Granke Mathilde, Makowski Alexander J, Uppuganti Sasidhar, Nyman Jeffry S
Department of Orthopaedics Surgery & Rehabilitation, Vanderbilt University Medical Center, Nashville, TN 37232, United States; Center for Bone Biology, Vanderbilt University Medical Center, Nashville, TN 37232, United States; Department of Veterans Affairs, Tennessee Valley Healthcare System, Nashville, TN 37212, United States.
Department of Orthopaedics Surgery & Rehabilitation, Vanderbilt University Medical Center, Nashville, TN 37232, United States; Center for Bone Biology, Vanderbilt University Medical Center, Nashville, TN 37232, United States; Department of Veterans Affairs, Tennessee Valley Healthcare System, Nashville, TN 37212, United States; Department of Biomedical Engineering, Vanderbilt University, Nashville, TN 37232, United States.
J Biomech. 2016 Sep 6;49(13):2748-2755. doi: 10.1016/j.jbiomech.2016.06.009. Epub 2016 Jun 15.
Changes in the distribution of bone mineralization occurring with aging, disease, or treatment have prompted concerns that alterations in mineralization heterogeneity may affect the fracture resistance of bone. Yet, so far, studies assessing bone from hip fracture cases and fracture-free women have not reached a consensus on how heterogeneity in tissue mineralization relates to skeletal fragility. Owing to the multifactorial nature of toughening mechanisms occurring in bone, we assessed the relative contribution of heterogeneity in mineralization to fracture resistance with respect to age, porosity, and area fraction of osteonal tissue. The latter parameters were extracted from quantitative backscattered electron imaging of human cortical bone sections following R-curve tests of single-edge notched beam specimens to determine fracture toughness properties. Microstructural heterogeneity was determined as the width of the mineral distribution (bulk) and as the sill of the variogram (local). In univariate analyses of measures from 62 human donors (21 to 101 years), local but not bulk heterogeneity as well as pore clustering negatively correlated with fracture toughness properties. With age as covariate, heterogeneity was a significant predictor of crack initiation, though local had a stronger negative contribution than bulk. When considering all potential covariates, age, cortical porosity and area fraction of osteons explained up to 50% of the variance in bone׳s crack initiation toughness. However, including heterogeneity in mineralization did not improve upon this prediction. The findings of the present work stress the necessity to account for porosity and microstructure when evaluating the potential of matrix-related features to affect skeletal fragility.
随着衰老、疾病或治疗而发生的骨矿化分布变化引发了人们对矿化异质性改变可能影响骨抗骨折能力的担忧。然而,到目前为止,评估髋部骨折病例和未发生骨折女性的骨骼的研究尚未就组织矿化异质性与骨骼脆性之间的关系达成共识。由于骨中增韧机制具有多因素性质,我们评估了矿化异质性相对于年龄、孔隙率和骨单位组织面积分数对骨折抗性的相对贡献。后几个参数是从单边切口梁试样的R曲线测试后对人皮质骨切片进行的定量背散射电子成像中提取的,以确定断裂韧性特性。微观结构异质性被确定为矿物质分布(整体)的宽度和变异函数的基台值(局部)。在对62名人类供体(21至101岁)的测量进行单变量分析时,局部而非整体异质性以及孔隙聚集与断裂韧性特性呈负相关。以年龄作为协变量,异质性是裂纹萌生的显著预测因子,尽管局部的负贡献比整体更强。当考虑所有潜在协变量时,年龄、皮质孔隙率和骨单位面积分数解释了骨裂纹萌生韧性中高达50%的方差。然而,将矿化异质性纳入其中并没有改善这一预测。本研究结果强调在评估与基质相关的特征影响骨骼脆性的潜力时,考虑孔隙率和微观结构的必要性。