The assessment of eosinophilic chronic rhinosinusitis (eCRS) lacks accurate non-invasive preoperative prediction methods, relying primarily on invasive histopathological sections. This study aims to use computed tomography (CT) images and clinical parameters to develop an integrated deep learning model for the preoperative identification of eCRS and further explore the biological basis of its predictions. A total of 1098 patients with sinus CT images were included from two hospitals and were divided into training, internal, and external test sets. The region of interest of sinus lesions was manually outlined by an experienced radiologist. We utilized three deep learning models (3D-ResNet, 3D-Xception, and HR-Net) to extract features from CT images and calculate deep learning scores. The clinical signature and deep learning score were inputted into a support vector machine for classification. The receiver operating characteristic curve, sensitivity, specificity, and accuracy were used to evaluate the integrated deep learning model. Additionally, proteomic analysis was performed on 34 patients to explore the biological basis of the model's predictions. The area under the curve of the integrated deep learning model to predict eCRS was 0.851 (95% confidence interval [CI]: 0.77-0.93) and 0.821 (95% CI: 0.78-0.86) in the internal and external test sets. Proteomic analysis revealed that in patients predicted to be eCRS, 594 genes were dysregulated, and some of them were associated with pathways and biological processes such as chemokine signaling pathway. The proposed integrated deep learning model could effectively predict eCRS patients. This study provided a non-invasive way of identifying eCRS to facilitate personalized therapy, which will pave the way toward precision medicine for CRS.

AimsAortic stenosis (AS) is a progressive disease requiring timely monitoring and intervention. While transthoracic echocardiography (TTE) remains the diagnostic standard, deep learning (DL)-based approaches offer potential for improved disease tracking. This study examined the longitudinal changes in a previously developed DL-derived index for AS continuum (DLi-ASc) and assessed its value in predicting progression to severe AS. Methods and ResultsWe retrospectively analysed 2,373 patients a(7,371 TTEs) from two tertiary hospitals. DLi-ASc (scaled 0-100), derived from parasternal long- and/or short-axis views, was tracked longitudinally. DLi-ASc increased in parallel with worsening AS stages (p for trend <0.001) and showed strong correlations with AV maximal velocity (Vmax) (Pearson correlation coefficients [PCC] = 0.69, p<0.001) and mean pressure gradient (mPG) (PCC = 0.66, p<0.001). Higher baseline DLi-ASc was associated with a faster AS progression rate (p for trend <0.001). Additionally, the annualised change in DLi-ASc, estimated using linear mixed-effect models, correlated strongly with the annualised progression of AV Vmax (PCC = 0.71, p<0.001) and mPG (PCC = 0.68, p<0.001). In Fine-Gray competing risk models, baseline DLi-ASc independently predicted progression to severe AS, even after adjustment for AV Vmax or mPG (hazard ratio per 10-point increase = 2.38 and 2.80, respectively) ConclusionDLi-ASc increased in parallel with AS progression and independently predicted severe AS progression. These findings support its role as a non-invasive imaging-based digital marker for longitudinal AS monitoring and risk stratification.

