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用于收缩期心脏光学映射视频中运动伪影补偿和变形测量的无标记跟踪

Marker-Free Tracking for Motion Artifact Compensation and Deformation Measurements in Optical Mapping Videos of Contracting Hearts.

作者信息

Christoph Jan, Luther Stefan

机构信息

Biomedical Physics Group, Max Planck Institute for Dynamics and Self-Organization, Göttingen, Germany.

German Center for Cardiovascular Research, Göttingen, Germany.

出版信息

Front Physiol. 2018 Nov 2;9:1483. doi: 10.3389/fphys.2018.01483. eCollection 2018.

DOI:10.3389/fphys.2018.01483
PMID:30450053
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC6224482/
Abstract

Optical mapping is a high-resolution fluorescence imaging technique, which provides highly detailed visualizations of the electrophysiological wave phenomena, which trigger the beating of the heart. Recent advancements in optical mapping have demonstrated that the technique can now be performed with moving and contracting hearts and that motion and motion artifacts, once a major limitation, can now be overcome by numerically tracking and stabilizing the heart's motion. As a result, the optical measurement of electrical activity can be obtained from the moving heart surface in a co-moving frame of reference and motion artifacts can be reduced substantially. The aim of this study is to assess and validate the performance of a 2D marker-free motion tracking algorithm, which tracks motion and non-rigid deformations in video images. Because the tracking algorithm does not require markers to be attached to the tissue, it is necessary to verify that it accurately tracks the displacements of the cardiac tissue surface, which not only contracts and deforms, but also fluoresces and exhibits spatio-temporal physiology-related intensity changes. We used computer simulations to generate synthetic optical mapping videos, which show the contracting and fluorescing ventricular heart surface. The synthetic data reproduces experimental data as closely as possible and shows electrical waves propagating across the deforming tissue surface, as seen during voltage-sensitive imaging. We then tested the motion tracking and motion-stabilization algorithm on the synthetic as well as on experimental data. The motion tracking and motion-stabilization algorithm decreases motion artifacts approximately by 80% and achieves sub-pixel precision when tracking motion of 1-10 pixels (in a video image with 100 by 100 pixels), effectively inhibiting motion such that little residual motion remains after tracking and motion-stabilization. To demonstrate the performance of the algorithm, we present optical maps with a substantial reduction in motion artifacts showing action potential waves propagating across the moving and strongly deforming ventricular heart surface. The tracking algorithm reliably tracks motion if the tissue surface is illuminated homogeneously and shows sufficient contrast or texture which can be tracked or if the contrast is artificially or numerically enhanced. In this study, we also show how a reduction in dissociation-related motion artifacts can be quantified and linked to tracking precision. Our results can be used to advance optical mapping techniques, enabling them to image contracting hearts, with the ultimate goal of studying the mutual coupling of electrical and mechanical phenomena in healthy and diseased hearts.

摘要

光学映射是一种高分辨率荧光成像技术,它能提供引发心脏跳动的电生理波现象的高度详细可视化。光学映射的最新进展表明,该技术现在可以在运动和收缩的心脏上进行,并且运动和运动伪影(曾经是一个主要限制因素)现在可以通过对心脏运动进行数值跟踪和稳定来克服。因此,可以在共同移动的参考系中从移动的心脏表面获得电活动的光学测量值,并且运动伪影可以大幅减少。本研究的目的是评估和验证一种二维无标记运动跟踪算法的性能,该算法可跟踪视频图像中的运动和非刚性变形。由于跟踪算法不需要在组织上附着标记,因此有必要验证它能准确跟踪心脏组织表面的位移,该表面不仅会收缩和变形,还会发出荧光并呈现与时空生理相关的强度变化。我们使用计算机模拟生成合成光学映射视频,展示收缩和发出荧光的心室心脏表面。合成数据尽可能精确地再现了实验数据,并显示了电压敏感染像过程中在变形组织表面传播的电波。然后,我们在合成数据和实验数据上测试了运动跟踪和运动稳定算法。运动跟踪和运动稳定算法可将运动伪影减少约80%,在跟踪1 - 10像素(在100×100像素的视频图像中)的运动时实现亚像素精度,有效抑制运动,使得跟踪和运动稳定后几乎没有残留运动。为了展示该算法的性能,我们呈现了运动伪影大幅减少的光学映射图,显示了动作电位波在移动且强烈变形的心室心脏表面传播。如果组织表面被均匀照亮且显示出足够的对比度或可被跟踪的纹理,或者对比度通过人工或数值方式增强,跟踪算法就能可靠地跟踪运动。在本研究中,我们还展示了如何量化与解离相关的运动伪影的减少,并将其与跟踪精度联系起来。我们的结果可用于推进光学映射技术,使其能够对收缩的心脏进行成像,最终目标是研究健康和患病心脏中电现象和机械现象的相互耦合。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c157/6224482/d607cd155c71/fphys-09-01483-g0012.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c157/6224482/89379dc7c7d9/fphys-09-01483-g0009.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c157/6224482/48698135081d/fphys-09-01483-g0010.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c157/6224482/46a90c73e9e7/fphys-09-01483-g0011.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c157/6224482/d607cd155c71/fphys-09-01483-g0012.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c157/6224482/89379dc7c7d9/fphys-09-01483-g0009.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c157/6224482/48698135081d/fphys-09-01483-g0010.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c157/6224482/46a90c73e9e7/fphys-09-01483-g0011.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c157/6224482/d607cd155c71/fphys-09-01483-g0012.jpg

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