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Register a new userSemantic Segmentation Using Deep Learning to Extract Total Extraocular Muscles and Optic Nerve from Orbital Computed Tomography Images
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Fubao Zhu
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Objectives: Precise segmentation of total extraocular muscles (EOM) and optic nerve (ON) is essential to assess anatomical development and progression of thyroid-associated ophthalmopathy (TAO). We aim to develop a semantic segmentation method based on deep learning to extract the total EOM and ON from orbital CT images in patients with suspected TAO. Materials and Methods: A total of 7,879 images obtained from 97 subjects who underwent orbit CT scans due to suspected TAO were enrolled in this study. Eighty-eight patients were randomly selected into the training/validation dataset, and the rest were put into the test dataset. Contours of the total EOM and ON in all the patients were manually delineated by experienced radiologists as the ground truth. A three-dimensional (3D) end-to-end fully convolutional neural network called semantic V-net (SV-net) was developed for our segmentation task. Intersection over Union (IoU) was measured to evaluate the accuracy of the segmentation results, and Pearson correlation analysis was used to evaluate the volumes measured from our segmentation results against those from the ground truth. Results: Our model in the test dataset achieved an overall IoU of 0.8207; the IoU was 0.7599 for the superior rectus muscle, 0.8183 for the lateral rectus muscle, 0.8481 for the medial rectus muscle, 0.8436 for the inferior rectus muscle and 0.8337 for the optic nerve. The volumes measured from our segmentation results agreed well with those from the ground truth (all R>0.98, P<0.0001). Conclusion: The qualitative and quantitative evaluations demonstrate excellent performance of our method in automatically extracting the total EOM and ON and measuring their volumes in orbital CT images. There is a great promise for clinical application to assess these anatomical structures for the diagnosis and prognosis of TAO.
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Since the introduction of optical coherence tomography (OCT), it has been possible to study the complex 3D morphological changes of the optic nerve head (ONH) tissues that occur along with the progression of glaucoma. Although several deep learning (DL) techniques have been recently proposed for the automated extraction (segmentation) and quantification of these morphological changes, the device specific nature and the difficulty in preparing manual segmentations (training data) limit their clinical adoption. With several new manufacturers and next-generation OCT devices entering the market, the complexity in deploying DL algorithms clinically is only increasing. To address this, we propose a DL based 3D segmentation framework that is easily translatable across OCT devices in a label-free manner (i.e. without the need to manually re-segment data for each device). Specifically, we developed 2 sets of DL networks. The first (referred to as the enhancer) was able to enhance OCT image quality from 3 OCT devices, and harmonized image-characteristics across these devices. The second performed 3D segmentation of 6 important ONH tissue layers. We found that the use of the enhancer was critical for our segmentation network to achieve device independency. In other words, our 3D segmentation network trained on any of 3 devices successfully segmented ONH tissue layers from the other two devices with high performance (Dice coefficients > 0.92). With such an approach, we could automatically segment images from new OCT devices without ever needing manual segmentation data from such devices.
Purpose: To develop a deep learning approach to de-noise optical coherence tomography (OCT) B-scans of the optic nerve head (ONH). Methods: Volume scans consisting of 97 horizontal B-scans were acquired through the center of the ONH using a commercial OCT device (Spectralis) for both eyes of 20 subjects. For each eye, single-frame (without signal averaging), and multi-frame (75x signal averaging) volume scans were obtained. A custom deep learning network was then designed and trained with 2,328 clean B-scans (multi-frame B-scans), and their corresponding noisy B-scans (clean B-scans + gaussian noise) to de-noise the single-frame B-scans. The performance of the de-noising algorithm was assessed qualitatively, and quantitatively on 1,552 B-scans using the signal to noise ratio (SNR), contrast to noise ratio (CNR), and mean structural similarity index metrics (MSSIM). Results: The proposed algorithm successfully denoised unseen single-frame OCT B-scans. The denoised B-scans were qualitatively similar to their corresponding multi-frame B-scans, with enhanced visibility of the ONH tissues. The mean SNR increased from $4.02 pm 0.68$ dB (single-frame) to $8.14 pm 1.03$ dB (denoised). For all the ONH tissues, the mean CNR increased from $3.50 pm 0.56$ (single-frame) to $7.63 pm 1.81$ (denoised). The MSSIM increased from $0.13 pm 0.02$ (single frame) to $0.65 pm 0.03$ (denoised) when compared with the corresponding multi-frame B-scans. Conclusions: Our deep learning algorithm can denoise a single-frame OCT B-scan of the ONH in under 20 ms, thus offering a framework to obtain superior quality OCT B-scans with reduced scanning times and minimal patient discomfort.
