用流形对齐可视化不同定义对心肌应变分析的影响
Visualizing definitional divergence in high-dimensional data by manifold alignment: Application to 3D right ventricular strain computations
- 通过流形对齐匹配不同应变定义的潜在表示
- 构建高维参数图展示定义差异带来的变异,最大达18.7%
- 适合医学影像分析中需评估定义敏感性的研究者
医学影像研究常基于每个受试者单一样本,假设其能代表生理特征。然而,输入描述符的定义或计算方式差异(如领域内缺乏共识)可能对分析结果产生关键影响,实践中却很少被考虑。本文提出一种基于表征学习的新策略,用于估计反映此类定义差异对特定生理指标影响的参数图,该指标已从医学影像中提取。我们将不同定义或计算方式视为异质类型的高维数据,聚焦于心肌变形(应变)这一定义不统一的指标。首先利用流形对齐匹配不同定义对应的潜在表示;随后在潜空间中构建合理分布,以表征描述符间的定义差异,并重建高维参数图进行可视化。由于该临床应用缺乏真实标签,我们先在模拟实验中验证方法,再应用于3D超声心动图序列获取的右心室应变数据,这些数据在右心室心内膜表面网格的每个点上提供多种类型应变。除该示范应用外,本方法可推广至其他涉及异质高维描述符的人群分析。
原文摘要 · Abstract (English)
Medical imaging studies often rely on a single sample per subject, assuming it is representative of their physiological traits. However, variations in how input descriptors are defined or computed (e.g. due to a lack of consensus in the scientific field) may have a crucial impact on the analysis, and are hardly considered in practice. In this paper, we propose an original strategy based on representation learning to estimate a parametric map reflecting the impact of such definitional differences on a given physiological descriptor, previously extracted from medical images. We consider the different definitions or computations of such physiological descriptors as different high-dimensional data, potentially of heterogeneous types. We specifically focus on myocardial deformation (strain), for which there is limited agreement on its definition. We first use manifold alignment to match the latent representations associated with the different definitions of this descriptor. Then, we formulate plausible distributions in the latent space to represent definitional divergence across descriptors, from which we reconstruct a high-dimensional parametric map to visualize such definitional divergence. Due to the lack of proper ground truth for this specific clinical application, we first demonstrate this methodology on toy experiments and then expand the evaluation on right ventricular strain data from subjects obtained from 3D echocardiographic image sequences, for which different types of strain are available at each point of the right ventricle endocardial surface mesh. Beyond this illustrative application, our methodology has the potential to be generalised to many other population analyses considering heterogeneous high-dimensional descriptors.
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