With the rapid development of artificial intelligence (AI), AI-assisted medical imaging analysis demonstrates remarkable performance in early lung cancer screening. However, the costly annotation process and privacy concerns limit the construction of large-scale medical datasets, hampering the further application of AI in healthcare. To address the data scarcity in lung cancer screening, we propose Lung-DDPM, a thoracic CT image synthesis approach that effectively generates high-fidelity 3D synthetic CT images, which prove helpful in downstream lung nodule segmentation tasks. Our method is based on semantic layout-guided denoising diffusion probabilistic models (DDPM), enabling anatomically reasonable, seamless, and consistent sample generation even from incomplete semantic layouts. Our results suggest that the proposed method outperforms other state-of-the-art (SOTA) generative models in image quality evaluation and downstream lung nodule segmentation tasks. Specifically, Lung-DDPM achieved superior performance on our large validation cohort, with a Fréchet inception distance (FID) of 0.0047, maximum mean discrepancy (MMD) of 0.0070, and mean squared error (MSE) of 0.0024. These results were 7.4×, 3.1×, and 29.5× better than the second-best competitors, respectively. Furthermore, the lung nodule segmentation model, trained on a dataset combining real and Lung-DDPM-generated synthetic samples, attained a Dice Coefficient (Dice) of 0.3914 and sensitivity of 0.4393. This represents 8.8% and 18.6% improvements in Dice and sensitivity compared to the model trained solely on real samples. The experimental results highlight Lung-DDPM's potential for a broader range of medical imaging applications, such as general tumor segmentation, cancer survival estimation, and risk prediction. The code and pretrained models are available at https://github.com/Manem-Lab/Lung-DDPM/.

Tractometry uses diffusion-weighted magnetic resonance imaging (dMRI) to assess physical properties of brain connections. Here, we present an integrative ecosystem of software that performs all steps of tractometry: post-processing of dMRI data, delineation of major white matter pathways, and modeling of the tissue properties within them. This ecosystem also provides a set of interoperable and extensible tools for visualization and interpretation of the results that extract insights from these measurements. These include novel machine learning and statistical analysis methods adapted to the characteristic structure of tract-based data. We benchmark the performance of these statistical analysis methods in different datasets and analysis tasks, including hypothesis testing on group differences and predictive analysis of subject age. We also demonstrate that computational advances implemented in the software offer orders of magnitude of acceleration. Taken together, these open-source software tools-freely available at https://tractometry.org-provide a transformative environment for the analysis of dMRI data.

Recent innovations in medical imaging have markedly improved brain tumor identification, surpassing conventional diagnostic approaches that suffer from low resolution, radiation exposure, and limited contrast. Magnetic Resonance Imaging (MRI) is pivotal in precise and accurate tumor characterization owing to its high-resolution, non-invasive nature. This study investigates the synergy among multiple feature representation schemes such as local Binary Patterns (LBP), Gabor filters, Discrete Wavelet Transform, Fast Fourier Transform, Convolutional Neural Networks (CNN), and Gray-Level Run Length Matrix alongside five learning algorithms namely: k-nearest Neighbor, Random Forest, Support Vector Classifier (SVC), and probabilistic neural network (PNN), and CNN. Empirical findings indicate that LBP in conjunction with SVC and CNN obtained high specificity and accuracy, rendering it a promising method for MRI-based tumor diagnosis. Further to investigate the contribution of LBP, Statistical analysis chi-square and p-value tests are used to confirm the significant impact of LBP feature space for identification of brain Tumor. In addition, The SHAP analysis was used to identify the most important features in classification. In a small dataset, CNN obtained 97.8% accuracy while SVC yielded 98.06% accuracy. In subsequent analysis, a large benchmark dataset is also utilized to evaluate the performance of learning algorithms in order to investigate the generalization power of the proposed model. CNN achieves the highest accuracy of 98.9%, followed by SVC at 96.7%. These results highlight CNN's effectiveness in automated, high-precision tumor diagnosis. This achievement is ascribed with MRI-based feature extraction by combining high resolution, non-invasive imaging capabilities with the powerful analytical abilities of CNN. CNN demonstrates superiority in medical imaging owing to its ability to learn intricate spatial patterns and generalize effectively. This interaction enhances the accuracy, speed, and consistency of brain tumor detection, ultimately leading to better patient outcomes and more efficient healthcare delivery. https://github.com/asifrahman557/BrainTumorDetection .

