Alekel D Lee, Peterson Charles T, Werner Roy K, Mortillaro Erica, Ahmed Noreen, Kukreja Subhash C
Department of Food Science & Human Nutrition, Iowa State University, Ames, Iowa 50011, USA.
J Clin Densitom. 2002 Summer;5(2):175-86. doi: 10.1385/jcd:5:2:175.
Published data on the spinal bone mineral density (BMD) of premenopausal women originating from the Indian subcontinent (Indian/Pakistani) are few. We compared anteroposterior (AP) and lateral areal BMD (aBMD) using dual X-ray absorptiometry and calculated volumetric BMD (vBMD) in Indian/Pakistani (n = 47) vs American (n = 47) women with dissimilar statures and skeletal sizes. To account for differences, we "adjusted" lumbar aBMD separately for vertebral size (aBMD/the square root of the projected area), height (aBMD/height), and hip skeletal width (aBMD/hip width). We "corrected" bone mineral content (BMC), aBMD, and vBMD for frame size, collectively using height, hip width, and vertebral size. Unadjusted mean aBMD values for AP lumbar (L1-L4, p = 0.0086; L3-L4, p = 0.044) spine were higher in Americans than Indians/Pakistanis,whereas lateral vBMD (p = 0.56) or aBMD (p = 0.060) values were not different. After adjusting for height, hip width, or vertebral size, or correcting for frame size, differences in aBMD disappeared. Regression analyses indicated that the best measures to correct for frame size were: vertebral area for BMC, hip width for aBMD, and vertebral width for lateral vBMD. Height was not significant in any model. In correcting for frame size, we accounted for 73-85% of the variability in BMC, 22-28% in aBMD, and 27% in lateral vBMD. After frame size was corrected, we accounted for 34% of the variability in AP BMC and aBMD, in contrast with 6-9% in the lateral models. Five significant biologic and lifestyle factors remained in AP models; only body weight remained for lateral spine. Upon accounting for frame size using regression, much variability in BMD, aBMD, and vBMD was explained by lifestyle and biologic factors, not by ethnicity.
源自印度次大陆(印度/巴基斯坦)的绝经前女性脊柱骨密度(BMD)的已发表数据很少。我们使用双能X线吸收法比较了前后位(AP)和侧位面积骨密度(aBMD),并计算了印度/巴基斯坦(n = 47)和美国(n = 47)身高和骨骼大小不同的女性的体积骨密度(vBMD)。为了考虑差异,我们分别针对椎体大小(aBMD/投影面积的平方根)、身高(aBMD/身高)和髋部骨骼宽度(aBMD/髋部宽度)对腰椎aBMD进行了“调整”。我们使用身高、髋部宽度和椎体大小共同对骨矿物质含量(BMC)、aBMD和vBMD进行了框架大小的“校正”。美国人腰椎AP(L1-L4,p = 0.0086;L3-L4,p = 0.044)的未调整平均aBMD值高于印度人/巴基斯坦人,而侧位vBMD(p = 0.56)或aBMD(p = 0.060)值没有差异。在对身高、髋部宽度或椎体大小进行调整后,或对框架大小进行校正后,aBMD的差异消失了。回归分析表明,校正框架大小的最佳指标是:BMC用椎体面积,aBMD用髋部宽度,侧位vBMD用椎体宽度。身高在任何模型中均无显著意义。在校正框架大小时,我们解释了BMC变异性的73-85%、aBMD变异性的22-28%和侧位vBMD变异性的27%。校正框架大小后,我们解释了AP BMC和aBMD变异性的34%,而侧位模型中为6-9%。AP模型中有五个显著的生物学和生活方式因素;侧位脊柱仅体重因素留存。通过回归考虑框架大小后,BMD、aBMD和vBMD的许多变异性是由生活方式和生物学因素解释的,而非种族因素。