Multi-detector row CT imaging of vertebral microstructure for evaluation of fracture risk

被引:173
作者
Ito, M
Ikeda, K
Nishiguchi, M
Shindo, H
Uetani, M
Hosoi, T
Orimo, H
机构
[1] Nagasaki Univ, Sch Med, Dept Radiol, Nagasaki 852, Japan
[2] Natl Ctr Geriatr & Gerontol, Res Inst, Dept Bone & Joint Dis, Obu, Aichi, Japan
[3] Japan Ekisai Kai Nagasaki Hosp, Dept Orthoped Surg, Nagasaki, Japan
[4] Nagasaki Univ, Sch Med, Dept Orthoped Surg, Nagasaki 852, Japan
[5] Tokyo Metropolitan Inst Gerontol & Geriatr Hosp, Dept Internal Med, Tokyo, Japan
[6] Hlth Sci Univ, Tokyo, Japan
关键词
osteoporosis; fracture; CT; microstructure;
D O I
10.1359/JBMR.050610
中图分类号
R5 [内科学];
学科分类号
1002 [临床医学]; 100201 [内科学];
摘要
We applied MDCT for in vivo evaluation of the microarchitecture of human vertebrae. Microstructure parameters, such as structure model index, Euler's number, and bone volume fraction, revealed higher relative risk for prevalent vertebral fracture than did BMD obtained by DXA. Thus, microstructure analysis by MDCT, together with simultaneously obtained volumetric BMD values, is useful for clinical assessment of fracture risk. Introduction: BMD measurement by DXA alone has limitations in predicting fracture, and methods for clinical assessment of bone quality, such as microstructure, are awaited. This study was undertaken to examine the applicability of multidetector row CT (MDCT) for in vivo evaluation of trabecular microstructure. Materials and Methods: Optimal conditions for MDCT scanning were determined at a spatial resolution of 250 x 250 x 500 mu m, using RCT data of excised human vertebra specimens as a reference. We analyzed the trabecular microstructure of the vertebrae of 82 postmenopausal women (55-76 years old), including 39 women with and 43 without a recent vertebral fracture. Results: Microstructure indices obtained by MDCT scanning revealed higher relative risk for prevalent vertebral fracture (OR: 16.0 for structure model index, 13.6 for bone volume fraction, and 13.1 for Euler's number) than did spinal BMD obtained by DXA (OR: 4.8). MDCT could also provide volumetric BMD data, which had higher diagnostic value (OR: 12.7) than did DXA. Conclusion: Vertebral microarchitecture can be visualized by MDCT, and microstructure parameters obtained by MDCT, together with volumetric BMD, provided better diagnostic performance for assessing fracture risk than DXA measurement.
引用
收藏
页码:1828 / 1836
页数:9
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