To evaluate image quality and diagnostic interchangeability of synth short-tau inversion recovery (STIR) generated by deep learning in comparison with standard STIR. This prospective study recruited participants between July 2023 and August 2023. Participants were scanned with T1WI and T2WI, then generated Synth-STIR. Signal-to-noise ratios (SNR), contrast-to-noise ratios (CNR) were calculated for quantitative evaluation. Four independent, blinded radiologists performed subjective quality and lesion characteristic assessment. Wilcoxon tests were used to assess the differences in SNR, CNR, and subjective image quality. Various diagnostic findings pertinent to the spine were tested for interchangeability using the individual equivalence index (IEI). Inter-reader and intra-reader agreement and concordance were computed, and McNemar tests were performed for comprehensive evaluation. One hundred ninety-nine participants (106 male patients, mean age 46.8 ± 16.9 years) were included. Compared to standard-STIR, Synth-STIR reduces sequence scanning time by approximately 180 s, has significantly higher SNR and CNR (p < 0.001). For artifacts, noise, sharpness, and diagnostic confidence, all readers agreed that Synth-STIR was significantly better than standard-STIR (all p < 0.001). In addition, the IEI was less than 1.61%. Kappa and Kendall showed a moderate to excellent agreement in the range of 0.52-0.97. There was no significant difference in the frequencies of the major features as reported with standard-STIR and Synth-STIR (p = 0.211-1). Synth-STIR shows significantly higher SNR and CNR, and is diagnostically interchangeable with standard-STIR with a substantial overall reduction in the imaging time, thereby improving efficiency without sacrificing diagnostic value. Question Can generating STIR improve image quality while reducing spine MRI acquisition time in order to increase clinical spine MRI throughput? Findings With reduced acquisition time, Synth-STIR has significantly higher SNR and CNR than standard-STIR and can be interchangeably diagnosed with standard-STIR in detecting spinal abnormalities. Clinical relevance Our Synth-STIR provides the same high-quality images for clinical diagnosis as standard-STIR, while reducing scanning time for spine MRI protocols. Increase clinical spine MRI throughput.

Advancements in diagnostic technology are required to improve patient outcomes and facilitate early diagnosis, as breast cancer is a substantial global health concern. This research discusses the creation of a unique Deep Learning (DL) Ensemble Deep Learning based on a Clinical Decision Support System (EDL-CDSS) that enables the precise and expeditious diagnosis of breast cancer. Numerous DL models are combined in the proposed EDL-CDSS to create an ensemble method that optimizes the advantages and reduces the disadvantages of individual techniques. The team improves its capacity to extricate intricate patterns and features from medical imaging data by incorporating the Kelm Extreme Learning Machine (KELM), Deep Belief Network (DBN), and other DL architectures. Comprehensive testing has been conducted across various datasets to assess the efficacy of this system in comparison to individual DL models and traditional diagnostic methods. Among other objectives, the evaluation prioritizes precision, sensitivity, specificity, F1-score, accuracy, and overall accuracy to mitigate false positives and negatives. The experiment's conclusion exhibits a remarkable accuracy of 96.14% in comparison to prior advanced methodologies.

Artificial intelligence (AI) is already having a significant impact on healthcare. For example, AI-guided imaging can improve the diagnosis/treatment of vascular diseases, which affect over 200 million people globally. Recently, Chiu and colleagues (2024) developed an AI algorithm that supports nurses with no ultrasound training in diagnosing abdominal aortic aneurysms (AAA) with similar accuracy as ultrasound-trained physicians. This technology can therefore improve AAA screening; however, achieving clinical impact with new AI technologies requires careful consideration of commercialization strategies, including funding, compliance with safety and regulatory frameworks, health technology assessment, regulatory approval, reimbursement, and clinical guideline integration.

The integration of artificial intelligence (AI) into [¹⁸F]FDG PET/CT imaging continues to expand, offering new opportunities for more precise, consistent, and personalized oncologic evaluations. Building on the foundation established in Part I, this second part explores AI-driven innovations across a broader range of malignancies, including hematological, genitourinary, melanoma, and central nervous system tumors as well applications of AI in pediatric oncology. Radiomics and machine learning algorithms are being explored for their ability to enhance diagnostic accuracy, reduce interobserver variability, and inform complex clinical decision-making, such as identifying patients with refractory lymphoma, assessing pseudoprogression in melanoma, or predicting brain metastases in extracranial malignancies. Additionally, AI-assisted lesion segmentation, quantitative feature extraction, and heterogeneity analysis are contributing to improved prediction of treatment response and long-term survival outcomes. Despite encouraging results, variability in imaging protocols, segmentation methods, and validation strategies across studies continues to challenge reproducibility and remains a barrier to clinical translation. This review evaluates recent advancements of AI, its current clinical applications, and emphasizes the need for robust standardization and prospective validation to ensure the reproducibility and generalizability of AI tools in PET imaging and clinical practice.

