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Purpose: This study aimed to establish a novel index, three-dimensional Hounsfield unit (3D-HU), to assess bone density, and evaluated its correlation with dual-energy X-ray absorptiometry (DXA) scores.
Methods: This study reviewed the electronic medical records of patients who underwent lumbar spine computed tomography (CT) and DXA at our hospital within one week. Patients were divided into osteoporotic and non-osteoporotic groups according to T-score. Demographics information and radiological parameters were compared. Using preoperative CT scanning of the lumbar spine, the novel 3D-HU was measured for each patient. DXA scores were obtained and were compared to 3D-HU using multivariate logistic regression analyses and Pearson correlation.
Results: This study involved 612 vertebrae from 191 patients. Among them, 134 were found to have a T-score ≤ -2.5. Multivariate analysis showed that lower 3D-HU and body mass index (BMI) were independent predictors for osteoporosis. Correlation analysis revealed that 3D-HU was highly correlated with bone mineral density (BMD) measured by DXA, and this correlation was consistently stronger than that of traditional HU. Receiver operating characteristic curve (ROC) analysis showed that 3D-HU has high accuracy, excellent sensitivity, and specificity in the diagnosis of osteoporosis.
Conclusions: This is the first study to directly correlate the novel 3D-HU with the diagnosis of osteoporosis. We identified this novel index as a significant predictor of osteoporosis, and established a strong correlation between 3D-HU and the BMD of the lumbar spine.
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http://dx.doi.org/10.1007/s00586-025-09010-9 | DOI Listing |
Gait Posture
September 2025
Beth Israel Deaconess Medical Center, 330 Brookline Avenue, RN115, Boston, MA 02215, USA.
Prog Neurobiol
September 2025
Age-Related and Brain Diseases Research Center, School of Medicine, Kyung Hee University, Seoul, Republic of Korea; Department of Biochemistry and Molecular Biology, School of Medicine, Kyung Hee University, Seoul, Republic of Korea; Biomedical Science Institute, Kyung Hee University, Seoul, Republi
Lumbar spinal stenosis (LSS) is one of the most common spinal disorders in elderly people and is often accompanied by neuropathic pain. Although our previous studies have demonstrated that infiltrating macrophage contribute to chronic neuropathic pain in LSS rat model, the molecular mechanisms underlying macrophage activation and infiltration have not been fully elucidated. In this study, we examined the critical role of platelet-derived growth factor receptor (PDGFR) signaling pathway in neuropathic pain associated with macrophage infiltration and activation in LSS rats.
View Article and Find Full Text PDFGlobal Spine J
September 2025
Department of Neurosurgery, Brain and Spine, Morsani College of Medicine, University of South Florida, Tampa, FL, USA.
DesignRandomized Controlled Trial.ObjectivePostoperative pain after lumbar spine surgery remains a clinical challenge. Fluoroscopy-guided erector spinae plane block (ESPB) has been proposed as a feasible technique for reducing pain and opioid use, particularly when ultrasound guidance is not available.
View Article and Find Full Text PDFEur Spine J
September 2025
Department of Biomedical Engineering, National Yang Ming Chiao Tung University, Taipei, Taiwan.
Purpose: This study aims to address the limitations of radiographic imaging and single-task learning models in adolescent idiopathic scoliosis assessment by developing a noninvasive, radiation-free diagnostic framework.
Methods: A multi-task deep learning model was trained using structured back surface data acquired via fringe projection three-dimensional imaging. The model was designed to simultaneously predict the Cobb angle, curve type (thoracic, lumbar, mixed, none), and curve direction (left, right, none) by learning shared morphological features.
J Bone Miner Res
September 2025
Department of Medicine, Indiana University School of Medicine, Indianapolis, IN, United States.
Autosomal Dominant Osteopetrosis (ADO) is a rare, osteosclerotic disorder usually caused by missense variants in the CLCN7 gene, resulting in impaired osteoclastic bone resorption. Penetrance is incomplete and disease severity varies widely, even among relatives within the same family. Although ADO can cause visual loss, osteonecrosis, osteomyelitis, and bone marrow failure, the most common complication of ADO is fracture.
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