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Magnetic resonance imaging-based computational modelling of blood flow and nanomedicine deposition in patients with peripheral arterial disease

机译:基于磁共振成像的外周动脉疾病患者血流和纳米药物沉积的计算模型

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摘要

Peripheral arterial disease (PAD) is generally attributed to the progressive vascular accumulation of lipoproteins and circulating monocytes in the vessel walls leading to the formation of atherosclerotic plaques. This is known to be regulated by the local vascular geometry, haemodynamics and biophysical conditions. Here, an isogeometric analysis framework is proposed to analyse the blood flow and vascular deposition of circulating nanoparticles (NPs) into the superficial femoral artery (SFA) of a PAD patient. The local geometry of the blood vessel and the haemodynamic conditions are derived from magnetic resonance imaging (MRI), performed at baseline and at 24 months post intervention. A dramatic improvement in blood flow dynamics is observed post intervention. A 500% increase in peak flow rate is measured in vivo as a consequence of luminal enlargement. Furthermore, blood flow simulations reveal a 32% drop in the mean oscillatory shear index, indicating reduced disturbed flow post intervention. The same patient information (vascular geometry and blood flow) is used to predict in silico in a simulation of the vascular deposition of systemically injected nanomedicines. NPs, targeted to inflammatory vascular molecules including VCAM-1, E-selectin and ICAM-1, are predicted to preferentially accumulate near the stenosis in the baseline configuration, with VCAM-1 providing the highest accumulation (approx. 1.33 and 1.50 times higher concentration than that of ICAM-1 and E-selectin, respectively). Such selective deposition of NPs within the stenosis could be effectively used for the detection and treatment of plaques forming in the SFA. The presented MRI-based computational protocol can be used to analyse data from clinical trials to explore possible correlations between haemodynamics and disease progression in PAD patients, and potentially predict disease occurrence as well as the outcome of an intervention.
机译:周围动脉疾病(PAD)通常归因于脂蛋白和循环单核细胞在血管壁中的进行性血管蓄积,导致形成动脉粥样硬化斑块。已知这受局部血管几何形状,血液动力学和生物物理条件的调节。在这里,提出了一种等几何分析框架,以分析循环中的纳米颗粒(NPs)进入PAD患者的股浅动脉(SFA)的血流和血管沉积。血管的局部几何形状和血液动力学状况来自于磁共振成像(MRI),在基线和干预后24个月进行。干预后观察到血流动力学的显着改善。由于管腔增大,体内峰值流速增加了500%。此外,血流模拟显示平均振荡剪切指数下降了32%,表明干预后血流减少。在系统注射纳米药物的血管沉积模拟中,使用相同的患者信息(血管几何形状和血流)来预测计算机模拟。预测靶向VCAM-1,E-选择素和ICAM-1等炎症性血管分子的NPs在基线状态下优先在狭窄附近积聚,其中VCAM-1提供最高的积聚(浓度高约1.33和1.50倍分别比ICAM-1和E-selectin高)。狭窄内NPs的这种选择性沉积可有效地用于SFA中斑块形成的检测和治疗。提出的基于MRI的计算协议可用于分析来自临床试验的数据,以探索PAD患者血液动力学与疾病进展之间的可能相关性,并可能预测疾病的发生以及干预的结果。

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