Evidence map›Paper›PMID 37791298›Full record

ReviewJACC. Basic to translational science2023

Inflammasome Signaling, Thromboinflammation, and Venous Thromboembolism.

Nicola Potere, Antonio Abbate, Yogendra Kanthi, Marc Carrier, Stefano Toldo, Ettore Porreca, Marcello Di Nisio

Open access · goldAbstract readReview
In one paragraph

Review in JACC. Basic to translational science, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 37 papers.

0numbers the graph read from it
0cells of the map it votes in
37citing papers in PubMed
10.0field-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

37 citing papers in PubMed, 57 citations in OpenAlex.

  1. Article
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  5. Article
  6. Review
  7. Article
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  10. Article
  11. Review
  12. Article
  13. Regulation of histones in thromboinflammation.Frontiers in immunology · 2026
    Review
  14. Article
  15. Toward targeting of inflammasome signaling in venous thrombosis.Journal of thrombosis and haemostasis : JTH · 2025
    Review
  16. Article
  17. Article
  18. Review
  19. Bridging worlds: a narrative review of IL-17 at the crossroads of inflammation and thrombosis.Inflammation research : official journal of the European Histamine Research Society ... [et al.] · 2025
    Review
  20. Review
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

7 authors at 4 institutions in 3 countries.

Nicola PotereDepartment of Medicine and Ageing Sciences, "G. d'Annunzio" University, Chieti, Italy.
Antonio AbbateRobert M. Berne Cardiovascular Research Center, Department of Medicine, Division of Cardiovascular Medicine, University of Virginia, Charlottesville, Virginia, USA.
Yogendra KanthiVascular Thrombosis & Inflammation Section, Division of Intramural Research, National Heart, Lung, and Blood Institute, National Institutes of Health, Bethesda, Maryland, USA.
Marc CarrierDepartment of Medicine, Ottawa Hospital Research Institute, University of Ottawa, Ottawa, Ontario, Canada.
Stefano ToldoRobert M. Berne Cardiovascular Research Center, Department of Medicine, Division of Cardiovascular Medicine, University of Virginia, Charlottesville, Virginia, USA.
Ettore PorrecaDepartment of Innovative Technologies in Medicine and Dentistry, School of Medicine and Health Sciences, "G. d'Annunzio" University, Chieti, Italy.
Marcello Di NisioDepartment of Medicine and Ageing Sciences, "G. d'Annunzio" University, Chieti, Italy.
University of Chieti-Pescara · ITUniversity of Virginia · USNational Institutes of Health · USUniversity of Ottawa · CA

Funding

Unconventional IL-1 Signaling in Heart failureR01HL150115 · NHLBI · VIRGINIA COMMONWEALTH UNIVERSITY · PI ABBATE, ANTONIO, TOLDO, STEFANO · 2020 to 2024
$1.9M
NHLBI NIH HHS R01 HL150115
6 · The paper itself

Abstract

Venous thromboembolism (VTE) remains a major health burden despite anticoagulation advances, suggesting incomplete management of pathogenic mechanisms. The NLRP3 (NACHT-, LRR- and pyrin domain-containing protein 3) inflammasome, interleukin (IL)-1, and pyroptosis are emerging contributors to the inflammatory pathogenesis of VTE. Inflammasome pathway activation occurs in patients with VTE. In preclinical models, inflammasome signaling blockade reduces venous thrombogenesis and vascular injury, suggesting that this therapeutic approach may potentially maximize anticoagulation benefits, protecting from VTE occurrence, recurrence, and ensuing post-thrombotic syndrome. The nonselective NLRP3 inhibitor colchicine and the anti-IL-1β agent canakinumab reduce atherothrombosis without increasing bleeding. Rosuvastatin reduces primary venous thrombotic events at least in part through lipid-lowering independent mechanisms, paving the way to targeted anti-inflammatory strategies in VTE. This review outlines recent preclinical and clinical evidence supporting a role for inflammasome pathway activation in venous thrombosis, and discusses the, yet unexplored, therapeutic potential of modulating inflammasome signaling to prevent and manage VTE.

Indexed as

anti-inflammatory agentsblood coagulationembolism and thrombosisinflammationinterleukin-1post-thrombotic syndrome

Identifiers

PMID37791298
PMCPMC10544095
OpenAlexW4379616735

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.