Intracranial and abdominal aortic aneurysms: Similarities, differences, and need for a new class of computational models

被引:247
作者
Humphrey, J. D. [1 ,2 ]
Taylor, C. A. [3 ,4 ]
机构
[1] Texas A&M Univ, Dept Biomed Engn, College Stn, TX 77843 USA
[2] Texas A&M Univ, ME DeBakey Inst, College Stn, TX USA
[3] Stanford Univ, Dept Bioengn, Stanford, CA 94305 USA
[4] Stanford Univ, Dept Surg, Stanford, CA 94305 USA
关键词
hemodynamics; wall stress; saccular aneurysm; growth and remodeling; cell and matrix turnover; patient-specific modeling;
D O I
10.1146/annurev.bioeng.10.061807.160439
中图分类号
R318 [生物医学工程];
学科分类号
0831 ;
摘要
Intracranial saccular and abdominal aortic aneurysms (ISAs and AAAs, respectively) result from different underlying disease processes and exhibit different rupture potentials, yet they share many histopathological and biornechanical characteristics. Moreover, as in other vascular diseases, heniodynamics and wall mechanics play important roles in the natural history and possible treatment of these two ty es of lesions. The goals of this review, p are twofold: first, to contrast the biology and mechanics of intracranial and abdominal aortic aneurVsms to emphasize that separate advances in our understanding of each disease can aid in our understanding of the other disease, and second, to suggest that research on the biomechanics of aneurysms must embrace a new paradigm for analysis. That is, past bioniechanical studies have provided tremendous insight but have progressed along separate lines, focusing on either the hemodynainics or the wall mechanics. We submit that there is a pressing need to couple in a new way the separate advances in vascular biology, medical imaging, and computational biofluld and biosolid mechanics to understand better the inechanobiology, pathophysiology, and treatment of these lesions, which continue to be responsible for significant inorbiditv and mortality. We refer to this needed new class of computational tools as fluid-solid-growth (FSG) models.
引用
收藏
页码:221 / 246
页数:26
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