Abstract:Background: Pericardial adipose tissue (PAT) may represent a novel risk marker for cardiovascular disease. However, absence of rapid radiation-free PAT quantification methods has precluded its examination in large cohorts.Objectives: We developed a fully automated quality-controlled tool for cardiovascular magnetic resonance (CMR) PAT quantification in the UK Biobank (UKB).Methods: Image analysis comprised contouring an en-bloc PAT area on four-chamber cine images. We created a ground truth manual analysis dat… Show more
“…Recently, automatic total pericardial fat quantification has been developed in 4Ch cine MRI. Bard, Raisi-Estabragh et al [ 23 ] obtained segmentation performances (DSC EAT+PAT = 0.8) very similar to ours (DSC EAT+PAT = 0.88) on their respective test-set. In their study, only the end-diastolic frame had been segmented while we segmented the full 4Ch cine MRI and trained on three consecutive cine frames to leverage cine temporal information.…”
Section: Discussionsupporting
confidence: 82%
“…Second, while the pericardial fascia is not clearly visible on short axis views, which was often reduced to a thin line that may be blurred by partial volume effects, on four-chamber (4Ch) views, the pericardium is generally less affected by partial volume effects resulting in better visualization. As such, the four-chamber view is recommended for evaluating pericarditis [ 21 ] and is a frequent choice of orientation to quantify EAT, PAT, and pericardial fat [ 22 , 23 , 24 , 25 , 26 , 27 ]. Consequently, the EAT analysis in this study were based on quantification of its 2D area representation in 4Ch long-axis cine MRI views.…”
Section: Introductionmentioning
confidence: 99%
“…Indeed, fully automated methods applied on routine images, such as cine MRI, could be rapidly translated to the clinics. Bard et al [ 23 ] developed a deep learning method to quantify pericardial fat in 4Ch long-axis cine MRI and evaluated it on the UK BioBank dataset. However, the segmentation of pericardial fat (EAT + PAT) limits the evaluation of the distinct roles and clinical implications of epicardial fat compared to paracardial fat.…”
In magnetic resonance imaging (MRI), epicardial adipose tissue (EAT) overload remains often overlooked due to tedious manual contouring in images. Automated four-chamber EAT area quantification was proposed, leveraging deep-learning segmentation using multi-frame fully convolutional networks (FCN). The investigation involved 100 subjects—comprising healthy, obese, and diabetic patients—who underwent 3T cardiac cine MRI, optimized U-Net and FCN (noted FCNB) were trained on three consecutive cine frames for segmentation of central frame using dice loss. Networks were trained using 4-fold cross-validation (n = 80) and evaluated on an independent dataset (n = 20). Segmentation performances were compared to inter-intra observer bias with dice (DSC) and relative surface error (RSE). Both systole and diastole four-chamber area were correlated with total EAT volume (r = 0.77 and 0.74 respectively). Networks’ performances were equivalent to inter-observers’ bias (EAT: DSCInter = 0.76, DSCU-Net = 0.77, DSCFCNB = 0.76). U-net outperformed (p < 0.0001) FCNB on all metrics. Eventually, proposed multi-frame U-Net provided automated EAT area quantification with a 14.2% precision for the clinically relevant upper three quarters of EAT area range, scaling patients’ risk of EAT overload with 70% accuracy. Exploiting multi-frame U-Net in standard cine provided automated EAT quantification over a wide range of EAT quantities. The method is made available to the community through a FSLeyes plugin.
“…Recently, automatic total pericardial fat quantification has been developed in 4Ch cine MRI. Bard, Raisi-Estabragh et al [ 23 ] obtained segmentation performances (DSC EAT+PAT = 0.8) very similar to ours (DSC EAT+PAT = 0.88) on their respective test-set. In their study, only the end-diastolic frame had been segmented while we segmented the full 4Ch cine MRI and trained on three consecutive cine frames to leverage cine temporal information.…”
Section: Discussionsupporting
confidence: 82%
“…Second, while the pericardial fascia is not clearly visible on short axis views, which was often reduced to a thin line that may be blurred by partial volume effects, on four-chamber (4Ch) views, the pericardium is generally less affected by partial volume effects resulting in better visualization. As such, the four-chamber view is recommended for evaluating pericarditis [ 21 ] and is a frequent choice of orientation to quantify EAT, PAT, and pericardial fat [ 22 , 23 , 24 , 25 , 26 , 27 ]. Consequently, the EAT analysis in this study were based on quantification of its 2D area representation in 4Ch long-axis cine MRI views.…”
Section: Introductionmentioning
confidence: 99%
“…Indeed, fully automated methods applied on routine images, such as cine MRI, could be rapidly translated to the clinics. Bard et al [ 23 ] developed a deep learning method to quantify pericardial fat in 4Ch long-axis cine MRI and evaluated it on the UK BioBank dataset. However, the segmentation of pericardial fat (EAT + PAT) limits the evaluation of the distinct roles and clinical implications of epicardial fat compared to paracardial fat.…”
In magnetic resonance imaging (MRI), epicardial adipose tissue (EAT) overload remains often overlooked due to tedious manual contouring in images. Automated four-chamber EAT area quantification was proposed, leveraging deep-learning segmentation using multi-frame fully convolutional networks (FCN). The investigation involved 100 subjects—comprising healthy, obese, and diabetic patients—who underwent 3T cardiac cine MRI, optimized U-Net and FCN (noted FCNB) were trained on three consecutive cine frames for segmentation of central frame using dice loss. Networks were trained using 4-fold cross-validation (n = 80) and evaluated on an independent dataset (n = 20). Segmentation performances were compared to inter-intra observer bias with dice (DSC) and relative surface error (RSE). Both systole and diastole four-chamber area were correlated with total EAT volume (r = 0.77 and 0.74 respectively). Networks’ performances were equivalent to inter-observers’ bias (EAT: DSCInter = 0.76, DSCU-Net = 0.77, DSCFCNB = 0.76). U-net outperformed (p < 0.0001) FCNB on all metrics. Eventually, proposed multi-frame U-Net provided automated EAT area quantification with a 14.2% precision for the clinically relevant upper three quarters of EAT area range, scaling patients’ risk of EAT overload with 70% accuracy. Exploiting multi-frame U-Net in standard cine provided automated EAT quantification over a wide range of EAT quantities. The method is made available to the community through a FSLeyes plugin.