Understanding the impact of epilepsy on pediatric brain tumors is crucial to diagnostic precision and optimal treatment selection. This study investigated MRI radiomics features, tumor location, voxel-based morphometry (VBM) for gray matter density, and tumor volumetry to differentiate between children with low grade glioma (LGG)-associated epilepsies and those without, and further identified key radiomics features for predicting of epilepsy risk in children with supratentorial LGG to construct an epilepsy prediction model. A total of 206 radiomics features of tumors and voxel-based morphometric analysis of tumor location features were extracted from T2-FLAIR images in a primary cohort of 48 children with LGG with epilepsy (N = 23) or without epilepsy (N = 25), prior to surgery. Feature selection was performed using the minimum redundancy maximum relevance algorithm, and leave-one-out cross-validation was applied to assess the predictive performance of radiomics and tumor location signatures in differentiating epilepsy-associated LGG from non-epilepsy cases. Voxel-based morphometric analysis showed significant positive t-scores within bilateral temporal cortex and negative t-scores in basal ganglia between epilepsy and non-epilepsy groups. Eight radiomics features were identified as significant predictors of epilepsy in LGG, encompassing characteristics of 2 locations, 2 shapes, 1 image gray scale intensity, and 3 textures. The most important predictor was temporal lobe involvement, followed by high dependence high grey level emphasis, elongation, area density, information correlation 1, midbrain and intensity range. The Linear Support Vector Machine (SVM) model yielded the best prediction performance, when implemented with a combination of radiomics features and tumor location features, as evidenced by the following metrics: precision (0.955), recall (0.913), specificity (0.960), accuracy (0.938), F-1 score (0.933), and area under curve (AUC) (0.950). Our findings demonstrated the efficacy of machine learning models based on radiomics features and voxel-based anatomical locations in predicting the risk of epilepsy in supratentorial LGG. This model provides a highly accurate tool for distinguishing epilepsy-associated LGG in children, supporting precise treatment planning. Not applicable.

This study aims to develop and validate a multiregional radiomics model to predict pathological complete response (pCR) to neoadjuvant chemoimmunotherapy in non-small cell lung cancer (NSCLC), and further evaluate the performance of the model in different specific subgroups (N2 stage and anti-PD-1/PD-L1). 216 patients with NSCLC who underwent neoadjuvant chemoimmunotherapy followed by surgical intervention were included and assigned to training and validation sets randomly. From pre-treatment baseline CT, one intratumoral (T) and two peritumoral regions (P₃: 0-3 mm; P₆: 0-6 mm) were extracted. Five radiomics models were developed using machine learning algorithms to predict pCR, utilizing selected features from intratumoral (T), peritumoral (P₃, P₆), and combined intra- and peritumoral regions (T + P₃, T + P₆). Additionally, the predictive efficacy of the optimal model was specifically assessed for patients in the N2 stage and anti-PD-1/PD-L1 subgroups. A total of 51.4 % (111/216) of patients exhibited pCR following neoadjuvant chemoimmunotherapy. Multivariable analysis identified that only the T + P₃ radiomics signature served as independent predictor of pCR (P < 0.001). The multiregional radiomics model (T + P₃) exhibited superior predictive performance for pCR, achieving an area under the curve (AUC) of 0.75 in the validation cohort. Furthermore, this multiregional model maintained robust predictive accuracy in both N2 stage and anti-PD-1/PD-L1 subgroups, with an AUC of 0.829 and 0.833, respectively. The proposed multiregional radiomics model showed potential in predicting pCR in NSCLC after neoadjuvant chemoimmunotherapy, and demonstrated good predictive performance in different specific subgroups. This capability may assist clinicians in identifying suitable candidates for neoadjuvant chemoimmunotherapy and promote the advancement in precision therapy.

Development of a deep learning model for accurate preoperative identification of glioblastoma and solitary brain metastases by combining multi-centre and multi-sequence magnetic resonance images and comparison of the performance of different deep learning models. Clinical data and MR images of a total of 236 patients with pathologically confirmed glioblastoma and single brain metastases were retrospectively collected from January 2019 to May 2024 at Provincial Hospital of Shandong First Medical University, and the data were randomly divided into a training set and a test set according to the ratio of 8:2, in which the training set contained 197 cases and the test set contained 39 cases; the images were preprocessed and labeled with the tumor regions. The images were pre-processed and labeled with tumor regions, and different MRI sequences were input individually or in combination to train the deep learning model 3D ResNet-18, and the optimal sequence combinations were obtained by five-fold cross-validation enhancement of the data inputs and training of the deep learning models 3D Vision Transformer (3D Vit), 3D DenseNet, and 3D VGG; the working characteristic curves (ROCs) of subjects were plotted, and the area under the curve (AUC) was calculated. The area under the curve (AUC), accuracy, precision, recall and F1 score were used to evaluate the discriminative performance of the models. In addition, 48 patients with glioblastoma and single brain metastases from January 2020 to December 2022 were collected from the Affiliated Cancer Hospital of Shandong First Medical University as an external test set to compare the discriminative performance, robustness and generalization ability of the four deep learning models. In the comparison of the discriminative effect of different MRI sequences, the three sequence combinations of T1-CE, T2, and T2-Flair gained discriminative effect, with the accuracy and AUC values of 0.8718 and 0.9305, respectively; after the four deep learning models were inputted into the aforementioned sequence combinations, the accuracy and AUC of the external validation of the 3D ResNet-18 model were 0.8125, respectively, 0.8899, all of which are the highest among all models. A combination of multi-sequence MR images and a deep learning model can efficiently identify glioblastoma and solitary brain metastases preoperatively, and the deep learning model 3D ResNet-18 has the highest efficacy in identifying the two types of tumours.

