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Impact of image resolution on neural network based automatic scar segmentation in cardiovascular magnetic resonance imaging
Isabel Margolis1, Tobias Hoh1, Jonathan Weine1, Thomas Joyce1, Robert Manka1, Miriam Weisskopf2, Nikola Cesarovic3, Maximilian Fuetterer1, and Sebastian Kozerke1
1Institute for Biomedical Engineering, University and ETH Zurich, Zurich, Switzerland, 2Center of Surgical Research, University Hospital Zurich, Zurich, Switzerland, 3Department of Health Sciences and Technology, ETH Zurich, Zurich, Switzerland

Synopsis

Keywords: Diagnosis/Prediction, Machine Learning/Artificial Intelligence

Motivation: Deep learning for myocardial scar segmentation offers an alternative to time-consuming and observer-dependent semi-automatic approaches.

Goal(s): The objective of this study was to assess the impact of effective image resolution on neural network training for ventricular scar segmentation.

Approach: Convolutional neural networks were trained on magnetic resonance images with constant matrix size and field-of-view but differing resolutions, and tested on a range of resolutions to investigate the effects.

Results: Neural networks trained on a specific resolution indicated a bias of the scar area estimation when employed to lower -or higher-resolution images. Deploying a network trained on multiple resolutions resulted in reduced resolution dependency.

Impact: The effective image resolution, with constant matrix size and field-of-view, should be considered when training a segmentation model to alleviate unwanted bias in the estimation. Training on multiple resolutions has been shown to increase network precision and robustness.

Introduction

Myocardial scar mass derived from cardiovascular magnetic resonance (CMR) late gadolinium enhancement (LGE) imaging is considered the gold standard for non-invasive myocardial viability assessment in the context of acute and chronic myocardial infarction (MI) 1-4. Myocardial scar mass is of prognostic value in patients with ischemic and non-ischemic cardiomyopathies 5-14. Generally, manual segmentation is time-consuming and requires well-trained observers as well as standardized criteria to account for variations in MRI sequences and hardware. In a multi-center study, significant interobserver differences in %LV mass were reported, indicating limited generalization of the classification of scar data 15. Several deep learning approaches to limit human interactions in scar segmentation have been proposed 16.
The standard data processing approach for CNN-based segmentation includes resampling or interpolation of image data to obtain training and test data with constant field-of-view (FOV) and matrix size, i.e. constant apparent in-plane resolution, as well as normalized contrast 11,17-20. The imaging point spread function (PSF) depends on various factors, including sequence and reconstruction parameters, as well as post-processing steps before image-domain data is saved as DICOM files for further processing. The objective of the present work was to systematically assess network performance degradation due to a mismatch of point-spread function between training and testing data using a representative U-Net-type network 21.

Methods

Thirty-six high-resolution (0.7 x 0.7 x 2.0 mm3) LGE k-space datasets were acquired post-mortem in porcine models of myocardial infarction. The in-plane point-spread function and hence in-plane resolution Δx was retrospectively degraded using k-space lowpass filtering, while field-of-view and matrix size were kept constant. Manual segmentation of the left ventricle (LV) and healthy remote myocardium was performed to quantify the location and area (% of myocardium) of scar tissue by thresholding (≥ SD5 above remote). The data processing pipeline is illustrated in Fig. 1.
Three standard U-Nets were trained on training resolutions Δxtrain = 0.7, 1.2, and 1.7 mm to predict endo- and epicardial borders of LV myocardium and scar. A five-fold cross-validation scheme was applied to increase the statistical meaning of the reported errors. The scar prediction of the three networks for varying test resolutions (Δxtest = 0.7 to 1.7 mm) was compared against the reference SD5 thresholding at 0.7 mm. Finally, a fourth network trained on a combination of resolutions (Δxtrain = 0.7 to 1.7 mm) was tested. Fig. 2 shows an example case of the network predictions on varying test resolutions.

