Evidence map›Paper›PMID 34585299›Full record

ArticleBiomechanics and modeling in mechanobiology2021

Computational simulation-derived hemodynamic and biomechanical properties of the pulmonary arterial tree early in the course of ventricular septal defects.

Melody L Dong, Ingrid S Lan, Weiguang Yang, Marlene Rabinovitch, Jeffrey A Feinstein, Alison L Marsden

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In one paragraph

Article in Biomechanics and modeling in mechanobiology, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers.

0numbers the graph read from it
0cells of the map it votes in
12citing papers in PubMed
1.6field-weighted citation impact, top 15% 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

12 citing papers in PubMed, 16 citations in OpenAlex.

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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 1 institution in 1 country.

Melody L DongDepartment of Bioengineering, Stanford University, Stanford, CA, USA.
Ingrid S LanDepartment of Bioengineering, Stanford University, Stanford, CA, USA.
Weiguang YangDepartment of Pediatrics, Stanford University, Stanford, CA, USA.
Marlene RabinovitchDepartment of Pediatrics, Stanford University, Stanford, CA, USA.
Jeffrey A FeinsteinDepartment of Pediatrics and Bioengineering, Stanford University, Stanford, CA, USA.
Alison L MarsdenDepartment of Pediatrics and Bioengineering, Stanford University, Stanford, CA, USA. amarsden@stanford.edu.
Stanford University · US

Funding

High Shear Stress Alters Gene Regulation in Pulmonary Arterial HypertensionR01HL152134 · NHLBI · STANFORD UNIVERSITY · PI RABINOVITCH, MARLENE · 2021 to 2024
$2.9M
SCH: INT: A Virtual Surgery Simulator to Accelerate Medical Training in Cardiovascular Disease R01EB029362 · NIBIB · STANFORD UNIVERSITY · PI MARSDEN, ALISON L · 2019 to 2022
$1.4M
Automated data curation to ensure model credibility in the Vascular Model RepositoryR01LM013120 · NLM · STANFORD UNIVERSITY · PI MARSDEN, ALISON L · 2019 to 2021
$1.0M
NHLBI NIH HHS R01 HL152134NIBIB NIH HHS R01 EB029362NLM NIH HHS R01 LM013120
6 · The paper itself

Abstract

Untreated ventricular septal defects (VSDs) can lead to pulmonary arterial hypertension (PAH) characterized by elevated pulmonary artery (PA) pressure and vascular remodeling, known as PAH associated with congenital heart disease (PAH-CHD). Though previous studies have investigated hemodynamic effects on vascular mechanobiology in late-stage PAH, hemodynamics leading to PAH-CHD initiation have not been fully quantified. We hypothesize that abnormal hemodynamics from left-to-right shunting in early stage VSDs affects PA biomechanical properties leading to PAH initiation. To model PA hemodynamics in healthy, small, moderate, and large VSD conditions prior to the onset of vascular remodeling, computational fluid dynamics simulations were performed using a 3D finite element model of a healthy 1-year-old's proximal PAs and a body-surface-area-scaled 0D distal PA tree. VSD conditions were modeled with increased pulmonary blood flow to represent degrees of left-to-right shunting. In the proximal PAs, pressure, flow, strain, and wall shear stress (WSS) increased with increasing VSD size; oscillatory shear index decreased with increasing VSD size in the larger PA vessels. WSS was higher in smaller diameter vessels and increased with VSD size, with the large VSD condition exhibiting WSS >100 dyn/cm[Formula: see text], well above values typically used to study dysfunctional mechanotransduction pathways in PAH. This study is the first to estimate hemodynamic and biomechanical metrics in the entire pediatric PA tree with VSD severity at the stage leading to PAH initiation and has implications for future studies assessing effects of abnormal mechanical stimuli on endothelial cells and vascular wall mechanics that occur during PAH-CHD initiation and progression.

Indexed as

Computer SimulationBiomechanical PhenomenaHeart Septal Defects, VentricularHemodynamicsHumansInfantMaleModels, BiologicalPulmonary ArteryComputational cardiovascular biomechanicsCongenital heart defectPulmonary arterial hypertensionPulmonary arterial treeVentricular septal defect

Identifiers

PMID34585299
PMCPMC9704055
OpenAlexW3203033704

What Socratic holds

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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.