The limited availability of bronchoscopy images makes image synthesis particularly interesting for training deep learning models. Robust image translation across different domains -- virtual bronchoscopy, phantom as well as in-vivo and ex-vivo image data -- is pivotal for clinical applications. This paper proposes BronchoGAN introducing anatomical constraints for image-to-image translation being integrated into a conditional GAN. In particular, we force bronchial orifices to match across input and output images. We further propose to use foundation model-generated depth images as intermediate representation ensuring robustness across a variety of input domains establishing models with substantially less reliance on individual training datasets. Moreover our intermediate depth image representation allows to easily construct paired image data for training. Our experiments showed that input images from different domains (e.g. virtual bronchoscopy, phantoms) can be successfully translated to images mimicking realistic human airway appearance. We demonstrated that anatomical settings (i.e. bronchial orifices) can be robustly preserved with our approach which is shown qualitatively and quantitatively by means of improved FID, SSIM and dice coefficients scores. Our anatomical constraints enabled an improvement in the Dice coefficient of up to 0.43 for synthetic images. Through foundation models for intermediate depth representations, bronchial orifice segmentation integrated as anatomical constraints into conditional GANs we are able to robustly translate images from different bronchoscopy input domains. BronchoGAN allows to incorporate public CT scan data (virtual bronchoscopy) in order to generate large-scale bronchoscopy image datasets with realistic appearance. BronchoGAN enables to bridge the gap of missing public bronchoscopy images.

Estimating brain age from structural MRI has emerged as a powerful tool for characterizing normative and pathological aging. In this work, we explore contrastive learning as a scalable and robust alternative to supervised approaches for brain age estimation. We introduce a novel contrastive loss function, $\mathcal{L}^{exp}$, and evaluate it across multiple public neuroimaging datasets comprising over 20,000 scans. Our experiments reveal four key findings. First, scaling pre-training on diverse, multi-site data consistently improves generalization performance, cutting external mean absolute error (MAE) nearly in half. Second, $\mathcal{L}^{exp}$ is robust to site-related confounds, maintaining low scanner-predictability as training size increases. Third, contrastive models reliably capture accelerated aging in patients with cognitive impairment and Alzheimer's disease, as shown through brain age gap analysis, ROC curves, and longitudinal trends. Lastly, unlike supervised baselines, $\mathcal{L}^{exp}$ maintains a strong correlation between brain age accuracy and downstream diagnostic performance, supporting its potential as a foundation model for neuroimaging. These results position contrastive learning as a promising direction for building generalizable and clinically meaningful brain representations.

<b>Background:</b> Chest radiographs play a crucial role in tuberculosis screening in high-prevalence regions, although widespread radiographic screening requires expertise that may be unavailable in settings with limited medical resources. <b>Objectives:</b> To evaluate a multimodal generative artificial intelligence (AI) model for detecting tuberculosis-associated abnormalities on chest radiography in patients undergoing tuberculosis screening. <b>Methods:</b> This retrospective study evaluated 800 chest radiographs obtained from two public datasets originating from tuberculosis screening programs. A generative AI model was used to create free-text reports for the radiographs. AI-generated reports were classified in terms of presence versus absence and laterality of tuberculosis-related abnormalities. Two radiologists independently reviewed the radiographs for tuberculosis presence and laterality in separate sessions, without and with use of AI-generated reports and recorded if they would accept the report without modification. Two additional radiologists reviewed radiographs and clinical readings from the datasets to determine the reference standard. <b>Results:</b> By the reference standard, 422/800 radiographs were positive for tuberculosis-related abnormalities. For detection of tuberculosis-related abnormalities, sensitivity, specificity, and accuracy were 95.2%, 86.7%, and 90.8% for AI-generated reports; 93.1%, 93.6%, and 93.4% for reader 1 without AI-generated reports; 93.1%, 95.0%, and 94.1% for reader 1 with AI-generated reports; 95.8%, 87.2%, and 91.3% for reader 2 without AI-generated reports; and 95.8%, 91.5%, and 93.5% for reader 2 with AI-generated reports. Accuracy was significantly lower for AI-generated reports than for both readers alone (p<.001), but significantly higher with than without AI-generated reports for one reader (reader 1: p=.47; reader 2: p=.47). Localization performance was significantly lower (p<.001) for AI-generated reports (63.3%) than for reader 1 (79.9%) and reader 2 (77.9%) without AI-generated reports and did not significantly change for either reader with AI-generated reports (reader 1: 78.7%, p=.71; reader 2: 81.5%, p=.23). Among normal and abnormal radiographs, reader 1 accepted 91.7% and 52.4%, while reader 2 accepted 83.2% and 37.0%, respectively, of AI-generated reports. <b>Conclusion:</b> While AI-generated reports may augment radiologists' diagnostic assessments, the current model requires human oversight given inferior standalone performance. <b>Clinical Impact:</b> The generative AI model could have potential application to aid tuberculosis screening programs in medically underserved regions, although technical improvements remain required.

