The new artificial intelligence-based software, Roadmap (HeartFlow), may assist in evaluating coronary artery stenosis during cardiac computed tomography (CT) for transcatheter aortic valve replacement (TAVR). Consecutive TAVR candidates who underwent both cardiac CT angiography (CTA) and invasive coronary angiography were enrolled. We evaluated the ability of three methods to predict obstructive coronary artery disease (CAD), defined as ≥50 ​% stenosis on quantitative coronary angiography (QCA), and the need for percutaneous coronary intervention (PCI) within one year: Roadmap, clinician CT specialists with Roadmap, and CT specialists alone. The area under the curve (AUC) for predicting QCA ≥50 ​% stenosis was similar for CT specialists with or without Roadmap (0.93 [0.85-0.97] vs. 0.94 [0.88-0.98], p ​= ​0.82), both significantly higher than Roadmap alone (all p ​< ​0.05). For PCI prediction, no significant differences were found between QCA and CT specialists, with or without Roadmap, while Roadmap's AUC was lower (all p ​< ​0.05). The negative predictive value (NPV) of CT specialists with Roadmap for ≥50 ​% stenosis was 97 ​%, and for PCI prediction, the NPV was comparable to QCA (p ​= ​1.00). In contrast, the positive predictive value (PPV) of Roadmap alone for ≥50 ​% stenosis was 49 ​%, the lowest among all approaches, with a similar trend observed for PCI prediction. While Roadmap alone is insufficient for clinical decision-making due to low PPV, Roadmap may serve as a "second observer", providing a supportive tool for CT specialists by flagging lesions for careful review, thereby enhancing workflow efficiency and maintaining high diagnostic accuracy with excellent NPV.

The severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) causes Coronavirus Disease 2019 (COVID-19) and induces activation of inflammatory pathways, including the inflammasome. The aim was to construct Machine Learning (ML) models to predict critical disease and death in patients with COVID-19. A total of 528 individuals with SARS-CoV-2 infection were included, comprising 308 with critical and 220 with non-critical COVID-19. The ML models included imaging, demographic, inflammatory biomarkers, NLRP3 (rs10754558 and rs10157379) and IL18 (rs360717 and rs187238) inflammasome variants. Individuals with critical COVID-19 were older, higher male/female ratio, body mass index (BMI), rate of type 2 diabetes mellitus (T2DM), hypertension, inflammatory biomarkers, need of orotracheal intubation, intensive care unit admission, incidence of death, and sickness symptom complex (SSC) scores and lower peripheral oxygen saturation (SpO₂) compared to those with non-critical disease. We found that 49.5 % of the variance in the severity of critical COVID-19 was explained by SpO₂ and SSC (negatively associated), chest computed tomography alterations (CCTA), inflammatory biomarkers, severe acute respiratory syndrome (SARS), BMI, T2DM, and age (positively associated). In this model, the NLRP3/IL18 variants showed indirect effects on critical COVID-19 that were mediated by inflammatory biomarkers, SARS, and SSC. Neural network models yielded a prediction of critical disease and death due to COVID-19 with an area under the receiving operating characteristic curve of 0.930 and 0.927, respectively. These ML methods increase the accuracy of predicting severity, critical illness, and mortality caused by COVID-19 and show that the genetic variants contribute to the predictive power of the ML models.

Computer-aided surgical simulation is a critical component of orthognathic surgical planning, where accurately simulating face-bone shape transformations is significant. The traditional biomechanical simulation methods are limited by their computational time consumption levels, labor-intensive data processing strategies and low accuracy. Recently, deep learning-based simulation methods have been proposed to view this problem as a point-to-point transformation between skeletal and facial point clouds. However, these approaches cannot process large-scale points, have limited receptive fields that lead to noisy points, and employ complex preprocessing and postprocessing operations based on registration. These shortcomings limit the performance and widespread applicability of such methods. Therefore, we propose a Transformer-based coarse-to-fine point movement network (TCFNet) to learn unique, complicated correspondences at the patch and point levels for dense face-bone point cloud transformations. This end-to-end framework adopts a Transformer-based network and a local information aggregation network (LIA-Net) in the first and second stages, respectively, which reinforce each other to generate precise point movement paths. LIA-Net can effectively compensate for the neighborhood precision loss of the Transformer-based network by modeling local geometric structures (edges, orientations and relative position features). The previous global features are employed to guide the local displacement using a gated recurrent unit. Inspired by deformable medical image registration, we propose an auxiliary loss that can utilize expert knowledge for reconstructing critical organs. Our framework is an unsupervised algorithm, and this loss is optional. Compared with the existing state-of-the-art (SOTA) methods on gathered datasets, TCFNet achieves outstanding evaluation metrics and visualization results. The code is available at https://github.com/Runshi-Zhang/TCFNet.

