Evidence map›Paper›PMID 33196292›Full record

ArticleArteriosclerosis, thrombosis, and vascular biology2021

COVID-19 and Sepsis Are Associated With Different Abnormalities in Plasma Procoagulant and Fibrinolytic Activity.

Emma G Bouck, Frederik Denorme, Lori A Holle, Elizabeth A Middelton, Antoinette M Blair, Bas de Laat, Joshua D Schiffman, Christian Con Yost, Matthew T Rondina, Alisa S Wolberg and 1 more

Open access · greenAbstract read
In one paragraph

Article in Arteriosclerosis, thrombosis, and vascular biology, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 95 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
95citing papers in PubMed, 2 pooled it
2.7field-weighted citation impact, top 6% 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

95 citing papers in PubMed, 2 syntheses or guidelines pooled it, 139 citations in OpenAlex.

  1. Endotheliopathy in Acute COVID-19 and Long COVID.International journal of molecular sciences · 2023
    Pooled it
  2. Guideline
  3. Trial
  4. Article
  5. Review
  6. Article
  7. Article
  8. Article
  9. Review
  10. Article
  11. Article
  12. Article
  13. Article
  14. Article
  15. Review
  16. Review
  17. Article
  18. Review
  19. Immunity and Coagulation in COVID-19.International journal of molecular sciences · 2024
    Review
  20. Review

35 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

11 authors at 3 institutions in 2 countries.

Emma G Bouck *Department of Pathology and Laboratory Medicine and UNC Blood Research Center, University of North Carolina, Chapel Hill (E.G.B., L.A.H., A.S.W.).
Frederik Denorme *University of Utah Molecular Medicine Program, Salt Lake City, UT (F.D., A.M.B., M.T.R., R.A.C.).
Lori A HolleDepartment of Pathology and Laboratory Medicine and UNC Blood Research Center, University of North Carolina, Chapel Hill (E.G.B., L.A.H., A.S.W.).
Elizabeth A MiddeltonDepartment of Internal Medicine (E.A.M., M.T.R., R.A.C.), University of Utah, Salt Lake City.
Antoinette M BlairUniversity of Utah Molecular Medicine Program, Salt Lake City, UT (F.D., A.M.B., M.T.R., R.A.C.).
Bas de LaatSynapse Research Institute, Maastricht, the Netherlands (B.d.L.).
Joshua D SchiffmanDepartment of Pediatrics (J.D.S., C.C.Y.), University of Utah, Salt Lake City.
Christian Con YostDepartment of Pediatrics (J.D.S., C.C.Y.), University of Utah, Salt Lake City.
Matthew T RondinaUniversity of Utah Molecular Medicine Program, Salt Lake City, UT (F.D., A.M.B., M.T.R., R.A.C.).
Alisa S Wolberg *Department of Pathology and Laboratory Medicine and UNC Blood Research Center, University of North Carolina, Chapel Hill (E.G.B., L.A.H., A.S.W.).
Robert A Campbell *University of Utah Molecular Medicine Program, Salt Lake City, UT (F.D., A.M.B., M.T.R., R.A.C.).
University of Utah · USUniversity of North Carolina at Chapel Hill · USSynapse (Netherlands) · NL

