Evidence map›Paper›PMID 26993683›Full record

ArticleJournal of vascular surgery. Venous and lymphatic disorders2015

Recanalization and flow regulate venous thrombus resolution and matrix metalloproteinase expression in vivo.

Christine Chabasse, Suzanne A Siefert, Mohammed Chaudry, Mark H Hoofnagle, Brajesh K Lal, Rajabrata Sarkar

Open access · greenAbstract read
In one paragraph

Article in Journal of vascular surgery. Venous and lymphatic disorders, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed
0.4field-weighted citation impact, top 31% 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

4 citing papers in PubMed, 10 citations in OpenAlex.

  1. Article
  2. Article
  3. Serpins in Venous Thrombosis and Venous Thrombus Resolution.Methods in molecular biology (Clifton, N.J.) · 2018
    Article
  4. 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

6 authors at 1 institution in 1 country.

Christine ChabasseCenter for Vascular and Inflammatory Diseases, School of Medicine, University of Maryland, Baltimore, Md; Department of Surgery, School of Medicine, University of Maryland, Baltimore, Md.
Suzanne A SiefertCenter for Vascular and Inflammatory Diseases, School of Medicine, University of Maryland, Baltimore, Md; Department of Surgery, School of Medicine, University of Maryland, Baltimore, Md.
Mohammed ChaudryCenter for Vascular and Inflammatory Diseases, School of Medicine, University of Maryland, Baltimore, Md; Department of Surgery, School of Medicine, University of Maryland, Baltimore, Md.
Mark H HoofnagleCenter for Vascular and Inflammatory Diseases, School of Medicine, University of Maryland, Baltimore, Md; Department of Surgery, School of Medicine, University of Maryland, Baltimore, Md.
Brajesh K LalDepartment of Surgery, School of Medicine, University of Maryland, Baltimore, Md.
Rajabrata SarkarCenter for Vascular and Inflammatory Diseases, School of Medicine, University of Maryland, Baltimore, Md; Department of Surgery, School of Medicine, University of Maryland, Baltimore, Md. Electronic address: rsarkar@smail.umaryland.edu.
University of Maryland, Baltimore · US

Funding

Vascular Biology Training ProgramT32HL007698 · NHLBI · UNIVERSITY OF MARYLAND BALTIMORE · PI Rosemary A Kozar, Dudley K. Strickland · 1991 to 2026
$8.7M
Training Grant in Cancer BiologyT32CA154274 · NCI · UNIVERSITY OF MARYLAND BALTIMORE · PI Toni M Antalis, CURT I CIVIN · 2011 to 2026
$6.8M
Fibrotic effects and regulation of MMP proteins in thrombus resolutionR01HL083917 · NHLBI · UNIVERSITY OF MARYLAND BALTIMORE · PI SARKAR, RAJABRATA · 2006 to 2009
$1.7M
Role of a Novel Exercise Program to Prevent Post-thrombotic SyndromeI01RX000995 · VA · BALTIMORE VA MEDICAL CENTER · PI LAL, BRAJESH K · 2015 to 2020
–
NCI NIH HHS T32 CA154274NHLBI NIH HHS R01 HL083917NHLBI NIH HHS R01HL083917NHLBI NIH HHS T32 HL007698RRD VA I01 RX000995
6 · The paper itself

Abstract

objectiveWe examined the role of thrombus recanalization and ongoing blood flow in the process of thrombus resolution by comparing two murine in vivo models of deep venous thrombosis.

methodsIn CD1 mice, we performed surgical inferior vena cava ligation (stasis thrombosis), stenosis (thrombosis with recanalization), or sham procedure. We analyzed thrombus weight over time as a measure of thrombus resolution and quantified the messenger RNA and protein levels of membrane-type matrix metalloproteinases (MT-MMPs) as well as effectors of the plasmin complex at days 4, 8, and 12 after surgery.

resultsDespite similar initial thrombus size, the presence of ongoing blood flow (stenosis model) was associated with a 45.91% subsequent improvement in thrombus resolution at day 8 and 12.57% at day 12 compared with stasis thrombosis (ligation model). Immunoblot and real-time polymerase chain reaction analysis demonstrated a difference in MMP-2 and MMP-9 activity at day 8 between the two models (P = .03 and P = .006, respectively) as well as a difference in MT2-MMP gene expression at day 8 (P = .044) and day 12 (P = .03) and MT1-MMP protein expression at day 4 (P = .021). Histologic analyses revealed distinct areas of recanalization in the thrombi of the stenosis model compared with the ligation model as well as the recruitment of inflammatory cells, especially macrophages, and a focal pattern of localized expression of MT1-MMP and MT3-MMP proteins surrounding the areas of recanalization in the stenosis model.

conclusionsRecanalization and ongoing blood flow accelerate deep venous thrombus resolution in vivo and are associated with distinct patterns of MT1-MMP and MT3-MMP expression and macrophage localization in areas of intrathrombus recanalization.

Indexed as

AnimalsDisease Models, AnimalMatrix Metalloproteinase 2Matrix MetalloproteinasesMatrix Metalloproteinases, Membrane-AssociatedMetallothionein 3MiceRNA, MessengerVena Cava, InferiorVenous ThrombosisMatrix Metalloproteinase 2Matrix MetalloproteinasesMatrix Metalloproteinases, Membrane-AssociatedMetallothionein 3Mt3 protein, mouseRNA, Messenger

Identifiers

PMID26993683
PMCPMC4892699
OpenAlexW2130173332

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.