Evidence map›Paper›PMID 40286630›Full record

ArticleJournal of biomechanics2025

Constrained optimization of scaffold behavior for improving tissue engineered vascular grafts.

Ryan M Hsu, Jason M Szafron, Camila C Carvalho, Jay D Humphrey, Alison L Marsden

Abstract read
In one paragraph

Article in Journal of biomechanics, 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.

Ryan M HsuDepartment of Biomedical Engineering, Yale University, United States of America. Electronic address: ryan.hsu@yale.edu.
Jason M SzafronDepartment of Pediatrics, Stanford University, United States of America; Cardiovascular Institute, Stanford University, United States of America; Department of Biomedical Engineering, Carnegie Mellon University, United States of America. Electronic address: jszafron@andrew.cmu.edu.
Camila C CarvalhoDepartment of Bioengineering, Stanford University, United States of America. Electronic address: camila_carvalho@brown.edu.
Jay D HumphreyDepartment of Biomedical Engineering, Yale University, United States of America. Electronic address: jay.humphrey@yale.edu.
Alison L MarsdenDepartment of Pediatrics, Stanford University, United States of America; Cardiovascular Institute, Stanford University, United States of America; Department of Bioengineering, Stanford University, United States of America. Electronic address: amarsden@stanford.edu.

Funding

Improving Tissue Engineered Vascular Graft Performance via Computational ModelingR01HL139796 · NHLBI · RESEARCH INST NATIONWIDE CHILDREN'S HOSP · PI BREUER, CHRISTOPHER KANE, HUMPHREY, JAY D. · 2018 to 2025
$6.4M
NHLBI NIH HHS R01 HL139796
6 · The paper itself

Abstract

Tissue engineered vascular grafts can offer long-term benefits in matching the geometry, properties, and function of native blood vessels. Yet, choosing appropriate design parameters for biodegradeable scaffolds such that they evolve into neovessels with favorable characteristics is challenging with iterative experimental testing alone. Herein, we present an in silico framework for constrained optimization of scaffold microstructure, mechanical behavior, and degradation kinetics. Our approach combines a biomechanical model of growth and remodeling informed by large animal experiments with numerical optimization to identify design parameters that limit clinically relevant failure modes, including stenosis and dilatation, and improve functional matching to native vessel compliance. Towards this end, constraints on geometry were introduced as a straightforward way to prevent adverse remodeling outcomes and shown to be useful in shaping desired outcomes in graft remodeling. Our simulations of long-term graft evolution suggest the need for a modest initial immune response to ensure graded load transfer from polymer to neotissue and to prevent extreme changes in diameter. Optimized designs showed less sensitivity to simulated variability in their design parameters, which could limit subject-to-subject variability. Together, these findings highlight the utility of computational modeling in identifying candidate designs for improved outcomes in tissue engineered vascular grafts - elimination of stenosis/aneurysm, better compliance matching, and consistent changes in behavior over time.

Indexed as

Blood Vessel ProsthesisModels, CardiovascularTissue EngineeringTissue ScaffoldsAnimalsBiomechanical PhenomenaComputer SimulationHumansComputational optimizationGrowth and remodelingMechanobiologyScaffoldVascular graft

Identifiers

PMID40286630
PMCPMC12085276

What OpenQuestion holds

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Registered trials

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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.