Chronic liver disease (CLD) is a substantial cause of morbidity and mortality worldwide. Liver stiffness, as measured by MR elastography (MRE), is well-accepted as a surrogate marker of liver fibrosis. To develop and validate deep learning (DL) models for predicting MRE-derived liver stiffness using routine clinical non-contrast abdominal T1-weighted (T1w) and T2-weighted (T2w) data from multiple institutions/system manufacturers in pediatric and adult patients. We identified pediatric and adult patients with known or suspected CLD from four institutions, who underwent clinical MRI with MRE from 2011 to 2022. We used T1w and T2w data to train DL models for liver stiffness classification. Patients were categorized into two groups for binary classification using liver stiffness thresholds (≥ 2.5 kPa, ≥ 3.0 kPa, ≥ 3.5 kPa, ≥ 4 kPa, or ≥ 5 kPa), reflecting various degrees of liver stiffening. We identified 4695 MRI examinations from 4295 patients (mean ± SD age, 47.6 ± 18.7 years; 428 (10.0%) pediatric; 2159 males [50.2%]). With a primary liver stiffness threshold of 3.0 kPa, our model correctly classified patients into no/minimal (< 3.0 kPa) vs moderate/severe (≥ 3.0 kPa) liver stiffness with AUROCs of 0.83 (95% CI: 0.82, 0.84) in our internal multi-site cross-validation (CV) experiment, 0.82 (95% CI: 0.80, 0.84) in our temporal hold-out validation experiment, and 0.79 (95% CI: 0.75, 0.81) in our external leave-one-site-out CV experiment. The developed model is publicly available ( https://github.com/almahdir1/Multi-channel-DeepLiverNet2.0.git ). Our DL models exhibited reasonable diagnostic performance for categorical classification of liver stiffness on a large diverse dataset using T1w and T2w MRI data. Question Can DL models accurately predict liver stiffness using routine clinical biparametric MRI in pediatric and adult patients with CLD? Findings DeepLiverNet2.0 used biparametric MRI data to classify liver stiffness, achieving AUROCs of 0.83, 0.82, and 0.79 for multi-site CV, hold-out validation, and external CV. Clinical relevance Our DeepLiverNet2.0 AI model can categorically classify the severity of liver stiffening using anatomic biparametric MR images in children and young adults. Model refinements and incorporation of clinical features may decrease the need for MRE.

To establish morphological and radiomic models for early prediction of cognitive impairment associated with cerebrovascular disease (CI-CVD) in an elderly cohort based on cerebral magnetic resonance angiography (MRA). One-hundred four patients with CI-CVD and 107 control subjects were retrospectively recruited from the 14-year elderly MRA cohort, and 63 subjects were enrolled for external validation. Automated quantitative analysis was applied to analyse the morphological features, including the stenosis score, length, relative length, twisted angle, and maximum deviation of cerebral arteries. Clinical and morphological risk factors were screened using univariate logistic regression. Radiomic features were extracted via least absolute shrinkage and selection operator (LASSO) regression. The predictive models of CI-CVD were established in the training set and verified in the external testing set. A history of stroke was demonstrated to be a clinical risk factor (OR 2.796, 1.359-5.751). Stenosis ≥ 50% in the right middle cerebral artery (RMCA) and left posterior cerebral artery (LPCA), maximum deviation of the left internal carotid artery (LICA), and twisted angles of the right internal carotid artery (RICA) and LICA were identified as morphological risk factors, with ORs of 4.522 (1.237-16.523), 2.851 (1.438-5.652), 1.373 (1.136-1.661), 0.981 (0.966-0.997) and 0.976 (0.958-0.994), respectively. Overall, 33 radiomic features were screened as risk factors. The clinical-morphological-radiomic model demonstrated optimal performance, with an AUC of 0.883 (0.838-0.928) in the training set and 0.843 (0.743-0.943) in the external testing set. Radiomics features combined with morphological indicators of cerebral arteries were effective indicators for early signs of CI-CVD in elderly individuals. Question The relationship between morphological features of cerebral arteries and cognitive impairment associated with cerebrovascular disease (CI-CVD) deserves to be explored. Findings The multipredictor model combining with stroke history, vascular morphological indicators and radiomic features of cerebral arteries demonstrated optimal performance for the early warning of CI-CVD. Clinical relevance Stenosis percentage and tortuosity score of the cerebral arteries are important risk factors for cognitive impairment. The radiomic features combined with morphological quantification analysis based on cerebral MRA provide higher predictive performance of CI-CVD.