“…In addition, CMR opens the possibility to a combined evaluation of potential underlying myocardial ischemia, storage diseases like amyloidosis, diffuse myocardial fibrosis (extracellular volume), and epicardial fat. Recently, a growing number of publications also demonstrate the easiness of epicardial fat quantification using artificial intelligence (AI) algorithms (69). Beside the heart, the same approach can also be applied to other organ regions in patients with HFpEF like the abdomen (70).…”
Section: Diagnosis Of Epicardial Adipose Tissue Expansionmentioning
Graphical AbstractEpicardial adipose tissue (EAT)-related heart failure with preserved ejection fraction (HFpEF). Obesity and type 2 diabetes mellitus (T2DM) are common triggers of HFpEF, frequently associated with EAT expansion. EAT plays metabolic and mechanical roles in HFpEF development via para/vasocrine factors and pericardial restrain, respectively. Life-style modifications including healthy diet and regular exercise can quash the EAT expansion. Statins, proprotein convertase subtilisin/kexin type 9 (PCSK9) inhibitors and fat-modulating antidiabetics including metformin, sodium-glucose cotransporter 2 (SGLT2) inhibitors and glucagon-like peptide-1 (GLP-1) agonists can target EAT. FFA, free fatty acids; AGEs, advanced glycation end-products; NO, nitric oxide; ROS, reactive oxygen species; Ang-II, angiotensin II; TGF-β, Transforming growth factor beta; MCP-1, monocyte chemoattractant protein 1; IL-6, interleukin 6; TNF-α, tumor necrosis factor alpha. Figure created via Servier Medical Art and BioRender tools.
“…Some frameworks additionally provide myocardial strain measures (299,342). Automated segmentation methods have also been proposed to quantitatively derive other important markers of cardiovascular disease such as volume of pericardial adipose tissue (343), and scarred tissue areas (from LGE images) (344)(345)(346)(347)(348). Moreover, few DL-based methods have proposed to automatically quantify myocardial tissue from native T 1 mapping (349,350) and myocardial blood flow from contrast-enhanced perfusion CMR (351,352).…”
Cardiovascular disease (CVD) is the leading single cause of morbidity and mortality, causing over 17. 9 million deaths worldwide per year with associated costs of over $800 billion. Improving prevention, diagnosis, and treatment of CVD is therefore a global priority. Cardiovascular magnetic resonance (CMR) has emerged as a clinically important technique for the assessment of cardiovascular anatomy, function, perfusion, and viability. However, diversity and complexity of imaging, reconstruction and analysis methods pose some limitations to the widespread use of CMR. Especially in view of recent developments in the field of machine learning that provide novel solutions to address existing problems, it is necessary to bridge the gap between the clinical and scientific communities. This review covers five essential aspects of CMR to provide a comprehensive overview ranging from CVDs to CMR pulse sequence design, acquisition protocols, motion handling, image reconstruction and quantitative analysis of the obtained data. (1) The basic MR physics of CMR is introduced. Basic pulse sequence building blocks that are commonly used in CMR imaging are presented. Sequences containing these building blocks are formed for parametric mapping and functional imaging techniques. Commonly perceived artifacts and potential countermeasures are discussed for these methods. (2) CMR methods for identifying CVDs are illustrated. Basic anatomy and functional processes are described to understand the cardiac pathologies and how they can be captured by CMR imaging. (3) The planning and conduct of a complete CMR exam which is targeted for the respective pathology is shown. Building blocks are illustrated to create an efficient and patient-centered workflow. Further strategies to cope with challenging patients are discussed. (4) Imaging acceleration and reconstruction techniques are presented that enable acquisition of spatial, temporal, and parametric dynamics of the cardiac cycle. The handling of respiratory and cardiac motion strategies as well as their integration into the reconstruction processes is showcased. (5) Recent advances on deep learning-based reconstructions for this purpose are summarized. Furthermore, an overview of novel deep learning image segmentation and analysis methods is provided with a focus on automatic, fast and reliable extraction of biomarkers and parameters of clinical relevance.
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