The rapid integration of artificial intelligence (AI) into healthcare has enhanced diagnostic accuracy; however, patient engagement and satisfaction remain significant challenges that hinder the widespread acceptance and effectiveness of AI-driven clinical tools. This study introduces CareAssist-GPT, a novel AI-assisted diagnostic model designed to improve both diagnostic accuracy and the patient experience through real-time, understandable, and empathetic communication. CareAssist-GPT combines high-resolution X-ray images, real-time physiological vital signs, and clinical notes within a unified predictive framework using deep learning. Feature extraction is performed using convolutional neural networks (CNNs), gated recurrent units (GRUs), and transformer-based NLP modules. Model performance was evaluated in terms of accuracy, precision, recall, specificity, and response time, alongside patient satisfaction through a structured user feedback survey. CareAssist-GPT achieved a diagnostic accuracy of 95.8%, improving by 2.4% over conventional models. It reported high precision (94.3%), recall (93.8%), and specificity (92.7%), with an AUC-ROC of 0.97. The system responded within 500 ms-23.1% faster than existing tools-and achieved a patient satisfaction score of 9.3 out of 10, demonstrating its real-time usability and communicative effectiveness. CareAssist-GPT significantly enhances the diagnostic process by improving accuracy and fostering patient trust through transparent, real-time explanations. These findings position it as a promising patient-centered AI solution capable of transforming healthcare delivery by bridging the gap between advanced diagnostics and human-centered communication.

The processing of medical images plays a central role in modern diagnostics and therapy. Automated processing and analysis of medical images can efficiently accelerate clinical workflows and open new opportunities for improved patient care. However, the high variability, complexity, and varying quality of medical image data pose significant challenges. In recent years, the greatest progress in medical image analysis has been achieved through artificial intelligence (AI), particularly by using deep neural networks in the context of deep learning. These methods are successfully applied in medical image analysis, including segmentation, registration, and image synthesis.AI-based segmentation allows for the precise delineation of organs, tissues, or pathological changes. The application of AI-based image registration supports the accelerated creation of 3D planning models for complex surgeries by aligning relevant anatomical structures from different imaging modalities (e.g., CT, MRI, and PET) or time points. Generative AI methods can be used to generate additional image data for the improved training of AI models, thereby expanding the potential applications of deep learning methods in medicine. Examples from radiology, ophthalmology, dermatology, and surgery are described to illustrate their practical relevance and the potential of AI in image-based diagnostics and therapy.

We propose a compositional graph-based Machine Learning (ML) framework for Alzheimer's disease (AD) detection that constructs complex ML predictors from modular components. In our directed computational graph, datasets are represented as nodes [Formula: see text], and deep learning (DL) models are represented as directed edges [Formula: see text], allowing us to model complex image-processing pipelines [Formula: see text] as end-to-end DL predictors. Each directed path in the graph functions as a DL predictor, supporting both forward propagation for transforming data representations, as well as backpropagation for model finetuning, saliency map computation, and input data optimization. We demonstrate our model on Alzheimer's disease prediction, a complex problem that requires integrating multimodal data containing scans of different modalities and contrasts, genetic data and cognitive tests. We built a graph of 11 nodes (data) and 14 edges (ML models), where each model has been trained on handling a specific task (e.g. skull-stripping MRI scans, AD detection,image2image translation, ...). By using a modular and adaptive approach, our framework effectively integrates diverse data types, handles distribution shifts, and scales to arbitrary complexity, offering a practical tool that remains accurate even when modalities are missing for advancing Alzheimer's disease diagnosis and potentially other complex medical prediction tasks.

Multimodal neuroimaging data modeling has become a widely used approach but confronts considerable challenges due to their heterogeneity, which encompasses variability in data types, scales, and formats across modalities. This variability necessitates the deployment of advanced computational methods to integrate and interpret diverse datasets within a cohesive analytical framework. In our research, we combine functional magnetic resonance imaging (fMRI), diffusion tensor imaging (DTI), and structural MRI (sMRI) for joint analysis. This integration capitalizes on the unique strengths of each modality and their inherent interconnections, aiming for a comprehensive understanding of the brain's connectivity and anatomical characteristics. Utilizing the Glasser atlas for parcellation, we integrate imaging-derived features from multiple modalities - functional connectivity from fMRI, structural connectivity from DTI, and anatomical features from sMRI - within consistent regions. Our approach incorporates a masking strategy to differentially weight neural connections, thereby facilitating an amalgamation of multimodal imaging data. This technique enhances interpretability at the connectivity level, transcending traditional analyses centered on singular regional attributes. The model is applied to the Human Connectome Project's Development study to elucidate the associations between multimodal imaging and cognitive functions throughout youth. The analysis demonstrates improved prediction accuracy and uncovers crucial anatomical features and neural connections, deepening our understanding of brain structure and function. This study not only advances multimodal neuroimaging analytics by offering a novel method for integrative analysis of diverse imaging modalities but also improves the understanding of intricate relationships between brain's structural and functional networks and cognitive development.