Funding

Utah Center for Clinical and Translational ScienceUL1TR002538 · NCATS · UNIVERSITY OF UTAH · PI HESS, RACHEL, MAJERSIK, JENNIFER JUHL · 2018 to 2022
$26.0M
Pre-doctoral Training Program in Integrative Vascular BiologyT32HL069768 · NHLBI · UNIV OF NORTH CAROLINA CHAPEL HILL · PI Christopher P. Mack · 2002 to 2026
$9.7M
Using genomics and functional biology to understand fibrinogen and its effect on thrombotic and atherosclerotic outcomesR01HL141291 · NHLBI · UNIVERSITY OF TEXAS HLTH SCI CTR HOUSTON · PI Alanna C Morrison, Alisa S. Wolberg · 2019 to 2026
$4.6M
Fibrinogen and Factor XIII in Venous ThrombosisR01HL126974 · NHLBI · UNIV OF NORTH CAROLINA CHAPEL HILL · PI Alisa S. Wolberg · 2016 to 2026
$4.4M
Targeting the Plasminogen Activation System to Limit Pancreatic Cancer Progression and Associated ThrombosisU01HL143403 · NHLBI · UNIV OF NORTH CAROLINA CHAPEL HILL · PI FISHEL, MELISSA L., FLICK, MATTHEW J. · 2018 to 2022
$4.2M
New Therapies to Restore Vascular Integrity During SepsisR01HL130541 · NHLBI · UNIVERSITY OF UTAH · PI ODELBERG, SHANNON J, WEYRICH, ANDREW S · 2016 to 2020
$3.7M
UT StrokeNet Administrative SupplementU24NS107228 · NINDS · UTAH STATE HIGHER EDUCATION SYSTEM--UNIVERSITY OF UTAH · PI Jennifer Juhl Majersik · 2018 to 2026
$3.0M
NETs: Protection or Harm in Neonatal Inflammation and InfectionR01HD093826 · NICHD · UTAH STATE HIGHER EDUCATION SYSTEM--UNIVERSITY OF UTAH · PI CHRISTIAN CON YOST · 2018 to 2026
$2.6M
Translational Control of Megakaryocyte and Platelet Function in SepsisR01HL142804 · NHLBI · UNIVERSITY OF UTAH · PI RONDINA, MATTHEW THOMAS · 2018 to 2021
$1.9M
Platelet Immune Responses in Aging and InfluenzaR01AG048022 · NIA · UNIVERSITY OF UTAH · PI RONDINA, MATTHEW THOMAS · 2014 to 2018
$1.8M
Interferon-Induced Transmembrane Protein 3 (IFITM3) Regulates Thrombosis During Inflammation in AgingK01AG059892 · NIA · UNIVERSITY OF UTAH · PI CAMPBELL, ROBERT A · 2019 to 2022
$400k
Novel Regulatory Mechanisms of Inflammation-Induced ThrombosisR56AG059877 · NIA · UNIVERSITY OF UTAH · PI RONDINA, MATTHEW THOMAS · 2018 to 2018
$381k
CSRD VA I01 CX001696NCATS NIH HHS UL1 TR002538NHLBI NIH HHS R01 HL126974NHLBI NIH HHS R01 HL130541NHLBI NIH HHS R01 HL141291NHLBI NIH HHS R01 HL142804NHLBI NIH HHS T32 HL069768NHLBI NIH HHS U01 HL143403NIA NIH HHS K01 AG059892NIA NIH HHS R01 AG048022NIA NIH HHS R56 AG059877NICHD NIH HHS R01 HD093826NINDS NIH HHS U24 NS107228
6 · The paper itself

Abstract

objectiveCoronavirus disease 2019 (COVID-19) is associated with derangement in biomarkers of coagulation and endothelial function and has been likened to the coagulopathy of sepsis. However, clinical laboratory metrics suggest key differences in these pathologies. We sought to determine whether plasma coagulation and fibrinolytic potential in patients with COVID-19 differ compared with healthy donors and critically ill patients with sepsis. Approach and Results: We performed comparative studies on plasmas from a single-center, cross-sectional observational study of 99 hospitalized patients (46 with COVID-19 and 53 with sepsis) and 18 healthy donors. We measured biomarkers of endogenous coagulation and fibrinolytic activity by immunoassays, thrombin, and plasmin generation potential by fluorescence and fibrin formation and lysis by turbidity. Compared with healthy donors, patients with COVID-19 or sepsis both had elevated fibrinogen, d-dimer, soluble TM (thrombomodulin), and plasmin-antiplasmin complexes. Patients with COVID-19 had increased thrombin generation potential despite prophylactic anticoagulation, whereas patients with sepsis did not. Plasma from patients with COVID-19 also had increased endogenous plasmin potential, whereas patients with sepsis showed delayed plasmin generation. The collective perturbations in plasma thrombin and plasmin generation permitted enhanced fibrin formation in both COVID-19 and sepsis. Unexpectedly, the lag times to thrombin, plasmin, and fibrin formation were prolonged with increased disease severity in COVID-19, suggesting a loss of coagulation-initiating mechanisms accompanies severe COVID-19.

conclusionsBoth COVID-19 and sepsis are associated with endogenous activation of coagulation and fibrinolysis, but these diseases differently impact plasma procoagulant and fibrinolytic potential. Dysregulation of procoagulant and fibrinolytic pathways may uniquely contribute to the pathophysiology of COVID-19 and sepsis.

Indexed as

SARS-CoV-2BiomarkersBlood CoagulationBlood Coagulation DisordersCOVID-19Cross-Sectional StudiesFemaleFibrinolysinHumansMaleMiddle AgedPandemicsSepsisBiomarkersFibrinolysinfibrinfibrinogenfibrinolysissepsisthrombin

Identifiers

PMID33196292
PMCPMC7942774
OpenAlexW3105146261

What OpenQuestion holds

Textmetadata
LicenceTDM
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.