Advancements in cardiac computed tomography angiography (CCTA) have enabled the extraction of physiological data from an anatomy-based imaging modality. This review outlines the key methodologies for deriving fractional flow reserve (FFR) from CCTA, with a focus on two primary methods: 1) computational fluid dynamics-based FFR (CT-FFR) and 2) plaque-derived ischemia assessment using artificial intelligence and quantitative plaque metrics. These techniques have expanded the role of CCTA beyond anatomical assessment, allowing for concurrent evaluation of coronary physiology without the need for invasive testing. This review provides an overview of the principles, workflows, and limitations of each technique and aims to inform on the current state and future direction of non-invasive coronary physiology assessment.

To evaluate image quality and diagnostic performance of prostate biparametric MRI (bi-MRI) with deep learning reconstruction (DLR). This prospective study included 61 adult male urological patients undergoing prostate MRI with standard-of-care (SOC) and fast protocols. Sequences included T2-weighted imaging (T2WI), diffusion-weighted imaging (DWI), and apparent diffusion coefficient (ADC) maps. DLR images were generated from FAST datasets. Three groups (SOC, FAST, DLR) were compared using: (1) five-point Likert scale, (2) signal-to-noise ratio (SNR), contrast-to-noise ratio (CNR), (3) lesion slope profiles, (4) dorsal capsule edge rise distance (ERD). PI-RADS scores were assigned to dominant lesions. ADC values were measured in histopathologically confirmed cases. Diagnostic performance was analyzed via receiver operating characteristic (ROC) curves (accuracy/sensitivity/specificity). Statistical tests included Friedman test, one-way ANOVA with post hoc analyses, and DeLong test for ROC comparisons (P<0.05). FAST scanning protocols reduced acquisition time by nearly half compared to the SOC scanning protocol. When compared to T2WI_FAST, DLR significantly improved SNR, CNR, slope profile, and ERD (P < 0.05). Similarly, DLR significantly enhanced SNR, CNR, and image sharpness when compared to DWI_FAST (P < 0.05). No significant differences were observed in PI-RADS scores and ADC values between groups (P > 0.05). The areas under the ROC curves, sensitivity, and specificity of ADC values for distinguishing benign and malignant lesions remained consistent (P > 0.05). DLR enhances image quality in fast prostate bi-MRI while preserving PI-RADS classification accuracy and ADC diagnostic performance.

This study aimed to systematically map the development methods, scope, and limitations of existing artificial intelligence (AI) reporting guidelines in medicine and to explore their applicability to generative AI (GAI) tools, such as large language models (LLMs). We reported a scoping review adhering to the Preferred Reporting Items for Systematic Reviews and Meta-Analyses Extension for Scoping Reviews (PRISMA-ScR). Five information sources were searched, including MEDLINE (via PubMed), EQUATOR Network, CNKI, FAIRsharing, and Google Scholar, from inception to December 31, 2024. Two reviewers independently screened records and extracted data using a predefined Excel template. Data included guideline characteristics (e.g., development methods, target audience, AI domain), adherence to EQUATOR Network recommendations, and consensus methodologies. Discrepancies were resolved by a third reviewer. 68 AI reporting guidelines were included. 48.5% focused on general AI, while only 7.4% addressed GAI/LLMs. Methodological rigor was limited: 39.7% described development processes, 42.6% involved multidisciplinary experts, and 33.8% followed EQUATOR recommendations. Significant overlap existed, particularly in medical imaging (20.6% of guidelines). GAI-specific guidelines (14.7%) lacked comprehensive coverage and methodological transparency. Existing AI reporting guidelines in medicine have suboptimal methodological rigor, redundancy, and insufficient coverage of GAI applications. Future and updated guidelines should prioritize standardized development processes, multidisciplinary collaboration, and expanded focus on emerging AI technologies like LLMs.

