This study aimed to develop and validate a clinical-radiomics deep learning (DL) model based on MRI for endometrial cancer (EC) molecular subtypes classification. This multicenter retrospective study included EC patients undergoing surgery, MRI, and molecular pathology diagnosis across three institutions from January 2020 to March 2024. Patients were divided into training, internal, and external validation cohorts. A total of 386 handcrafted radiomics features were extracted from each MR sequence, and MoCo-v2 was employed for contrastive self-supervised learning to extract 2048 DL features per patient. Feature selection integrated selected features into 12 machine learning methods. Model performance was evaluated with the AUC. A total of 526 patients were included (mean age, 55.01 ± 11.07). The radiomics model and clinical model demonstrated comparable performance across the internal and external validation cohorts, with macro-average AUCs of 0.70 vs 0.69 and 0.70 vs 0.67 (p = 0.51), respectively. The radiomics DL model, compared to the radiomics model, improved AUCs for POLEmut (0.68 vs 0.79), NSMP (0.71 vs 0.74), and p53abn (0.76 vs 0.78) in the internal validation (p = 0.08). The clinical-radiomics DL Model outperformed both the clinical model and radiomics DL model (macro-average AUC = 0.79 vs 0.69 and 0.73, in the internal validation [p = 0.02], 0.74 vs 0.67 and 0.69 in the external validation [p = 0.04]). The clinical-radiomics DL model based on MRI effectively distinguished EC molecular subtypes and demonstrated strong potential, with robust validation across multiple centers. Future research should explore larger datasets to further uncover DL's potential. Our clinical-radiomics DL model based on MRI has the potential to distinguish EC molecular subtypes. This insight aids in guiding clinicians in tailoring individualized treatments for EC patients. Accurate classification of EC molecular subtypes is crucial for prognostic risk assessment. The clinical-radiomics DL model outperformed both the clinical model and the radiomics DL model. The MRI features exhibited better diagnostic performance for POLEmut and p53abn.

Early and precise diagnosis of dyslexia is crucial for implementing timely intervention to reduce its effects. Timely identification can improve the individual's academic and cognitive performance. Traditional dyslexia detection (DD) relies on lengthy, subjective, restricted behavioral evaluations and interviews. Due to the limitations, deep learning (DL) models have been explored to improve DD by analyzing complex neurological, behavioral, and visual data. DL architectures, including convolutional neural networks (CNNs) and vision transformers (ViTs), encounter challenges in extracting meaningful patterns from cross-modality data. The lack of model interpretability and limited computational power restricts these models' generalizability across diverse datasets. To overcome these limitations, we propose an innovative model for DD using magnetic resonance imaging (MRI), electroencephalography (EEG), and handwriting images. We introduce a model, leveraging hybrid transformer-based feature extraction, including SWIN-Linformer for MRI, LeViT-Performer for handwriting images, and graph transformer networks (GTNs) with multi-attention mechanisms for EEG data. A multi-modal attention-based feature fusion network was used to fuse the extracted features in order to guarantee the integration of key multi-modal features. We enhance Dartbooster XGBoost (DXB)-based classification using Bayesian optimization with Hyperband (BOHB) algorithm. In order to reduce computational overhead, we employ a quantization-aware training technique. The local interpretable model-agnostic explanations (LIME) technique and gradient-weighted class activation mapping (Grad-CAM) were adopted to enable model interpretability. Five public repositories were used to train and test the proposed model. The experimental outcomes demonstrated that the proposed model achieves an accuracy of 99.8% with limited computational overhead, outperforming baseline models. It sets a novel standard for DD, offering potential for early identification and timely intervention. In the future, advanced feature fusion and quantization techniques can be utilized to achieve optimal results in resource-constrained environments.

In the field of healthcare, the acquisition and annotation of medical images present significant challenges, resulting in a scarcity of trainable samples. This data limitation hinders the performance of deep learning models, creating bottlenecks in clinical applications. To address this issue, we construct a framework (EScarcityS) aimed at enhancing the success rate of disease diagnosis in scarcity of trainable medical image scenarios. Firstly, considering that Transformer-based deep learning networks rely on a large amount of trainable data, this study takes into account the unique characteristics of pathological regions. By extracting the feature representations of all particles in medical images at different granularities, a multi-granularity Transformer network (MGVit) is designed. This network leverages additional prior knowledge to assist the Transformer network during training, thereby reducing the data requirement to some extent. Next, the importance maps of particles at different granularities, generated by MGVit, are fused to construct disease probability maps corresponding to the images. Based on these maps, a disease probability map-guided diffusion generation model is designed to generate more realistic and interpretable synthetic data. Subsequently, authentic and synthetical data are mixed and used to retrain MGVit, aiming to enhance the accuracy of medical image classification in scarcity of trainable medical image scenarios. Finally, we conducted detailed experiments on four real medical image datasets to validate the effectiveness of EScarcityS and its specific modules.