Quantitative analysis of cell structures is essential for biomedical and pharmaceutical research. The standard imaging approach relies on fluorescence microscopy, where cell structures of interest are labeled by chemical staining techniques. However, these techniques are often invasive and sometimes even toxic to the cells, in addition to being time-consuming, labor-intensive, and expensive. Here, we introduce an alternative deep-learning-powered approach based on the analysis of brightfield images by a conditional generative adversarial neural network (cGAN). We show that this approach can extract information from the brightfield images to generate virtually-stained images, which can be used in subsequent downstream quantitative analyses of cell structures. Specifically, we train a cGAN to virtually stain lipid droplets, cytoplasm, and nuclei using brightfield images of human stem-cell-derived fat cells (adipocytes), which are of particular interest for nanomedicine and vaccine development. Subsequently, we use these virtually-stained images to extract quantitative measures about these cell structures. Generating virtually-stained fluorescence images is less invasive, less expensive, and more reproducible than standard chemical staining; furthermore, it frees up the fluorescence microscopy channels for other analytical probes, thus increasing the amount of information that can be extracted from each cell.
Purpose: To develop a deep learning approach to digitally-stain optical coherence tomography (OCT) images of the optic nerve head (ONH). Methods: A horizontal B-scan was acquired through the center of the ONH using OCT (Spectralis) for 1 eye of each of 100 subjects (40 normal & 60 glaucoma). All images were enhanced using adaptive compensation. A custom deep learning network was then designed and trained with the compensated images to digitally stain (i.e. highlight) 6 tissue layers of the ONH. The accuracy of our algorithm was assessed (against manual segmentations) using the Dice coefficient, sensitivity, and specificity. We further studied how compensation and the number of training images affected the performance of our algorithm. Results: For images it had not yet assessed, our algorithm was able to digitally stain the retinal nerve fiber layer + prelamina, the retinal pigment epithelium, all other retinal layers, the choroid, and the peripapillary sclera and lamina cribrosa. For all tissues, the mean dice coefficient was $0.84 pm 0.03$, the mean sensitivity $0.92 pm 0.03$, and the mean specificity $0.99 pm 0.00$. Our algorithm performed significantly better when compensated images were used for training. Increasing the number of images (from 10 to 40) to train our algorithm did not significantly improve performance, except for the RPE. Conclusion. Our deep learning algorithm can simultaneously stain neural and connective tissues in ONH images. Our approach offers a framework to automatically measure multiple key structural parameters of the ONH that may be critical to improve glaucoma management.
For conventional computed tomography (CT) image reconstruction tasks, the most popular method is the so-called filtered-back-projection (FBP) algorithm. In it, the acquired Radon projections are usually filtered first by a ramp kernel before back-projected to generate CT images. In this work, as a contrary, we realized the idea of image-domain backproject-filter (BPF) CT image reconstruction using the deep learning techniques for the first time. With a properly designed convolutional neural network (CNN), preliminary results demonstrate that it is feasible to reconstruct CT images with maintained high spatial resolution and accurate pixel values from the highly blurred back-projection image, i.e., laminogram. In addition, experimental results also show that this deconvolution-based CT image reconstruction network has the potential to reduce CT image noise (up to 20%), indicating that patient radiation dose may be reduced. Due to these advantages, this proposed CNN-based image-domain BPF type CT image reconstruction scheme provides promising prospects in generating high spatial resolution, low-noise CT images for future clinical applications.
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