School of Aerospace, Mechanical and Manufacturing Engineering, and Health Innovations Research Institute (HIRi), RMIT University, Australia.
BMC Cardiovasc Disord. 2012 Feb 15;12:7. doi: 10.1186/1471-2261-12-7.
This study characterizes the distribution and components of plaque structure by presenting a three-dimensional blood-vessel modelling with the aim of determining mechanical properties due to the effect of lipid core and calcification within a plaque. Numerical simulation has been used to answer how cap thickness and calcium distribution in lipids influence the biomechanical stress on the plaque.
Modelling atherosclerotic plaque based on structural analysis confirms the rationale for plaque mechanical examination and the feasibility of our simulation model. Meaningful validation of predictions from modelled atherosclerotic plaque model typically requires examination of bona fide atherosclerotic lesions. To analyze a more accurate plaque rupture, fluid-structure interaction is applied to three-dimensional blood-vessel carotid bifurcation modelling. A patient-specific pressure variation is applied onto the plaque to influence its vulnerability.
Modelling of the human atherosclerotic artery with varying degrees of lipid core elasticity, fibrous cap thickness and calcification gap, which is defined as the distance between the fibrous cap and calcification agglomerate, form the basis of our rupture analysis. Finite element analysis shows that the calcification gap should be conservatively smaller than its threshold to maintain plaque stability. The results add new mechanistic insights and methodologically sound data to investigate plaque rupture mechanics.
Structural analysis using a three-dimensional calcified model represents a more realistic simulation of late-stage atherosclerotic plaque. We also demonstrate that increases of calcium content that is coupled with a decrease in lipid core volume can stabilize plaque structurally.
本研究通过呈现三维血管建模来描述斑块结构的分布和组成,目的是确定由于斑块内脂质核心和钙化的影响而导致的机械性能。数值模拟已被用于回答帽厚度和脂质中钙分布如何影响斑块的生物力学应力。
基于结构分析的动脉粥样硬化斑块建模证实了斑块力学检查的合理性和我们模拟模型的可行性。对模拟动脉粥样硬化斑块模型的预测进行有意义的验证通常需要检查真实的动脉粥样硬化病变。为了更准确地分析斑块破裂,应用流固耦合对三维血管颈动脉分叉建模。将特定于患者的压力变化施加到斑块上以影响其脆弱性。
用不同程度的脂质核心弹性、纤维帽厚度和钙化间隙(定义为纤维帽和钙化团块之间的距离)对人类动脉粥样硬化动脉进行建模,这是我们破裂分析的基础。有限元分析表明,钙化间隙应保守地小于其阈值以保持斑块稳定性。结果为研究斑块破裂力学提供了新的机制见解和方法上合理的数据。
使用三维钙化模型进行结构分析代表了对晚期动脉粥样硬化斑块的更现实模拟。我们还证明,钙含量的增加伴随着脂质核心体积的减少可以稳定斑块的结构。