Lung diseases represent one of the most prevalent health challenges globally, necessitating accurate diagnosis to improve patient outcomes. This work presents a novel deep learning-aided lung disease classification framework comprising three key phases: image acquisition, segmentation, and classification. Initially, chest X-ray images are taken from standard datasets. The lung regions are segmented using an Adaptive Recurrent Residual U-Net (AR2-UNet), whose parameters are optimised using Enhanced Pufferfish Optimisation Algorithm (EPOA) to enhance segmentation accuracy. The segmented images are processed using "Attention-based Densenet with Long Short Term Memory(ADNet-LSTM)" for robust categorisation. Investigational results demonstrate that the proposed model achieves the highest classification accuracy of 93.92%, significantly outperforming several baseline models including ResNet with 90.77%, Inception with 89.55%, DenseNet with 89.66%, and "Long Short Term Memory (LSTM)" with 91.79%. Thus, the proposed framework offers a dependable and efficient solution for lung disease detection, supporting clinicians in early and accurate diagnosis.

AI-driven scan time reduction is rapidly transforming medical imaging with benefits such as improved patient comfort and enhanced efficiency. A Dual Contrastive Learning Generative Adversarial Network (DCLGAN) was developed to predict full-time PET scans from shorter, noisier scans, improving challenges in imaging patients with movement disorders. 18F FP-CIT PET/CT data from 391 patients with suspected Parkinsonism were used [250 training/validation, 141 testing (hospital A)]. Ground truth (GT) images were reconstructed from 15-minute scans, while denoised images (DIs) were generated from 1-, 3-, 5-, and 10-minute scans. Image quality was assessed using normalized root mean square error (NRMSE), peak signal-to-noise ratio (PSNR), structural similarity index measure (SSIM), visual analysis, and clinical metrics like BPND and ISR for diagnosis of non-neurodegenerative Parkinson disease (NPD), idiopathic PD (IPD), and atypical PD (APD). External validation used data from 2 hospitals with different scanners (hospital B: 1-, 3-, 5-, and 10-min; hospital C: 1-, 3-, and 5-min). In addition, motion artifact reduction was evaluated using the Dice similarity coefficient (DSC). In hospital A, NRMSE, PSNR, and SSIM values improved with scan duration, with the 5-minute DIs achieving optimal quality (NRMSE 0.008, PSNR 42.13, SSIM 0.98). Visual analysis rated DIs from scans ≥3 minutes as adequate or higher. The mean BPND differences (95% CI) for each DIs were 0.19 (-0.01, 0.40), 0.11 (-0.02, 0.24), 0.08 (-0.03, 0.18), and 0.01 (-0.06, 0.07), with the CIs significantly decreasing. ISRs with the highest effect sizes for differentiating NPD, IPD, and APD (PP/AP, PP/VS, PC/VP) remained stable post-denoising. External validation showed 10-minute DIs (hospital B) and 1-minute DIs (hospital C) reached benchmarks of hospital A's image quality metrics, with similar trends in visual analysis and BPND CIs. Furthermore, motion artifact correction in 9 patients yielded DSC improvements from 0.89 to 0.95 in striatal regions. The DL-model is capable of generating high-quality 18F FP-CIT PET images from shorter scans to enhance patient comfort, minimize motion artifacts, and maintain diagnostic precision. Furthermore, our study plays an important role in providing insights into how imaging quality assessment metrics can be used to determine the appropriate scan duration for different scanners with varying sensitivities.

Advancements in coronary computed tomography angiography (CCTA) facilitated the transition from traditional histological approaches to comprehensive plaque burden assessment. Recent updates in the European Society of Cardiology (ESC) guidelines emphasize CCTA's role in managing chronic coronary syndrome by enabling detailed monitoring of atherosclerotic plaque progression. Limitations of conventional CCTA, such as spatial resolution challenges in accurately characterizing plaque components like thin-cap fibroatheromas and necrotic lipid-rich cores, are addressed with photon-counting detector CT (PCD-CT) technology. PCD-CT offers enhanced spatial resolution and spectral imaging, improving the detection and characterization of high-risk plaque features while reducing artifacts. The integration of artificial intelligence (AI) in plaque analysis enhances diagnostic accuracy through automated plaque characterization and radiomics. These technological advancements support a comprehensive approach to plaque assessment, incorporating hemodynamic evaluations, morphological metrics, and AI-driven analysis, thereby enabling personalized patient care and improved prediction of acute clinical events.

