Wang X, Shen X, Li X, Agrawal C Mauli
Department of Mechanical Engineering, University of Texas Health Science Center at San Antonio, San Antonio, TX, USA.
Bone. 2002 Jul;31(1):1-7. doi: 10.1016/s8756-3282(01)00697-4.
The hypothesis of this study is that the mechanical integrity of the collagen network in bone deteriorates with age, and such adverse changes correlate with the decreased toughness of aged bone. To test the hypothesis, 30 human cadaveric femurs from donors ranging from 19 to 89 years of age were tested to determine the age-related changes in the mechanical properties of demineralized bone and fresh bone samples. Along with bone porosity, bone density, and weight fractions of the mineral and organic phases, collagen denaturation and concentrations of collagen cross-links (HP, hydroxylysylpyridinoline; LP, lysylpyridinoline; PE, pentosidine) were determined for these bone specimens as a function age. Analysis of variance (ANOVA) showed that age-dependent changes were reflected in the decreased strength, work to fracture, and fracture toughness of bone; in the decreased strength, elastic modulus, and work to fracture of the collagen network; as well as in the increased concentration of pentosidine (a marker of nonenzymatic glycation) and increased bone porosity. Regression analyses of the measured parameters showed that the age-related decrease in work to fracture of bone (especially its postyield portion) correlated significantly with deterioration in the mechanical integrity of the collagen network. The results of this study indicate that the adverse changes in the collagen network occur as people age and such changes may lead to the decreased toughness of bone. Also, the results suggest that nonenzymatic glycation may be an important contributing factor causing changes in collagen and, consequently, leading to the age-related deterioration of bone quality.
本研究的假设是,骨骼中胶原蛋白网络的机械完整性会随着年龄增长而恶化,且这种不利变化与老年骨骼韧性下降相关。为验证该假设,对30具年龄在19岁至89岁之间的人类尸体股骨进行了测试,以确定脱矿骨和新鲜骨样本力学性能的年龄相关变化。除了骨孔隙率、骨密度以及矿物质和有机相的重量分数外,还测定了这些骨标本中胶原蛋白变性情况以及胶原蛋白交联物(HP,羟赖氨酰吡啶啉;LP,赖氨酰吡啶啉;PE,戊糖苷)的浓度随年龄的变化。方差分析(ANOVA)表明,年龄依赖性变化体现在骨骼强度、断裂功和断裂韧性的降低;胶原蛋白网络强度、弹性模量和断裂功的降低;以及戊糖苷浓度增加(非酶糖基化的标志物)和骨孔隙率增加。对测量参数的回归分析表明,骨骼断裂功(尤其是屈服后部分)的年龄相关下降与胶原蛋白网络机械完整性的恶化显著相关。本研究结果表明,随着人们年龄增长,胶原蛋白网络会出现不利变化,且这些变化可能导致骨骼韧性下降。此外,结果表明非酶糖基化可能是导致胶原蛋白变化的一个重要因素,进而导致与年龄相关的骨质恶化。