Inaccuracies inherent in patient-specific dual-energy X-ray absorptiometry bone mineral density measurements:: Comprehensive phantom-based evaluation

被引:92
作者
Bolotin, HH [1 ]
Sievänen, H
Grashuis, JL
Kuiper, JW
Järvinen, TLN
机构
[1] Univ Melbourne, Sch Phys, Parkville, Vic 3010, Australia
[2] UKK Inst, Bone Res Grp, Tampere, Finland
[3] Erasmus Univ, Dept Med Informat & Radiol, Rotterdam, Netherlands
[4] Acad Hosp Rotterdam Dijkzigt, Dept Radiol, NL-3000 DR Rotterdam, Netherlands
[5] Tampere Univ Hosp, Dept Surg, Tampere, Finland
[6] Univ Tampere, Sch Med, FIN-33101 Tampere, Finland
[7] Univ Tampere, Inst Med Technol, FIN-33101 Tampere, Finland
关键词
bone mineral density inaccuracies; marrow; dual-energy X-ray absorptiometry; soft tissue anthropometrics; phantoms;
D O I
10.1359/jbmr.2001.16.2.417
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
An extensive series of dual-energy X-ray absorptiometry (DXA) scans and dual polyenergetic X-ray simulation studies of 150 different phantom arrays were carried out to evaluate quantitatively the extent of systematic inaccuracies inherent in DXA in vivo bone mineral density (BMD). These measurements are particularly relevant to lumbar vertebral and proximal femoral sites, The phantoms were specially fabricated near perfect absorptiometric representations of bone material, red marrow (RM) and yellow marrow (YM), and estraosseous mixtures of fat (F) and lean muscle that spanned the full range of soft tissue anthropometrics encountered clinically. In each case, the DXA-measured BMD values obtained using Hologic, Lunar, and Norland densitometers were found to be virtually the same and to be in excellent agreement with the corresponding quantitative simulation study BMD results. Comparisons of the known phantom BMD values and DXA-measured BMD in each case allowed the BMD inaccuracies to be evaluated, These present findings show that these ubiquitous inaccuracies in DXA BMD methodology are of in vivo soft tissue anthropometric genesis. It is found that patient-specific DXA-measured in vivo BMD inaccuracies as high as 20% or more can be readily anticipated clinically, particularly in cases of osteopenic, osteoporotic, and elderly patients. As these inaccuracies exceed considerably DXA precision errors, they may compromise patient-specific evaluations of fracture risk and, in prospective studies, mask or exaggerate clinically significant true changes in BMD. It is concluded that the magnitudes and variability of inherent inaccuracies in DXA-measured in vivo BMD underscore the need for prudence and circumspection in interpretations and assessments of DXA-based clinical studies.
引用
收藏
页码:417 / 426
页数:10
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