ISSN 1004-4140
CN 11-3017/P

基于胸部CT的人工智能骨密度测量系统机会性筛查骨质疏松症的可行性研究

崔璨, 温庆祥, 刘妮, 李民, 李俊秋, 刘军莲, 霍健伟

崔璨, 温庆祥, 刘妮, 等. 基于胸部CT的人工智能骨密度测量系统机会性筛查骨质疏松症的可行性研究[J]. CT理论与应用研究(中英文), xxxx, x(x): 1-5. DOI: 10.15953/j.ctta.2024.289.
引用本文: 崔璨, 温庆祥, 刘妮, 等. 基于胸部CT的人工智能骨密度测量系统机会性筛查骨质疏松症的可行性研究[J]. CT理论与应用研究(中英文), xxxx, x(x): 1-5. DOI: 10.15953/j.ctta.2024.289.
CUI C, WEN Q X, LIU N, et al. Feasibility of opportunistic osteoporosis screening using an artificial intelligence-based bone density measurement on chest CT scans[J]. CT Theory and Applications, xxxx, x(x): 1-5. DOI: 10.15953/j.ctta.2024.289. (in Chinese).
Citation: CUI C, WEN Q X, LIU N, et al. Feasibility of opportunistic osteoporosis screening using an artificial intelligence-based bone density measurement on chest CT scans[J]. CT Theory and Applications, xxxx, x(x): 1-5. DOI: 10.15953/j.ctta.2024.289. (in Chinese).

基于胸部CT的人工智能骨密度测量系统机会性筛查骨质疏松症的可行性研究

详细信息
    作者简介:

    崔璨,女,硕士,放射科主治医师,主要从事骨密度测量方面的研究,E-mail:540545201@qq.com

    通讯作者:

    刘军莲✉,女,副主任技师,主要从事骨密度测量方面的研究,E-mail:13501192985@163.com

    霍健伟✉,男,主任医师,主要从事影像诊断工作,E-mail:huojianwei@bjzhongyi.com

  • 中图分类号: R 814

Feasibility of opportunistic osteoporosis screening using an artificial intelligence-based bone density measurement on chest CT scans

  • 摘要:

    探讨基于胸部CT的人工智能(AI)骨密度测量系统机会性筛查骨质疏松症的可行性。回顾性分析于我科2023年8月至2024年7月同时行双光能X线吸收测定法(DXA)和胸部CT的462名患者的资料,其中绝经后的女性317例、50岁以上的男性145例。比较两种方法测量骨密度之间的差异;以DXA测量的T值为参考标准,分析基于胸部CT的AI系统与DXA测量结果的一致性和相关性。绝经后女性和50岁以上男性的身高、体重、DXA T值及AI BMD有统计学差异;AI测量的BMD与DXA T值之间的相关系数为0.767;二者的κ值为0.697;AI诊断骨质疏松的ROC曲线下面积为0.941(95%CI 0.914~0.968),敏感性85.71%,特异性93.84%。AI骨密度测量系统与DXA测定骨密度具有高度相关性及良好一致性,可以帮助机会性筛查骨质疏松症。

    Abstract:

    This study explores the feasibility of opportunistic osteoporosis screening using an artificial intelligence (AI)-based bone mineral density (BMD) measurement system on chest computed tomography (CT) scans. A retrospective analysis was conducted on 462 patients who underwent both dual-energy X-ray absorptiometry (DXA) and chest CT in our department between August 2023 and July 2024. The cohort included 317 postmenopausal women and 145 men aged > 50 years. BMD measurements from the AI system and DXA were compared. Using the T-value measured by DXA as the reference standard, the consistency and correlation between AI-based and DXA-measured BMD were analyzed. Significant differences in height, weight, DXA T-value, and AI-derived BMD were observed between men aged > 50 years and postmenopausal women. The AI-derived BMD showed a correlation coefficient of 0.767 with DXA T-values and a κ value of 0.697. The area under the ROC curve for AI-based diagnosis of osteoporosis was 0.941(95% CI 0.914–0.968), with a sensitivity of 85.71% and a specificity of 93.84%. The AI-based BMD measurement system demonstrates strong correlation and good agreement with DXA, supporting its feasibility for opportunistic osteoporosis screening.

  • 图  1   AI测量BMD与DXA测量T值的相关性散点图

    Figure  1.   Scatter plot of correlation between BMD measured by AI and T value measured by DXA

    图  2   AI诊断骨质疏松症的ROC曲线

    Figure  2.   ROC curve of AI diagnosis of osteoporosis

    表  1   462名受试者基本资料

    Table  1   Demographic data from 462 subjects

    变量 全部(n=462) 女性(n=317) 男性(n=145) P
    年龄(岁) 64.94±8.547 64.99±8.221 64.81±9.249 0.837
    身高(cm) 162.98±7.278 159.35±4.855 170.90±5.065 <0.001
    体重(kg) 65.91±11.065 62.52±9.609 73.34±10.412 <0.001
    BMI(kg/m2 24.75±3.385 24.60±3.492 25.08±3.125 0.160
    DXA T值 −1.79±0.855 −1.98±0.839 −1.36±0.726 <0.001
    AI BMD(mg/cm3 111.33±33.522 106.66±32.886 121.53±32.732 <0.001
    下载: 导出CSV

    表  2   DXA和AI诊断类型的分布

    Table  2   Distributions of DXA and AI diagnostic types

    AI
    骨量正常 骨量减少 骨质疏松 总计
    DXA 骨量正常 67(14.5%) 23(5.0%)a 1(0.2%)b 91(19.7%)
    骨量减少 21(4.5%)a 225(48.7%) 20(4.3%)a 266(57.6%)
    骨质疏松 0(0%)b 16(3.5%)a 89(19.3%) 105(22.7%)
    总计   88(19.0%) 264(57.1%) 110(23.8%) 462(100%)
    注:黑体字为一致;a为轻度不一致:一种方法显示骨密度正常,而另一种则显示骨量减少或一种方法显示骨量减少,而另一种则显示骨质疏松;b为重度不一致:一种方法显示骨密度正常,而另一种则显示骨质疏松。
    下载: 导出CSV
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  • 收稿日期:  2024-12-04
  • 修回日期:  2025-01-25
  • 录用日期:  2025-02-05
  • 网络出版日期:  2025-03-12

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