Evidence map›Paper›PMID 37699504›Full record

ArticleActa biomaterialia2023

A viscoelastic constitutive model for human femoropopliteal arteries.

Will Zhang, Majid Jadidi, Sayed Ahmadreza Razian, Gerhard A Holzapfel, Alexey Kamenskiy, David A Nordsletten

Open access · greenAbstract read
In one paragraph

Article in Acta biomaterialia, 2023. 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
1.8field-weighted citation impact, top 16% 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

6 citing papers in PubMed, 16 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Mechanical, structural, and morphological differences in the iliac arteries.Journal of the mechanical behavior of biomedical materials · 2024
    Article
  5. Review
  6. 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

6 authors at 4 institutions in 4 countries.

Will ZhangDepartment of Biomedical Engineering, University of Michigan, Ann Arbor, MI, USA. Electronic address: willwz@umich.edu.
Majid JadidiDepartment of Biomechanics, University of Nebraska at Omaha, Omaha, NE, USA. Electronic address: mjadidi@unomaha.edu.
Sayed Ahmadreza RazianDepartment of Biomechanics, University of Nebraska at Omaha, Omaha, NE, USA. Electronic address: srazian@unomaha.edu.
Gerhard A HolzapfelInstitute of Biomechanics, Graz Univerisity of Technology, Graz, Austria; Department of Structural Engineering, Norwegian University of Science and Technology, Trondheim, Norway. Electronic address: holzapfel@tugraz.at.
Alexey KamenskiyDepartment of Biomechanics, University of Nebraska at Omaha, Omaha, NE, USA. Electronic address: akamenskiy@unomaha.edu.
David A NordslettenDepartment of Biomedical Engineering, University of Michigan, Ann Arbor, MI, USA; Division of Biomedical Engineering and Imaging Sciences, Department of Biomedical Engineering, King's College London, London, UK. Electronic address: nordslet@umich.edu.
University of Nebraska at Omaha · USKing's College London · GBNorwegian University of Science and Technology · NOUniversity of Michigan · US

Funding

Optimized Stents for the Femoropopliteal ArteryR01HL125736 · NHLBI · UNIVERSITY OF NEBRASKA OMAHA · PI KAMENSKIY, ALEXEY, MACTAGGART, JASON · 2015 to 2024
$6.3M
Effect of cell-based therapies on functional, hemodynamic, and histologic outcomes in a porcine model of peripheral arterial diseaseR01AG062198 · NIA · UNIVERSITY OF NEBRASKA MEDICAL CENTER · PI CARLSON, MARK A, PIPINOS, IRAKLIS ILIAS · 2019 to 2023
$3.1M
Effects of aortic compliance and Windkessel reduction on cardiac and aortic pathophysiologyR01HL147128 · NHLBI · UNIVERSITY OF NEBRASKA OMAHA · PI DESYATOVA, ANASTASIA S · 2019 to 2023
$3.0M
NHLBI NIH HHS R01 HL125736NHLBI NIH HHS R01 HL147128NIA NIH HHS R01 AG062198
6 · The paper itself

Abstract

High failure rates present challenges for surgical and interventional therapies for peripheral artery disease of the femoropopliteal artery (FPA). The FPA's demanding biomechanical environment necessitates complex interactions with repair devices and materials. While a comprehensive understanding of the FPA's mechanical characteristics could improve medical treatments, the viscoelastic properties of these muscular arteries remain poorly understood, and the constitutive model describing their time-dependent behavior is absent. We introduce a new viscoelastic constitutive model for the human FPA grounded in its microstructural composition. The model is capable of detailing the contributions of each intramural component to the overall viscoelastic response. Our model was developed utilizing fractional viscoelasticity and tested using biaxial experimental data with hysteresis and relaxation collected from 10 healthy human subjects aged 57 to 65 and further optimized for high throughput and automation. The model accurately described the experimental data, capturing significant nonlinearity and hysteresis that were particularly pronounced circumferentially, and tracked the contribution of passive smooth muscle cells to viscoelasticity that was twice that of the collagen fibers. The high-throughput parameter estimation procedure we developed included a specialized objective function and modifications to enhance convergence for the common exponential-type fiber laws, facilitating computational implementation. Our new model delineates the time-dependent behavior of human FPAs, which will improve the fidelity of computational simulations investigating device-artery interactions and contribute to their greater physical accuracy. Moreover, it serves as a useful tool to investigate the contribution of arterial constituents to overall tissue viscoelasticity, thereby expanding our knowledge of arterial mechanophysiology. STATEMENT OF SIGNIFICANCE: The demanding biomechanical environment of the femoropopliteal artery (FPA) necessitates complex interactions with repair devices and materials, but the viscoelastic properties of these muscular arteries remain poorly understood with the constitutive model describing their time-dependent behavior being absent. We hereby introduce the first viscoelastic constitutive model for the human FPA grounded in its microstructures. This model was tested using biaxial mechanical data collected from 10 healthy human subjects between the ages of 57 to 65. It can detail the contributions of each intramural component to the overall viscoelastic response, showing that the contribution of passive smooth muscle cells to viscoelasticity is twice that of collagen fibers. The usefulness of this model as tool to better understand arterial mechanophysiology was demonstrated.

Indexed as

Femoral ArteryPeripheral Arterial DiseaseAgedBiomechanical PhenomenaCollagenElasticityHumansMiddle AgedModels, BiologicalStress, MechanicalViscosityCollagenConstitutive modelingHuman femoropopliteal arteryNonlinear elasticity,Tissue mechanicsViscoelasticity

Identifiers

PMID37699504
PMCPMC10802972
OpenAlexW4386588959

What OpenQuestion holds

Textmetadata
LicenceTDM
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.