An Implementation of Patient-Specific Biventricular Mechanics Simulations With a Deep Learning and Computational Pipeline

被引:16
|
作者
Miller, Renee [1 ]
Kerfoot, Eric [1 ]
Mauger, Charlene [2 ]
Ismail, Tevfik F. [1 ]
Young, Alistair A. [1 ,2 ]
Nordsletten, David A. [1 ,3 ]
机构
[1] Kings Coll London, Sch Biomed Engn & Imaging Sci, London, England
[2] Univ Auckland, Auckland MR Res Grp, Auckland, New Zealand
[3] Univ Michigan, Dept Biomed Engn & Cardiac Surg, Ann Arbor, MI 48109 USA
基金
英国工程与自然科学研究理事会;
关键词
personalised modelling; biventricular mechanics; parameter identification; automatic segmentation; valve landmark identification; IDIOPATHIC DILATED CARDIOMYOPATHY; MATERIAL PARAMETER-ESTIMATION; LEFT-VENTRICULAR MECHANICS; HYPERTROPHIC CARDIOMYOPATHY; AUTOMATIC SEGMENTATION; IN-VIVO; HEART; MODEL; QUANTIFICATION; ORIENTATION;
D O I
10.3389/fphys.2021.716597
中图分类号
Q4 [生理学];
学科分类号
071003 ;
摘要
Parameterised patient-specific models of the heart enable quantitative analysis of cardiac function as well as estimation of regional stress and intrinsic tissue stiffness. However, the development of personalised models and subsequent simulations have often required lengthy manual setup, from image labelling through to generating the finite element model and assigning boundary conditions. Recently, rapid patient-specific finite element modelling has been made possible through the use of machine learning techniques. In this paper, utilising multiple neural networks for image labelling and detection of valve landmarks, together with streamlined data integration, a pipeline for generating patient-specific biventricular models is applied to clinically-acquired data from a diverse cohort of individuals, including hypertrophic and dilated cardiomyopathy patients and healthy volunteers. Valve motion from tracked landmarks as well as cavity volumes measured from labelled images are used to drive realistic motion and estimate passive tissue stiffness values. The neural networks are shown to accurately label cardiac regions and features for these diverse morphologies. Furthermore, differences in global intrinsic parameters, such as tissue anisotropy and normalised active tension, between groups illustrate respective underlying changes in tissue composition and/or structure as a result of pathology. This study shows the successful application of a generic pipeline for biventricular modelling, incorporating artificial intelligence solutions, within a diverse cohort.</p>
引用
收藏
页数:19
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