Evidence map›Paper›PMID 23976792›Full record

ArticleJournal of the mechanics and physics of solids2013

On the effect of prestrain and residual stress in thin biological membranes.

Manuel K Rausch, Ellen Kuhl

Abstract read
In one paragraph

Article in Journal of the mechanics and physics of solids, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 37 papers.

0numbers the graph read from it
0cells of the map it votes in
37citing 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

37 citing papers in PubMed.

  1. Trial
  2. Article
  3. Article
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  5. Article
  6. Article
  7. Article
  8. A design-based model of the aortic valve for fluid-structure interaction.Biomechanics and modeling in mechanobiology · 2021
    Article
  9. Review
  10. Article
  11. Article
  12. Article
  13. Article
  14. Tricuspid valve leaflet strains in the beating ovine heart.Biomechanics and modeling in mechanobiology · 2019
    Article
  15. Increased Cell Traction-Induced Prestress in Dynamically Cultured Microtissues.Frontiers in bioengineering and biotechnology · 2019
    Article
  16. Improving tissue expansion protocols through computational modeling.Journal of the mechanical behavior of biomedical materials · 2018
    Article
  17. Article
  18. Review
  19. Computational virtual evaluation of the effect of annuloplasty ring shape.International journal for numerical methods in biomedical engineering · 2017
    Article
  20. Modeling molecular mechanisms in the axon.Computational mechanics · 2017
    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

2 authors.

Manuel K RauschDepartment of Mechanical Engineering, Stanford, California, USA.
Ellen Kuhl

Funding

Physics-based Simulation of Biological Structures(RMI)U54GM072970 · NIGMS · STANFORD UNIVERSITY · PI ALTMAN, RUSS BIAGIO · 2004 to 2013
$33.5M
NIGMS NIH HHS U54 GM072970
6 · The paper itself

Abstract

Understanding the difference between ex vivo and in vivo measurements is critical to interpret the load carrying mechanisms of living biological systems. For the past four decades, the ex vivo stiffness of thin biological membranes has been characterized using uniaxial and biaxial tests with remarkably consistent stiffness parameters, even across different species. Recently, the in vivo stiffness was characterized using combined imaging techniques and inverse finite element analyses. Surprisingly, ex vivo and in vivo stiffness values differed by up to three orders of magnitude. Here, for the first time, we explain this tremendous discrepancy using the concept of prestrain. We illustrate the mathematical modeling of prestrain in nonlinear continuum mechanics through the multiplicative decomposition of the total elastic deformation into prestrain-induced and load-induced parts. Using in vivo measured membrane kinematics and associated pressure recordings, we perform an inverse finite element analysis for different prestrain levels and show that the resulting membrane stiffness may indeed differ by four orders of magnitude depending on the prestrain level. Our study motivates the hypothesis that prestrain is important to position thin biological membranes in vivo into their optimal operating range, right at the transition point of the stiffening regime. Understanding the effect of prestrain has direct clinical implications in regenerative medicine, medical device design, and and tissue engineering of replacement constructs for thin biological membranes.

Indexed as

finite element methodmitral leafletparameter identificationprestrainresidual strainresidual stress

Identifiers

PMID23976792
PMCPMC3747014

What OpenQuestion holds

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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.