Evidence map›Paper›PMID 33568740›Full record

ArticleScientific reports2021

A pilot study on biaxial mechanical, collagen microstructural, and morphological characterizations of a resected human intracranial aneurysm tissue.

Devin W Laurence, Hannah Homburg, Feng Yan, Qinggong Tang, Kar-Ming Fung, Bradley N Bohnstedt, Gerhard A Holzapfel, Chung-Hao Lee

Open access · goldAbstract readCase Reports
In one paragraph

Article in Scientific reports, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers.

0numbers the graph read from it
0cells of the map it votes in
13citing papers in PubMed
2.3field-weighted citation impact, top 10% 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

13 citing papers in PubMed, 28 citations in OpenAlex.

  1. Article
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  6. Article
  7. Computational Fluid Dynamic Simulations of Cerebral Aneurysms.Advances in experimental medicine and biology · 2024
    Review
  8. Article
  9. 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

8 authors at 4 institutions in 3 countries.

Devin W LaurenceBiomechanics and Biomaterials Design Laboratory (BBDL), School of Aerospace and Mechanical Engineering, The University of Oklahoma, 865 Asp Ave., Felgar Hall 219C, Norman, 73019, USA.
Hannah HomburgDepartment of Neurosurgery, The University of Oklahoma Health Sciences Center, Oklahoma City, 73104, USA.
Feng YanBiophotonic Imaging Laboratory, Stephenson School of Biomedical Engineering, The University of Oklahoma, Norman, 73019, USA.
Qinggong TangBiophotonic Imaging Laboratory, Stephenson School of Biomedical Engineering, The University of Oklahoma, Norman, 73019, USA.
Kar-Ming FungDepartment of Pathology, The University of Oklahoma Health Sciences Center, Oklahoma City, 73104, USA.
Bradley N BohnstedtDepartment of Neurological Surgery, Indiana University School of Medicine, Indianapolis, IN, 46202, USA.
Gerhard A HolzapfelInstitute of Biomechanics, Graz University of Technology, 8010, Graz, Austria.
Chung-Hao LeeBiomechanics and Biomaterials Design Laboratory (BBDL), School of Aerospace and Mechanical Engineering, The University of Oklahoma, 865 Asp Ave., Felgar Hall 219C, Norman, 73019, USA. ch.lee@ou.edu.
University of Oklahoma · USUniversity of Oklahoma Health Sciences Center · USGraz University of Technology · ATNeurological Surgery · US

Funding

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

Abstract

Intracranial aneurysms (ICAs) are focal dilatations that imply a weakening of the brain artery. Incidental rupture of an ICA is increasingly responsible for significant mortality and morbidity in the American's aging population. Previous studies have quantified the pressure-volume characteristics, uniaxial mechanical properties, and morphological features of human aneurysms. In this pilot study, for the first time, we comprehensively quantified the mechanical, collagen fiber microstructural, and morphological properties of one resected human posterior inferior cerebellar artery aneurysm. The tissue from the dome of a right posterior inferior cerebral aneurysm was first mechanically characterized using biaxial tension and stress relaxation tests. Then, the load-dependent collagen fiber architecture of the aneurysm tissue was quantified using an in-house polarized spatial frequency domain imaging system. Finally, optical coherence tomography and histological procedures were used to quantify the tissue's microstructural morphology. Mechanically, the tissue was shown to exhibit hysteresis, a nonlinear stress-strain response, and material anisotropy. Moreover, the unloaded collagen fiber architecture of the tissue was predominantly aligned with the testing Y-direction and rotated towards the X-direction under increasing equibiaxial loading. Furthermore, our histological analysis showed a considerable damage to the morphological integrity of the tissue, including lack of elastin, intimal thickening, and calcium deposition. This new unified characterization framework can be extended to better understand the mechanics-microstructure interrelationship of aneurysm tissues at different time points of the formation or growth. Such specimen-specific information is anticipated to provide valuable insight that may improve our current understanding of aneurysm growth and rupture potential.

Indexed as

Stress, MechanicalAnisotropyBiomechanical PhenomenaCollagenElastinHumansIntracranial AneurysmPilot ProjectsTensile StrengthCollagenElastin

Identifiers

PMID33568740
PMCPMC7876029
OpenAlexW3126587070

What OpenQuestion holds

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LicenceCC BY
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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.