End-to-End Semi-Supervised Opportunistic Osteoporosis Screening Using Computed Tomography.

BACKGRUOUND: Osteoporosis is the most common metabolic bone disease and can cause fragility fractures. Despite this, screening utilization rates for osteoporosis remain low among populations at risk. Automated bone mineral density (BMD) estimation using computed tomography (CT) can help bridge this gap and serve as an alternative screening method to dual-energy X-ray absorptiometry (DXA). METHODS: The feasibility of an opportunistic and population agnostic screening method for osteoporosis using abdominal CT scans without bone densitometry phantom-based calibration was investigated in this retrospective study. A total of 268 abdominal CT-DXA pairs and 99 abdominal CT studies without DXA scores were obtained from an oncology specialty clinic in the Republic of Korea. The center axial CT slices from the L1, L2, L3, and L4 lumbar vertebrae were annotated with the CT slice level and spine segmentation labels for each subject. Deep learning models were trained to localize the center axial slice from the CT scan of the torso, segment the vertebral bone, and estimate BMD for the top four lumbar vertebrae. RESULTS: Automated vertebra-level DXA measurements showed a mean absolute error (MAE) of 0.079, Pearson's r of 0.852 (P<0.001), and R2 of 0.714. Subject-level predictions on the held-out test set had a MAE of 0.066, Pearson's r of 0.907 (P<0.001), and R2 of 0.781. CONCLUSION: CT scans collected during routine examinations without bone densitometry calibration can be used to generate DXA BMD predictions.

Unpaired deep learning for pharmacokinetic parameter estimation from dynamic contrast-enhanced MRI without AIF measurements.

DCE-MRI provides information about vascular permeability and tissue perfusion through the acquisition of pharmacokinetic parameters. However, traditional methods for estimating these pharmacokinetic parameters involve fitting tracer kinetic models, which often suffer from computational complexity and low accuracy due to noisy arterial input function (AIF) measurements. Although some deep learning approaches have been proposed to tackle these challenges, most existing methods rely on supervised learning that requires paired input DCE-MRI and labeled pharmacokinetic parameter maps. This dependency on labeled data introduces significant time and resource constraints and potential noise in the labels, making supervised learning methods often impractical. To address these limitations, we present a novel unpaired deep learning method for estimating pharmacokinetic parameters and the AIF using a physics-driven CycleGAN approach. Our proposed CycleGAN framework is designed based on the underlying physics model, resulting in a simpler architecture with a single generator and discriminator pair. Crucially, our experimental results indicate that our method does not necessitate separate AIF measurements and produces more reliable pharmacokinetic parameters than other techniques.

Generative Adversarial Network-Based Image Conversion Among Different Computed Tomography Protocols and Vendors: Effects on Accuracy and Variability in Quantifying Regional Disease Patterns of Interstitial Lung Disease.

OBJECTIVE: To assess whether computed tomography (CT) conversion across different scan parameters and manufacturers using a routable generative adversarial network (RouteGAN) can improve the accuracy and variability in quantifying interstitial lung disease (ILD) using a deep learning-based automated software. MATERIALS AND METHODS: This study included patients with ILD who underwent thin-section CT. Unmatched CT images obtained using scanners from four manufacturers (vendors A-D), standard- or low-radiation doses, and sharp or medium kernels were classified into groups 1-7 according to acquisition conditions. CT images in groups 2-7 were converted into the target CT style (Group 1: vendor A, standard dose, and sharp kernel) using a RouteGAN. ILD was quantified on original and converted CT images using a deep learning-based software (Aview, Coreline Soft). The accuracy of quantification was analyzed using the dice similarity coefficient (DSC) and pixel-wise overlap accuracy metrics against manual quantification by a radiologist. Five radiologists evaluated quantification accuracy using a 10-point visual scoring system. RESULTS: Three hundred and fifty CT slices from 150 patients (mean age: 67.6 ± 10.7 years; 56 females) were included. The overlap accuracies for quantifying total abnormalities in groups 2-7 improved after CT conversion (original vs. converted: 0.63 vs. 0.68 for DSC, 0.66 vs. 0.70 for pixel-wise recall, and 0.68 vs. 0.73 for pixel-wise precision; P < 0.002 for all). The DSCs of fibrosis score, honeycombing, and reticulation significantly increased after CT conversion (0.32 vs. 0.64, 0.19 vs. 0.47, and 0.23 vs. 0.54, P < 0.002 for all), whereas those of ground-glass opacity, consolidation, and emphysema did not change significantly or decreased slightly. The radiologists' scores were significantly higher (P < 0.001) and less variable on converted CT. CONCLUSION: CT conversion using a RouteGAN can improve the accuracy and variability of CT images obtained using different scan parameters and manufacturers in deep learning-based quantification of ILD.

