Quantitative ultrasound of the calcaneus - An in vivo comparison with dual-energy X-ray absorptiometry and magnetic resonance imaging

Citation
O. Louis et al., Quantitative ultrasound of the calcaneus - An in vivo comparison with dual-energy X-ray absorptiometry and magnetic resonance imaging, J CLIN DENS, 3(1), 2000, pp. 43-48
Citations number
25
Categorie Soggetti
Endocrynology, Metabolism & Nutrition
Journal title
JOURNAL OF CLINICAL DENSITOMETRY
ISSN journal
10946950 → ACNP
Volume
3
Issue
1
Year of publication
2000
Pages
43 - 48
Database
ISI
SICI code
1094-6950(200021)3:1<43:QUOTC->2.0.ZU;2-N
Abstract
This study was performed in a clinical setting and aimed to evaluate the re lationship between quantitative ultrasound (QUS) of the calcaneus with bone mineral density (BMD) assessed with dual-energy X-ray absorptiometry (DXA) and with variables derived from magnetic resonance imaging (MRI). Thirty-t wo post menopausal women (mean age 61 yr) were studied at the level of the nondominant calcaneus. QUS was performed using a DTU-one device, including parametric imaging and yielded speed of sound (SOS) and broad-band ultrasou nd attenuation (BUA) data. DXA was performed at a matched region of interes t (ROI) in the calcaneus, using a Hologic QDR 4500 device. MRI, also perfor med at a matched ROI, yielded, using a Siemens Magnetom Vision device, the inverse of the transverse relaxation time (1/T-2*) and the phase standard d eviation (PSD). The strongest relationship between QUS and the other variab les involved BUA and BMD (r = 0.677, p < 0.001); 1/T-2* showed a trend to c orrelation with SOS (r = 0.359, p = 0.044) and with BMD (r = 0.364, p = 0.0 40), whereas the relationship between 1/T-2* and BUA, PSD and BUA, PSD and SOS, and PSD and BMD remained far from significant. Regression analysis of QUS, DXA, and MRI variables versus age showed a trend to significant declin e only for 1/T-2* (r= -0.409, p = 0.020). In conclusion, this study shows t hat BUA of the calcaneus has the best correlation with BMD, and that, at le ast in a clinical setting, the ability of QUS to give information about bon e structure is limited.