In pancreatic stereotactic body radiotherapy (SBRT), accurate motion management is crucial for the safe delivery of high doses per fraction. Intra-fraction tracking with magnetic resonance imaging-guidance for gated SBRT has shown potential for improved local control. Visualisation of pancreas (and surrounding organs) remains challenging in intra-fraction kilo-voltage (kV) imaging, requiring implanted fiducials. In this study, we investigate patient-specific deep-learning approaches to track the gross-tumour-volume (GTV), pancreas-head and the whole-pancreas in intra-fraction kV images. Conditional-generative-adversarial-networks were trained and tested on data from 25 patients enrolled in an ethics-approved pancreatic SBRT trial for contour prediction on intra-fraction 2D kV images. Labelled digitally-reconstructed-radiographs (DRRs) were generated from contoured planning-computed-tomography (CTs) (CT-DRRs) and cone-beam-CTs (CBCT-DRRs). A population model was trained using CT-DRRs of 19 patients. Two patient-specific model types were created for six additional patients by fine-tuning the population model using CBCT-DRRs (CBCT-models) or CT-DRRs (CT-models) acquired in exhale-breath-hold. Model predictions on unseen triggered-kV images from the corresponding six patients were evaluated against projected-contours using Dice-Similarity-Coefficient (DSC), centroid-error (CE), average Hausdorff-distance (AHD), and Hausdorff-distance at 95th-percentile (HD95). The mean ± 1SD (standard-deviation) DSCs were 0.86 ± 0.09 (CBCT-models) and 0.78 ± 0.12 (CT-models). For AHD and CE, the CBCT-model predicted contours within 2.0 mm ≥90.3 % of the time, while HD95 was within 5.0 mm ≥90.0 % of the time, and had a prediction time of 29.2 ± 3.7 ms per contour. The patient-specific CBCT-models outperformed the CT-models and predicted the three contours with 90th-percentile error ≤2.0 mm, indicating the potential for clinical real-time application.

The accurate and early evaluation of response to neoadjuvant chemotherapy (NAC) in breast cancer is crucial for optimizing treatment strategies and minimizing unnecessary interventions. While deep learning (DL)-based approaches have shown promise in medical imaging analysis, existing models often fail to comprehensively integrate spatial and temporal tumor dynamics. This study aims to develop and validate a spatiotemporal interaction (STI) model based on longitudinal MRI data to predict pathological complete response (pCR) to NAC in breast cancer patients. This study included retrospective and prospective datasets from five medical centers in China, collected from June 2018 to December 2024. These datasets were assigned to the primary cohort (including training and internal validation sets), external validation cohorts, and a prospective validation cohort. DCE-MRI scans from both pre-NAC (T0) and early-NAC (T1) stages were collected for each patient, along with surgical pathology results. A Siamese network-based STI model was developed, integrating spatial features from tumor segmentation with temporal dependencies using a transformer-based multi-head attention mechanism. This model was designed to simultaneously capture spatial heterogeneity and temporal dynamics, enabling accurate prediction of NAC response. The STI model's performance was evaluated using the area under the ROC curve (AUC) and Precision-Recall curve (AP), accuracy, sensitivity, and specificity. Additionally, the I-SPY1 and I-SPY2 datasets were used for Kaplan-Meier survival analysis and to explore the biological basis of the STI model, respectively. The prospective cohort was registered with Chinese Clinical Trial Registration Centre (ChiCTR2500102170). A total of 1044 patients were included in this study, with the pCR rate ranging from 23.8% to 35.9%. The STI model demonstrated good performance in early prediction of NAC response in breast cancer. In the external validation cohorts, the AUC values were 0.923 (95% CI: 0.859-0.987), 0.892 (95% CI: 0.821-0.963), and 0.913 (95% CI: 0.835-0.991), all outperforming the single-timepoint T0 or T1 models, as well as models with spatial information added (all p < 0.05, Delong test). Additionally, the STI model significantly outperformed the clinical model (p < 0.05, Delong test) and radiologists' predictions. In the prospective validation cohort, the STI model identified 90.2% (37/41) of non-pCR and 82.6% (19/23) of pCR patients, reducing misclassification rates by 58.7% and 63.3% compared to radiologists. This indicates that these patients might benefit from treatment adjustment or continued therapy in the early NAC stage. Survival analysis showed a significant correlation between the STI model and both recurrence-free survival (RFS) and overall survival (OS) in breast cancer patients. Further investigation revealed that favorable NAC responses predicted by the STI model were closely linked to upregulated immune-related genes and enhanced immune cell infiltration. Our study established a novel noninvasive STI model that integrates the spatiotemporal evolution of MRI before and during NAC to achieve early and accurate pCR prediction, offering potential guidance for personalized treatment. This study was supported by the National Natural Science Foundation of China (82302314, 62271448, 82171920, 81901711), Basic and Applied Basic Research Foundation of Guangdong Province (2022A1515110792, 2023A1515220097, 2024A1515010653), Medical Scientific Research Foundation of Guangdong Province (A2023073, A2024116), Science and Technology Projects in Guangzhou (2023A04J1275, 2024A03J1030, 2025A03J4163, 2025A03J4162); Guangzhou First People's Hospital Frontier Medical Technology Project (QY-C04).

