Evidence map›Paper›PMID 29715364›Full record

ArticleJournal of biomechanical engineering2018

Quantitative Analysis of Tissue Damage Evolution in Porcine Liver With Interrupted Mechanical Testing Under Tension, Compression, and Shear.

Joseph Chen, Bryn Brazile, Raj Prabhu, Sourav S Patnaik, Robbin Bertucci, Hongjoo Rhee, M F Horstemeyer, Yi Hong, Lakiesha N Williams, Jun Liao

Abstract read
In one paragraph

Article in Journal of biomechanical engineering, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing 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

6 citing papers in PubMed.

  1. Article
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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

10 authors.

Joseph ChenDepartment of Biological Engineering, Mississippi State University, Mississippi State, MS 39762.
Bryn BrazileDepartment of Biological Engineering, Mississippi State University, Mississippi State, MS 39762.
Raj PrabhuDepartment of Biological Engineering, Mississippi State University, Mississippi State, MS 39762.
Sourav S PatnaikDepartment of Biological Engineering, Mississippi State University, Mississippi State, MS 39762.
Robbin BertucciDepartment of Biological Engineering, Mississippi State University, Mississippi State, MS 39762.
Hongjoo RheeCenter for Advanced Vehicular Systems, Mississippi State University, Mississippi State, MS 39762.
M F HorstemeyerCenter for Advanced Vehicular Systems, Mississippi State University, Mississippi State, MS 39762.
Yi HongDepartment of Bioengineering, University of Texas at Arlington, Arlington, TX 79010.
Lakiesha N WilliamsDepartment of Biological Engineering, Mississippi State University, Mississippi State, MS 39762.
Jun LiaoDepartment of Biological Engineering, Mississippi State University, Mississippi State, MS 39762.

Funding

CONTROL OF CARDIAC FIBROSIS TO PREVENT CARDIAC FUNCTION DETERIORATIONR01EB022018 · NIBIB · WASHINGTON UNIVERSITY · PI GUAN, JIANJUN · 2016 to 2018
$1.1M
NIBIB NIH HHS R01 EB022018
6 · The paper itself

Abstract

In this study, the damage evolution of liver tissue was quantified at the microstructural level under tensile, compression, and shear loading conditions using an interrupted mechanical testing method. To capture the internal microstructural changes in response to global deformation, the tissue samples were loaded to different strain levels and chemically fixed to permanently preserve the deformed tissue geometry. Tissue microstructural alterations were analyzed to quantify the accumulated damages, with damage-related parameters such as number density, area fraction, mean area, and mean nearest neighbor distance (NND). All three loading states showed a unique pattern of damage evolution, in which the damages were found to increase in number and size, but decrease in NND as strain level increased. To validate the observed damage features as true tissue microstructural damages, more samples were loaded to the above-mentioned strain levels and then unloaded back to their reference state, followed by fixation. The most major damage-relevant features at higher strain levels remained after the release of the external loading, indicating the occurrence of permanent inelastic deformation. This study provides a foundation for future structure-based constitutive material modeling that can capture and predict the stress-state dependent damage evolution in liver tissue.

Indexed as

Compressive StrengthMaterials TestingShear StrengthStress, MechanicalAnimalsBiomechanical PhenomenaLiverSwineTensile Strength

Identifiers

PMID29715364
PMCPMC5938066

What OpenQuestion holds

Textmetadata
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.