Mokhtari-Dizaji M, Dadras M R, Larijani B
Department of Medical Physics, Tarbiat Modares University, Tehran, Iran.
Pak J Biol Sci. 2007 Feb 15;10(4):545-52. doi: 10.3923/pjbs.2007.545.552.
DXA and QUS assessments in vivo have been shown to be predictive of osteoporosis and future fractures. In clinical measurements, bone thickness can affect bone mineral density and ultrasound parameters. Previous in vitro studies have demonstrated contradictory reports about relationship between bone mineral density and so ultrasound parameters with bone thickness, separately. In this study, DXA, phalangeal QUS and calcaneus QUS measurements were conducted on rabbit bone in vivo using clinical instruments. We have selected rabbit's bones that have low BMD and more collagen tissue to predict structure not only measures BMD, but is also sensitive to the structure of the bone. To investigate the effect of bone thickness on the measured parameters, two regions of femur and tibia bones (N = 44) were processed: up (1/3 of length) and down (2/3 of length) for BMC, areal BMD, volumetric BMD, AD-SOS, UBPI, BTT, SOS, BUA and SI measurements and bone thickness-corrected SOS and bone thickness corrected BUA. The paired student's t-test analysis of densitometric and ultrasonic characteristics extracted by DXA, Phalangeal and calcaneus quantitative ultrasound showed significant differences (p < 0.05) between densitometric and ultrasonic parameters of two groups of up and down of the femur and two groups of up and down of the tibia, with the exception of SOS and SI (p > 0.05). It shows that BMC, BMD(a), AD-SOS, UBPI, BTT and BUA correlate well with the bone thickness of the tibia and the femur. Among the femur parameters, the highest correlation (r = 0.755) was obtained for BMC parameter. But in the tibia, measurements at AD-SOS, UBPI and BUA inversely correlated with bone thickness, that could be arise from the tibia bone structure. This bone has collagen and non mineral structures more than bone mineral density. Correlation analyses of the bone thickness with the thickness-corrected DXA and ultrasound parameters revealed that corrected BMD (BMD(v)) is independent from thickness, but corrected parameters excluding SOSc and BUA(c) showed significant correlation coefficient than uncorrected. Linear regression analyses were used to examine the relationship between DXA and ultrasound parameters with bone thickness and the regression functions for each parameters (with correlated significant) is given. We concluded that BMD(v), SOS and SI are independent from bone thickness (with range of 5-9 mm). Thus, the ability of these parameters to discriminate low density or osteoporotic bone from normal bone may be limited if differences in bone thickness are not accounted for. This result may be at least in part due to large precision error measurement of the bone thickness, in vivo study.
体内双能X线吸收法(DXA)和定量超声(QUS)评估已被证明可预测骨质疏松症和未来骨折情况。在临床测量中,骨厚度会影响骨矿物质密度和超声参数。此前的体外研究分别就骨矿物质密度以及超声参数与骨厚度之间的关系给出了相互矛盾的报告。在本研究中,使用临床仪器对兔骨进行了体内DXA、指骨QUS和跟骨QUS测量。我们选择了骨密度低且胶原组织较多的兔骨,以预测不仅能测量骨密度,还对骨结构敏感的结构。为研究骨厚度对测量参数的影响,对股骨和胫骨的两个区域(N = 44)进行了处理:上端(长度的1/3)和下端(长度的2/3),用于测量骨矿含量(BMC)、面积骨密度、体积骨密度、轴向声速(AD - SOS)、超声骨密度指数(UBPI)、骨小梁厚度(BTT)、声速(SOS)、宽带超声衰减(BUA)和结构指数(SI),以及骨厚度校正后的SOS和骨厚度校正后的BUA。对DXA、指骨定量超声和跟骨定量超声提取的密度测定和超声特征进行配对学生t检验分析,结果显示股骨上下两组和胫骨上下两组的密度测定和超声参数之间存在显著差异(p < 0.05),但SOS和SI除外(p > 0.05)。这表明BMC、面积骨密度(BMD(a))、AD - SOS、UBPI、BTT和BUA与胫骨和股骨的骨厚度密切相关。在股骨参数中,BMC参数的相关性最高(r = 0.755)。但在胫骨中,AD - SOS、UBPI和BUA的测量值与骨厚度呈负相关,这可能源于胫骨的骨结构。该骨的胶原和非矿物质结构比骨矿物质密度更多。骨厚度与经厚度校正的DXA和超声参数的相关性分析表明,校正后的骨密度(BMD(v))与厚度无关,但除SOSc和BUA(c)外的校正参数显示出比未校正参数更高的相关系数。使用线性回归分析来检验DXA和超声参数与骨厚度之间的关系,并给出了每个参数的回归函数(具有显著相关性)。我们得出结论,BMD(v)、SOS和SI与骨厚度无关(骨厚度范围为5 - 9毫米)。因此,如果不考虑骨厚度差异,这些参数区分低密度或骨质疏松性骨与正常骨的能力可能会受到限制。这一结果可能至少部分归因于体内研究中骨厚度测量的较大精度误差。