Osteoporosis (OP), a systemic skeletal disease characterized by compromised bone strength and elevated fracture susceptibility, represents a growing global health challenge that necessitates early detection and accurate risk stratification. With the exponential growth of multidimensional biomedical data in OP research, feature selection has become an indispensable machine learning paradigm that improves model generalizability. At the same time, it preserves clinical interpretability and enhances predictive accuracy. This perspective article systematically reviews the transformative role of feature selection methodologies across three critical domains of OP investigation: 1) multi-omics biomarker identification, 2) diagnostic pattern recognition, and 3) fracture risk prognostication. In biomarker discovery, advanced feature selection algorithms systematically refine high-dimensional multi-omics datasets (genomic, proteomic, metabolomic) to isolate key molecular signatures correlated with bone mineral density (BMD) trajectories and microarchitectural deterioration. For clinical diagnostics, these techniques enable efficient extraction of discriminative pattern from multimodal imaging data, including dual-energy X-ray absorptiometry (DXA), quantitative computed tomography (CT), and emerging dental radiographic biomarkers. In prognostic modeling, strategic variable selection optimizes prognostic accuracy by integrating demographic, biochemical, and biomechanical predictors while migrating overfitting in heterogeneous patient cohorts. Current challenges include heterogeneity in dataset quality and dimensionality, translational gaps between algorithmic outputs and clinical decision parameters, and limited reproducibility across diverse populations. Future directions should prioritize the development of adaptive feature selection frameworks capable of dynamic multi-omics data integration, coupled with hybrid intelligence systems that synergize machine-derived biomarkers with clinician expertise. Addressing these challenges requires coordinated interdisciplinary efforts to establish standardized validation protocols and create clinician-friendly decision support interfaces, ultimately bridging the gap between computational OP research and personalized patient care.

To establish a comprehensive reference range for OxNNet-derived first-trimester placental volume (FTPV), based on values observed in healthy pregnancies. Data were obtained from the First Trimester Placental Ultrasound Study, an observational cohort study in which three-dimensional placental ultrasound imaging was performed between 11 + 2 and 14 + 1 weeks' gestation, alongside otherwise routine care. A subgroup of singleton pregnancies resulting in term live birth, without neonatal unit admission or major chromosomal or structural abnormality, were included. Exclusion criteria were fetal growth restriction, maternal diabetes mellitus, hypertensive disorders of pregnancy or other maternal medical conditions (e.g. chronic hypertension, antiphospholipid syndrome, systemic lupus erythematosus). Placental images were processed using the OxNNet toolkit, a software solution based on a fully convolutional neural network, for automated placental segmentation and volume calculation. Quantile regression and the lambda-mu-sigma (LMS) method were applied to model the distribution of FTPV, using both crown-rump length (CRL) and gestational age as predictors. Model fit was assessed using the Akaike information criterion (AIC), and centile curves were constructed for visual inspection. The cohort comprised 2547 cases. The distribution of FTPV across gestational ages was positively skewed, with variation in the distribution at different gestational timepoints. In model comparisons, the LMS method yielded lower AIC values compared with quantile regression models. For predicting FTPV from CRL, the LMS model with the Sinh-Arcsinh distribution achieved the best performance, with the lowest AIC value. For gestational-age-based prediction, the LMS model with the Box-Cox Cole and Green original distribution achieved the lowest AIC value. The LMS models were selected to construct centile charts for FTPV based on both CRL and gestational age. Evaluation of the centile charts revealed strong agreement between predicted and observed centiles, with minimal deviations. Both models demonstrated excellent calibration, and the Z-scores derived using each of the models confirmed normal distribution. This study established reference ranges for FTPV based on both CRL and gestational age in healthy pregnancies. The LMS method provided the best model fit, demonstrating excellent calibration and minimal deviations between predicted and observed centiles. These findings should facilitate the exploration of FTPV as a potential biomarker for adverse pregnancy outcome and provide a foundation for future research into its clinical applications. © 2025 The Author(s). Ultrasound in Obstetrics & Gynecology published by John Wiley & Sons Ltd on behalf of International Society of Ultrasound in Obstetrics and Gynecology.

