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Cardiac magnetic resonance imaging (MRI) provides 3D images with high-resolution in-plane information, however, they are known to have low through-plane resolution due to the trade-off between resolution, image acquisition time and signal-to-noise ratio. This results in anisotropic 3D images which could lead to difficulty in diagnosis, especially in late gadolinium enhanced (LGE) cardiac MRI, which is the reference imaging modality for locating the extent of myocardial fibrosis in various cardiovascular diseases like myocardial infarction and atrial fibrillation. To address this issue, we propose a self-supervised deep learning-based approach to enhance the through-plane resolution of the LGE MRI images. We train a convolutional neural network (CNN) model on randomly extracted patches of short-axis LGE MRI images and this trained CNN model is used to leverage the information learnt from the high-resolution in-plane data to improve the through-plane resolution. We conducted experiments on LGE MRI dataset made available through the 2018 atrial segmentation challenge. Our proposed method achieved a mean peak signal-to-noise-ratio (PSNR) of 36.99 and 35.92 and a mean structural similarity index measure (SSIM) of 0.9 and 0.84 on training the CNN model using low-resolution images downsampled by a scale factor of 2 and 4, respectively.
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http://dx.doi.org/10.23919/cinc53138.2021.9662790 | DOI Listing |
Neurol Neuroimmunol Neuroinflamm
November 2025
Departments of Neurology and Ophthalmology, NYU Grossman School of Medicine, NY; and.
Background And Objectives: While reductions in optical coherence tomography (OCT) pRNFL and ganglion cell-inner plexiform layer thicknesses have been shown to be associated with brain atrophy in adult-onset MS (AOMS) cohorts, the relationship between OCT and brain MRI measures is less established in pediatric-onset MS (POMS). Our aim was to examine the associations of OCT measures with volumetric MRI in a cohort of patients with POMS to determine whether OCT measures reflect CNS neurodegeneration in this patient population, as is seen in AOMS cohorts.
Methods: This was a cross-sectional study with retrospective ascertainment of patients with POMS evaluated at a single center with expertise in POMS and neuro-ophthalmology.
J Pediatr Hematol Oncol
September 2025
Department of Biostatistics, All India Institute of Medical Sciences, New Delhi, India.
Purpose: In children with Langerhans Cell Histiocytosis (LCH), FDG-PET/CT is used for staging and response assessment. Whole-body MRI (WB-MRI) can serve as an ionizing radiation-free alternative for repeated whole-body imaging. The aim of this study was to compare WB-MRI with FDG-PET/CT for staging and response assessment in pediatric LCH.
View Article and Find Full Text PDFEur Heart J Cardiovasc Imaging
September 2025
Department of Diagnostic and Interventional Radiology, University Hospital Bonn, Venusberg-Campus 1, 53127, Bonn, Germany.
Aims: Fetal circulation undergoes complex changes in congenital heart disease (CHD) that are challenging to assess with fetal echocardiography. This study aimed to assess clinical feasibility and diagnostic value of 4D flow cardiac magnetic resonance (CMR) in fetal CHD.
Methods And Results: Pregnant women in advanced third trimester pregnancy with fetal CHD were prospectively recruited for fetal CMR between 08/2021 and 11/2024.
Int J Surg Pathol
September 2025
Department of Pathology, The Thirteenth People's Hospital of Chongqing, Chongqing, China.
Soft tissue sarcomas are a heterogeneous group of malignancies arising from mesenchymal cells. Recent advancements in genomic profiling have identified novel gene fusions in these tumors, offering new insights into their pathogenesis and potential therapeutic targets. Here, we describe a spindle cell sarcoma harboring a novel gene fusion.
View Article and Find Full Text PDFJ Alzheimers Dis
September 2025
Frontotemporal Disorders Unit, Department of Neurology, Massachusetts General Hospital and Harvard Medical School, Charlestown, MA, USA.
Compared with more typical late-onset Alzheimer's disease (AD), the mechanisms of young-onset AD (YOAD; age of symptom onset <65 years) remain less understood. Using resting-state functional MRI data and dynamic causal modeling techniques, Sacu et al. demonstrate that individuals with YOAD (amnestic AD or posterior cortical atrophy) exhibit alterations in effective (i.
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