To date, indications for a surgical approach of small pancreatic neuroendocrine tumours (PanNETs) remain controversial. This cohort study aimed to identify the pseudocapsule status preoperatively to estimate the rationality of enucleation and survival prognosis of PanNETs, particularly in small tumours. Clinicopathological data were collected from patients with PanNETs who underwent the first pancreatectomy at our hospital (n = 578) between February 2012 and September 2023. Kaplan-Meier curves were constructed to visualise prognostic differences. Five distinct tissue samples were obtained for single-cell RNA sequencing (scRNA-seq) to evaluate variations in the tumour microenvironment. Radiological features were extracted from preoperative arterial-phase contrast-enhanced computed tomography. The performance of the pseudocapsule radiomics model was assessed using the area under the curve (AUC) metric. 475 cases (mean [SD] age, 53.01 [12.20] years; female vs male, 1.24:1) were eligible for this study. The mean pathological diameter of tumour was 2.99 cm (median: 2.50 cm; interquartile range [IQR]: 1.50-4.00 cm). These cases were stratified into complete (223, 46.95%) and incomplete (252, 53.05%) pseudocapsule groups. A statistically significant difference in aggressive indicators was observed between the two groups (P < 0.001). Through scRNA-seq analysis, we identified that the incomplete group presented a markedly immunosuppressive microenvironment. Regarding the impact on recurrence-free survival, the 3-year and 5-year rates were 94.8% and 92.5%, respectively, for the complete pseudocapsule group, compared to 76.7% and 70.4% for the incomplete pseudocapsule group. The radiomics-predictive model has a significant discrimination for the state of the pseudocapsule, particularly in small tumours (AUC, 0.744; 95% CI, 0.652-0.837). By combining computed tomography-based radiomics and machine learning for preoperative identification of pseudocapsule status, the intact group is more likely to benefit from enucleation.

BRAF V600E mutation status detection facilitates prognosis prediction in papillary thyroid carcinoma (PTC). We developed a deep-learning model to determine the BRAF V600E status in PTC. PTC from three centers were collected as the training set (1341 patients), validation set (148 patients), and external test set (135 patients). After testing the performance of the ResNeSt-50, Vision Transformer, and Swin Transformer V2 (SwinT) models, SwinT was chosen as the optimal backbone. An integrated BrafSwinT model was developed by combining the backbone with a radiomics feature branch and a clinical parameter branch. BrafSwinT demonstrated an AUC of 0.869 in the external test set, outperforming the original SwinT, Vision Transformer, and ResNeSt-50 models (AUC: 0.782-0.824; <i>p</i> value: 0.017-0.041). BrafSwinT showed promising results in determining BRAF V600E mutation status in PTC based on routinely acquired ultrasound images and basic clinical information, thus facilitating risk stratification.

Imaging holds a pivotal yet contentious role in the early diagnosis of axial spondyloarthritis. Although MRI has enhanced our ability to detect early inflammatory changes, particularly bone marrow oedema in the sacroiliac joints, the poor specificity of this finding introduces a substantial risk of overdiagnosis. The well intentioned push by rheumatologists towards earlier intervention could inadvertently lead to the misclassification of mechanical or degenerative conditions (eg, osteitis condensans ilii) as inflammatory disease, especially in the absence of structural lesions. Diagnostic uncertainty is further fuelled by anatomical variability, sex differences, and suboptimal imaging protocols. Current strategies-such as quantifying bone marrow oedema and analysing its distribution patterns, and integrating clinical and laboratory data-offer partial guidance for avoiding overdiagnosis but fall short of resolving the core diagnostic dilemma. Emerging imaging technologies, including high-resolution sequences, quantitative MRI, radiomics, and artificial intelligence, could improve diagnostic precision, but these tools remain exploratory. This Viewpoint underscores the need for a shift in imaging approaches, recognising that although timely diagnosis and treatment is essential to prevent long-term structural damage, robust and reliable imaging criteria are also needed. Without such advances, the imaging field risks repeating past missteps seen in other rheumatological conditions.

