Computed tomography coronary angiography provides a non-invasive evaluation of coronary artery disease that includes phenotyping of atherosclerotic plaques and the surrounding perivascular adipose tissue (PVAT). Image analysis techniques have been developed to quantify atherosclerotic plaque burden and morphology as well as the associated PVAT attenuation, and emerging radiomic approaches can add further contextual information. PVAT attenuation might provide a novel measure of vascular health that could be indicative of the pathogenetic processes implicated in atherosclerosis such as inflammation, fibrosis or increased vascularity. Bidirectional signalling between the coronary artery and adjacent PVAT has been hypothesized to contribute to coronary artery disease progression and provide a potential novel measure of the risk of future cardiovascular events. However, despite the development of more advanced radiomic and artificial intelligence-based algorithms, studies involving large datasets suggest that the measurement of PVAT attenuation contributes only modest additional predictive discrimination to standard cardiovascular risk scores. In this Review, we explore the pathobiology of coronary atherosclerotic plaques and PVAT, describe their phenotyping with computed tomography coronary angiography, and discuss potential future applications in clinical risk prediction and patient management.

Cardiovascular disease (CVD) is the leading cause of death worldwide. Coronary artery disease (CAD), a prevalent form of CVD, is typically assessed using catheter coronary angiography (CCA), an invasive, costly procedure with associated risks. While cardiac computed tomography angiography (CTA) presents a less invasive alternative, it suffers from limited temporal resolution, often resulting in motion artifacts that degrade diagnostic quality. Traditional ECG-based gating methods for CTA inadequately capture cardiac mechanical motion. To address this, we propose a novel multimodal approach that enhances CTA imaging by predicting cardiac quiescent periods using seismocardiogram (SCG) and ECG data, integrated through a weighted fusion (WF) approach and artificial neural networks (ANNs). We developed a regression-based ANN framework (r-ANN WF) designed to improve prediction accuracy and reduce computational complexity, which was compared with a classification-based framework (c-ANN WF), ECG gating, and US data. Our results demonstrate that the r-ANN WF approach improved overall diastolic and systolic cardiac quiescence prediction accuracy by 52.6% compared to ECG-based predictions, using ultrasound (US) as the ground truth, with an average prediction time of 4.83 ms. Comparative evaluations based on reconstructed CTA images show that both r-ANN WF and c-ANN WF offer diagnostic quality comparable to US-based gating, underscoring their clinical potential. Additionally, the lower computational complexity of r-ANN WF makes it suitable for real-time applications. This approach could enhance CTA's diagnostic quality, offering a more accurate and efficient method for CVD diagnosis and management.

Medical image classification using convolutional neural networks (CNNs) is promising but often requires extensive manual tuning for optimal model definition. Neural architecture search (NAS) automates this process, reducing human intervention significantly. This study applies NAS to [18F]-Florbetaben PET cardiac images for classifying cardiac amyloidosis (CA) sub-types (amyloid light chain (AL) and transthyretin amyloid (ATTR)) and controls. Following data preprocessing and augmentation, an evolutionary cell-based NAS approach with a fixed network macro-structure is employed, automatically deriving cells' micro-structure. The algorithm is executed five times, evaluating 100 mutating architectures per run on an augmented dataset of 4048 images (originally 597), totaling 5000 architectures evaluated. The best network (NAS-Net) achieves 76.95% overall accuracy. K-fold analysis yields mean ± SD percentages of sensitivity, specificity, and accuracy on the test dataset: AL subjects (98.7 ± 2.9, 99.3 ± 1.1, 99.7 ± 0.7), ATTR-CA subjects (93.3 ± 7.8, 78.0 ± 2.9, 70.9 ± 3.7), and controls (35.8 ± 14.6, 77.1 ± 2.0, 96.7 ± 4.4). NAS-derived network performance rivals manually determined networks in the literature while using fewer parameters, validating its automatic approach's efficacy.

