Evidence map›Paper›PMID 34135399›Full record

ArticleScientific reports2021

Assessment with clinical data of a coupled bio-hemodynamics numerical model to predict leukocyte adhesion in coronary arteries.

Umberto Ciri, Ruth L Bennett, Rita Bhui, David S Molony, Habib Samady, Clark A Meyer, Heather N Hayenga, Stefano Leonardi

Open access · goldAbstract read
In one paragraph

Article in Scientific reports, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
0.8field-weighted citation impact, top 27% 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

1 citing paper in PubMed, 4 citations in OpenAlex.

  1. 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

8 authors at 2 institutions in 1 country.

Umberto CiriDepartment of Mechanical Engineering, The University of Texas at Dallas, Richardson, TX, 75080, USA. umberto.ciri@utdallas.edu.
Ruth L BennettDepartment of Mechanical Engineering, The University of Texas at Dallas, Richardson, TX, 75080, USA.
Rita BhuiDepartment of Bioengineering, The University of Texas at Dallas, Richardson, TX, 75080, USA.
David S MolonySchool of Medicine, Emory University, Atlanta, GA, 30303, USA.
Habib SamadySchool of Medicine, Emory University, Atlanta, GA, 30303, USA.
Clark A MeyerDepartment of Bioengineering, The University of Texas at Dallas, Richardson, TX, 75080, USA.
Heather N HayengaDepartment of Bioengineering, The University of Texas at Dallas, Richardson, TX, 75080, USA.
Stefano LeonardiDepartment of Mechanical Engineering, The University of Texas at Dallas, Richardson, TX, 75080, USA.
The University of Texas at Dallas · USEmory University · US

Funding

A computational model of the G&R during atherosclerosis: Integrating mechanics and biologyR01HL136776 · NHLBI · UNIVERSITY OF TEXAS DALLAS · PI HAYENGA, HEATHER NAOMI · 2018 to 2022
$1.9M
6 · The paper itself

Abstract

Numerical simulations of coupled hemodynamics and leukocyte transport and adhesion inside coronary arteries have been performed. Realistic artery geometries have been obtained for a set of four patients from intravascular ultrasound and angiography images. The numerical model computes unsteady three-dimensional blood hemodynamics and leukocyte concentration in the blood. Wall-shear stress dependent leukocyte adhesion is also computed through agent-based modeling rules, fully coupled to the hemodynamics and leukocyte transport. Numerical results have a good correlation with clinical data. Regions where high adhesion is predicted by the simulations coincide to a good approximation with artery segments presenting plaque increase, as documented by clinical data from baseline and six-month follow-up exam of the same artery. In addition, it is observed that the artery geometry and, in particular, the tortuosity of the centerline are a primary factor in determining the spatial distribution of wall-shear stress, and of the resulting leukocyte adhesion patterns. Although further work is required to overcome the limitations of the present model and ultimately quantify plaque growth in the simulations, these results are encouraging towards establishing a predictive methodology for atherosclerosis progress.

Indexed as

Cell AdhesionHemodynamicsModels, CardiovascularCoronary AngiographyCoronary Artery DiseaseCoronary CirculationCoronary VesselsHumansLeukocytesStress, MechanicalUltrasonography

Identifiers

PMID34135399
PMCPMC8208986
OpenAlexW3172353823

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.