Inter reader variability and cross site domain shift challenge the automatic segmentation of prostate anatomy using T2 weighted MRI images. This study investigates whether transformer models can retain precision amid such heterogeneity. We compare the performance of UNETR and SwinUNETR in prostate gland segmentation against our previous 3D UNet model [1], based on 546 MRI (T2weighted) volumes annotated by two independent experts. Three training strategies were analyzed: single cohort dataset, 5 fold cross validated mixed cohort, and gland size based dataset. Hyperparameters were tuned by Optuna. The test set, from an independent population of readers, served as the evaluation endpoint (Dice Similarity Coefficient). In single reader training, SwinUNETR achieved an average dice score of 0.816 for Reader#1 and 0.860 for Reader#2, while UNETR scored 0.8 and 0.833 for Readers #1 and #2, respectively, compared to the baseline UNets 0.825 for Reader #1 and 0.851 for Reader #2. SwinUNETR had an average dice score of 0.8583 for Reader#1 and 0.867 for Reader#2 in cross-validated mixed training. For the gland size-based dataset, SwinUNETR achieved an average dice score of 0.902 for Reader#1 subset and 0.894 for Reader#2, using the five-fold mixed training strategy (Reader#1, n=53; Reader#2, n=87) at larger gland size-based subsets, where UNETR performed poorly. Our findings demonstrate that global and shifted-window self-attention effectively reduces label noise and class imbalance sensitivity, resulting in improvements in the Dice score over CNNs by up to five points while maintaining computational efficiency. This contributes to the high robustness of SwinUNETR for clinical deployment.

Synthesizing high quality CT projection data remains a significant challenge due to the limited availability of annotated data and the complex nature of CT imaging. In this work, we present PRO, a projection domain synthesis foundation model for CT imaging. To the best of our knowledge, this is the first study that performs CT synthesis in the projection domain. Unlike previous approaches that operate in the image domain, PRO learns rich structural representations from raw projection data and leverages anatomical text prompts for controllable synthesis. This projection domain strategy enables more faithful modeling of underlying imaging physics and anatomical structures. Moreover, PRO functions as a foundation model, capable of generalizing across diverse downstream tasks by adjusting its generative behavior via prompt inputs. Experimental results demonstrated that incorporating our synthesized data significantly improves performance across multiple downstream tasks, including low-dose and sparse-view reconstruction. These findings underscore the versatility and scalability of PRO in data generation for various CT applications. These results highlight the potential of projection domain synthesis as a powerful tool for data augmentation and robust CT imaging. Our source code is publicly available at: https://github.com/yqx7150/PRO.

Kernel size selection in Convolutional Neural Networks (CNNs) is a critical but often overlooked design decision that affects receptive field, feature extraction, computational cost, and model accuracy. This paper proposes the Best Kernel Size Estimation Function (BKSEF), a mathematically grounded and empirically validated framework for optimal, layer-wise kernel size determination. BKSEF balances information gain, computational efficiency, and accuracy improvements by integrating principles from information theory, signal processing, and learning theory. Extensive experiments on CIFAR-10, CIFAR-100, ImageNet-lite, ChestX-ray14, and GTSRB datasets demonstrate that BKSEF-guided architectures achieve up to 3.1 percent accuracy improvement and 42.8 percent reduction in FLOPs compared to traditional models using uniform 3x3 kernels. Two real-world case studies further validate the approach: one for medical image classification in a cloud-based setup, and another for traffic sign recognition on edge devices. The former achieved enhanced interpretability and accuracy, while the latter reduced latency and model size significantly, with minimal accuracy trade-off. These results show that kernel size can be an active, optimizable parameter rather than a fixed heuristic. BKSEF provides practical heuristics and theoretical support for researchers and developers seeking efficient and application-aware CNN designs. It is suitable for integration into neural architecture search pipelines and real-time systems, offering a new perspective on CNN optimization.

High tumor recurrence after surgery remains a significant challenge in managing hepatocellular carcinoma (HCC). We aimed to construct a multimodal model to forecast the early recurrence of HCC after surgical resection and explore the associated biological mechanisms. Overall, 519 patients with HCC were included from three medical centers. 433 patients from Nanfang Hospital were used as the training cohort, and 86 patients from the other two hospitals comprised validation cohort. Radiomics and deep learning (DL) models were developed using contrast-enhanced computed tomography images. Radiomics feature visualization and gradient-weighted class activation mapping were applied to improve interpretability. A multimodal model (MM-RDLM) was constructed by integrating radiomics and DL models. Associations between MM-RDLM and recurrence-free survival (RFS) and overall survival were analyzed. Gene set enrichment analysis (GSEA) and multiplex immunohistochemistry (mIHC) were used to investigate the biological mechanisms. Models based on hepatic arterial phase images exhibited the best predictive performance, with radiomics and DL models achieving areas under the curve (AUCs) of 0.770 (95 % confidence interval [CI]: 0.725-0.815) and 0.846 (95 % CI: 0.807-0.886), respectively, in the training cohort. MM-RDLM achieved an AUC of 0.955 (95 % CI: 0.937-0.972) in the training cohort and 0.930 (95 % CI: 0.876-0.984) in the validation cohort. MM-RDLM (high vs. low) was notably linked to RFS in the training (hazard ratio [HR] = 7.80 [5.74 - 10.61], P < 0.001) and validation (HR = 10.46 [4.96 - 22.68], P < 0.001) cohorts. GSEA revealed enrichment of the natural killer cell-mediated cytotoxicity pathway in the MM-RDLM low cohort. mIHC showed significantly higher percentages of CD3-, CD56-, and CD8-positive cells in the MM-RDLM low group. The MM-RDLM model demonstrated strong predictive performance for early postoperative recurrence of HCC. These findings contribute to identifying patients at high risk for early recurrence and provide insights into the potential underlying biological mechanisms.