Chronological age, although commonly used in clinical practice, fails to capture individual variations in rates of ageing and physiological decline. Recent advances in artificial intelligence (AI) have transformed the estimation of biological age using various imaging techniques. This Review consolidates AI developments in age prediction across brain, chest, abdominal, bone, and facial imaging using diverse methods, including MRI, CT, x-ray, and photographs. The difference between predicted and chronological age-often referred to as age deviation-is a promising biomarker for assessing health status and predicting disease risk. In this Review, we highlight consistent associations between age deviation and various health outcomes, including mortality risk, cognitive decline, and cardiovascular prognosis. We also discuss the technical challenges in developing unbiased models and ethical considerations for clinical application. This Review highlights the potential of AI-based age estimation in personalised medicine as it offers a non-invasive, interpretable biomarker that could transform health risk assessment and guide preventive interventions.

Vascular aging is an important phenotype characterized by structural and geometric remodeling. Some individuals exhibit supernormal vascular aging, associated with improved cardiovascular outcomes; others experience early vascular aging, linked to adverse cardiovascular outcomes. The aorta is the artery that exhibits the most prominent age-related changes; however, the biological mechanisms underlying aortic aging, its genetic architecture, and its relationship with cardiovascular structure, function, and disease states remain poorly understood. We developed sex-specific models to quantify aortic age on the basis of aortic geometric phenotypes derived from 3-dimensional tomographic imaging data in 2 large biobanks: the UK Biobank and the Penn Medicine BioBank. Convolutional neural ne2rk-assisted 3-dimensional segmentation of the aorta was performed in 56 104 magnetic resonance imaging scans in the UK Biobank and 6757 computed tomography scans in the Penn Medicine BioBank. Aortic vascular age index (AVAI) was calculated as the difference between the vascular age predicted from geometric phenotypes and the chronological age, expressed as a percent of chronological age. We assessed associations with cardiovascular structure and function using multivariate linear regression and examined the genetic architecture of AVAI through genome-wide association studies, followed by Mendelian randomization to assess causal associations. We also constructed a polygenic risk score for AVAI. AVAI displayed numerous associations with cardiac structure and function, including increased left ventricular mass (standardized β=0.144 [95% CI, 0.138, 0.149]; <i>P</i><0.0001), wall thickness (standardized β=0.061 [95% CI, 0.054, 0.068]; <i>P</i><0.0001), and left atrial volume maximum (standardized β=0.060 [95% CI, 0.050, 0.069]; <i>P</i><0.0001). AVAI exhibited high genetic heritability (<i>h</i>²=40.24%). We identified 54 independent genetic loci (<i>P</i><5×10^-⁸) associated with AVAI, which further exhibited gene-level associations with the fibrillin-1 (<i>FBN1</i>) and elastin (<i>ELN1</i>) genes. Mendelian randomization supported causal associations between AVAI and atrial fibrillation, vascular dementia, aortic aneurysm, and aortic dissection. A polygenic risk score for AVAI was associated with an increased prevalence of atrial fibrillation, hypertension, aortic aneurysm, and aortic dissection. Early aortic aging is significantly associated with adverse cardiac remodeling and important cardiovascular disease states. AVAI exhibits a polygenic, highly heritable genetic architecture. Mendelian randomization analyses support a causal association between AVAI and cardiovascular diseases, including atrial fibrillation, vascular dementia, aortic aneurysms, and aortic dissection.

Propose and evaluate an automatic approach for predicting the optimal inversion time (TI) for dark and gray blood images for flow-independent dark-blood delayed-enhancement (FIDDLE) acquisition based on free-breathing FIDDLE TI-scout images. In 267 patients, the TI-scout sequence acquired single-shot magnetization-prepared and associated reference images (without preparation) on a 3 T Magnetom Vida and a 1.5 T Magnetom Sola scanner. Data were reconstructed into phase-corrected TI-scout images typically covering TIs from 140 to 440 ms (20 ms increment). A deep learning network was trained to segment the myocardium and blood pool in reference images. These segmentation masks were transferred to the TI-scout images to derive intensity features of myocardium and blood, with which T₁-recovery curves were determined by logarithmic fitting. The optimal TI for dark and gray blood images were derived as linear functions of the TI in which both T₁-curves cross. This TI-prediction pipeline was evaluated in 64 clinical subjects. The pipeline predicted optimal TIs with an average error less than 10 ms compared to manually annotated optimal TIs. The presented approach reliably and automatically predicted optimal TI for dark and gray blood FIDDLE acquisition, with an average error less than the TI increment of the FIDDLE TI-scout sequence.