Recently, a hepatic arterial infusion chemotherapy (HAIC)-associated combination therapeutic regimen, comprising HAIC and systemic therapies (molecular targeted therapy plus immunotherapy), referred to as HAIC combination therapy, has demonstrated promising anticancer effects. Identifying individuals who may potentially benefit from HAIC combination therapy could contribute to improved treatment decision-making for patients with advanced hepatocellular carcinoma (HCC). This dual-center study was a retrospective analysis of prospectively collected data with advanced HCC patients who underwent HAIC combination therapy and pretreatment contrast-enhanced ultrasound (CEUS) evaluations from March 2019 to March 2023. Two deep learning models, AE-3DNet and 3DNet, along with a time-intensity curve-based model, were developed for predicting therapeutic responses from pretreatment CEUS cine images. Diagnostic metrics, including the area under the receiver-operating-characteristic curve (AUC), were calculated to compare the performance of the models. Survival analysis was used to assess the relationship between predicted responses and prognostic outcomes. The model of AE-3DNet was constructed on the top of 3DNet, with innovative incorporation of spatiotemporal attention modules to enhance the capacity for dynamic feature extraction. 326 patients were included, 243 of whom formed the internal validation cohort, which was utilized for model development and fivefold cross-validation, while the rest formed the external validation cohort. Objective response (OR) or non-objective response (non-OR) were observed in 63% (206/326) and 37% (120/326) of the participants, respectively. Among the three efficacy prediction models assessed, AE-3DNet performed superiorly with AUC values of 0.84 and 0.85 in the internal and external validation cohorts, respectively. AE-3DNet's predicted response survival curves closely resembled actual clinical outcomes. The deep learning model of AE-3DNet developed based on pretreatment CEUS cine performed satisfactorily in predicting the responses of advanced HCC to HAIC combination therapy, which may serve as a promising tool for guiding combined therapy and individualized treatment strategies. Trial Registration: NCT02973685.

The differential diagnosis of invasive pulmonary aspergillosis (IPA), pulmonary mucormycosis (PM), bacterial pneumonia (BP) and pulmonary tuberculosis (PTB) are challenging due to overlapping clinical and imaging features. Manual CT lesion segmentation is time-consuming, deep-learning (DL)-based segmentation models offer a promising solution, yet disease-specific models for these infections remain underexplored. We aimed to develop and validate dedicated CT segmentation models for IPA, PM, BP and PTB to enhance diagnostic accuracy. Methods：Retrospective multi-centre data (115 IPA, 53 PM, 130 BP, 125 PTB) were used for training/internal validation, with 21 IPA, 8PM, 30 BP and 31 PTB cases for external validation. Expert-annotated lesions served as ground truth. An improved 3D U-Net architecture was employed for segmentation, with preprocessing steps including normalisations, cropping and data augmentation. Performance was evaluated using Dice coefficients. Results：Internal validation achieved Dice scores of 78.83% (IPA), 93.38% (PM), 80.12% (BP) and 90.47% (PTB). External validation showed slightly reduced but robust performance: 75.09% (IPA), 77.53% (PM), 67.40% (BP) and 80.07% (PTB). The PM model demonstrated exceptional generalisability, scoring 83.41% on IPA data. Cross-validation revealed mutual applicability, with IPA/PTB models achieving > 75% Dice for each other's lesions. BP segmentation showed lower but clinically acceptable performance ( ＞72%), likely due to complex radiological patterns. Disease-specific DL segmentation models exhibited high accuracy, particularly for PM and PTB. While IPA and BP models require refinement, all demonstrated cross-disease utility, suggesting immediate clinical value for preliminary lesion annotation. Future efforts should enhance datasets and optimise models for intricate cases.

