Evidence map›Paper›PMID 35931818›Full record

ReviewNature reviews. Immunology2022

Understanding COVID-19-associated coagulopathy.

Edward M Conway, Nigel Mackman, Ronald Q Warren, Alisa S Wolberg, Laurent O Mosnier, Robert A Campbell, Lisa E Gralinski, Matthew T Rondina, Frank L van de Veerdonk, Karin M Hoffmeister and 4 more

Open access · bronzeAbstract readReview
In one paragraph

Review in Nature reviews. Immunology, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 220 papers, 5 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
220citing papers in PubMed, 5 pooled it
33.0field-weighted citation impact, top 1% 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

220 citing papers in PubMed, 5 syntheses or guidelines pooled it, 343 citations in OpenAlex.

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160 more citing papers are in PubMed but not listed here.

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

14 authors at 9 institutions in 3 countries.

Edward M ConwayCentre for Blood Research, Life Sciences Institute, Department of Medicine, University of British Columbia, Vancouver, British Columbia, Canada.
Nigel MackmanDepartment of Medicine, UNC Blood Research Center, University of North Carolina at Chapel Hill, Chapel Hill, NC, USA.ORCID 0000-0002-9170-7700
Ronald Q WarrenMolecular Cellular and Systems Blood Science Branch, Division of Blood Diseases and Resources, National Heart, Lung, and Blood Institute, Bethesda, MD, USA.
Alisa S WolbergDepartment of Pathology and Laboratory Medicine, UNC Blood Research Center, University of North Carolina at Chapel Hill, Chapel Hill, NC, USA.
Laurent O MosnierDepartment of Molecular Medicine, The Scripps Research Institute, La Jolla, CA, USA.
Robert A CampbellDepartment of Internal Medicine, Division of General Medicine, University of Utah, Salt Lake City, UT, USA.
Lisa E GralinskiDepartment of Epidemiology, University of North Carolina at Chapel Hill, Chapel Hill, NC, USA.ORCID 0000-0003-1374-8002
Matthew T RondinaDepartment of Internal Medicine, Division of General Medicine, University of Utah, Salt Lake City, UT, USA.
Frank L van de VeerdonkDepartment of Internal Medicine, Radboud University Medical Center, Nijmegen, the Netherlands.
Karin M HoffmeisterVersiti Translational Glycomics Center, Blood Research Institute and Medical College of Wisconsin, Milwaukee, WI, USA.
John H GriffinDepartment of Molecular Medicine, The Scripps Research Institute, La Jolla, CA, USA.
Diane NugentDepartment of Paediatrics, School of Medicine, University of California at Irvine, Irvine, CA, USA.
Kyung MoonMolecular Cellular and Systems Blood Science Branch, Division of Blood Diseases and Resources, National Heart, Lung, and Blood Institute, Bethesda, MD, USA. kyung.moon@nih.gov.ORCID 0000-0001-5809-1601
James H MorrisseyDepartment of Biological Chemistry, University of Michigan Medical School, Ann Arbor, MI, USA. jhmorris@umich.edu.ORCID 0000-0002-1570-1569
University of North Carolina at Chapel Hill · USNational Heart Lung and Blood Institute · USScripps Research Institute · USUniversity of Utah · USMedical College of Wisconsin · USRadboud University Nijmegen · NLUniversity of British Columbia · CAUniversity of California, Irvine · USUniversity of Michigan · US

Funding

ACTIV Integration of Host-targeting Therapies for COVID-19 Administrative Coordinating CenterOT2HL156812 · NHLBI · RESEARCH TRIANGLE INSTITUTE · PI NOLEN, TRACY L, THOMAS, SONIA M · 2020 to 2024
$1270.7M
Regulation of Protein C PathwaysR01HL142975 · NHLBI · SCRIPPS RESEARCH INSTITUTE, THE · PI GRIFFIN, JOHN H, MOSNIER, LAURENT OLIVIER · 2018 to 2025
$7.3M
Structure-function of cytoprotective coagulation proteases and their receptorsR01HL104165 · NHLBI · SCRIPPS RESEARCH INSTITUTE, THE · PI MOSNIER, LAURENT OLIVIER · 2011 to 2024
$6.1M
Mechanisms in Blood ClottingR35HL135823 · NHLBI · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI MORRISSEY, JAMES H. · 2017 to 2023
$4.8M
Novel functions of Thrombin Activatable Fibrinolysis Inhibitor (TAFI)R01HL148096 · NHLBI · SCRIPPS RESEARCH INSTITUTE, THE · PI MOSNIER, LAURENT OLIVIER · 2020 to 2023
$2.6M
Mechanisms linking the plasminogen/fibrinogen axis to the pathogenesis of COVID-19R01HL160046 · NHLBI · UNIV OF NORTH CAROLINA CHAPEL HILL · PI FLICK, MATTHEW J., GRALINSKI, LISA · 2021 to 2024
$2.2M
Platelet-Mediated Neutrophil Extracellular Traps Regulate Ischemic Stroke InjuryR01HL163019 · NHLBI · WASHINGTON UNIVERSITY · PI CAMPBELL, ROBERT A · 2022 to 2025
$2.2M
Interferon-Induced Transmembrane Protein 3 (IFITM3) Regulates Thrombosis During Inflammation in AgingK01AG059892 · NIA · UNIVERSITY OF UTAH · PI CAMPBELL, ROBERT A · 2019 to 2022
$400k
CIHRNHLBI NIH HHS OT2 HL156812NHLBI NIH HHS R01 HL104165NHLBI NIH HHS R01 HL142975NHLBI NIH HHS R01 HL148096NHLBI NIH HHS R01 HL160046NHLBI NIH HHS R01 HL163019NHLBI NIH HHS R35 HL135823NIA NIH HHS K01 AG059892
6 · The paper itself

Abstract

COVID-19-associated coagulopathy (CAC) is a life-threatening complication of SARS-CoV-2 infection. However, the underlying cellular and molecular mechanisms driving this condition are unclear. Evidence supports the concept that CAC involves complex interactions between the innate immune response, the coagulation and fibrinolytic pathways, and the vascular endothelium, resulting in a procoagulant condition. Understanding of the pathogenesis of this condition at the genomic, molecular and cellular levels is needed in order to mitigate thrombosis formation in at-risk patients. In this Perspective, we categorize our current understanding of CAC into three main pathological mechanisms: first, vascular endothelial cell dysfunction; second, a hyper-inflammatory immune response; and last, hypercoagulability. Furthermore, we pose key questions and identify research gaps that need to be addressed to better understand CAC, facilitate improved diagnostics and aid in therapeutic development. Finally, we consider the suitability of different animal models to study CAC.

Indexed as

Blood Coagulation DisordersCOVID-19ThrombosisAnimalsEndothelium, VascularSARS-CoV-2

Identifiers

PMID35931818
PMCPMC9362465
OpenAlexW4289918655

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.