Experimentally-induced CTEPH significantly increased pulmonary artery wall stiffness and the percentage of the intralobar arterial network with low time-averaged wall shear stress and high oscillatory shear index.
A 1D computational fluid dynamics model demonstrates that CTEPH increases pulmonary artery stiffness and alters shear stress, providing potential mechanobiological markers for disease progression.
p-value: p=0.023
Abstract Chronic thromboembolic pulmonary hypertension (CTEPH) develops due to the accumulation of blood clots in the lung vasculature that obstructs flow and increases pressure. The mechanobiological factors that drive progression of CTEPH are not understood, in part because mechanical and hemodynamic changes in the small pulmonary arteries due to CTEPH are not easily measurable. Using previously published hemodynamic measurements and imaging from a large animal model of CTEPH, we applied a subject-specific one-dimensional (1D) computational fluid dynamic (CFD) approach to investigate the impact of CTEPH on pulmonary artery stiffening, time-averaged wall shear stress (TAWSS), and oscillatory shear index (OSI) in extralobar (main, right, and left) pulmonary arteries and intralobar (distal to the extralobar) arteries. Our results demonstrate that CTEPH increases pulmonary artery wall stiffness and decreases TAWSS in extralobar and intralobar arteries. Moreover, CTEPH increases the percentage of the intralobar arterial network with both low TAWSS and high OSI, quantified by the novel parameter φ, which is related to thrombogenicity. Our analysis reveals a strong positive correlation between increases in mean pulmonary artery pressure (mPAP) and φ from baseline to CTEPH in individual subjects, which supports the suggestion that increased φ drives disease severity. This subject-specific experimental–computational framework shows potential as a predictor of the impact of CTEPH on pulmonary arterial hemodynamics and pulmonary vascular mechanics. By leveraging advanced modeling techniques and calibrated model parameters, we predict spatial distributions of flow and pressure, from which we can compute potential physiomarkers of disease progression. Ultimately, this approach can lead to more spatially targeted interventions that address the needs of individual CTEPH patients.
Kachabi et al. (Tue,) conducted a other in Chronic thromboembolic pulmonary hypertension (CTEPH) (n=5). CTEPH induction via microspheres vs. Baseline was evaluated on Percentage of intralobar arterial network with low TAWSS and high OSI (ϕ) (p=0.023). Experimentally-induced CTEPH significantly increased pulmonary artery wall stiffness and the percentage of the intralobar arterial network with low time-averaged wall shear stress and high oscillatory shear index.