To compare the image quality and fat attenuation index (FAI) of coronary artery CT angiography (CCTA) under different tube voltages between deep learning image reconstruction (DLIR) and adaptive statistical iterative reconstruction V (ASIR-V). Three hundred one patients who underwent CCTA with automatic tube current modulation were prospectively enrolled and divided into two groups: 120 kV group and low tube voltage group. Images were reconstructed using ASIR-V level 50% (ASIR-V50%) and high-strength DLIR (DLIR-H). In the low tube voltage group, the voltage was selected according to Chinese BMI classification: 70 kV (BMI < 24 kg/m²), 80 kV (24 kg/m² ≤ BMI < 28 kg/m²), 100 kV (BMI ≥ 28 kg/m²). At the same tube voltage, the subjective and objective image quality, edge rise distance (ERD), and FAI between different algorithms were compared. Under different tube voltages, we used DLIR-H to compare the differences between subjective, objective image quality, and ERD. Compared with the 120 kV group, the DLIR-H image noise of 70 kV, 80 kV, and 100 kV groups increased by 36%, 25%, and 12%, respectively (all P < 0.001); contrast-to-noise ratio (CNR), subjective score, and ERD were similar (all P > 0.05). In the 70 kV, 80 kV, 100 kV, and 120 kV groups, compared with ASIR-V50%, DLIR-H image noise decreased by 50%, 53%, 47%, and 38-50%, respectively; CNR, subjective score, and FAI value increased significantly (all P < 0.001), ERD decreased. Compared with 120 kV tube voltage, the combination of DLIR-H and low tube voltage maintains image quality. At the same tube voltage, compared with ASIR-V, DLIR-H improves image quality and FAI value.

The prevalence of coronary artery disease (CAD) has become the major cause of death across the world in recent years. The accurate segmentation of coronary artery is important in clinical diagnosis and treatment of coronary artery disease (CAD) such as stenosis detection and plaque analysis. Deep learning techniques have been shown to assist medical experts in diagnosing diseases using biomedical imaging. There are many methods which employ 2D DL models for medical image segmentation. The 2D Pyramid Scene Parsing Neural Network (PSPNet) has potential in this domain but not explored for the segmentation of coronary arteries from 3D Coronary Computed Tomography Angiography (CCTA) images. The contribution of present research work is to propose the modification of 2D PSPNet into 3D PSPNet for segmenting the coronary arteries from 3D CCTA images. The innovative factor is to evaluate the network performance by employing Global processing and Patch based processing methods. The experimental results achieved a Dice Similarity Coefficient (DSC) of 0.76 for Global process method and 0.73 for Patch based method using a subset of 200 images from the ImageCAS dataset.

Long scan time significantly hinders the widespread applications of three-dimensional multi-contrast cardiac magnetic resonance (3D-MC-CMR) imaging. This study aims to accelerate 3D-MC-CMR acquisition by a novel method based on score-based diffusion models with self-supervised learning. Specifically, we first establish a mapping between the undersampled k-space measurements and the MR images, utilizing a self-supervised Bayesian reconstruction network. Secondly, we develop a joint score-based diffusion model on 3D-MC-CMR images to capture their inherent distribution. The 3D-MC-CMR images are finally reconstructed using the conditioned Langenvin Markov chain Monte Carlo sampling. This approach enables accurate reconstruction without fully sampled training data. Its performance was tested on the dataset acquired by a 3D joint myocardial $ \text {T}_{{1}}$ and $ \text {T}_{{1}\rho }$ mapping sequence. The $ \text {T}_{{1}}$ and $ \text {T}_{{1}\rho }$ maps were estimated via a dictionary matching method from the reconstructed images. Experimental results show that the proposed method outperforms traditional compressed sensing and existing self-supervised deep learning MRI reconstruction methods. It also achieves high quality $ \text {T}_{{1}}$ and $ \text {T}_{{1}\rho }$ parametric maps close to the reference maps, even at a high acceleration rate of 14.

Cardiovascular disease is a leading global cause of death, requiring accurate heart segmentation for diagnosis and surgical planning. Deep learning methods have been demonstrated to achieve superior performances in cardiac structures segmentation. However, there are still limitations in 3D whole heart segmentation, such as inadequate spatial context modeling, difficulty in capturing long-distance dependencies, high computational complexity, and limited representation of local high-level semantic information. To tackle the above problems, we propose a lightweight Pyramid Pooling Transformer-CNN (P2TC) network for accurate 3D whole heart segmentation. The proposed architecture comprises a dual encoder-decoder structure with a 3D pyramid pooling Transformer for multi-scale information fusion and a lightweight large-kernel Convolutional Neural Network (CNN) for local feature extraction. The decoder has two branches for precise segmentation and contextual residual handling. The first branch is used to generate segmentation masks for pixel-level classification based on the features extracted by the encoder to achieve accurate segmentation of cardiac structures. The second branch highlights contextual residuals across slices, enabling the network to better handle variations and boundaries. Extensive experimental results on the Multi-Modality Whole Heart Segmentation (MM-WHS) 2017 challenge dataset demonstrate that P2TC outperforms the most advanced methods, achieving the Dice scores of 92.6% and 88.1% in Computed Tomography (CT) and Magnetic Resonance Imaging (MRI) modalities respectively, which surpasses the baseline model by 1.5% and 1.7%, and achieves state-of-the-art segmentation results.

