Quantitative ultrasound or clinical risk factors - which best identifies women at risk of osteoporosis?

Citation
A. Stewart et Dm. Reid, Quantitative ultrasound or clinical risk factors - which best identifies women at risk of osteoporosis?, BR J RADIOL, 73(866), 2000, pp. 165-171
Citations number
28
Categorie Soggetti
Radiology ,Nuclear Medicine & Imaging","Medical Research Diagnosis & Treatment
Journal title
BRITISH JOURNAL OF RADIOLOGY
ISSN journal
00071285 → ACNP
Volume
73
Issue
866
Year of publication
2000
Pages
165 - 171
Database
ISI
SICI code
Abstract
Dual energy X-ray absorptiometry (DXA) is the current technique of choice t o assess risk of future fracture and to diagnose osteoporosis as defined by bone mineral density (BMD). Guidelines for bone densitometry referral have been published listing clinical risk factors that might be considered grou nds for assessment. However, these factors are known to be poorly predictiv e of subsequent BMD measurement and, accordingly, new inexpensive methods o f selecting subjects for assessment should be sought. Quantitative ultrasou nd (QUS) of bone may be such a technique. Women (n=250) considered by their general practitioners to be at risk of osteoporosis and who had been refer red for DXA measurements of the spine and hip were recruited into the study . All underwent a QUS scan of the heel using a McCue CUBA Clinical machine, which measures broadband ultrasound attenuation (BUA) and velocity of soun d (VOS), a clinical risk factor questionnaire, and spine and hip BMD measur ement by a Norland XR-26 bone densitometer. Patients were categorized accor ding to published diagnostic criteria for BMD, and these were also applied to the QUS parameters. Risk factors were arbitrarily categorized into "low" , "medium" and "high" risk groups. Kappa scores were calculated to analyse the agreement between different techniques. Receiver operator characteristi c (ROC) analyses were undertaken to demonstrate the technique with the best sensitivity and specificity for the detection of low BMD at the spine and hip. Analysis of the bone mass data demonstrated only moderate agreement (k appa 0.33) between femoral neck and spine BMD with femoral neck BMD and BUA showing a very similar level of agreement (kappa 0.31). ROC analysis demon strated that VOS followed by BUA was the best predictor of low BMD, with ri sk factors alone being significantly poorer; QUS parameters are better pred ictors than clinical risk factors for women with low BMD and could be used effectively at the primary care level to indicate those who should be consi dered for full osteoporosis assessment. However, further study into the cos t effectiveness of this approach is required.