National Medical Research Center for Hematology, Moscow, Russia.
Moscow Institute of Physics and Technology, Dolgoprudny, Russia.
PLoS One. 2022 Oct 3;17(10):e0272342. doi: 10.1371/journal.pone.0272342. eCollection 2022.
Shear-induced platelet activation (SIPAct) is an important mechanism of thrombosis initiation under high blood flow. This mechanism relies on the interaction of platelets with the von Willebrand factor (VWF) capable of unfolding under high shear stress. High shear stress occurs in the arteriovenous fistula (AVF) commonly used for haemodialysis. A novel patient-specific approach for the modelling of SIPAct in the AVF was proposed. This enabled us to estimate the SIPAct level via computational fluid dynamics. The suggested approach was applied for the SIPAct analysis in AVF geometries reconstructed from medical images. The approach facilitates the determination of the SIPAct level dependence on both biomechanical (AVF flow rate) and biochemical factors (VWF multimer size). It was found that the dependence of the SIPAct level on the AVF flow rate can be approximated by a power law. The critical flow rate was a decreasing function of the VWF multimer size. Moreover, the critical AVF flow rate highly depended on patient-specific factors, e.g., the vessel geometry. This indicates that the approach may be adopted to elucidate patient-specific thrombosis risk factors in haemodialysis patients.
剪切诱导的血小板激活(SIPAct)是血流高时血栓形成起始的一个重要机制。该机制依赖于血小板与能够在高切应力下展开的血管性血友病因子(VWF)相互作用。高剪切应力发生在常用于血液透析的动静脉瘘(AVF)中。提出了一种新的用于模拟 AVF 中 SIPAct 的患者特异性方法。这使我们能够通过计算流体动力学来估计 SIPAct 水平。该方法应用于从医学图像重建的 AVF 几何形状的 SIPAct 分析。该方法有助于确定 SIPAct 水平对生物力学(AVF 流速)和生化因素(VWF 多聚体大小)的依赖性。结果表明,SIPAct 水平对 AVF 流速的依赖性可以用幂律来近似。临界流速是 VWF 多聚体大小的递减函数。此外,临界 AVF 流速高度依赖于患者特异性因素,例如血管几何形状。这表明该方法可用于阐明血液透析患者的特定患者血栓形成危险因素。