The volume of image data generated in the medical field is continuously increasing. Manual annotation is both costly and prone to human error. Additionally, deep learning-based medical image algorithms rely on large, accurately annotated training datasets, which are expensive to produce and often result in instability. This study introduces LR-COBRAS, an interactive computer-aided data annotation algorithm designed for medical experts. LR-COBRAS aims to assist healthcare professionals in achieving more precise annotation outcomes through interactive processes, thereby optimizing medical image annotation tasks. The algorithm enhances must-link and cannot-link constraints during interactions through a logic reasoning module. It automatically generates potential constraint relationships, reducing the frequency of user interactions and improving clustering accuracy. By utilizing rules such as symmetry, transitivity, and consistency, LR-COBRAS effectively balances automation with clinical relevance. Experimental results based on the MedMNIST＋ dataset and ChestX-ray8 dataset demonstrate that LR-COBRAS significantly outperforms existing methods in clustering accuracy, efficiency, and interactive burden, showcasing superior robustness and applicability. This algorithm provides a novel solution for intelligent medical image analysis. The source code for our implementation is available on https://github.com/cjw-bbxc/MILR-COBRAS.

Computed tomography (CT) is one of the most widely used non-invasive imaging modalities for medical diagnosis. In clinical practice, CT images are usually acquired with large slice thicknesses due to the high cost of memory storage and operation time, resulting in an anisotropic CT volume with much lower inter-slice resolution than in-plane resolution. Since such inconsistent resolution may lead to difficulties in disease diagnosis, deep learning-based volumetric super-resolution methods have been developed to improve inter-slice resolution. Most existing methods conduct single-image super-resolution on the through-plane or synthesize intermediate slices from adjacent slices; however, the anisotropic characteristic of 3D CT volume has not been well explored. In this paper, we propose a novel cross-view texture transfer approach for CT slice interpolation by fully utilizing the anisotropic nature of 3D CT volume. Specifically, we design a unique framework that takes high-resolution in-plane texture details as a reference and transfers them to low-resolution through-plane images. To this end, we introduce a multi-reference non-local attention module that extracts meaningful features for reconstructing through-plane high-frequency details from multiple in-plane images. Through extensive experiments, we demonstrate that our method performs significantly better in CT slice interpolation than existing competing methods on public CT datasets including a real-paired benchmark, verifying the effectiveness of the proposed framework. The source code of this work is available at https://github.com/khuhm/ACVTT.

Chronological age is an important component of medical risk scores and decision-making. However, there is considerable variability in how individuals age. We recently published an open-source deep learning model to assess biological age from chest radiographs (CXR-Age), which predicts all-cause and cardiovascular mortality better than chronological age. Here, we compare CXR-Age to two established epigenetic aging clocks (First generation-Horvath Age; Second generation-DNAm PhenoAge) to test which is more strongly associated with cardiopulmonary disease and frailty. Our cohort consisted of 2,097 participants from the Project Baseline Health Study, a prospective cohort study of individuals from four US sites. We compared the association between the different aging clocks and measures of cardiopulmonary disease, frailty, and protein abundance collected at the participant's first annual visit using linear regression models adjusted for common confounders. We found that CXR-Age was associated with coronary calcium, cardiovascular risk factors, worsening pulmonary function, increased frailty, and abundance in plasma of two proteins implicated in neuroinflammation and aging. Associations with DNAm PhenoAge were weaker for pulmonary function and all metrics in middle-age adults. We identified thirteen proteins that were associated with DNAm PhenoAge, one (CDH13) of which was also associated with CXR-Age. No associations were found with Horvath Age. These results suggest that CXR-Age may serve as a better metric of cardiopulmonary aging than epigenetic aging clocks, especially in midlife adults.

Machine learning models have utilized semantic features, deep features, or both to assess lung nodule malignancy. However, their reliance on manual annotation during inference, limited interpretability, and sensitivity to imaging variations hinder their application in real-world clinical settings. Thus, this research aims to integrate semantic features derived from radiologists' assessments of nodules, guiding the model to learn clinically relevant, robust, and explainable imaging features for predicting lung cancer. We obtained 938 low-dose CT scans from the National Lung Screening Trial (NLST) with 1,246 nodules and semantic features. Additionally, the Lung Image Database Consortium dataset contains 1,018 CT scans, with 2,625 lesions annotated for nodule characteristics. Three external datasets were obtained from UCLA Health, the LUNGx Challenge, and the Duke Lung Cancer Screening. We fine-tuned a pretrained Contrastive Language-Image Pretraining (CLIP) model with a parameter-efficient fine-tuning approach to align imaging and semantic text features and predict the one-year lung cancer diagnosis. Our model outperformed state-of-the-art (SOTA) models in the NLST test set with an AUROC of 0.901 and AUPRC of 0.776. It also showed robust results in external datasets. Using CLIP, we also obtained predictions on semantic features through zero-shot inference, such as nodule margin (AUROC: 0.812), nodule consistency (0.812), and pleural attachment (0.840). Our approach surpasses the SOTA models in predicting lung cancer across datasets collected from diverse clinical settings, providing explainable outputs, aiding clinicians in comprehending the underlying meaning of model predictions. This approach also prevents the model from learning shortcuts and generalizes across clinical settings. The code is available at https://github.com/luotingzhuang/CLIP_nodule.