The preoperative human epidermal growth factor receptor type 2 (HER2) status of breast cancer is typically determined by pathological examination of a core needle biopsy, which influences the efficacy of neoadjuvant chemotherapy (NAC). However, the highly heterogeneous nature of breast cancer and the limitations of needle aspiration biopsy increase the instability of pathological evaluation. The aim of this study was to predict HER2 status in preoperative breast cancer using deep learning (DL) models based on ultrasound (US) and magnetic resonance imaging (MRI). The study included women with invasive breast cancer who underwent US and MRI at our institution between January 2021 and July 2024. US images and dynamic contrast-enhanced T1-weighted MRI images were used to construct DL models (DL-US: the DL model based on US; DL-MRI: the model based on MRI; and DL-MRI&US: the combined model based on both MRI and US). All classifications were based on postoperative pathological evaluation. Receiver operating characteristic analysis and the DeLong test were used to compare the diagnostic performance of the DL models. In the test cohort, DL-US differentiated the HER2 status of breast cancer with an AUC of 0.842 (95% CI: 0.708-0.931), and sensitivity and specificity of 89.5% and 79.3%, respectively. DL-MRI achieved an AUC of 0.800 (95% CI: 0.660-0.902), with sensitivity and specificity of 78.9% and 79.3%, respectively. DL-MRI&US yielded an AUC of 0.898 (95% CI: 0.777-0.967), with sensitivity and specificity of 63.2% and 100.0%, respectively.

To evaluate the prognosis of patients with traumatic brain injury according to the Computed Tomography (CT) findings of skull fracture and cerebral parenchymal hemorrhage. Retrospectively collected data from adult patients who received non-surgical or surgical treatment after the first CT scan with craniocerebral injuries from January 2020 to August 2021. The radiomics features were extracted by Pyradiomics. Dimensionality reduction was then performed using the max relevance and min-redundancy algorithm (mRMR) and the least absolute shrinkage and selection operator (LASSO), with ten-fold cross-validation to select the best radiomics features. Three parsimonious machine learning classifiers, multinomial logistic regression (LR), a support vector machine (SVM), and a naive Bayes (Gaussian distribution), were used to construct radiomics models. A personalized emergency prognostic nomogram for cranial injuries was erected using a logistic regression model based on selected radiomic labels and patients' baseline information at emergency admission. The mRMR algorithm and the LASSO regression model finally extracted 22 top-ranked radiological features and based on these image histological features, the emergency brain injury prediction model was built with SVM, LG, and naive Bayesian classifiers, respectively. The SVM model showed the largest AUC area in training cohort for the three classifications, indicating that the SVM model is more stable and accurate. Moreover, a nomogram prediction model for GOS prognostic score in patients was constructed. We established a nomogram for predicting patients' prognosis through radiomic features and clinical characteristics, provides some data support and guidance for clinical prediction of patients' brain injury prognosis and intervention.

Foundation models, pretrained on extensive datasets, have significantly advanced machine learning by providing robust and transferable embeddings applicable to various domains, including medical imaging diagnostics. This study evaluates the utility of embeddings derived from both general-purpose and medical domain-specific foundation models for training lightweight adapter models in multi-class radiography classification, focusing specifically on tube placement assessment. A dataset comprising 8842 radiographs classified into seven distinct categories was employed to extract embeddings using six foundation models: DenseNet121, BiomedCLIP, Med-Flamingo, MedImageInsight, Rad-DINO, and CXR-Foundation. Adapter models were subsequently trained using classical machine learning algorithms. Among these combinations, MedImageInsight embeddings paired with an support vector machine adapter yielded the highest mean area under the curve (mAUC) at 93.8%, followed closely by Rad-DINO (91.1%) and CXR-Foundation (89.0%). In comparison, BiomedCLIP and DenseNet121 exhibited moderate performance with mAUC scores of 83.0% and 81.8%, respectively, whereas Med-Flamingo delivered the lowest performance at 75.1%. Notably, most adapter models demonstrated computational efficiency, achieving training within one minute and inference within seconds on CPU, underscoring their practicality for clinical applications. Furthermore, fairness analyses on adapters trained on MedImageInsight-derived embeddings indicated minimal disparities, with gender differences in performance within 2% and standard deviations across age groups not exceeding 3%. These findings confirm that foundation model embeddings-especially those from MedImageInsight-facilitate accurate, computationally efficient, and equitable diagnostic classification using lightweight adapters for radiographic image analysis.