98%
921
2 minutes
20
Objective: This study aims to develop a fully automated, computed tomography (CT)-based deep learning (DL) model to segment ossified lesions of the posterior longitudinal ligament and to measure the thickness of the ossified material and calculate the cervical spinal cord compression factor.
Methods: A total of 307 patients were enrolled, with 260 patients from Shanghai Changzheng Hospital, and 47 patients from the Traditional Chinese Medicine Hospital of Southwest Medical University. CT images were used to manually segment the Ossification of the posterior longitudinal ligament (OPLL) by 4 experienced radiologists. The DL model employing a 3-dimensional U-Net framework was developed to segment the OPLLs. The system also measures the thickness of the ossified material at its thickest point and the diameter of the spinal canal at the corresponding level. Segmentation performance was evaluated using the Dice Similarity Coefficient, Average Surface Distance, and intraclass correlation coefficient (ICC) between ground truth and segmentation volumes. Concordance between the radiologists' and the DL system's measurements of the ossified material thickness, residual spinal canal diameter at maximum compression, and cervical spinal cord compression coefficient was assessed in a randomly selected subset of 30 cases from the training set using ICCs and Bland-Altman plots.
Results: The DL system demonstrated average Dice Similarity Coefficient of 0.81, 0.75, and 0.71 for the training, internal validation, and external test sets, respectively. The mean Average Surface Distance was 1.30 for the training set, 2.35 for the internal validation set, and 2.63 for the external test set. The ICC values of 0.958 for the thickness of the ossified material and 0.974 for the residual canal diameter measurement.
Conclusions: The proposed DL model effectively detects and separates ossification foci in OPLL on CT images. It exhibits comparable performance to radiologists in quantifying spinal cord compression metrics.
Download full-text PDF |
Source |
---|---|
http://dx.doi.org/10.1016/j.wneu.2024.123567 | DOI Listing |
Neurol Neuroimmunol Neuroinflamm
November 2025
Department of Clinical Neuroscience, Karolinska Institutet, Stockholm, Sweden.
Background And Objectives: Myelitis is a relatively common clinical entity for neurologists, with diverse underlying causes. The aim of this study was to describe the incidence of myelitis, its causes, clinical presentation, and factors predicting functional outcomes and relapses.
Methods: Using the Swedish National Patient Registry, we identified all adult patients in Stockholm County between 2008 and 2018 using International Classification of Diseases, 10th Edition (ICD-10) codes likely to include myelitis.
J Spinal Cord Med
September 2025
Department of Surgery, Hôpital du Sacré-Coeur de Montréal, Montréal, Québec, Canada.
Study Design: A retrospective study with a crossover design.
Objectives: Maintaining mean arterial pressure (MAP) is crucial in the early management of SCI, yet the role of oral midodrine in this setting remains unclear. This study evaluates whether midodrine facilitates IV vasopressor weaning within 24 hours of initiation.
Sci Prog
September 2025
Department of Neurology, University of Afyonkarahisar Health Sciences, Afyonkarahisar, Türkiye.
A considerable number of individuals are diagnosed with idiopathic trigeminal neuralgia. In order to achieve a more complete understanding of the pathophysiology, it is essential to adopt a range of novel approaches and utilize new animal models. This study investigated changes in the messenger RNA (mRNA) expression of ion-channels in a newly developed animal model of trigeminal neuropathic pain induced by cervical spinal dorsal horn compression.
View Article and Find Full Text PDFEur Spine J
September 2025
Consultant Neurosurgeon, Centre for Functional Neurosurgery, University Hospital Southampton NHS Foundation Trust, Southampton, UK.
Stem Cell Rev Rep
September 2025
Stem Cells and Metabolism Research Program (STEMM), Research Programs Unit, Faculty of Medicine, University of Helsinki, Helsinki, 00014, Finland.
Mutations in Delta Like Non-Canonical Notch Ligand 1 (DLK1), a paternally expressed imprinted gene, underlie central precocious puberty (CPP), yet the mechanism remains unclear. To test the hypothesis that DLK1 plays a role in gonadotropin releasing hormone (GnRH) neuron ontogeny, 75 base pairs were deleted in both alleles of DLK1 exon 3 with CRISPR-Cas9 in human pluripotent stem cells (hPSCs). This line, exhibiting More than 80% loss of DLK1 protein, was differentiated into GnRH neurons by dual SMAD inhibition (dSMADi), FGF8 treatment and Notch inhibition, as previously described, however, it did not exhibit accelerated GNRH1 expression.
View Article and Find Full Text PDF