Due to the inductive bias of convolutions, CNNs perform hierarchical feature extraction efficiently in the field of medical image segmentation. However, the local correlation assumption of inductive bias limits the ability of convolutions to focus on global information, which has led to the performance of Transformer-based methods surpassing that of CNNs in some segmentation tasks in recent years. Although combining with Transformers can solve this problem, it also introduces computational complexity and considerable parameters. In addition, narrowing the encoder-decoder semantic gap for high-quality mask generation is a key challenge, addressed in recent works through feature aggregation from different skip connections. However, this often results in semantic mismatches and additional noise. In this paper, we propose a novel segmentation method, X-UNet, whose backbones employ the CFGC (Collaborative Fusion with Global Context-aware) module. The CFGC module enables multi-scale feature extraction and effective global context modeling. Simultaneously, we employ the CSPF (Cross Split-channel Progressive Fusion) module to progressively align and fuse features from corresponding encoder and decoder stages through channel-wise operations, offering a novel approach to feature integration. Experimental results demonstrate that X-UNet, with fewer computations and parameters, exhibits superior performance on various medical image datasets.The code and models are available on https://github.com/XSJ0410/X-UNet.

Transformers and state space sequence models (SSMs) have attracted interest in biomedical image segmentation for their ability to capture long-range dependency. However, traditional visual state space (VSS) methods suffer from the incompatibility of image tokens with autoregressive assumption. Although Transformer attention does not require this assumption, its high computational cost limits effective channel-wise information utilization. To overcome these limitations, we propose the Mamba-Like Aggregated UNet (MLAgg-UNet), which introduces Mamba-inspired mechanism to enrich Transformer channel representation and exploit implicit autoregressive characteristic within U-shaped architecture. For establishing dependencies among image tokens in single scale, the Mamba-Like Aggregated Attention (MLAgg) block is designed to balance representational ability and computational efficiency. Inspired by the human foveal vision system, Mamba macro-structure, and differential attention, MLAgg block can slide its focus over each image token, suppress irrelevant tokens, and simultaneously strengthen channel-wise information utilization. Moreover, leveraging causal relationships between consecutive low-level and high-level features in U-shaped architecture, we propose the Multi-Scale Mamba Module with Implicit Causality (MSMM) to optimize complementary information across scales. Embedded within skip connections, this module enhances semantic consistency between encoder and decoder features. Extensive experiments on four benchmark datasets, including AbdomenMRI, ACDC, BTCV, and EndoVis17, which cover MRI, CT, and endoscopy modalities, demonstrate that the proposed MLAgg-UNet consistently outperforms state-of-the-art CNN-based, Transformer-based, and Mamba-based methods. Specifically, it achieves improvements of at least 1.24%, 0.20%, 0.33%, and 0.39% in DSC scores on these datasets, respectively. These results highlight the model's ability to effectively capture feature correlations and integrate complementary multi-scale information, providing a robust solution for medical image segmentation. The implementation is publicly available at https://github.com/aticejiang/MLAgg-UNet.

Enhancing domain generalization (DG) is a crucial and compelling research pursuit within the field of medical image segmentation, owing to the inherent heterogeneity observed in medical images. The recent success with large-scale pre-trained vision models (PVMs), such as Vision Transformer (ViT), inspires us to explore their application in this specific area. While a straightforward strategy involves fine-tuning the PVM using supervised signals from the source domains, this approach overlooks the domain shift issue and neglects the rich knowledge inherent in the instances themselves. To overcome these limitations, we introduce a novel framework enhanced by global and local prompts (GLPs). Specifically, to adapt PVM in the medical DG scenario, we explicitly separate domain-shared and domain-specific knowledge in the form of GLPs. Furthermore, we develop an individualized domain adapter to intricately investigate the relationship between each target domain sample and the source domains. To harness the inherent knowledge within instances, we devise two innovative regularization terms from both the consistency and anatomy perspectives, encouraging the model to preserve instance discriminability and organ position invariance. Extensive experiments and in-depth discussions in both vanilla and semi-supervised DG scenarios deriving from five diverse medical datasets consistently demonstrate the superior segmentation performance achieved by GLP. Our code and datasets are publicly available at https://github.com/xmed-lab/GLP.