Evidence map›Paper›PMID 23533576›Full record

ArticlePloS one2013

Rule-based model of vein graft remodeling.

Minki Hwang, Marc Garbey, Scott A Berceli, Rongling Wu, Zhihua Jiang, Roger Tran-Son-Tay

Open access · goldAbstract read
In one paragraph

Article in PloS one, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 15 papers.

0numbers the graph read from it
0cells of the map it votes in
15citing papers in PubMed
2.0field-weighted citation impact, top 14% 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

15 citing papers in PubMed, 18 citations in OpenAlex.

  1. Article
  2. Article
  3. Review
  4. Article
  5. A computational bio-chemo-mechanical model of in vivo tissue-engineered vascular graft development.Integrative biology : quantitative biosciences from nano to macro · 2020
    Article
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  12. Review
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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 4 institutions in 1 country.

Minki HwangDepartment of Mechanical Engineering, University of Florida, Gainesville, Florida, United States of America.
Marc Garbey
Scott A Berceli
Rongling Wu
Zhihua Jiang
Roger Tran-Son-Tay
University of Florida · USFlorida College · USPennsylvania State University · USUniversity of Houston · US

Funding

Constitutive and Agent-Based Multiscale Models to Improve Vein Graft SurvivalU01HL119178 · NHLBI · UNIVERSITY OF FLORIDA · PI BERCELI, SCOTT A, GARBEY, MARC · 2013 to 2018
$2.7M
The Dichotomy of Alk1 and Alk5 Signaling Pathways in Vascular Response to InjuryR01HL105764 · NHLBI · UNIVERSITY OF FLORIDA · PI JIANG, ZHIHUA · 2011 to 2015
$1.6M
Multiscale Network Modeling of Hemodynamically-Driven Vascular AdaptationR01HL095508 · NHLBI · UNIVERSITY OF FLORIDA · PI BERCELI, SCOTT A · 2009 to 2012
$1.5M
NHLBI NIH HHS 1R01 HL095508NHLBI NIH HHS R01 HL095508NHLBI NIH HHS R01 HL105764NHLBI NIH HHS U01 HL119178
6 · The paper itself

Abstract

When vein segments are implanted into the arterial system for use in arterial bypass grafting, adaptation to the higher pressure and flow of the arterial system is accomplished thorough wall thickening and expansion. These early remodeling events have been found to be closely coupled to the local hemodynamic forces, such as shear stress and wall tension, and are believed to be the foundation for later vein graft failure. To further our mechanistic understanding of the cellular and extracellular interactions that lead to global changes in tissue architecture, a rule-based modeling method is developed through the application of basic rules of behaviors for these molecular and cellular activities. In the current method, smooth muscle cell (SMC), extracellular matrix (ECM), and monocytes are selected as the three components that occupy the elements of a grid system that comprise the developing vein graft intima. The probabilities of the cellular behaviors are developed based on data extracted from in vivo experiments. At each time step, the various probabilities are computed and applied to the SMC and ECM elements to determine their next physical state and behavior. One- and two-dimensional models are developed to test and validate the computational approach. The importance of monocyte infiltration, and the associated effect in augmenting extracellular matrix deposition, was evaluated and found to be an important component in model development. Final model validation is performed using an independent set of experiments, where model predictions of intimal growth are evaluated against experimental data obtained from the complex geometry and shear stress patterns offered by a mid-graft focal stenosis, where simulation results show good agreements with the experimental data.

Indexed as

AlgorithmsAnimalsApoptosisCell DivisionExtracellular MatrixIn Situ Nick-End LabelingModels, TheoreticalMonocytesMyocytes, Smooth MuscleRabbitsVeins

Identifiers

PMID23533576
PMCPMC3606352
OpenAlexW1974774503

What OpenQuestion holds

Textmetadata
LicenceCC0
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.