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Application of Deep Learning-Based Medical Image Segmentation via Orbital Computed Tomography
Published on: November 30, 2022
Open-source pre-clinical image segmentation: mouse cardiac magnetic resonance imaging datasets with a deep learning
Wan Shah1, Daniel J Stuckey2, Tina Yao3
1UCL Centre for Translational Cardiovascular Imaging, Institute of Cardiovascular Science, University College London, London, UK; UCL Centre for Advanced Biomedical Imaging, University College London, London, UK.
Background:
Longitudinal cardiovascular magnetic resonance (CMR) in small animal models is essential for studying cardiovascular disease mechanisms and assessing new therapies. However, conventional manual segmentation of ventricular structures from cine short-axis images is slow, labor-intensive, and subject to substantial observer variability, limiting reproducibility in large-scale pre-clinical studies. While deep learning (DL) segmentation has become standard in human CMR, existing models do not generalize to pre-clinical datasets. Current mouse-specific approaches have been constrained by small private cohorts, where the DL segmentation models are not published.
Methods:
Here, we present the first publicly available pre-clinical CMR dataset, along with an open-source DL segmentation model and a web-based interface for easy deployment. The dataset comprises complete cine short-axis CMR images from 130 mice with diverse phenotypes, acquired at 9.4T. The dataset also contains expert manual segmentations of left ventricular (LV) blood pool and myocardium at end-diastole, end-systole, as well as additional timeframes with artifacts to improve robustness. Using this resource, we developed an open-source DL segmentation model based on the UNet3+ architecture. The model was evaluated against an independent internal test dataset (9.4T, n = 25 mice), as well as two external test datasets (n = 15 mice at 7T, and n = 10 mice at 11.7T) and compared to expert manual segmentations in terms of Dice and functional parameters.
Results:
At inference, the DL segmentation model took <20 ms per 2D image, enabling complete cine stack segmentation in ∼4.6 s-over 6,000-fold speed-up over manual analysis. It achieved high segmentation accuracy in both the blood pool and myocardium in all test datasets (overall Dice ≥ 0.91). In addition, functional parameters showed excellent agreement with manual ground-truth measurements (intraclass correlation coefficient (ICC) ≥ 0.89 for the internal test dataset, and ICC > 0.85 for the external test datasets), with ICC values comparable to human inter-observer variability.
Conclusion:
This work provides the first open-access mouse cardiac MRI dataset, an open-source DL segmentation model, and an accessible inference platform. These tools establish a benchmark for pre-clinical CMR, enabling reproducible, scalable, and community-driven development of DL methods to accelerate cardiovascular research.