We aimed to develop a machine-learning(ML) algorithm consisting of physical examination, sonographic findings, and laboratory markers. The data of 70 patients with confirmed ovarian torsion followed and treated in our clinic for ovarian torsion and 73 patients for control group that presented to the emergency department with similar complaints but didn't have ovarian torsion detected on ultrasound as the control group between 2013-2023 were retrospectively analyzed. Sonographic findings, laboratory values, and clinical status of patients were examined and fed into three supervised ML systems to identify and develop viable decision algorithms. Presence of nausea/vomiting and symptom duration was statistically significant(p<0.05) for ovarian torsion. Presence of abdominal pain and palpable mass on physical examination weren't significant(p>0.05). White blood cell count(WBC), neutrophile/lymphocyte ratio(NLR), systemic immune-inflammation index(SII) and systemic inflammation response index(SIRI), high values of C-reactive protein was highly significant in prediction of torsion( p<0.001,p<0.05). Ovarian size ratio, medialization, follicular ring sign, presence of free fluid in pelvis in ultrasound demonstrated statistical significance in the torsion group(p<0.001). We used supervised ML algorithms, including decision trees, random forests, and LightGBM, to classify patients as either control or having torsion. We evaluated the models using 5-fold cross-validation, achieving an average F1-score of 98%, an accuracy of 98%, and a specificity of 100% across each fold with the decision tree model. This study represents the first development of a ML algorithm that integrates clinical, laboratory and ultrasonographic findings for the diagnosis of pediatric ovarian torsion with over 98% accuracy.

The human brain exhibits intricate spatiotemporal dynamics, which can be described and understood through the framework of complex dynamic systems theory. In this study, we leverage functional magnetic resonance imaging (fMRI) data to investigate reaction-diffusion processes in the brain. A reaction-diffusion process refers to the interaction between two or more substances that spread through space and react with each other over time, often resulting in the formation of patterns or waves of activity. Building on this empirical foundation, we apply a reaction-diffusion framework inspired by theoretical physics to simulate the emergence of brain spacetime vortices within the brain. By exploring this framework, we investigate how reaction-diffusion processes can serve as a compelling model to govern the formation and propagation of brain spacetime vortices, which are dynamic, swirling patterns of brain activity that emerge and evolve across both time and space within the brain. Our approach integrates computational modeling with fMRI data to investigate the spatiotemporal properties of these vortices, offering new insights into the fundamental principles of brain organization. This work highlights the potential of reaction-diffusion models as an alternative framework for understanding brain spacetime dynamics.

Background and purposeAccurate estimation of Overall Survival (OS) in Non-Small Cell Lung Cancer (NSCLC) patients provides critical insights for treatment planning. While previous studies showed that radiomics and Deep Learning (DL) features increased prediction accuracy, this study aimed to examine whether a model that combines the radiomics and DL features with the clinical and dosimetric features outperformed other models. Materials and methodsWe collected pre-treatment lung CT scans and clinical data for 225 NSCLC patients from the Maastro Clinic: 180 for training and 45 for testing. Radiomics features were extracted using the Python radiomics feature extractor, and DL features were obtained using a 3D ResNet model. An ensemble model comprising XGB and NN classifiers was developed using: (1) clinical features only; (2) clinical and radiomics features; (3) clinical and DL features; and (4) clinical, radiomics, and DL features. The performance metrics were evaluated for the test and K-fold cross-validation data sets. ResultsThe prediction model utilizing only clinical variables provided an Area Under the Receiver Operating Characteristic Curve (AUC) of 0.64 and a test accuracy of 77.55%. The best performance came from combining clinical, radiomics, and DL features (AUC: 0.84, accuracy: 85.71%). The prediction improvement of this model was statistically significant compared to models trained with clinical features alone or with a combination of clinical and radiomics features. ConclusionIntegrating radiomics and DL features with clinical characteristics improved the prediction of OS after radiotherapy for NSCLC patients. The increased accuracy of our integrated model enables personalized, risk-based treatment planning, guiding clinicians toward more effective interventions, improved patient outcomes and enhanced quality of life.