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一种基于深度学习的多视图方法用于下肢自动三维地标定位和畸形评估。

A deep learning-based multi-view approach to automatic 3D landmarking and deformity assessment of lower limb.

作者信息

Rostamian Reyhaneh, Shariat Panahi Masoud, Karimpour Morad, Kashani Hadi G, Abi Amirhossein

机构信息

School of Mechanical Engineering, College of Engineering, University of Tehran, Tehran, Iran.

出版信息

Sci Rep. 2025 Jan 2;15(1):534. doi: 10.1038/s41598-024-84387-z.

DOI:10.1038/s41598-024-84387-z
PMID:39747979
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11697423/
Abstract

Anatomical Landmark detection in CT-Scan images is widely used in the identification of skeletal disorders. However, the traditional process of manually detecting anatomical landmarks, especially in three dimensions, is both time-consuming and prone to human errors. We propose a novel, deep-learning-based approach to automatic detection of 3D landmarks in CT images of the lower limb. We generate multiple view renderings of the scanned limb and then integrate them, using a pyramid-style convolutional neural network, to build a 3D model of the bone and to determine the spatial coordinates of the landmarks. Those landmarks are then used to calculate key anatomical indicators that would enable the reliable diagnosis of skeletal disorders. To evaluate the performance of the proposed approach we compare its predicted landmark coordinates and resulting anatomical indicators (both 2D and 3D) with those determined by human experts. The average coordinate error (difference between automatically and manually determined coordinates) of the landmarks was 2.05 ± 1.36 mm on test data, whereas the average angular error (difference between automatically and manually calculated angles in three and two dimensions) on the same dataset was 0.53 ± 0.66° and 0.74 ± 0.87°, respectively. Our proposed deep-learning-based approach not only outperforms the traditional landmark detection and indicator assessment methods in terms of speed and accuracy but also improves the credibility of the ensuing diagnoses by avoiding manual landmarking errors.

摘要

CT扫描图像中的解剖标志点检测在骨骼疾病的识别中被广泛应用。然而,传统的手动检测解剖标志点的过程,尤其是在三维空间中,既耗时又容易出现人为误差。我们提出了一种基于深度学习的新颖方法,用于自动检测下肢CT图像中的三维标志点。我们生成扫描肢体的多个视图渲染图,然后使用金字塔式卷积神经网络将它们整合起来,以构建骨骼的三维模型并确定标志点的空间坐标。然后使用这些标志点来计算关键的解剖学指标,从而能够可靠地诊断骨骼疾病。为了评估所提出方法的性能,我们将其预测的标志点坐标和由此得出的解剖学指标(二维和三维)与人类专家确定的指标进行比较。在测试数据上,标志点的平均坐标误差(自动确定的坐标与手动确定的坐标之间的差异)为2.05±1.36毫米,而在同一数据集上,平均角度误差(三维和二维中自动计算的角度与手动计算的角度之间的差异)分别为0.53±0.66°和0.74±0.87°。我们提出的基于深度学习的方法不仅在速度和准确性方面优于传统的标志点检测和指标评估方法,而且通过避免手动标志点误差提高了后续诊断的可信度。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/bbc3/11697423/e7b43bb11a85/41598_2024_84387_Fig7_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/bbc3/11697423/a3ba5f2e86a5/41598_2024_84387_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/bbc3/11697423/ca7be9a6ba88/41598_2024_84387_Fig2_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/bbc3/11697423/2a83c900838d/41598_2024_84387_Figa_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/bbc3/11697423/b246f486ee2d/41598_2024_84387_Fig3_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/bbc3/11697423/83958f7cf190/41598_2024_84387_Fig4_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/bbc3/11697423/71848420b95f/41598_2024_84387_Fig5_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/bbc3/11697423/091440f574c8/41598_2024_84387_Fig6_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/bbc3/11697423/e7b43bb11a85/41598_2024_84387_Fig7_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/bbc3/11697423/a3ba5f2e86a5/41598_2024_84387_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/bbc3/11697423/ca7be9a6ba88/41598_2024_84387_Fig2_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/bbc3/11697423/2a83c900838d/41598_2024_84387_Figa_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/bbc3/11697423/b246f486ee2d/41598_2024_84387_Fig3_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/bbc3/11697423/83958f7cf190/41598_2024_84387_Fig4_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/bbc3/11697423/71848420b95f/41598_2024_84387_Fig5_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/bbc3/11697423/091440f574c8/41598_2024_84387_Fig6_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/bbc3/11697423/e7b43bb11a85/41598_2024_84387_Fig7_HTML.jpg

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