胎儿主动脉瓣成形术对心肌生物力学的影响

IF 3 3区 医学 Q2 BIOPHYSICS
Laura Green, Wei Xuan Chan, Andreas Tulzer, Gerald Tulzer, Choon Hwai Yap
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引用次数: 0

摘要

胎儿重度主动脉瓣狭窄伴左心发育不全综合征(CAS-eHLHS)可发展为单室(UV)出生畸形。基于导管的胎儿主动脉瓣成形术(FAV)可以解决狭窄问题,并降低畸形进展的可能性。然而,我们对 FAV 的生物力学影响和随后的左心室反应了解有限。因此,我们对 4 个 CAS-eHLHS 胎儿心脏进行了基于图像的有限元(FE)建模,通过迭代模拟来匹配基于图像的特征,然后反向计算生理参数。我们使用FAV前的模拟来进行虚拟FAV(vFAV),并对FAV前和FAV后的模拟进行比较。vFAV模拟通常能使一些生理特征部分恢复到健康水平,包括增加每搏量和心肌应变、降低主动脉瓣(AV)和二尖瓣反流(MVr)速度、降低左心室和左心室压以及降低肌纤维应力峰值。主动脉瓣反流通常会导致主动脉瓣反流(AVr)。我们的模拟显示,主动脉瓣反流会影响左心室和洛杉矶减压,但也会显著增加每搏量和心肌变形刺激。FAV后扫描和模拟显示,FAV只能部分降低房室耗散系数。此外,左心室收缩力和外周血管阻力也会因FAV而发生变化,从而阻止房室速度和左心室压力的降低,这与狭窄缓解的预期效果不同。这表明,需要针对具体病例建立FAV后模型,以全面反映心脏功能。总之,基于图像的 FE 建模可以提供 FAV 效果的机理细节,但由于患者对 FAV 的生理反应具有依赖性,因此很难通过计算预测急性预后。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Myocardial biomechanical effects of fetal aortic valvuloplasty

Myocardial biomechanical effects of fetal aortic valvuloplasty

Fetal critical aortic stenosis with evolving hypoplastic left heart syndrome (CAS-eHLHS) can progress to a univentricular (UV) birth malformation. Catheter-based fetal aortic valvuloplasty (FAV) can resolve stenosis and reduce the likelihood of malformation progression. However, we have limited understanding of the biomechanical impact of FAV and subsequent LV responses. Therefore, we performed image-based finite element (FE) modeling of 4 CAS-eHLHS fetal hearts, by performing iterative simulations to match image-based characteristics and then back-computing physiological parameters. We used pre-FAV simulations to conduct virtual FAV (vFAV) and compared pre-FAV and post-FAV simulations. vFAV simulations generally enabled partial restoration of several physiological features toward healthy levels, including increased stroke volume and myocardial strains, reduced aortic valve (AV) and mitral valve regurgitation (MVr) velocities, reduced LV and LA pressures, and reduced peak myofiber stress. FAV often leads to aortic valve regurgitation (AVr). Our simulations showed that AVr could compromise LV and LA depressurization but it could also significantly increase stroke volume and myocardial deformational stimuli. Post-FAV scans and simulations showed FAV enabled only partial reduction of the AV dissipative coefficient. Furthermore, LV contractility and peripheral vascular resistance could change in response to FAV, preventing decreases in AV velocity and LV pressure, compared with what would be anticipated from stenosis relief. This suggested that case-specific post-FAV modeling is required to fully capture cardiac functionality. Overall, image-based FE modeling could provide mechanistic details of the effects of FAV, but computational prediction of acute outcomes was difficult due to a patient-dependent physiological response to FAV.

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来源期刊
Biomechanics and Modeling in Mechanobiology
Biomechanics and Modeling in Mechanobiology 工程技术-工程:生物医学
CiteScore
7.10
自引率
8.60%
发文量
119
审稿时长
6 months
期刊介绍: Mechanics regulates biological processes at the molecular, cellular, tissue, organ, and organism levels. A goal of this journal is to promote basic and applied research that integrates the expanding knowledge-bases in the allied fields of biomechanics and mechanobiology. Approaches may be experimental, theoretical, or computational; they may address phenomena at the nano, micro, or macrolevels. Of particular interest are investigations that (1) quantify the mechanical environment in which cells and matrix function in health, disease, or injury, (2) identify and quantify mechanosensitive responses and their mechanisms, (3) detail inter-relations between mechanics and biological processes such as growth, remodeling, adaptation, and repair, and (4) report discoveries that advance therapeutic and diagnostic procedures. Especially encouraged are analytical and computational models based on solid mechanics, fluid mechanics, or thermomechanics, and their interactions; also encouraged are reports of new experimental methods that expand measurement capabilities and new mathematical methods that facilitate analysis.
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