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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血动脉疾病患者血流和纳米胺沉积的计算模型

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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:外周动脉疾病(垫)通常归因于脂蛋白的逐步血管积累和血管壁中的循环单核细胞,导致形成动脉粥样硬化斑块。已知这是由局部血管几何形状,血管动力学和生物物理条件调节。这里,提出了一种异步分析框架,分析循环纳米颗粒(NPS)进入垫患者的表面股动脉(SFA)的血流量和血管沉积。血管和血管动力学条件的局部几何形状源自磁共振成像(MRI),在基线和24个月后介入干预。介入后,观察到血流动力学的显着改善。由于腔扩大,在体内测量了500%的峰值流量增加。此外,血流量模拟显示平均振荡剪切指数中的32%下降,表明减少干扰后介入。相同的患者信息(血管几何和血流)用于预测硅的血管沉积在系统上注射纳米丝胺的血管沉积中。靶向包括VCAM-1,E-SELECTIN和ICAM-1的炎症血管分子的NPS,预计将优先积聚在基线配置中的狭窄附近,VCAM-1提供最高的积累(约1.33和1.5.50倍浓度比ICAM-1和E-SELETIN的那个)。在狭窄内的这种选择性沉积NP可以有效地用于在SFA中形成噬斑的检测和治疗。所呈现的基于MRI的计算协议可用于分析来自临床试验的数据,以探讨垫患者血液动力学和疾病进展之间的可能相关性,并且可能预测疾病发生以及干预的结果。

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