (hiPSCs) infected with SARS-CoV-2 in the presence of interleukins, with clinical findings, to investigate plausible mechanisms of cardiac disease in COVID-19 patients. We infected hiPSC-derived cardiomyocytes, from healthy human subjects, with SARS-CoV-2 in the absence and presence of interleukins. We find that interleukin treatment and infection results in disorganization of myofibrils, extracellular release of troponin-I, and reduced and erratic beating. Although interleukins do not increase the extent, they increase the severity of viral infection of cardiomyocytes resulting in cessation of beating. Clinical data from hospitalized patients from the Mount Sinai Health system show that a significant portion of COVID-19 patients without prior history of heart disease, have elevated troponin and interleukin levels. A substantial subset of these patients showed reduced left ventricular function by echocardiography. Our laboratory observations, combined with the clinical data, indicate that direct effects on cardiomyocytes by interleukins and SARS-CoV-2 infection can underlie the heart disease in COVID-19 patients.

Identifiers

PMID33200140
PMCPMC7668750
OpenAlexW3105493778

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.