When antispasmodics are unavailable, the periodically rotated overlapping parallel lines with enhanced reconstruction (PROPELLER; called BLADE by Siemens Healthineers) or half Fourier single-shot turbo spin echo (HASTE) is clinically used in gynecologic MRI. However, their imaging qualities are limited compared to Turbo Spin Echo (TSE) with antispasmodics. Even with antispasmodics, TSE can be artifact-affected, necessitating a rapid backup sequence. This study aimed to investigate the utility of HASTE with deep learning reconstruction and variable flip angle evolution (iHASTE) compared to conventional sequences with and without antispasmodics. This retrospective study included MRI scans without antispasmodics for 79 patients who underwent iHASTE, HASTE, and BLADE and MRI scans with antispasmodics for 79 case-control matched patients who underwent TSE. Three radiologists qualitatively evaluated image quality, robustness to artifacts, tissue contrast, and uterine lesion margins. Tissue contrast was also quantitatively evaluated. Quantitative evaluations revealed that iHASTE exhibited significantly superior tissue contrast to HASTE and BLADE. Qualitative evaluations indicated that iHASTE outperformed HASTE in overall quality. Two of three radiologists judged iHASTE to be significantly superior to BLADE, while two of three judged TSE to be significantly superior to iHASTE. iHASTE demonstrated greater robustness to artifacts than both BLADE and TSE. Lesion margins in iHASTE had lower scores than BLADE and TSE. iHASTE is a viable clinical option in patients undergoing gynecologic MRI with anti-spasmodics. iHASTE may also be considered as a useful add-on sequence in patients undergoing MRI with antispasmodics.

Some sarcomas are highly malignant, associated with high recurrence despite treatment. This multicenter study aimed to develop and validate a radiomics signature to estimate sarcoma progression-free survival (PFS). The study retrospectively enrolled 202 consecutive patients with pathologically diagnosed sarcoma, who had pre-treatment axial fat-suppressed T2-weighted images (FS-T2WI), and included them in the ROI-Net model for training. Among them, 120 patients were included in the radiomics analysis, all of whom had pre-treatment axial T1-weighted and transverse FS-T2WI images, and were randomly divided into a development group (n = 96) and a validation group (n = 24). In the development cohort, Least Absolute Shrinkage and Selection Operator (LASSO) Cox regression was used to develop the radiomics features for PFS prediction. By combining significant clinical features with radiomics features, a nomogram was constructed using Cox regression. The proposed ROI-Net framework achieved a Dice coefficient of 0.820 (0.791-0.848). The radiomics signature based on 21 features could distinguish high-risk patients with poor PFS. Univariate Cox analysis revealed that peritumoral edema, metastases, and the radiomics score were associated with poor PFS and were included in the construction of the nomogram. The Radiomics-T1WI-Clinical model exhibited the best performance, with AUC values of 0.947, 0.907, and 0.924 at 300 days, 600 days, and 900 days, respectively. The proposed ROI-Net framework demonstrated high consistency between its segmentation results and expert annotations. The radiomics features and the combined nomogram have the potential to aid in predicting PFS for patients with sarcoma.

Accurate and robust segmentation of anatomical structures in brain MRI provides a crucial basis for the subsequent observation, analysis, and treatment planning of various brain diseases. Deep learning foundation models trained and designed on large-scale natural scene image datasets experience significant performance degradation when applied to subcortical brain structure segmentation in MRI, limiting their direct applicability in clinical diagnosis. This paper proposes a subcortical brain structure segmentation algorithm based on Low-Rank Adaptation (LoRA) to fine-tune SAM (Segment Anything Model) by freezing SAM's image encoder and applying LoRA to approximate low-rank matrix updates to the encoder's training weights, while also fine-tuning SAM's lightweight prompt encoder and mask decoder. The fine-tuned model's learnable parameters (5.92 MB) occupy only 6.39% of the original model's parameter size (92.61 MB). For training, model preheating is employed to stabilize the fine-tuning process. During inference, adaptive prompt learning with point or box prompts is introduced to enhance the model's accuracy for arbitrary brain MRI segmentation. This interactive prompt learning approach provides clinicians with a means of intelligent segmentation for deep brain structures, effectively addressing the challenges of limited data labels and high manual annotation costs in medical image segmentation. We use five MRI datasets of IBSR, MALC, LONI, LPBA, Hammers and CANDI for experiments across various segmentation scenarios, including cross-domain settings with inference samples from diverse MRI datasets and supervised fine-tuning settings, demonstrate the proposed segmentation algorithm's generalization and effectiveness when compared to current mainstream and supervised segmentation algorithms.