The lumbar spine and pelvis are critical stress-bearing structures of the human body, and their rapid and accurate segmentation plays a vital role in clinical diagnosis and intervention. However, conventional CT imaging poses significant challenges due to the low contrast of sacral and bilateral hip tissues and the complex and highly similar intervertebral space structures within the lumbar spine. To address these challenges, we propose a general-purpose segmentation network that integrates a cross-scale feature fusion strategy with a linear self-attention mechanism. The proposed network effectively extracts multi-scale features and fuses them along the channel dimension, enabling both structural and boundary information of lumbar and pelvic regions to be captured within the encoder-decoder architecture.Furthermore, we introduce a linear mapping strategy to approximate the traditional attention matrix with a low-rank representation, allowing the linear attention mechanism to significantly reduce computational complexity while maintaining segmentation accuracy for vertebrae and pelvic bones. Comparative and ablation experiments conducted on the CTSpine1K and CTPelvic1K datasets demonstrate that our method achieves improvements of 1.5% in Dice Similarity Coefficient (DSC) and 2.6% in Hausdorff Distance (HD) over state-of-the-art models, validating the effectiveness of our approach in enhancing boundary segmentation quality and segmentation accuracy in homogeneous anatomical regions.

The objective of this study was to develop a deep learning model for automated pituitary adenoma segmentation in MRI scans for stereotactic radiosurgery planning and to assess its accuracy and efficiency in clinical settings. An nnU-Net-based model was trained on MRI scans with expert segmentations of 582 patients treated with Leksell Gamma Knife over the course of 12 years. The accuracy of the model was evaluated by a human expert on a separate dataset of 146 previously unseen patients. The primary outcome was the comparison of expert ratings between the predicted segmentations and a control group consisting of original manual segmentations. Secondary outcomes were the influence of tumor volume, previous surgery, previous stereotactic radiosurgery (SRS), and endocrinological status on expert ratings, performance in a subgroup of nonfunctioning macroadenomas (measuring 1000-4000 mm3) without previous surgery and/or radiosurgery, and influence of using additional MRI modalities as model input and time cost reduction. The model achieved Dice similarity coefficients of 82.3%, 63.9%, and 79.6% for tumor, normal gland, and optic nerve, respectively. A human expert rated 20.6% of the segmentations as applicable in treatment planning without any modifications, 52.7% as applicable with minor manual modifications, and 26.7% as inapplicable. The ratings for predicted segmentations were lower than for the control group of original segmentations (p < 0.001). Larger tumor volume, history of a previous radiosurgery, and nonfunctioning pituitary adenoma were associated with better expert ratings (p = 0.005, p = 0.007, and p < 0.001, respectively). In the subgroup without previous surgery, although expert ratings were more favorable, the association did not reach statistical significance (p = 0.074). In the subgroup of noncomplex cases (n = 9), 55.6% of the segmentations were rated as applicable without any manual modifications and no segmentations were rated as inapplicable. Manually improving inaccurate segmentations instead of creating them from scratch led to 53.6% reduction of the time cost (p < 0.001). The results were applicable for treatment planning with either no or minor manual modifications, demonstrating a significant increase in the efficiency of the planning process. The predicted segmentations can be loaded into the planning software used in clinical practice for treatment planning. The authors discuss some considerations of the clinical utility of the automated segmentation models, as well as their integration within established clinical workflows, and outline directions for future research.

The primary goal in neuro-oncology is the maximally safe resection of high-grade glioma (HGG). A more extensive resection improves both overall and disease-free survival, while a complication-free surgery enables better tolerance to adjuvant therapies such as chemotherapy and radiotherapy. Techniques such as 5-aminolevulinic acid (5-ALA) fluorescence and intraoperative ultrasound (ioUS) are valuable for safe resection and cost-effective. However, the benefits of combining these techniques remain undocumented. The aim of this study was to investigate outcomes when combining 5-ALA and ioUS. From January 2019 to January 2024, 72 patients (mean age 62.2 years, 62.5% male) underwent HGG resection at a single hospital. Tumor histology included glioblastoma (90.3%), grade IV astrocytoma (4.1%), grade III astrocytoma (2.8%), and grade III oligodendroglioma (2.8%). Tumor resection was performed under natural light, followed by using 5-ALA and ioUS to detect residual tumor. Biopsies from the surgical bed were analyzed for tumor presence and categorized based on 5-ALA and ioUS results. Results of 5-ALA and ioUS were classified into positive, weak/doubtful, or negative. Histological findings of the biopsies were categorized into solid tumor, infiltration, or no tumor. Sensitivity, specificity, and predictive values for both techniques, separately and combined, were calculated. A machine learning algorithm (HGGPredictor) was developed to predict tumor presence in biopsies. The overall sensitivities of 5-ALA and ioUS were 84.9% and 76%, with specificities of 57.8% and 84.5%, respectively. The combination of both methods in a positive/positive scenario yielded the highest performance, achieving a sensitivity of 91% and specificity of 86%. The positive/doubtful combination followed, with sensitivity of 67.9% and specificity of 95.2%. Area under the curve analysis indicated superior performance when both techniques were combined, in comparison to each method used individually. Additionally, the HGGPredictor tool effectively estimated the quantity of tumor cells in surgical margins. Combining 5-ALA and ioUS enhanced diagnostic accuracy for HGG resection, suggesting a new surgical standard. An intraoperative predictive algorithm could further automate decision-making.