The effectiveness of deep neural networks (DNNs) for the ultrasound image analysis depends on the availability and accuracy of the training data. However, the large-scale data collection and annotation, particularly in medical fields, is often costly and time consuming, especially when healthcare professionals are already burdened with their clinical responsibilities. Ensuring that a model remains robust across different imaging conditions-such as variations in ultrasound devices and manual transducer operation-is crucial in the ultrasound image analysis. The data augmentation is a widely used solution, as it increases both the size and diversity of datasets, thereby enhancing the generalization performance of DNNs. With the advent of generative networks such as generative adversarial networks (GANs) and diffusion-based models, the synthetic data generation has emerged as a promising augmentation technique. However, comprehensive studies comparing classic and generative method-based augmentation methods are lacking, particularly in ultrasound-based breast cancer imaging, where variability in breast density, tumor morphology, and operator skill poses significant challenges. This study aims to compare the effectiveness of classic and generative network-based data augmentation techniques in improving the performance and robustness of breast ultrasound image classification models. Specifically, we seek to determine whether the computational intensity of generative networks is justified in data augmentation. This analysis will provide valuable insights into the role and benefits of each technique in enhancing the diagnostic accuracy of DNN for breast cancer diagnosis. The code for this work will be available at: ht.tps://github.com/yasamin-med/SCDA.git.

Brachial plexopathies (BPs) encompass a complex spectrum of nerve injuries affecting motor and sensory function in the upper extremities. Diagnosis is challenging due to the intricate anatomy and symptom overlap with other neuropathies. Magnetic Resonance Neurography (MRN) provides advanced imaging but requires specialized interpretation. This study proposes an AI-based framework that combines deep learning (DL) with the modified Hiking Optimization Algorithm (MHOA) enhanced by a Comprehensive Learning (CL) technique to improve the classification of nerve injuries (neuropraxia, axonotmesis, neurotmesis) using MRN data. The framework utilizes MobileNetV4 for feature extraction and MHOA for optimized feature selection across different MRI sequences (STIR, T2, T1, and DWI). A dataset of 39 patients diagnosed with BP was used. The framework classifies injuries based on Seddon's criteria, distinguishing between normal and abnormal conditions as well as injury severity. The model achieved excellent performance, with 1.0000 accuracy in distinguishing normal from abnormal conditions using STIR and T2 sequences. For injury severity classification, accuracy was 0.9820 in STIR, outperforming the original HOA and other metaheuristic algorithms. Additionally, high classification accuracy (0.9667) was observed in DWI. The proposed framework outperformed traditional methods and demonstrated high sensitivity and specificity. The proposed AI-based framework significantly improves the diagnosis of BP by accurately classifying nerve injury types. By integrating DL and optimization techniques, it reduces diagnostic variability, making it a valuable tool for clinical settings with limited specialized neuroimaging expertise. This framework has the potential to enhance clinical decision-making and optimize patient outcomes through precise and timely diagnoses.

To explore the feasibility of deep learning (DL)-enhanced, fully automated bone mineral density (BMD) measurement using the ultralow-voltage 80 kV chest CT scans performed for lung cancer screening. This study involved 987 patients who underwent 80 kV chest and 120 kV lumbar CT from January to July 2024. Patients were collected from six CT scanners and divided into the training, validation, and test sets 1 and 2 (561: 177: 112: 137). Four convolutional neural networks (CNNs) were employed for automated segmentation (3D VB-Net and SCN), region of interest extraction (3D VB-Net), and BMD calculation (DenseNet and ResNet) of the target vertebrae (T12-L2). The BMD values of T12-L2 were obtained using 80 and 120 kV quantitative CT (QCT), the latter serving as the standard reference. Linear regression and Bland-Altman analyses were used to compare BMD values between 120 kV QCT and 80 kV CNNs, and between 120 kV QCT and 80 kV QCT. Receiver operating characteristic curve analysis was used to assess the diagnostic performance of the 80 kV CNNs and 80 kV QCT for osteoporosis and low BMD from normal BMD. Linear regression and Bland-ltman analyses revealed a stronger correlation (R²=0.991-0.998 and 0.990-0.991, P<0.001) and better agreement (mean error, -1.36 to 1.62 and 1.72 to 2.27 mg/cm³; 95% limits of agreement, -9.73 to 7.01 and -5.71 to 10.19mg/cm³) for BMD between 120 kV QCT and 80 kV CNNs than between 120 kV QCT and 80 kV QCT. The areas under the curve of the 80 kV CNNs and 80 kV QCT in detecting osteoporosis and low BMD were 0.997-1.000 and 0.997-0.998, and 0.998-1.000 and 0.997, respectively. The DL method could achieve fully automated BMD calculation for opportunistic osteoporosis screening with high accuracy using ultralow-voltage 80 kV chest CT performed for lung cancer screening.