This study introduces an ensemble framework that integrates Vision Transformer (ViT) and Convolutional Neural Networks (CNN) models to leverage their complementary strengths, generating visualized and decision-transparent recommendations for dual-energy X-ray absorptiometry (DXA) scans from chest low-dose computed tomography (LDCT). The framework was developed using data from 321 individuals and validated with an independent test cohort of 186 individuals. It addresses two classification tasks: (1) distinguishing normal from abnormal bone mineral density (BMD) and (2) differentiating osteoporosis from non-osteoporosis. Three field-of-view (FOV) settings-fitFOV (entire vertebra), halfFOV (vertebral body only), and largeFOV (fitFOV + 20 %)-were analyzed to assess their impact on model performance. Model predictions were weighted and combined to enhance classification accuracy, and visualizations were generated to improve decision transparency. DXA scans were recommended for individuals classified as having abnormal BMD or osteoporosis. The ensemble framework significantly outperformed individual models in both classification tasks (McNemar test, p < 0.001). In the development cohort, it achieved 91.6 % accuracy for task 1 with largeFOV (area under the receiver operating characteristic curve [AUROC]: 0.97) and 86.0 % accuracy for task 2 with fitFOV (AUROC: 0.94). In the test cohort, it demonstrated 86.6 % accuracy for task 1 (AUROC: 0.93) and 76.9 % accuracy for task 2 (AUROC: 0.99). DXA recommendation accuracy was 91.6 % and 87.1 % in the development and test cohorts, respectively, with notably high accuracy for osteoporosis detection (98.7 % and 100 %). This combined ViT-CNN framework effectively assesses bone status from LDCT images, particularly when utilizing fitFOV and largeFOV settings. By visualizing classification confidence and vertebral abnormalities, the proposed framework enhances decision transparency and supports clinicians in making informed DXA recommendations following opportunistic osteoporosis screening.

Idiopathic Pulmonary Fibrosis (IPF) is a progressive lung disease that continuously scars and thickens lung tissue, leading to respiratory difficulties. Timely assessment of IPF progression is essential for developing treatment plans and improving patient survival rates. However, current clinical standards require multiple (usually two) CT scans at certain intervals to assess disease progression. This presents a dilemma: the disease progression is identified only after the disease has already progressed. To address this issue, a feasible solution is to generate the follow-up CT image from the patient's initial CT image to achieve early prediction of IPF. To this end, we propose a lung structure and function information-guided residual diffusion model. The key components of our model include (1) using a 2.5D generation strategy to reduce computational cost of generating 3D images with the diffusion model; (2) designing structural attention to mitigate negative impact of spatial misalignment between the two CT images on generation performance; (3) employing residual diffusion to accelerate model training and inference while focusing more on differences between the two CT images (i.e., the lesion areas); and (4) developing a CLIP-based text extraction module to extract lung function test information and further using such extracted information to guide the generation. Extensive experiments demonstrate that our method can effectively predict IPF progression and achieve superior generation performance compared to state-of-the-art methods.

Lung cancer remains the leading cause of cancer-related mortality worldwide, with its early detection and effective treatment posing significant clinical challenges. Radiomics, the extraction of quantitative features from medical imaging, has emerged as a promising approach for enhancing diagnostic accuracy, predicting treatment responses, and personalising patient care. This review explores the role of radiomics in lung cancer diagnosis and management, with methods ranging from handcrafted radiomics to deep learning techniques that can capture biological intricacies. The key applications are highlighted across various stages of lung cancer care, including nodule detection, histology prediction, and disease staging, where artificial intelligence (AI) models demonstrate superior specificity and sensitivity. The article also examines future directions, emphasising the integration of large language models, explainable AI (XAI), and super-resolution imaging techniques as transformative developments. By merging diverse data sources and incorporating interpretability into AI models, radiomics stands poised to redefine clinical workflows, offering more robust and reliable tools for lung cancer diagnosis, treatment planning, and outcome prediction. These advancements underscore radiomics' potential in supporting precision oncology and improving patient outcomes through data-driven insights.