Evidence map›Paper›PMID 31734412›Full record

ArticleActa biomaterialia2020

Integration of polarized spatial frequency domain imaging (pSFDI) with a biaxial mechanical testing system for quantification of load-dependent collagen architecture in soft collagenous tissues.

Samuel V Jett, Luke T Hudson, Ryan Baumwart, Bradley N Bohnstedt, Arshid Mir, Harold M Burkhart, Gerhard A Holzapfel, Yi Wu, Chung-Hao Lee

Open access · greenAbstract read
In one paragraph

Article in Acta biomaterialia, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 24 papers.

0numbers the graph read from it
0cells of the map it votes in
24citing papers in PubMed
6.6field-weighted citation impact, top 2% 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

24 citing papers in PubMed, 48 citations in OpenAlex.

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  8. Spatial frequency domain Mueller matrix imaging.Journal of biomedical optics · 2022
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  13. AnData in brief · 2021
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  15. Parameterization, geometric modeling, and isogeometric analysis of tricuspid valves.Computer methods in applied mechanics and engineering · 2021
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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

9 authors at 4 institutions in 3 countries.

Samuel V JettBiomechanics and Biomaterials Design Laboratory, School of Aerospace and Mechanical Engineering, Affiliated Faculty Member, Institute for Biomedical Engineering, Science, and Technology, The University of Oklahoma, 865 Asp Ave., Felgar Hall Rm. 219C, Norman, OK 73019-3609, United States.
Luke T HudsonBiomechanics and Biomaterials Design Laboratory, School of Aerospace and Mechanical Engineering, Affiliated Faculty Member, Institute for Biomedical Engineering, Science, and Technology, The University of Oklahoma, 865 Asp Ave., Felgar Hall Rm. 219C, Norman, OK 73019-3609, United States.
Ryan BaumwartCenter for Veterinary Health Sciences, Oklahoma State University, 2065 W. Farm Rd., Stillwater, OK 74078, United States.
Bradley N BohnstedtDepartment of Neurosurgery, The University of Oklahoma Health Sciences Center, 1000 N Lincoln Blvd #400, Oklahoma City, OK 73104, United States.
Arshid MirDivision of Pediatric Cardiology, Department of Pediatrics, The University of Oklahoma Health Sciences Center, 1200 Children's Ave., Suite 2F, Oklahoma City, OK 73104, United States.
Harold M BurkhartDivision of Cardiothoracic Surgery, Department of Surgery, The University of Oklahoma Health Sciences Center, 800 Stanton L. Young Blvd. Suite 9000, Oklahoma City, OK 73104, United States.
Gerhard A HolzapfelInstitute of Biomechanics, Graz University of Technology, Stremayrgasse 16/2 8010 Graz, Austria; Department of Structural Engineering, Norwegian University of Science and Technology (NTNU), 7491 Trondheim, Norway.
Yi WuBiomechanics and Biomaterials Design Laboratory, School of Aerospace and Mechanical Engineering, Affiliated Faculty Member, Institute for Biomedical Engineering, Science, and Technology, The University of Oklahoma, 865 Asp Ave., Felgar Hall Rm. 219C, Norman, OK 73019-3609, United States.
Chung-Hao LeeBiomechanics and Biomaterials Design Laboratory, School of Aerospace and Mechanical Engineering, Affiliated Faculty Member, Institute for Biomedical Engineering, Science, and Technology, The University of Oklahoma, 865 Asp Ave., Felgar Hall Rm. 219C, Norman, OK 73019-3609, United States; Institute for Biomedical Engineering, Science and Technology, The University of Oklahoma, 202 West Boyd St., Norman, OK 73019, United States. Electronic address: ch.lee@ou.edu.
University of Oklahoma · USUniversity of Oklahoma Health Sciences Center · USNorwegian University of Science and Technology · NOOklahoma State University · US

Funding

American Heart Association-American Stroke Association 16SDG27760143
6 · The paper itself

Abstract

Collagen fiber networks provide the structural strength of tissues, such as tendons, skin and arteries. Quantifying the fiber architecture in response to mechanical loads is essential towards a better understanding of the tissue-level mechanical behaviors, especially in assessing disease-driven functional changes. To enable novel investigations into these load-dependent fiber structures, a polarized spatial frequency domain imaging (pSFDI) device was developed and, for the first time, integrated with a biaxial mechanical testing system. The integrated instrument is capable of a wide-field quantification of the fiber orientation and the degree of optical anisotropy (DOA), representing the local degree of fiber alignment. The opto-mechanical instrument''s performance was assessed through uniaxial loading on tendon tissues with known collagen fiber microstructures. Our results revealed that the bulk fiber orientation angle of the tendon tissue changed minimally with loading (median ± 0.5*IQR of 52.7° ± 3.3° and 51.9° ± 3.3° under 0 and 3% longitudinal strains, respectively), whereas on a micro-scale, the fibers became better aligned with the direction of loading: the DOA (mean ± SD) increased from 0.149 ± 0.032 to 0.198 ± 0.056 under 0 and 3% longitudinal strains, respectively, p < 0.001. The integrated instrument was further applied to study two representative mitral valve anterior leaflet (MVAL) tissues subjected to various biaxial loads. The fiber orientations within these representative MVAL tissue specimens demonstrated noticeable heterogeneity, with the local fiber orientations dependent upon the sample, the spatial and transmural locations, and the applied loading. Our results also showed that fibers were generally better aligned under equibiaxial (DOA = 0.089 ± 0.036) and circumferentially-dominant loading (DOA = 0.086 ± 0.037) than under the radially-dominant loading (DOA = 0.077 ± 0.034), indicating circumferential predisposition. These novel findings exemplify a deeper understanding of the load-dependent collagen fiber microstructures obtained through the use of the integrated opto-mechanical instrument. STATEMENT OF SIGNIFICANCE: In this study, a novel quantitative opto-mechanical system was developed by combining a polarized Spatial Frequency Domain Imaging (pSFDI) device with a biaxial mechanical tester. The integrated system was used to quantify the load-dependent collagen fiber microstructures in representative tendon and mitral valve anterior leaflet (MVAL) tissues. Our results revealed that MVAL's fiber architectures exhibited load-dependent spatial and transmural heterogeneities, suggesting further microstructural complexity than previously reported in heart valve tissues. These novel findings were possible through the system's ability to, for the first time, capture the load-dependent collagen architecture in the mitral valve anterior leaflet tissue over a wide field of view (e.g., 10 × 10 mm for the MVAL tissue specimens). Such capabilities afford unique future opportunities to improve patient outcomes through concurrent mechanical and microstructural assessments of healthy and diseased tissues in conditions such as heart valve regurgitation and calcification.

Indexed as

AnimalsBiomechanical PhenomenaCattleCollagenMechanical TestsMitral ValveOptical ImagingSwineTendonsCollagenBiaxial loadingCollagen fiber architectureHeart valveLoad-dependenceMicrostructurePolarization imagingQuantitative optical technique

Identifiers

PMID31734412
PMCPMC8101699
OpenAlexW2988602903

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.