Pancreatic Cancer (PC) is a highly aggressive tumor that is mainly diagnosed at later stages. Various imaging technologies, such as CT, MRI, and EUS, possess limitations in early PC diagnosis. Therefore, this review article explores the various innovative biomarkers for PC detection, such as DNA methylation, Noncoding RNAs, and proteomic biomarkers, and the role of AI in PC detection at early stages. Innovative biomarkers, such as DNA methylation genes, show higher specificity and sensitivity in PC diagnosis. Additionally, various non-coding RNAs, such as long non-coding RNAs (lncRNAs) and microRNAs, show high diagnostic accuracy and serve as diagnostic and prognostic biomarkers. Additionally, proteomic biomarkers retain higher diagnostic accuracy in different body fluids. Apart from this, the utilization of AI showed that AI surpassed the radiologist's diagnostic performance in PC detection. The combination of AI and advanced biomarkers can revolutionize early PC detection. However, large-scale, prospective studies are needed to validate its clinical utility. Further. standardization of biomarker panels and AI algorithms is a vital step toward their reliable applications in early PC detection, ultimately improving patient outcomes.

This retrospective study evaluates the diagnostic performance of an optimized comprehensive multi-stage framework based on the Segment Anything Model (SAM), which we named Dr-SAM, for detecting and grading vascular stenosis in the abdominal aorta and iliac arteries using digital subtraction angiography (DSA). A total of 100 DSA examinations were conducted on 100 patients. The infrarenal abdominal aorta (AAI), common iliac arteries (CIA), and external iliac arteries (EIA) were independently evaluated by two experienced radiologists using a standardized 5-point grading scale. Dr-SAM analyzed the same DSA images, and its assessments were compared with the average stenosis grading provided by the radiologists. Diagnostic accuracy was evaluated using Cohen's kappa, specificity, sensitivity, and Wilcoxon signed-rank tests. Interobserver agreement between radiologists, which established the reference standard, was strong (Cohen's kappa: CIA right = 0.95, CIA left = 0.94, EIA right = 0.98, EIA left = 0.98, AAI = 0.79). Dr-SAM showed high agreement with radiologist consensus for CIA (κ = 0.93 right, 0.91 left), moderate agreement for EIA (κ = 0.79 right, 0.76 left), and fair agreement for AAI (κ = 0.70). Dr-SAM demonstrated excellent specificity (up to 1.0) and robust sensitivity (0.67-0.83). Wilcoxon tests revealed no significant differences between Dr-SAM and radiologist grading (p > 0.05). Dr-SAM proved to be an accurate and efficient tool for vascular assessment, with the potential to streamline diagnostic workflows and reduce variability in stenosis grading. Its ability to deliver rapid and consistent evaluations may contribute to earlier detection of disease and the optimization of treatment strategies. Further studies are needed to confirm these findings in prospective settings and to enhance its capabilities, particularly in the detection of occlusions.

