University of Colorado Anschutz Medical Campus, 12700 E. 19th Avenue, Box B131, Aurora, CO, 80045, USA.
427 University of Colorado Boulder, 1111 Engineering Drive, ECME 114, Boulder, CO, 80309, USA.
Curr Hypertens Rep. 2016 Jan;18(1):4. doi: 10.1007/s11906-015-0609-2.
Stiffening of the pulmonary arterial bed with the subsequent increased load on the right ventricle is a paramount feature of pulmonary hypertension (PH). The pathophysiology of vascular stiffening is a complex and self-reinforcing function of extracellular matrix remodeling, driven by recruitment of circulating inflammatory cells and their interactions with resident vascular cells, and mechanotransduction of altered hemodynamic forces throughout the ventricular-vascular axis. New approaches to understanding the cell and molecular determinants of the pathophysiology combine novel biopolymer substrates, controlled flow conditions, and defined cell types to recapitulate the biomechanical environment in vitro. Simultaneously, advances are occurring to assess novel parameters of stiffness in vivo. In this comprehensive state-of-art review, we describe clinical hemodynamic markers, together with the newest translational echocardiographic and cardiac magnetic resonance imaging methods, to assess vascular stiffness and ventricular-vascular coupling. Finally, fluid-tissue interactions appear to offer a novel route of investigating the mechanotransduction processes and disease progression.
肺血管床的僵硬以及随之而来的右心室负荷增加是肺动脉高压(PH)的主要特征。血管僵硬的病理生理学是细胞外基质重塑的复杂和自我强化功能,由循环炎症细胞的募集及其与驻留血管细胞的相互作用以及整个心室-血管轴中改变的血流动力的机械转导驱动。理解病理生理学的细胞和分子决定因素的新方法结合了新型生物聚合物底物、受控的流动条件和定义明确的细胞类型,以在体外再现生物力学环境。同时,正在评估体内新的硬度参数。在这篇全面的综述中,我们描述了临床血流动力学标志物以及最新的转化超声心动图和心脏磁共振成像方法,以评估血管僵硬和心室-血管耦联。最后,流体-组织相互作用似乎为研究机械转导过程和疾病进展提供了一条新途径。