Abstract

Thoracic aortic aneurysm (TAA) is a focal enlargement of the thoracic aorta, but the etiology of this disease is not fully understood. Previous work suggests that various genetic syndromes, congenital defects such as bicuspid aortic valve, hypertension, and age are associated with TAA formation. Though occurrence of TAAs is rare, they can be life-threatening when dissection or rupture occurs. Prevention of these adverse events often requires surgical intervention through full aortic root replacement or implantation of endovascular stent grafts. Currently, aneurysm diameters and expansion rates are used to determine if intervention is warranted. Unfortunately, this approach oversimplifies the complex aortopathy. Improving treatment of TAAs will likely require an increased understanding of the biological and biomechanical factors contributing to the disease. Past studies have substantially contributed to our knowledge of TAAs using various ex vivo, in vivo, and computational methods to biomechanically characterize the thoracic aorta. However, any singular approach typically focuses on only material properties of the aortic wall, intra-aneurysmal hemodynamics, or in vivo vessel dynamics, neglecting combinatorial factors that influence aneurysm development and progression. In this review, we briefly summarize the current understanding of TAA causes, treatment, and progression, before discussing recent advances in biomechanical studies of TAAs and possible future directions. We identify the need for comprehensive approaches that combine multiple characterization methods to study the mechanisms contributing to focal weakening and rupture. We hope this summary and analysis will inspire future studies leading to improved prediction of thoracic aneurysm progression and rupture, improving patient diagnoses and outcomes.

Highlights

  • Thoracic aortic aneurysms (TAAs) are pathological dilations, often associated with genetic disorders or other factors leading to cellular changes, elastic fiber degradation, collagen deposition, and inflammation [1, 2]

  • Use of Fluid-structure interaction (FSI) modeling of the thoracic aorta will likely increase because the results demonstrate that large vessel deformations affect relevant hemodynamic metrics

  • The biomechanical analyses briefly presented in this review illustrate our current understanding of TAA development and progression

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Summary

Introduction

Thoracic aortic aneurysms (TAAs) are pathological dilations, often associated with genetic disorders or other factors leading to cellular changes, elastic fiber degradation, collagen deposition, and inflammation [1, 2]. In this review we present advances in the biomechanical characterization of human and animal TAAs including ex vivo and in vivo mechanical analyses, and modeling of blood flow and the vessel wall. Their findings demonstrate the importance of studying multiple models to increase translational potential as there is no exact phenocopy of human TAAs. Using porcine models has some benefits including sharing similar structure, thickness, and composition to human aortae (Supplementary Table 1) [67].

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