Multi-domain CT translation by a routable translation network.

Objective.To unify the style of computed tomography (CT) images from multiple sources, we propose a novel multi-domain image translation network to convert CT images from different scan parameters and manufacturers by simply changing a routing vector.Approach.Unlike the existing multi-domain translation techniques, our method is based on a shared encoder and a routable decoder architecture to maximize the expressivity and conditioning power of the network.Main results.Experimental results show that the proposed CT image conversion can minimize the variation of image characteristics caused by imaging parameters, reconstruction algorithms, and hardware designs. Quantitative results and clinical evaluation from radiologists also show that our method can provide accurate translation results.Significance.Quantitative evaluation of CT images from multi-site or longitudinal studies has been a difficult problem due to the image variation depending on CT scan parameters and manufacturers. The proposed method can be utilized to address this for the quantitative analysis of multi-domain CT images.

Unsupervised resolution-agnostic quantitative susceptibility mapping using adaptive instance normalization.

Quantitative susceptibility mapping (QSM) is a useful magnetic resonance imaging (MRI) technique that provides the spatial distribution of magnetic susceptibility values of tissues. QSMs can be obtained by deconvolving the dipole kernel from phase images, but the spectral nulls in the dipole kernel make the inversion ill-posed. In recent years, deep learning approaches have shown a comparable QSM reconstruction performance to the classic approaches, in addition to the fast reconstruction time. Most of the existing deep learning methods are, however, based on supervised learning, so matched pairs of input phase images and ground-truth maps are needed. Moreover, it was reported that the deep learning-based methods fail to reconstruct QSM when the resolution of test data is different from the trained resolution. To address this, here we propose an unsupervised resolution-agnostic QSM deep learning method. The proposed method does not require QSM labels for training and reconstructs QSM with various resolutions by using adaptive instance normalization. Experimental results and clinical validation confirm that the proposed method provides accurate QSM with various resolutions compared to other deep learning approaches, and shows competitive performance to the best classical approaches in addition to the ultra-fast reconstruction.

Unpaired MR Motion Artifact Deep Learning Using Outlier-Rejecting Bootstrap Aggregation.

Recently, deep learning approaches for MR motion artifact correction have been extensively studied. Although these approaches have shown high performance and lower computational complexity compared to classical methods, most of them require supervised training using paired artifact-free and artifact-corrupted images, which may prohibit its use in many important clinical applications. For example, transient severe motion (TSM) due to acute transient dyspnea in Gd-EOB-DTPA-enhanced MR is difficult to control and model for paired data generation. To address this issue, here we propose a novel unpaired deep learning scheme that does not require matched motion-free and motion artifact images. Specifically, the first step of our method is k -space random subsampling along the phase encoding direction that can remove some outliers probabilistically. In the second step, the neural network reconstructs fully sampled resolution image from a downsampled k -space data, and motion artifacts can be reduced in this step. Last, the aggregation step through averaging can further improve the results from the reconstruction network. We verify that our method can be applied for artifact correction from simulated motion as well as real motion from TSM successfully from both single and multi-coil data with and without k -space raw data, outperforming existing state-of-the-art deep learning methods.