Accurate quantification of the extent of bronchial damage across various airway levels in chronic obstructive pulmonary disease (COPD) remains a challenge. In this study, artificial intelligence (AI) was employed to develop an airway segmentation model to investigate the morphological changes of the central and peripheral airways in COPD patients and the effects of these airway changes on pulmonary function classification and acute COPD exacerbations. Clinical data from a total of 340 patients with COPD and 73 healthy volunteers were collected and compiled. An AI-driven airway segmentation model was constructed using Convolutional Neural Regressor (CNR) and Airway Transfer Network (ATN) algorithms. The efficacy of the model was evaluated through support vector machine (SVM) and random forest regression approaches. The area under the receiver operating characteristic (ROC) curve (AUC) of the SVM in evaluating the COPD airway segmentation model was 0.96, with a sensitivity of 97% and a specificity of 92%, however, the AUC value of the SVM was 0.81 when it was replaced the healthy group by non-COPD outpatients. Compared with the healthy group, the grade and the total number of airway segmentation were decreased and the diameters of the right main bronchus and bilateral lobar bronchi of patients with COPD were smaller and the airway walls were thinner (all P < 0.01). However, the diameters of the subsegmental and small airway bronchi were increased, and airway walls were thickened, and the arc lengths were shorter ( all P < 0.01), especially in patients with severe COPD (all P < 0.05). Correlation and regression analysis showed that FEV1%pre was positively correlated with the diameters and airway wall thickness of the main and lobar airway, and the arc lengths of small airway bronchi (all P < 0.05). Airway wall thickness of the subsegment and small airway were found to have the greatest impact on the frequency of COPD exacerbations. Artificial intelligence lung CT airway segmentation model is a non-invasive quantitative tool for measuring chronic obstructive pulmonary disease. The main changes in COPD patients are that the central airway diameter becomes narrower and the thickness becomes thinner. The arc length of the peripheral airway becomes shorter, and the diameter and airway wall thickness become larger, which is more obvious in severe patients. Pulmonary function classification and small and medium airway dysfunction are also affected by the diameter, thickness and arc length of large and small airways. Small airway remodeling is more significant in acute exacerbations of COPD.

Coronary CT angiography is widely implemented, with an estimated 2.2 million procedures in patients with stable chest pain every year in Europe alone. In parallel, artificial intelligence and machine learning are poised to transform coronary atherosclerotic plaque evaluation by improving reliability and speed. However, little is known about how to use coronary atherosclerosis imaging biomarkers to individualize recommendations for medical treatment. This Consensus Statement from the Quantitative Cardiovascular Imaging (QCI) Study Group outlines key recommendations derived from a three-step Delphi process that took place after the third international QCI Study Group meeting in September 2024. Experts from various fields of cardiovascular imaging agreed on the use of age-adjusted and gender-adjusted percentile curves, based on coronary plaque data from the DISCHARGE and SCOT-HEART trials. Two key issues were addressed: the need to harness the reliability and precision of artificial intelligence and machine learning tools and to tailor treatment on the basis of individualized plaque analysis. The QCI Study Group recommends that the presence of any atherosclerotic plaque should lead to a recommendation of pharmacological treatment, whereas the 70th percentile of total plaque volume warrants high-intensity treatment. The aim of these recommendations is to lay the groundwork for future trials and to unlock the potential of coronary CT angiography to improve patient outcomes globally.