Traditional clinical diagnostic methods of rapid eye movement sleep behavior disorder (RBD) have certain limitations, especially in the early stages. This study aims to develop and validate an magnetic resonance imaging (MRI) radiomics-based machine learning classifier to accurately detect RBD patients with Parkinson's disease (PD). Data from 183 subjects, including 63 PD patients with RBD, sourced from the PPMI database were utilized in this study. The data were randomly divided into training (70%) and testing (30%) sets. Quantitative radiomic features of white matter, gray matter, and cerebrospinal fluid were extracted from whole-brain structural MRI images. Feature reduction was performed on the training set data to construct radiomics signatures. Additionally, multi-factor logistic regression analysis identified clinical predictors associated with PD-RBD, and these clinical features were integrated with the radiomics signatures to develop predictive models using various machine learning algorithms. The model exhibiting the best performance was selected, and receiver operating characteristic (ROC) curves were used to evaluate its performance in both the training and testing sets. Furthermore, based on the optimal cut-off value of the model, subjects were categorized into low- and high-risk groups, and differences in the actual number of RBD patients between the two sets were compared to assess the clinical effectiveness of the model. The radiomics signatures achieved areas under the curve (AUC) of 0.754 and 0.707 in the training and testing sets, respectively. Multi-factor logistic regression analysis revealed that postural instability was an independent predictor of PD-RBD. The random forest model, which integrated radiomics signatures with postural instability, demonstrated superior performance in predicting PD-RBD. Specifically, its AUCs in the training and testing sets were 0.917 and 0.882, with sensitivities of 0.933 and 0.889, and specificities of 0.786 and 0.722, respectively. Based on the optimal cut-off value of 0.3772, significant differences in the actual number of PD-RBD patients were observed between low-risk and high-risk groups in both the training and testing sets (P < 0.05). MRI-based radiomic signatures have the potential to serve as biomarkers for PD-RBD. The random forest model, which integrates radiomic signatures with postural instability, and shows improved performance in identifying PD-RBD. This approach offers valuable insights for prognostic evaluation and preventive treatment strategies.

To improve the prediction of immune checkpoint inhibitors (ICIs) efficacy in hepatocellular carcinoma (HCC), this study categorized the tumor immune microenvironment (TIME) into two types: immune-activated (IA), characterized by a high CD8 + score and high PD-L1 combined positive score (CPS), and non-immune-activated (NIA), encompassing all other conditions. We aimed to develop an MRI-based radiomics model to predict TIME types and validate its predictive capability for ICIs efficacy in HCC patients receiving anti-PD-1/PD-L1 therapy. The study included 200 HCC patients who underwent preoperative/pretreatment multiparametric contrast-enhanced MRI (Cohort 1: 168 HCC patients with hepatectomy from two centres; Cohort 2: 42 advanced HCC patients on anti-PD-1/PD-L1 therapy). In Cohort 1, after feature selection, clinical, intratumoral radiomics, peritumoral radiomics, combined radiomics, and clinical-radiomics models were established using machine learning algorithms. In cohort 2, the clinical-radiomics model's predictive ability for ICIs efficacy was assessed. In Cohort 1, the AUC values for intratumoral, peritumoral, and combined radiomics models were 0.825, 0.809, and 0.868, respectively, in the internal validation set, and 0.73, 0.759, and 0.822 in the external validation set; the clinical-radiomics model incorporating neutrophil-to-lymphocyte ratio, tumor size, and combined radiomics score achieved an AUC of 0.887 in the internal validation set, outperforming clinical model (P = 0.049), and an AUC of 0.837 in the external validation set. In cohort 2, the clinical-radiomics model stratified patients into low- and high-score groups, demonstrating a significant difference in objective response rate (p = 0.003) and progression-free survival (p = 0.031). The clinical-radiomics model is effective in predicting TIME types and efficacy of ICIs in HCC, potentially aiding in treatment decision-making.

