Evidence map›Paper›PMID 40946806›Full record

ReviewJournal of thrombosis and haemostasis : JTH2025

Toward targeting of inflammasome signaling in venous thrombosis.

Rana Dhar, Rinaldo R Dos Passos, R Michael Gower, Abhishek Jain, Colin E Evans

Abstract readReview
In one paragraph

Review in Journal of thrombosis and haemostasis : JTH, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing 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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

5 authors.

Rana DharCardiovascular Translational Research Center, Department of Cell Biology and Anatomy, University of South Carolina School of Medicine, Columbia, South Carolina, USA.
Rinaldo R Dos PassosCardiovascular Translational Research Center, Department of Cell Biology and Anatomy, University of South Carolina School of Medicine, Columbia, South Carolina, USA.
R Michael GowerDepartment of Biomedical Engineering, University of South Carolina, Columbia, South Carolina, USA; Department of Chemical Engineering, University of South Carolina, Columbia, South Carolina, USA; Veterans Affairs Medical Center, Columbia, South Carolina, USA.
Abhishek JainDepartment of Biomedical Engineering, Texas A&M University, College Station, Texas, USA; Department of Cardiovascular Sciences, Houston Methodist Research Institute, Houston Methodist Hospital, Houston, Texas, USA; Department of Medical Physiology, Texas A&M Health Science Center, Bryan, Texas, USA.
Colin E EvansCardiovascular Translational Research Center, Department of Cell Biology and Anatomy, University of South Carolina School of Medicine, Columbia, South Carolina, USA; Department of Cell Biology and Anatomy, University of South Carolina School of Medicine, Columbia, South Carolina, USA; Institute on Cardiovascular Disease Research, University of South Carolina, Columbia, South Carolina, USA; Department of Biomedical Engineering, University of South Carolina, Columbia, South Carolina, USA. Electronic address: colin.evans@sc.edu.

Funding

South Carolina IDeA Networks of Biomedical Research (SC INBRE V)P20GM103499 · NIGMS · UNIVERSITY OF SOUTH CAROLINA AT COLUMBIA · PI EDIE C GOLDSMITH · 2012 to 2026
$61.0M
NIGMS NIH HHS P20 GM103499
6 · The paper itself

Abstract

Deep vein thrombosis (DVT) is a serious and debilitating vascular condition with sequelae that include postthrombotic syndrome and pulmonary embolism. Current treatments for DVT are limited by their contraindications and suboptimal safety profiles. Pharmacological approaches that safely and effectively reduce thrombus formation are being investigated in laboratory and clinical settings, including agents that aim to inhibit the interplay between thrombosis and inflammation. Recent studies have shown that inflammasome complexes-multiprotein inflammatory complexes activated by pathogen-associated molecular patterns and damage-associated molecular patterns-play a role in the development and propagation of DVT. Thus, inflammasome complexes have attracted considerable interest as possible therapeutic targets for the treatment of DVT. This review summarizes the current knowledge on inflammasome complexes and discusses studies on their role and therapeutic potential in DVT. An improved understanding of inflammasome-dependent regulation of DVT could lead to the development of safe and effective treatments for patients affected by this condition.

Indexed as

Anti-Inflammatory AgentsBlood CoagulationInflammasomesVenous ThrombosisAnimalsHumansInflammation MediatorsMolecular Targeted TherapySignal TransductionAnti-Inflammatory AgentsInflammasomesInflammation Mediatorsinflammasomeinflammationthrombosis

Identifiers

PMID40946806
PMCPMC12628352

What Socratic 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 Socratic graph.