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This Paper Explores How Deep Learning Enhances Osteoporosis Screening with Routine CT Scans Madhur Garg Artificial Intelligence Category – MarkTechPost

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The prevalence of osteoporosis, a condition that weakens bones due to decreased bone mass, is a significant concern due to the increasing global population. The current methods used to diagnose osteoporosis, primarily relying on central dual-energy X-ray absorptiometry (DXA), have limitations contributing to the underdiagnosis and undertreatment of the condition. Researchers have developed an innovative tool that utilizes deep learning technology to automate bone mineral density (DL-BMD) measurements to address these challenges. This tool aims to improve the screening process for osteoporosis by using routine computed tomography (CT) scans, providing a more accessible and accurate approach.

The detection of osteoporosis poses challenges for current methods, especially due to the decreasing popularity of central DXA. To address this issue, a team of researchers from Korea University College of Medicine has developed DL-BMD, a groundbreaking tool that utilizes advanced deep-learning algorithms. With DL-BMD, measuring bone mineral density on lumbar spine CT scans becomes automated, offering a highly efficient and precise solution. In contrast to conventional approaches, DL-BMD allows opportunistic osteoporosis screening by leveraging routine CT scans, eliminating the requirement for specialized imaging techniques.

https://www.nature.com/articles/s41598-023-45824-7

The DL-BMD tool is built upon a segmentation network called U-Net, specifically designed to locate the lumbar spine. The researchers included additional techniques such as field of view augmentation and CT denoising to make the tool more reliable in different scan settings. A diverse dataset of CT scans from other sources was used to train the model, and pre-processing steps and data augmentation were applied to improve its ability to generalize. When tested, the tool showed strong agreement with manually measured BMD and demonstrated a high accuracy level in diagnosing low BMD and osteoporosis.The researchers used several pre-processing approaches, such as window-level adjustments and normalization, to improve the quality of the CT images for accurate segmentation.

After the initial segmentation process, the tool uses a region of interest (ROI) placement algorithm to create an elliptical ROI. This ROI excludes the cortical bone and avoids the basivertebral vein. The specific slices that are selected, usually including the L1 and L2 vertebrae, then undergo a calculation of Hounsfield unit (HU) values within the ROI. The success of DL-BMD relies heavily on the conversion of these HU values into bone mineral density (BMD). The tool is calibrated against the European Spine Phantom to ensure accurate and reliable BMD measurements. Regression analysis is conducted based on the pre and post-contrast attenuation of the L1 trabecular bone.

https://www.nature.com/articles/s41598-023-45824-7

In conclusion, introducing the DL-BMD tool represents a meaningful advancement in osteoporosis screening, employing advanced deep-learning techniques to elevate the accuracy of diagnostic evaluations. By effectively tackling the shortcomings of traditional approaches, the dedicated research team has paved the way for more efficient and accessible opportunistic screening through routine CT scans. This remarkable breakthrough holds tremendous promise for the early identification and proactive prevention of osteoporotic fractures, thus propelling us forward in our mission to enhance bone health on a larger and more comprehensive level.

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 The prevalence of osteoporosis, a condition that weakens bones due to decreased bone mass, is a significant concern due to the increasing global population. The current methods used to diagnose osteoporosis, primarily relying on central dual-energy X-ray absorptiometry (DXA), have limitations contributing to the underdiagnosis and undertreatment of the condition. Researchers have developed an innovative
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