Evidence map›Paper›PMID 24210474›Full record

ArticleJournal of biomechanics2014

Computational model of the in vivo development of a tissue engineered vein from an implanted polymeric construct.

K S Miller, Y U Lee, Y Naito, C K Breuer, J D Humphrey

Abstract read
In one paragraph

Article in Journal of biomechanics, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 32 papers.

0numbers the graph read from it
0cells of the map it votes in
32citing 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

32 citing papers in PubMed.

  1. Postnatal pulmonary artery development from transcript to tissue.Journal of the Royal Society, Interface · 2026
    Article
  2. Article
  3. Article
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  6. Tissue Engineering of Vascular Grafts: A Case Report From Bench to Bedside and Back.Arteriosclerosis, thrombosis, and vascular biology · 2023
    Review
  7. Article
  8. Article
  9. Article
  10. Review
  11. Vascular adaptation in the presence of external support - A modeling study.Journal of the mechanical behavior of biomedical materials · 2020
    Article
  12. Review
  13. Cell signaling model for arterial mechanobiology.PLoS computational biology · 2020
    Article
  14. A computational bio-chemo-mechanical model of in vivo tissue-engineered vascular graft development.Integrative biology : quantitative biosciences from nano to macro · 2020
    Article
  15. Article
  16. Article
  17. Article
  18. Article
  19. Degradation andRegenerative medicine · 2019
    Article
  20. Mechanobiological Stability of Biological Soft Tissues.Journal of the mechanics and physics of solids · 2019
    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

5 authors.

K S MillerDepartment of Biomedical Engineering, Yale University, New Haven, CT, USA.
Y U LeeSurgical Research and Regenerative Medicine, Nationwide Children's Hospital, Columbus, OH, USA.
Y NaitoVascular Biology and Therapeutics Program, Yale School of Medicine, New Haven, CT, USA.
C K BreuerSurgical Research and Regenerative Medicine, Nationwide Children's Hospital, Columbus, OH, USA.
J D HumphreyDepartment of Biomedical Engineering, Yale University, New Haven, CT, USA; Vascular Biology and Therapeutics Program, Yale School of Medicine, New Haven, CT, USA. Electronic address: jay.humphrey@yale.edu.

Funding

Training In Multi-modality Molecular & Translational Cardiovascular ImagingT32HL098069 · NHLBI · YALE UNIVERSITY · PI JAMES S DUNCAN, Georges El Fakhri · 2010 to 2026
$5.2M
Mechanisms of Vascular Neotissue Formation In Tissue Engineered Vascular GraftsR01HL098228 · NHLBI · YALE UNIVERSITY · PI BREUER, CHRISTOPHER KANE · 2010 to 2018
$3.6M
Gender Specific Evolution of Abdominal Aortic Aneurysm Composition and PropertiesR21HL107768 · NHLBI · YALE UNIVERSITY · PI HUMPHREY, JAY D. · 2012 to 2013
$421k
NHLBI NIH HHS 5T32-HL098069NHLBI NIH HHS R01 HL098228NHLBI NIH HHS R01-HL098228NHLBI NIH HHS R21 HL107768NHLBI NIH HHS R21-HL107768NHLBI NIH HHS T32 HL098069
6 · The paper itself

Abstract

Advances in vascular tissue engineering have been tremendous over the past 15 years, yet there remains a need to optimize current constructs to achieve vessels having true growth potential. Toward this end, it has been suggested that computational models may help hasten this process by enabling time-efficient parametric studies that can reduce the experimental search space. In this paper, we present a first generation computational model for describing the in vivo development of a tissue engineered vein from an implanted polymeric scaffold. The model was motivated by our recent data on the evolution of mechanical properties and microstructural composition over 24 weeks in a mouse inferior vena cava interposition graft. It is shown that these data can be captured well by including both an early inflammatory-mediated and a subsequent mechano-mediated production of extracellular matrix. There remains a pressing need, however, for more data to inform the development of next generation models, particularly the precise transition from the inflammatory to the mechanobiological dominated production of matrix having functional capability.

Indexed as

Blood Vessel ProsthesisModels, CardiovascularVena Cava, InferiorAnimalsExtracellular MatrixMiceMice, SCIDPolymersTissue ScaffoldsPolymersConstrained mixture theoryInflammationInterposition graftMechanosensingMouse modelTissue engineering

Identifiers

PMID24210474
PMCPMC3994188

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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.