The study aimed to develop a single-stage deep learning (DL) screening system for automated binary and multiclass grading of lumbar central stenosis (LCS), lateral recess stenosis (LRS), and lumbar foraminal stenosis (LFS). Consecutive inpatients who underwent lumbar MRI at our center were retrospectively reviewed for the internal dataset. Axial and sagittal lumbar MRI scans were collected. Based on a new MRI diagnostic criterion, all MRI studies were labeled by two spine specialists and calibrated by a third spine specialist to serve as reference standard. Furthermore, two spine clinicians labeled all MRI studies independently to compare interobserver reliability with the DL model. Samples were assigned into training, validation, and test sets at a proportion of 8:1:1. Additional patients from another center were enrolled as the external test dataset. A modified single-stage YOLOv5 network was designed for simultaneous detection of regions of interest (ROIs) and grading of LCS, LRS, and LFS. Quantitative evaluation metrics of exactitude and reliability for the model were computed. In total, 420 and 50 patients were enrolled in the internal and external datasets. High recalls of 97.4%-99.8% were achieved for ROI detection of lumbar spinal stenosis (LSS). The system revealed multigrade area under curve (AUC) values of 0.93-0.97 in the internal test set and 0.85-0.94 in the external test set for LCS, LRS, and LFS. In binary grading, the DL model achieved high sensitivities of 0.97 for LCS, 0.98 for LRS, and 0.96 for LFS, slightly better than those achieved by spine clinicians in the internal test set. In the external test set, the binary sensitivities were 0.98 for LCS, 0.96 for LRS, and 0.95 for LFS. For reliability assessment, the kappa coefficients between the DL model and reference standard were 0.92, 0.88, and 0.91 for LCS, LRS, and LFS, respectively, slightly higher than those evaluated by nonexpert spine clinicians. The authors designed a novel DL system that demonstrated promising performance, especially in sensitivity, for automated diagnosis and grading of different types of lumbar spinal stenosis using spine MRI. The reliability of the system was better than that of spine surgeons. The authors' system may serve as a triage tool for LSS to reduce misdiagnosis and optimize routine processes in clinical work.

Given that resection of brainstem cavernous malformations (BSCMs) ends hemorrhaging but carries a high risk of neurological deficits, it is necessary to develop and validate a model predicting surgical outcomes. This study aimed to construct a BSCM surgery outcome prediction model based on clinical characteristics and T2-weighted MRI-based radiomics. Two separate cohorts of patients undergoing BSCM resection were included as discovery and validation sets. Patient characteristics and imaging data were analyzed. An unfavorable outcome was defined as a modified Rankin Scale score > 2 at the 12-month follow-up. Image features were extracted from regions of interest within lesions and adjacent brainstem. A nomogram was constructed using the risk score from the optimal model. The discovery and validation sets comprised 218 and 49 patients, respectively (mean age 40 ± 14 years, 127 females); 63 patients in the discovery set and 35 in the validation set had an unfavorable outcome. The eXtreme Gradient Boosting imaging model with selected radiomics features achieved the best performance (area under the receiver operating characteristic curve [AUC] 0.82). Patients were stratified into high- and low-risk groups based on risk scores computed from this model (optimal cutoff 0.37). The final integrative multimodal prognostic model attained an AUC of 0.90, surpassing both the imaging and clinical models alone. Inclusion of BSCM and brainstem subregion imaging data in machine learning models yielded significant predictive capability for unfavorable postoperative outcomes. The integration of specific clinical features enhanced prediction accuracy.

While conventional structural magnetic resonance imaging (MRI) can detect cruciate ligament anatomy and injuries, it has inherent limitations. Recently, novel MRI technologies such as quantitative MRI and artificial intelligence (AI) have emerged to mitigate these shortcomings, providing critical quantitative insights beyond gross morphological imaging and poised to expand current knowledge in assessing cruciate ligament injuries and to facilitate clinical decision making. Quantitative MRI serves as a noninvasive histological and quantification tool, which significantly improves the evaluation of degeneration and repair processes. AI plays a crucial role in automating radiological estimations and enabling data-driven predictions of future events. Despite the transformative impact of advanced MRI techniques on the analytical and diagnostic algorithms related to cruciate ligament disorders, future efforts are warranted to address challenges such as economic burdens and ethical considerations.