Subclinical atrial fibrillation (SCAF), also known as atrial high-rate episodes (AHREs), refers to asymptomatic heart rate elevations associated with increased risks of atrial fibrillation and cardiovascular events. Although deep learning (DL) models leveraging echocardiographic images from ultrasound are widely used for cardiac function analysis, their application to AHRE prediction remains unexplored. This study introduces a novel DL-based framework for automatic AHRE detection using echocardiograms. The approach encompasses left atrium (LA) segmentation, LA strain feature extraction, and AHRE classification. Data from 117 patients with cardiac implantable electronic devices undergoing echocardiography were analyzed, with 80% allocated to the development set and 20% to the test set. LA segmentation accuracy was quantified using the Dice coefficient, yielding scores of 0.923 for the LA cavity and 0.741 for the LA wall. For AHRE classification, metrics such as area under the curve (AUC), accuracy, sensitivity, and specificity were employed. A transformer-based model integrating patient characteristics demonstrated robust performance, achieving mean AUC of 0.815, accuracy of 0.809, sensitivity of 0.800, and specificity of 0.783 for a 24-h AHRE duration threshold. This framework represents a reliable tool for AHRE assessment and holds significant potential for early SCAF detection, enhancing clinical decision-making and patient outcomes.

Cardiac magnetic resonance (CMR) is a key investigation in clinical cardiovascular medicine and has been used extensively in population research. However, extracting clinically important measurements such as ejection fraction for diagnosing cardiovascular diseases remains time-consuming and subjective. We developed CineMA, a foundation AI model automating these tasks with limited labels. CineMA is a self-supervised autoencoder model trained on 74,916 cine CMR studies to reconstruct images from masked inputs. After fine-tuning, it was evaluated across eight datasets on 23 tasks from four categories: ventricle and myocardium segmentation, left and right ventricle ejection fraction calculation, disease detection and classification, and landmark localisation. CineMA is the first foundation model for cine CMR to match or outperform convolutional neural networks (CNNs). CineMA demonstrated greater label efficiency than CNNs, achieving comparable or better performance with fewer annotations. This reduces the burden of clinician labelling and supports replacing task-specific training with fine-tuning foundation models in future cardiac imaging applications. Models and code for pre-training and fine-tuning are available at https://github.com/mathpluscode/CineMA, democratising access to high-performance models that otherwise require substantial computational resources, promoting reproducibility and accelerating clinical translation.

Echocardiography is the most common modality for assessing cardiac structure and function. While cardiac magnetic resonance (CMR) imaging is less accessible, CMR can provide unique tissue characterization including late gadolinium enhancement (LGE), T1 and T2 mapping, and extracellular volume (ECV) which are associated with tissue fibrosis, infiltration, and inflammation. Deep learning has been shown to uncover findings not recognized by clinicians, however it is unknown whether CMR-based tissue characteristics can be derived from echocardiography videos using deep learning. To assess the performance of a deep learning model applied to echocardiography to detect CMR-specific parameters including LGE presence, and abnormal T1, T2 or ECV. In a retrospective single-center study, adult patients with CMRs and echocardiography studies within 30 days were included. A video-based convolutional neural network was trained on echocardiography videos to predict CMR-derived labels including LGE presence, and abnormal T1, T2 or ECV across echocardiography views. The model was also trained to predict presence/absence of wall motion abnormality (WMA) as a positive control for model function. The model performance was evaluated in a held-out test dataset not used for training. The study population included 1,453 adult patients (mean age 56±18 years, 42% female) with 2,556 paired echocardiography studies occurring at a median of 2 days after CMR (interquartile range 2 days prior to 6 days after). The model had high predictive capability for presence of WMA (AUC 0.873 [95%CI 0.816-0.922]) which was used for positive control. However, the model was unable to reliably detect the presence of LGE (AUC 0.699 [0.613-0.780]), abnormal native T1 (AUC 0.614 [0.500-0.715]), T2 0.553 [0.420-0.692], or ECV 0.564 [0.455-0.691]). Deep learning applied to echocardiography accurately identified CMR-based WMA, but was unable to predict tissue characteristics, suggesting that signal for these tissue characteristics may not be present within ultrasound videos, and that the use of CMR for tissue characterization remains essential within cardiology.