Inverse analysis of patient-specific parameters of a 3D-0D closed-loop cardiovascular model with an exemplary application to an adult tetralogy of Fallot case.

IF 2.7 3区 医学 Q2 BIOPHYSICS
Tahar Arjoune, Christian Bilas, Christian Meierhofer, Heiko Stern, Peter Ewert, Michael W Gee
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引用次数: 0

Abstract

Patient-specific computational models of the cardiovascular system can inform clinical decision-making by providing physics-based, non-invasive calculations of quantities that cannot be measured or are impractical to measure and by predicting physiological changes due to interventions. In particular, mixed-dimensional 3D-0D coupled models can represent spatially resolved 3D myocardial tissue mechanics and 0D pressure-flow relationships in heart valves and vascular system compartments, while accounting for their interactions in a closed-loop setting. We present an inverse analysis framework for the automated identification of a set of 3D and 0D patient-specific parameters based on flow, pressure, and cine cardiac MRI measurements. We propose a novel decomposition of the underlying large, nonlinear, and mixed-dimensional inverse problem into an equivalent set of independently solvable, computationally efficient, and well-posed inverse subproblems. This decomposition is enabled by the availability of measurement data of the coupling quantities and ensures a faster convergence toward a unique minimum. The inverse subproblems are solved with a L-BFGS optimization algorithm and an adjoint gradient evaluation. The proposed framework is demonstrated in a clinical case study of an adult repaired tetralogy of Fallot (ToF) patient with severe pulmonary regurgitation. The identified parameters provide a good agreement between measured and computed flows, pressures, and chamber volumes, ensuring a patient-specific model response. The outcome prediction of an in silico pulmonary valve replacement using the personalized model is physiologically consistent and correlates well with postoperative measurements. The proposed framework is essential for developing accurate and reliable cardiovascular digital twins and exploiting their predictive capabilities for intervention planning.

3D-0D闭环心血管模型患者特异性参数的逆分析,并以成人法洛四联症为例。
患者特定的心血管系统计算模型可以通过提供基于物理的、非侵入性的无法测量或无法测量的数量计算,以及通过预测干预引起的生理变化,为临床决策提供信息。特别是,混合维3D-0D耦合模型可以表示空间分辨的3D心肌组织力学和心脏瓣膜和血管系统室中的0D压力-流量关系,同时考虑它们在闭环设置中的相互作用。我们提出了一个逆分析框架,用于自动识别一组基于流量,压力和电影心脏MRI测量的3D和0D患者特定参数。我们提出了一种新的分解方法,将潜在的大型、非线性和混合维反问题分解为一组独立可解的、计算效率高的、适定的反子问题。耦合量的测量数据的可用性支持这种分解,并确保更快地收敛到唯一的最小值。利用L-BFGS优化算法和伴随梯度求解逆子问题。提出的框架在一个成人修复法洛四联症(ToF)患者严重肺反流的临床病例研究中得到证明。确定的参数在测量和计算的流量、压力和腔室容积之间提供了良好的一致性,确保了患者特定的模型响应。使用个性化模型预测人工肺瓣膜置换术的结果在生理学上是一致的,并且与术后测量结果有很好的相关性。所提出的框架对于开发准确可靠的心血管数字双胞胎以及利用其预测干预计划的能力至关重要。
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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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