In order to automate the centerline extraction of the coronary tree, three challenges must be addressed: tracking branches automatically, passing through plaques successfully, and detecting endpoints accurately. This study aims to develop a method to solve the three challenges. We propose a branch-endpoint-aware coronary centerline extraction framework. The framework consists of a deep reinforcement learning-based tracker and a 3D dilated CNN-based detector. The tracker is designed to predict the actions of an agent with the objective of tracking the centerline. The detector identifies bifurcation points and endpoints, assisting the tracker in tracking branches and terminating the tracking process automatically. The detector can also estimate the radius values of the coronary artery. The method achieves the state-of-the-art performance in both the centerline extraction and radius estimate. Furthermore, the method necessitates minimal user interaction to extract a coronary tree, a feature that surpasses other interactive methods. The method can track branches automatically, pass through plaques successfully and detect endpoints accurately. Compared with other interactive methods that require multiple seeds, our method only needs one seed to extract the entire coronary tree.

Cancer is considered one of the deadliest diseases worldwide. Early detection of cancer can significantly improve patient survival rates. In recent years, computer-aided diagnosis (CAD) systems have been increasingly employed in cancer diagnosis through various medical image modalities. These systems play a critical role in enhancing diagnostic accuracy, reducing physician workload, providing consistent second opinions, and contributing to the efficiency of the medical industry. Acute lymphoblastic leukemia (ALL) is a fast-progressing blood cancer that primarily affects children but can also occur in adults. Early and accurate diagnosis of ALL is crucial for effective treatment and improved outcomes, making it a vital area for CAD system development. In this research, a CAD system for ALL diagnosis has been developed. It contains four phases which are preprocessing, segmentation, feature extraction and selection phase, and classification of suspicious regions as normal or abnormal. The proposed system was applied to microscopic blood images to classify each case as ALL or normal. Three classifiers which are Naïve Bayes (NB), Support Vector Machine (SVM) and K-nearest Neighbor (K-NN) were utilized to classify the images based on selected features. Ant Colony Optimization (ACO) was combined with the classifiers as a feature selection method to identify the optimal subset of features among the extracted features from segmented cell parts that yield the highest classification accuracy. The NB classifier achieved the best performance, with accuracy, sensitivity, and specificity of 96.15%, 97.56, and 94.59%, respectively.

Subvariants of testicular germ cell tumor (TGCT) significantly affect therapeutic strategies and patient prognosis. However, preoperatively distinguishing seminoma (SE) from non-seminoma (n-SE) remains a challenge. This study aimed to evaluate the performance of a deep learning-based super-resolution (SR) US radiomics model for SE/n-SE differentiation. This international multicenter retrospective study recruited patients with confirmed TGCT between 2015 and 2023. A pre-trained SR reconstruction algorithm was applied to enhance native resolution (NR) images. NR and SR radiomics models were constructed, and the superior model was then integrated with clinical features to construct clinical-radiomics models. Diagnostic performance was evaluated by ROC analysis (AUC) and compared with radiologists' assessments using the DeLong test. A total of 486 male patients were enrolled for training (n = 338), domestic (n = 92), and international (n = 59) validation sets. The SR radiomics model achieved AUCs of 0.90, 0.82, and 0.91, respectively, in the training, domestic, and international validation sets, significantly surpassing the NR model (p < 0.001, p = 0.031, and p = 0.001, respectively). The clinical-radiomics model exhibited a significantly higher across both domestic and international validation sets compared to the SR radiomics model alone (0.95 vs 0.82, p = 0.004; 0.97 vs 0.91, p = 0.031). Moreover, the clinical-radiomics model surpassed the performance of experienced radiologists in both domestic (AUC, 0.95 vs 0.85, p = 0.012) and international (AUC, 0.97 vs 0.77, p < 0.001) validation cohorts. The SR-based clinical-radiomics model can effectively differentiate between SE and n-SE. This international multicenter study demonstrated that a radiomics model of deep learning-based SR reconstructed US images enabled effective differentiation between SE and n-SE. Clinical parameters and radiologists' assessments exhibit limited diagnostic accuracy for SE/n-SE differentiation in TGCT. Based on scrotal US images of TGCT, the SR radiomics models performed better than the NR radiomics models. The SR-based clinical-radiomics model outperforms both the radiomics model and radiologists' assessment, enabling accurate, non-invasive preoperative differentiation between SE and n-SE.