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The Materials Map is an open tool for improving networking and interdisciplinary exchange within materials research. It enables cross-database search for cooperation and network partners and discovering of the research landscape.

The dashboard provides detailed information about the selected scientist, e.g. publications. The dashboard can be filtered and shows the relationship to co-authors in different diagrams. In addition, a link is provided to find contact information.

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The Materials Map is still under development. In its current state, it is only based on one single data source and, thus, incomplete and contains duplicates. We are working on incorporating new open data sources like ORCID to improve the quality and the timeliness of our data. We will update Materials Map as soon as possible and kindly ask for your patience.

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in Cooperation with on an Cooperation-Score of 37%

Topics

Publications (1/1 displayed)

  • 2020In Vivo Aortic Magnetic Resonance Elastography in Abdominal Aortic Aneurysm14citations

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Chart of shared publication
Russell, Duncan
1 / 1 shared
Dong, Huiming
1 / 1 shared
Joseph, Matthew E.
1 / 1 shared
White, Richard D.
1 / 1 shared
Kolipaka, Arunark
1 / 1 shared
Mo, Xiaokui
1 / 2 shared
Chart of publication period
2020

Co-Authors (by relevance)

  • Russell, Duncan
  • Dong, Huiming
  • Joseph, Matthew E.
  • White, Richard D.
  • Kolipaka, Arunark
  • Mo, Xiaokui
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article

In Vivo Aortic Magnetic Resonance Elastography in Abdominal Aortic Aneurysm

  • Russell, Duncan
  • Dong, Huiming
  • Litsky, Alan S.
  • Joseph, Matthew E.
  • White, Richard D.
  • Kolipaka, Arunark
  • Mo, Xiaokui
Abstract

<jats:sec><jats:title>Objectives</jats:title><jats:p>Using maximum diameter of an abdominal aortic aneurysm (AAA) alone for management can lead to delayed interventions or unnecessary urgent repairs. Abdominal aortic aneurysm stiffness plays an important role in its expansion and rupture. In vivo aortic magnetic resonance elastography (MRE) was developed to spatially measure AAA stiffness in previous pilot studies and has not been thoroughly validated and evaluated for its potential clinical value. This study aims to evaluate noninvasive in vivo aortic MRE-derived stiffness in an AAA porcine model and investigate the relationships between MRE-derived AAA stiffness and (1) histopathology, (2) uniaxial tensile test, and (3) burst testing for assessing MRE's potential in evaluating AAA rupture risk.</jats:p></jats:sec><jats:sec><jats:title>Materials and Methods</jats:title><jats:p>Abdominal aortic aneurysm was induced in 31 Yorkshire pigs (n = 226 stiffness measurements). Animals were randomly divided into 3 cohorts: 2-week, 4-week, and 4-week-burst. Aortic MRE was sequentially performed. Histopathologic analyses were performed to quantify elastin, collagen, and mineral densities. Uniaxial tensile test and burst testing were conducted to measure peak stress and burst pressure for assessing the ultimate wall strength.</jats:p></jats:sec><jats:sec><jats:title>Results</jats:title><jats:p>Magnetic resonance elastography–derived AAA stiffness was significantly higher than the normal aorta. Significant reduction in elastin and collagen densities as well as increased mineralization was observed in AAAs. Uniaxial tensile test and burst testing revealed reduced ultimate wall strength. Magnetic resonance elastography–derived aortic stiffness correlated to elastin density (<jats:italic toggle="yes">ρ</jats:italic> = −0.68; <jats:italic toggle="yes">P</jats:italic> &lt; 0.0001; n = 60) and mineralization (<jats:italic toggle="yes">ρ</jats:italic> = 0.59; <jats:italic toggle="yes">P</jats:italic> &lt; 0.0001; n = 60). Inverse correlations were observed between aortic stiffness and peak stress (<jats:italic toggle="yes">ρ</jats:italic> = −0.32; <jats:italic toggle="yes">P</jats:italic> = 0.0495; n = 38) as well as burst pressure (<jats:italic toggle="yes">ρ</jats:italic> = −0.55; <jats:italic toggle="yes">P</jats:italic> = 0.0116; n = 20).</jats:p></jats:sec><jats:sec><jats:title>Conclusions</jats:title><jats:p>Noninvasive in vivo aortic MRE successfully detected aortic wall stiffening, confirming the extracellular matrix remodeling observed in the histopathologic analyses. These mural changes diminished wall strength. Inverse correlation between MRE-derived aortic stiffness and aortic wall strength suggests that MRE-derived stiffness can be a potential biomarker for clinically assessing AAA wall status and rupture potential.</jats:p></jats:sec>

Topics
  • density
  • mineral
  • strength
  • size-exclusion chromatography