This study aims to develop and validate a novel radiomics model utilizing magnetic resonance imaging (MRI) to predict progression-free survival (PFS) in patients with unresectable hepatocellular carcinoma (uHCC) who are receiving a combination of immune checkpoint inhibitors (ICIs) and antiangiogenic agents. This is an area that has not been previously explored using MRI-based radiomics. 111 patients with uHCC were enrolled in this study. After performing univariate cox regression and the least absolute shrinkage and selection operator (LASSO) algorithms to extract radiological features, the Rad-score was calculated through a Cox proportional hazards regression model and a random survival forest (RSF) model. The optimal calculation method was selected by comparing the Harrell's concordance index (C-index) values. The Rad-score was then combined with independent clinical risk factors to create a nomogram. C-index, time-dependent receiver operating characteristics (ROC) curves, calibration curves, and decision curve analysis were employed to assess the forecast ability of the risk models. The combined nomogram incorporated independent clinical factors and Rad-score calculated by RSF demonstrated better prognosis prediction for PFS, with C-index of 0.846, 0.845, separately in the training and the validation cohorts. This indicates that our model performs well and has the potential to enable more precise patient stratification and personalized treatment strategies. Based on the risk level, the participants were classified into two distinct groups: the high-risk signature (HRS) group and the low-risk signature (LRS) group, with a significant difference between the groups (P < 0.01). The effective clinical-radiomics nomogram based on MRI imaging is a promising tool in predicting the prognosis in uHCC patients receiving ICIs combined with anti-angiogenic agents, potentially leading to more effective clinical outcomes.

Machine learning (ML), a subset of artificial intelligence (AI), utilizes advanced algorithms to learn patterns from data, enabling accurate predictions and decision-making without explicit programming. In orthopedic surgery, ML is transforming clinical practice, particularly in shoulder arthroplasty and rotator cuff tears (RCTs) management. This review explores the fundamental paradigms of ML, including supervised, unsupervised, and reinforcement learning, alongside key algorithms such as XGBoost, neural networks, and generative adversarial networks. In shoulder arthroplasty, ML accurately predicts postoperative outcomes, complications, and implant selection, facilitating personalized surgical planning and cost optimization. Predictive models, including ensemble learning methods, achieve over 90% accuracy in forecasting complications, while neural networks enhance surgical precision through AI-assisted navigation. In RCTs treatment, ML enhances diagnostic accuracy using deep learning models on magnetic resonance imaging and ultrasound, achieving area under the curve values exceeding 0.90. ML models also predict tear reparability with 85% accuracy and postoperative functional outcomes, including range of motion and patient-reported outcomes. Despite remarkable advancements, challenges such as data variability, model interpretability, and integration into clinical workflows persist. Future directions involve federated learning for robust model generalization and explainable AI to enhance transparency. ML continues to revolutionize orthopedic care by providing data-driven, personalized treatment strategies and optimizing surgical outcomes.

The standard approach to diagnosing idiopathic pulmonary fibrosis (IPF) includes identifying the usual interstitial pneumonia (UIP) pattern via high resolution computed tomography (HRCT) or lung biopsy and excluding known causes of interstitial lung disease (ILD). However, limitations of manual interpretation of lung imaging, along with other reasons such as lack of relevant knowledge and non-specific symptoms have hindered the timely diagnosis of IPF. This review proposes the definition of early IPF, emphasizes the diagnostic urgency of early IPF, and highlights current diagnostic strategies and future prospects for early IPF. The integration of artificial intelligence (AI), specifically machine learning (ML) and deep learning (DL), is revolutionizing the diagnostic procedure of early IPF by standardizing and accelerating the interpretation of thoracic images. Innovative bronchoscopic techniques such as transbronchial lung cryobiopsy (TBLC), genomic classifier, and endobronchial optical coherence tomography (EB-OCT) provide less invasive diagnostic alternatives. In addition, chest auscultation, serum biomarkers, and susceptibility genes are pivotal for the indication of early diagnosis. Ongoing research is essential for refining diagnostic methods and treatment strategies for early IPF.