Ex Vivo mechanical tests and multiscale computational modeling highlight the importance of intramural shear stress in ascending thoracic aortic aneurysms

Christopher E. Korenczuk, Rohit Y. Dhume, Kenneth Liao, Victor H. Barocas

Research output: Contribution to journalArticlepeer-review

16 Scopus citations

Abstract

Ascending thoracic aortic aneurysms (ATAAs) are anatomically complex in terms of architecture and geometry, and both complexities contribute to unpredictability of ATAA dissection and rupture in vivo. The goal of this work was to examine the mechanism of ATAA failure using a combination of detailed mechanical tests on human tissue and a multiscale computational model. We used (1) multiple, geometrically diverse, mechanical tests to characterize tissue properties; (2) a multiscale computational model to translate those results into a broadly usable form; and (3) a model-based computer simulation of the response of an ATAA to the stresses generated by the blood pressure. Mechanical tests were performed in uniaxial extension, biaxial extension, shear lap, and peel geometries. ATAA tissue was strongest in circumferential extension and weakest in shear, presumably because of the collagen and elastin in the arterial lamellae. A multiscale, fiber-based model using different fiber properties for collagen, elastin, and interlamellar connections was specified to match all of the experimental data with one parameter set. Finally, this model was used to simulate ATAA inflation using a realistic geometry. The predicted tissue failure occurred in regions of high stress, as expected; initial failure events involved almost entirely interlamellar connections, consistent with arterial dissection-the elastic lamellae remain intact, but the connections between them fail.

Original languageEnglish (US)
Article number121010
JournalJournal of biomechanical engineering
Volume141
Issue number12
DOIs
StatePublished - Dec 2019
Externally publishedYes

Bibliographical note

Funding Information:
The authors acknowledge the Minnesota Supercomputing Institute (MSI) and UofM hospital at the University of Minnesota for providing high-performance computing resources and tissue, respectively, that contributed to the research results reported within this paper. The authors also recognize and appreciate the technical assistance of Colleen Witzenburg, Ryan Mahutga, Celeste Blum, and Kenzie Trewartha. This work was supported by NIH grants R01 EB005813 and U01 HL139471, and by the National Science Foundation Graduate Research Fellowship Program under Grant No. 00039202 (CEK). Any opinions, findings, and conclusions or recommendations expressed in this material are those of the author(s) and do not necessarily reflect the views of the National Science Foundation. CEK is a recipient of the Richard Pyle Scholar Award from the ARCS Foundation.

Publisher Copyright:
Copyright © 2019 by ASME.

Keywords

  • Artery
  • Biomechanics
  • Cardiovascular
  • Dissection
  • Finite element

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