Results

The networks were evaluated based on Dice scores and relative fractional errors of the estimated myocardial and scar areas compared to the reference, given as percentage points (p.p.) and corresponding interquartile ranges (IQR). Fig. 3 shows the results of the fractional errors across all investigated test resolutions, and Fig. 4 shows the distribution of the Dice scores. The median fractional scar errors and precisions (IQR) from networks trained and tested on the same resolution were 0.0p.p. (1.24 - 1.45), and -0.5 - 0.0p.p. (2.00 – 3.25) for networks trained and tested on the most differing resolutions, respectively. Deploying the network trained on multiple resolutions resulted in reduced resolution dependency with median scar errors and IQRs of 0.0p.p. (1.24 – 1.69) for all investigated test resolutions.

Discussion

Using a standard U-Net, network-based predictions of relative scar areas showed variability for fractional errors and Dice scores across the investigated test resolutions. All networks underestimated scar areas more often on high-resolution than on low-resolution test images. This is partly explained by the fact that reduced resolution corresponds to a wider PSF, which leads to spatial information being smeared out over neighbouring pixels, i.e., spatial signal variations occur on a larger scale and are smoother.
As pointed out by Heiberg et al., n-SD thresholding depends on the signal-to-noise ratio (SNR) in the data 22. Low SNR causes underestimation of the scar area, and high SNR results in overestimation. Given that reference scar masks were derived at the highest available resolution, where the SD5 thresholding is more likely to underestimate the true scar area, the networks trained on low-resolution images learned to segment the scar conservatively.
The PSF-dependent bias and variability demonstrated in our work indicate the importance of considering and reporting acquisition rather than reconstruction resolution as a crucial parameter, as well as SNR, when designing and evaluating scar segmentation networks.

Conclusion

A mismatch of the imaging point-spread function between training and test data can lead to degradation of scar segmentation when using current U-Net architectures, as demonstrated on LGE porcine myocardial infarction data. Training networks on multi-resolution data can alleviate the resolution dependency.

Acknowledgements

The authors are grateful for the support and advice on data acquisition, interpretation and curation of Dr. Mareike Cramer, Dr. Conny Waschkies, Dr. Christian Stoeck and Oliver Bludau.

References

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Figures

Figure 1: (a) LGE image acquisition and reconstruction. Reference scar segmentation using SD5 thresholding followed by morphological denoising of scar masks. (b) Resolution reduction by multiplication of k-space data with a low-pass filter while keeping FOV and matrix size constant. (c) Examples of resulting images with in-plane resolutions Δxtrain = 0.7 mm, 1.2 mm, and 1.7 mm. (d) Four segmentation networks are trained for the given resolutions. (e) Segmentation mask predictions for the network trained at Δxtrain = 0.7 mm, including identical (*) morphological denoising.

Figure 2: (a) Images with varying in-plane resolution Δx and reference SD5 thresholding segmentation masks. Corresponding predictions using networks trained on these resolutions are shown in (b-d), respectively. Predictions for a network trained on mixed resolutions from Δxtrain = 0.7 mm to 1.7 mm are shown in (e). Healthy myocardium is shown in green and scar (SD5) in red. Regional areas in mm2 for myocardium and scar are given as numbers in green and red, respectively. Dice scores relative to SD5 thresholding are given in the top right corner of the shown frames.

Figure 3: Boxplot analysis of fractional errors between network predictions and SD5 thresholding as a function of in-plane resolutions Δxtest from 0.7 mm to 1.7 mm is shown for networks trained on Δxtrain = 0.7 mm (a), 1.2 mm (b) and 1.7 mm (c), and multiple resolutions Δxtrain = 0.7 mm to 1.7 mm (d). Left and right columns show boxplots for myocardium (MYO) and scar (SCAR) predictions, respectively. Interquartile ranges (IQR), which indicate network precision, are given in the legend.

Figure 4: Boxplot analysis of Dice scores between network predictions and SD5 thresholding as a function of in-plane resolutions Δxtest = 0.7 mm to 1.7 mm are shown for networks trained at Δxtrain = 0.7 mm (a), 1.2 mm (b), 1.7 mm (c) and mixed multiple resolutions Δxtrain = 0.7 mm to 1.7 mm (d). Left and right columns show boxplots for myocardium (MYO) and scar (SCAR) predictions, respectively. Interquartile ranges (IQR), which indicate network precision, are given in the legend.

Proc. Intl. Soc. Mag. Reson. Med. 32 (2024)
3788
DOI: https://doi.org/10.58530/2024/3788