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Constitutive description of human femoropopliteal artery aging

本构方程 弹性蛋白 人口 材料科学 正交异性材料 生物医学工程 结构工程 医学 有限元法 病理 工程类 环境卫生
作者
Alexey Kamenskiy,Andreas Seas,Paul Deegan,William Poulson,Eric Anttila,Sylvie Sim,Anastasia Desyatova,Jason N. MacTaggart
出处
期刊:Biomechanics and Modeling in Mechanobiology [Springer Science+Business Media]
卷期号:16 (2): 681-692 被引量:39
标识
DOI:10.1007/s10237-016-0845-7
摘要

Femoropopliteal artery (FPA) mechanics play a paramount role in pathophysiology and the artery’s response to therapeutic interventions, but data on FPA mechanical properties are scarce. Our goal was to characterize human FPAs over a wide population to derive a constitutive description of FPA aging to be used for computational modeling. Fresh human FPA specimens ( $$n=579$$ ) were obtained from $$n=351$$ predominantly male (80 %) donors 54±15 years old (range 13–82 years). Morphometric characteristics including radius, wall thickness, opening angle, and longitudinal pre-stretch were recorded. Arteries were subjected to multi-ratio planar biaxial extension to determine constitutive parameters for an invariant-based model accounting for the passive contributions of ground substance, elastin, collagen, and smooth muscle. Nonparametric bootstrapping was used to determine unique sets of material parameters that were used to derive age-group-specific characteristics. Physiologic stress–stretch state was calculated to capture changes with aging. Morphometric and constitutive parameters were derived for seven age groups. Vessel radius, wall thickness, and circumferential opening angle increased with aging, while longitudinal pre-stretch decreased ( $$p<0.01$$ ). Age-group-specific constitutive parameters portrayed orthotropic FPA stiffening, especially in the longitudinal direction. Structural changes in artery wall elastin were associated with reduction of physiologic longitudinal and circumferential stretches and stresses with age. These data and the constitutive description of FPA aging shed new light on our understanding of peripheral arterial disease pathophysiology and arterial aging. Application of this knowledge might improve patient selection for specific treatment modalities in personalized, precision medicine algorithms and could assist in device development for treatment of peripheral artery disease.

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