Evidence map›Paper›PMID 31065952›Full record

ArticleBiomechanics and modeling in mechanobiology2019

A computational model for understanding the micro-mechanics of collagen fiber network in the tunica adventitia.

Venkat Ayyalasomayajula, Baptiste Pierrat, Pierre Badel

Open access · hybridAbstract read
In one paragraph

Article in Biomechanics and modeling in mechanobiology, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
0.9field-weighted citation impact, top 31% 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

2 citing papers in PubMed, 28 citations in OpenAlex.

  1. Article
  2. [Experimental measurement and modeling analysis of active and passive mechanical properties of arterial vessel wall].Sheng wu yi xue gong cheng xue za zhi = Journal of biomedical engineering = Shengwu yixue gongchengxue zazhi · 2020
    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

3 authors at 1 institution in 1 country.

Venkat AyyalasomayajulaMines Saint-Étienne, Univ Lyon, Univ Jean Monnet, INSERM, U1059 SAINBIOSE, Centre CIS, 42023, Saint-Étienne, France. radhakrishna300792@gmail.com.ORCID http://orcid.org/0000-0002-0158-6723
Baptiste PierratMines Saint-Étienne, Univ Lyon, Univ Jean Monnet, INSERM, U1059 SAINBIOSE, Centre CIS, 42023, Saint-Étienne, France.
Pierre BadelMines Saint-Étienne, Univ Lyon, Univ Jean Monnet, INSERM, U1059 SAINBIOSE, Centre CIS, 42023, Saint-Étienne, France.
Université Claude Bernard Lyon 1 · FR

Funding

H2020 European Research Council 638804
6 · The paper itself

Abstract

Abdominal aortic aneurysm is a prevalent cardiovascular disease with high mortality rates. The mechanical response of the arterial wall relies on the organizational and structural behavior of its microstructural components, and thus, a detailed understanding of the microscopic mechanical response of the arterial wall layers at loads ranging up to rupture is necessary to improve diagnostic techniques and possibly treatments. Following the common notion that adventitia is the ultimate barrier at loads close to rupture, in the present study, a finite element model of adventitial collagen network was developed to study the mechanical state at the fiber level under uniaxial loading. Image stacks of the rabbit carotid adventitial tissue at rest and under uniaxial tension obtained using multi-photon microscopy were used in this study, as well as the force-displacement curves obtained from previously published experiments. Morphological parameters like fiber orientation distribution, waviness, and volume fraction were extracted for one sample from the confocal image stacks. An inverse random sampling approach combined with a random walk algorithm was employed to reconstruct the collagen network for numerical simulation. The model was then verified using experimental stress-stretch curves. The model shows the remarkable capacity of collagen fibers to uncrimp and reorient in the loading direction. These results further show that at high stretches, collagen network behaves in a highly non-affine manner, which was quantified for each sample. A comprehensive parameter study to understand the relationship between structural parameters and their influence on mechanical behavior is presented. Through this study, the model was used to conclude important structure-function relationships that control the mechanical response. Our results also show that at loads close to rupture, the probability of failure occurring at the fiber level is up to 2%. Uncertainties in usually employed rupture risk indicators and the stochastic nature of the event of rupture combined with limited knowledge on the microscopic determinants motivate the development of such an analysis. Moreover, this study will advance the study of coupling microscopic mechanisms to rupture of the artery as a whole.

Indexed as

Models, CardiovascularAdventitiaAlgorithmsAnimalsBiomechanical PhenomenaComputer SimulationFibrillar CollagensFinite Element AnalysisMaleNonlinear DynamicsPorosityProbabilityRabbitsReproducibility of ResultsStress, MechanicalTensile StrengthFibrillar CollagensCollagen fibersFinite elementsRuptureTunica adventitia

Identifiers

PMID31065952
PMCPMC6748894
OpenAlexW2943865891

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.