Personalized evaluation of the passive myocardium in ischemic cardiomyopathy via computational modeling using Bayesian optimization

IF 3 3区 医学 Q2 BIOPHYSICS Biomechanics and Modeling in Mechanobiology Pub Date : 2024-07-02 DOI:10.1007/s10237-024-01856-0
Saeed Torbati, Alireza Daneshmehr, Hamidreza Pouraliakbar, Masoud Asgharian, Seyed Hossein Ahmadi Tafti, Dominique Shum-Tim, Alireza Heidari
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Abstract

Biomechanics-based patient-specific modeling is a promising approach that has proved invaluable for its clinical potential to assess the adversities caused by ischemic heart disease (IHD). In the present study, we propose a framework to find the passive material properties of the myocardium and the unloaded shape of cardiac ventricles simultaneously in patients diagnosed with ischemic cardiomyopathy (ICM). This was achieved by minimizing the difference between the simulated and the target end-diastolic pressure–volume relationships (EDPVRs) using black-box Bayesian optimization, based on the finite element analysis (FEA). End-diastolic (ED) biventricular geometry and the location of the ischemia were determined from cardiac magnetic resonance (CMR) imaging. We employed our pipeline to model the cardiac ventricles of three patients aged between 57 and 66 years, with and without the inclusion of valves. An excellent agreement between the simulated and the target EDPVRs has been reached. Our results revealed that the incorporation of valvular springs typically leads to lower hyperelastic parameters for both healthy and ischemic myocardium, as well as a higher fiber Green strain in the viable regions compared to models without valvular stiffness. Furthermore, the addition of valve-related effects did not result in significant changes in myofiber stress after optimization. We concluded that more accurate results could be obtained when cardiac valves were considered in modeling ventricles. The present novel and practical methodology paves the way for developing digital twins of ischemic cardiac ventricles, providing a non-invasive assessment for designing optimal personalized therapies in precision medicine.

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通过贝叶斯优化计算建模对缺血性心肌病的被动心肌进行个性化评估。
基于生物力学的患者特异性建模是一种很有前途的方法,它在评估缺血性心脏病(IHD)引起的逆境方面的临床潜力已被证明是无价之宝。在本研究中,我们提出了一个框架,可同时找到被诊断为缺血性心肌病(ICM)患者心肌的被动材料特性和心室的无负荷形状。为此,我们在有限元分析 (FEA) 的基础上,利用黑盒贝叶斯优化技术将模拟舒张末期压力-容积关系(EDPVR)与目标舒张末期压力-容积关系(EDPVR)之间的差异最小化。双心室舒张末期(ED)几何形状和缺血位置是通过心脏磁共振(CMR)成像确定的。我们使用我们的管道为年龄在 57 岁至 66 岁之间的三名患者的心室建模,包括包含和不包含瓣膜。模拟的 EDPVR 与目标的 EDPVR 非常吻合。我们的结果表明,与不包含瓣膜刚度的模型相比,包含瓣膜弹簧通常会导致健康和缺血心肌的高弹性参数降低,以及有活力区域的纤维格林应变增加。此外,增加瓣膜相关效应并不会导致优化后的肌纤维应力发生显著变化。我们的结论是,如果在心室建模时考虑到心脏瓣膜,就能获得更精确的结果。这种新颖实用的方法为开发缺血性心室的数字双胞胎铺平了道路,为设计精准医疗的最佳个性化疗法提供了无创评估。
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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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