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Wall shear stress is decreased in the pulmonary arteries of patients with pulmonary arterial hypertension: An image-based computational fluid dynamics study

机译:肺动脉高压患者的肺动脉壁切应力降低:基于图像的计算流体动力学研究

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摘要

Previous clinical studies in pulmonary arterial hypertension (PAH) have concentrated predominantly on distal pulmonary vascular resistance, its contribution to the disease process, and response to therapy. However, it is well known that biomechanical factors such as shear stress have an impact on endothelial health and dysfunction in other parts of the vasculature. This study tested the hypothesis that wall shear stress is reduced in the proximal pulmonary arteries of PAH patients with the belief that reduced shear stress may contribute to pulmonary endothelial cell dysfunction and as a result, PAH progression. A combined MRI and computational fluid dynamics (CFD) approach was used to construct subject-specific pulmonary artery models and quantify flow features and wall shear stress (WSS) in five PAH patients with moderate-to-severe disease and five age- and sex-matched controls. Three-dimensional model reconstruction showed PAH patients have significantly larger main, right, and left pulmonary artery diameters (3.5 ± 0.4 vs. 2.7 ± 0.1 cm, P = 0.01; 2.5 ± 0.4 vs. 1.9 ± 0.2 cm, P = 0.04; and 2.6 ± 0.4 vs. 2.0 ± 0.2 cm, P = 0.01, respectively), and lower cardiac output (3.7 ± 1.2 vs. 5.8 ± 0.6 L/min, P = 0.02.). CFD showed significantly lower time-averaged central pulmonary artery WSS in PAH patients compared to controls (4.3 ± 2.8 vs. 20.5 ± 4.0 dynes/cm2, P = 0.0004). Distal WSS was not significantly different. A novel method of measuring WSS was utilized to demonstrate for the first time that WSS is altered in some patients with PAH. Using computational modeling in patient-specific models, WSS was found to be significantly lower in the proximal pulmonary arteries of PAH patients compared to controls. Reduced WSS in proximal pulmonary arteries may play a role in the pathogenesis and progression of PAH. This data may serve as a basis for future in vitro studies of, for example, effects of WSS on gene expression.
机译:先前有关肺动脉高压(PAH)的临床研究主要集中于远端肺血管阻力,其对疾病过程的贡献以及对治疗的反应。但是,众所周知,诸如剪切应力之类的生物力学因素会影响血管系统其他部位的内皮健康和功能障碍。这项研究验证了PAH患者近端肺动脉壁切应力降低的假设,并认为切应力降低可能会导致肺内皮细胞功能障碍,进而导致PAH进展。 MRI和计算流体动力学(CFD)的组合方法用于构建特定于受试者的肺动脉模型,并量化5位中重度疾病和5位年龄和性别的PAH患者的血流特征和壁切应力(WSS)匹配的控件。三维模型重建显示PAH患者的主,右,左肺动脉直径明显更大(3.5±0.4 vs. 2.7±0.1 cm,P = 0.01; 2.5±0.4 vs. 1.9±0.2 cm,P = 0.04;和2.6±0.4 vs. 2.0±0.2 cm,P = 0.01)和较低的心排血量(3.7±1.2 vs. 5.8±0.6 L / min,P = 0.02。)与对照组相比,CFD显示PAH患者的平均时间平均中央肺动脉WSS显着降低(4.3±2.8与20.5±4.0达因/ cm 2 ,P = 0.0004)。 WSS远端无明显差异。一种新颖的WSS测量方法被用于首次证明某些PAH患者的WSS发生了改变。使用针对患者的模型中的计算模型,发现与对照组相比,PAH患者近端肺动脉中的WSS显着降低。近端肺动脉中WSS的减少可能在PAH的发病机理和进程中起作用。该数据可以用作例如WSS对基因表达的影响的未来体外研究的基础。

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