Abstract

Background: In the study of early cardiac development, it is essential to acquire accurate volume changes of the heart chambers. Although advanced imaging techniques, such as light-sheet fluorescent microscopy (LSFM), provide an accurate procedure for analyzing the heart structure, rapid, and robust segmentation is required to reduce laborious time and accurately quantify developmental cardiac mechanics.Methods: The traditional biomedical analysis involving segmentation of the intracardiac volume occurs manually, presenting bottlenecks due to enormous data volume at high axial resolution. Our advanced deep-learning techniques provide a robust method to segment the volume within a few minutes. Our U-net-based segmentation adopted manually segmented intracardiac volume changes as training data and automatically produced the other LSFM zebrafish cardiac motion images.Results: Three cardiac cycles from 2 to 5 days postfertilization (dpf) were successfully segmented by our U-net-based network providing volume changes over time. In addition to understanding each of the two chambers' cardiac function, the ventricle and atrium were separated by 3D erode morphology methods. Therefore, cardiac mechanical properties were measured rapidly and demonstrated incremental volume changes of both chambers separately. Interestingly, stroke volume (SV) remains similar in the atrium while that of the ventricle increases SV gradually.Conclusion: Our U-net-based segmentation provides a delicate method to segment the intricate inner volume of the zebrafish heart during development, thus providing an accurate, robust, and efficient algorithm to accelerate cardiac research by bypassing the labor-intensive task as well as improving the consistency in the results.

Highlights

  • Biomechanical analysis is vital during cardiac development, as assessment of biomechanics is closely associated with regulation of valve formation, ventricular septum, and trabecular morphology related to cardiogenic transcriptional and growth/differentiation factors [1, 2]

  • We explore the potential use of the U-Net architecture to expedite the segmentation of the intracardiac zebrafish heart, including the atrium and ventricle and further biomechanical analysis of the extracted results from the network

  • Manual segmentation was performed along the 2D axial plane of the zebrafish heart for each studied sample

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Summary

Introduction

Biomechanical analysis is vital during cardiac development, as assessment of biomechanics is closely associated with regulation of valve formation, ventricular septum, and trabecular morphology related to cardiogenic transcriptional and growth/differentiation factors [1, 2]. Volume change-based cardiac mechanics measurements (e.g., ejection fraction) from the complex trabeculated and beating heart are most commonly used and play an essential role in evaluating the cardiac health condition. Such measurement relies on the accurate reconstruction of the heart’s volume, which depends on the accurate segmentation of the biomedical images. Light-sheet fluorescent microscopy (LSFM) circumvents these challenges to capture in vivo dynamic samples, such as zebrafish heart, with a high axial resolution, deep axial scanning, fast image acquisition, and low photobleaching [12, 13]. Advanced imaging techniques, such as light-sheet fluorescent microscopy (LSFM), provide an accurate procedure for analyzing the heart structure, rapid, and robust segmentation is required to reduce laborious time and accurately quantify developmental cardiac mechanics

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