Bruno Alexander G, Broe Kerry E, Zhang Xiaochun, Samelson Elizabeth J, Meng Ching-An, Manoharan Rajaram, D'Agostino John, Cupples L Adrienne, Kiel Douglas P, Bouxsein Mary L
Harvard-MIT Health Sciences and Technology Program, Cambridge, MA, USA; Center for Advanced Orthopaedic Studies, Beth Israel Deaconess Medical Center, Boston, MA, USA.
J Bone Miner Res. 2014 Mar;29(3):562-9. doi: 10.1002/jbmr.2067.
To explore the possible mechanisms underlying sex-specific differences in skeletal fragility that may be obscured by two-dimensional areal bone mineral density (aBMD) measures, we compared quantitative computed tomography (QCT)-based vertebral bone measures among pairs of men and women from the Framingham Heart Study Multidetector Computed Tomography Study who were matched for age and spine aBMD. Measurements included vertebral body cross-sectional area (CSA, cm(2) ), trabecular volumetric BMD (Tb.vBMD, g/cm(3) ), integral volumetric BMD (Int.vBMD, g/cm(3) ), estimated vertebral compressive loading and strength (Newtons) at L3 , the factor-of-risk (load-to-strength ratio), and vertebral fracture prevalence. We identified 981 male-female pairs (1:1 matching) matched on age (± 1 year) and QCT-derived aBMD of L3 (± 1%), with an average age of 51 years (range 34 to 81 years). Matched for aBMD and age, men had 20% larger vertebral CSA, lower Int.vBMD (-8%) and Tb.vBMD (-9%), 10% greater vertebral compressive strength, 24% greater vertebral compressive loading, and 12% greater factor-of-risk than women (p < 0.0001 for all), as well as higher prevalence of vertebral fracture. After adjusting for height and weight, the differences in CSA and volumetric bone mineral density (vBMD) between men and women were attenuated but remained significant, whereas compressive strength was no longer different. In conclusion, vertebral size, morphology, and density differ significantly between men and women matched for age and spine aBMD, suggesting that men and women attain the same aBMD by different mechanisms. These results provide novel information regarding sex-specific differences in mechanisms that underlie vertebral fragility.
为了探究骨骼脆弱性性别差异背后可能被二维面积骨密度(aBMD)测量所掩盖的潜在机制,我们比较了来自弗雷明汉心脏研究多探测器计算机断层扫描研究中年龄和脊柱aBMD相匹配的男性和女性对之间基于定量计算机断层扫描(QCT)的椎体骨测量值。测量包括椎体横截面积(CSA,cm²)、小梁体积骨密度(Tb.vBMD,g/cm³)、整体体积骨密度(Int.vBMD,g/cm³)、L3处估计的椎体压缩负荷和强度(牛顿)、风险因素(负荷与强度比)以及椎体骨折患病率。我们确定了981对男性 - 女性对(1:1匹配),年龄匹配在(±1岁),L3的QCT衍生aBMD匹配在(±1%),平均年龄为51岁(范围34至81岁)。在aBMD和年龄匹配的情况下,男性的椎体CSA比女性大20%,Int.vBMD(-8%)和Tb.vBMD(-9%)更低,椎体压缩强度高10%,椎体压缩负荷高24%,风险因素高12%(所有p < 0.0001),以及椎体骨折患病率更高。在调整身高和体重后,男性和女性之间CSA和体积骨密度(vBMD)的差异有所减弱但仍然显著,而压缩强度不再有差异。总之,在年龄和脊柱aBMD相匹配的男性和女性之间,椎体大小、形态和密度存在显著差异,这表明男性和女性通过不同机制达到相同的aBMD。这些结果提供了关于椎体脆弱性潜在机制中性别差异的新信息。