Evidence map›Paper›PMID 33774926›Full record

ReviewJournal of thrombosis and haemostasis : JTH2021

Targeting von Willebrand factor in liver diseases: A novel therapeutic strategy?

Dafna J Groeneveld, Lauren G Poole, James P Luyendyk

Open access · greenAbstract readReview
In one paragraph

Review in Journal of thrombosis and haemostasis : JTH, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 25 papers.

0numbers the graph read from it
0cells of the map it votes in
25citing papers in PubMed
2.6field-weighted citation impact, top 8% 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

25 citing papers in PubMed, 33 citations in OpenAlex.

  1. Noninvasive Tests for Predicting Decompensation in Compensated Advanced Chronic Liver Disease: A Comprehensive Review.Liver international : official journal of the International Association for the Study of the Liver · 2026
    Review
  2. Article
  3. Article
  4. Article
  5. Review
  6. Allele-selective von Willebrand factor silencing.Research and practice in thrombosis and haemostasis · 2026
    Article
  7. Review
  8. Article
  9. Article
  10. Review
  11. Review
  12. [New targets for the prevention and treatment of cirrhotic portal vein thrombosis].Zhonghua gan zang bing za zhi = Zhonghua ganzangbing zazhi = Chinese journal of hepatology · 2024
    Review
  13. Article
  14. Review
  15. Article
  16. Article
  17. Article
  18. Article
  19. Mechanisms of ADAMTS13 regulation.Journal of thrombosis and haemostasis : JTH · 2022
    Review
  20. 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

3 authors at 1 institution in 1 country.

Dafna J GroeneveldDepartment of Pathobiology & Diagnostic Investigation, Michigan State University, East Lansing, MI, USA.ORCID 0000-0002-1207-5769
Lauren G PooleDepartment of Pathobiology & Diagnostic Investigation, Michigan State University, East Lansing, MI, USA.
James P LuyendykDepartment of Pathobiology & Diagnostic Investigation, Michigan State University, East Lansing, MI, USA.
Michigan State University · US

Funding

Novel anti-fibrotic mechanisms in chemical-induced liver injuryR01ES017537 · NIEHS · UNIVERSITY OF KANSAS MEDICAL CENTER · PI LUYENDYK, JAMES P · 2009 to 2019
$3.6M
Novel determinants of fibrinogen pro-repair activity in acetaminophen-induced liver toxicityR01DK120289 · NIDDK · MICHIGAN STATE UNIVERSITY · PI LUYENDYK, JAMES P · 2019 to 2023
$2.2M
Novel coagulation-dependent mechanisms of liver regeneration to detect and prevent liver dysfunction after partial hepatectomyR01DK122813 · NIDDK · MICHIGAN STATE UNIVERSITY · PI LUYENDYK, JAMES P · 2020 to 2024
$2.0M
Mechanisms of fibrin(ogen)-directed macrophage activation in liver toxicityF32DK121423 · NIDDK · MICHIGAN STATE UNIVERSITY · PI POOLE, LAUREN G · 2019 to 2019
$62k
NIDDK NIH HHS DK120289NIDDK NIH HHS DK122813NIDDK NIH HHS F32 DK121423NIDDK NIH HHS R01 DK120289NIDDK NIH HHS R01 DK122813NIEHS NIH HHS ES017537NIEHS NIH HHS R01 ES017537
6 · The paper itself

Abstract

Acute and chronic liver disease are associated with substantial alterations in the hemostatic system. Evidence from both experimental and clinical studies suggests that anticoagulants slow the progression of liver disease. Efficacy of those anticoagulant drugs is, in part, attributed to a reduction of microthrombi formation within the liver. Although anticoagulant drugs show promising results, bleeding risk associated with these drugs is an obvious drawback, particularly in patients with a complex coagulopathy driven by decreased liver function. Identifying therapies that reduce intrahepatic thrombosis with minimal bleeding risk would significantly advance the field. Among the hemostatic alterations observed in patients are substantially increased levels of the platelet-adhesive protein von Willebrand factor (VWF). In contrast, levels of A Disintegrin and Metalloproteinase with Thrombospondin motifs, the enzyme that regulates VWF activity, are significantly reduced in patients with liver disease. Highly elevated VWF levels are proposed to accelerate intrahepatic thrombus formation and thus be a driver of disease progression. Strong clinical evidence suggesting a link between liver disease and changes in VWF is now being matched by emerging mechanistic data showing a detrimental role for VWF in the progression of liver disease. This review focuses on clinical and experimental evidence supporting a connection between VWF function and the progression of acute and chronic liver diseases. Furthermore, with the recent anticipated approval of several novel therapies targeting VWF, we discuss potential strategies and benefits of targeting VWF as an innovative therapy for patients with liver disease.

Indexed as

Liver DiseasesThrombosisvon Willebrand DiseasesADAMTS13 ProteinBlood PlateletsHemostasisHumansvon Willebrand FactorADAMTS13 Proteinvon Willebrand FactorADAMTS13 proteinblood plateletsfibrosisliver failurevon Willebrand factor

Identifiers

PMID33774926
PMCPMC8582603
OpenAlexW3149553378

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.