Roschger Paul, Misof Barbara, Paschalis Eleftherios, Fratzl Peter, Klaushofer Klaus
1st Medical Department, Hanusch Hospital, Ludwig Boltzmann Institute of Osteology at the Hanusch Hospital of WGKK and AUVA Trauma Centre Meidling, Heinrich Collin Str. 30, A-1140, Vienna, Austria,
Curr Osteoporos Rep. 2014 Sep;12(3):338-50. doi: 10.1007/s11914-014-0218-z.
The diagnosis of osteoporosis is based on low bone mineral density (BMD) and/or the occurrence of fragility fractures. The majority of patients, however, have also abnormally low bone matrix mineralization. The latter is indicative of alterations in bone turnover rates and/or in kinetics of mineral accumulation within the newly formed bone matrix. Osteoporosis therapies can alter the bone matrix mineralization according to their action on bone turnover and/or mineralization kinetics. Antiresorptives, including the most widely used bisphosphonates, reduce the bone turnover rate resulting in a decrease in heterogeneity and an increase in the degree of mineralization toward to or even beyond normal values. Anabolic agents increase the bone volume and the amount of newly formed bone resulting in a likely transient decrease in mean degree and homogeneity of mineralization. Hence, the measurement of bone matrix mineralization is a sensitive tool to evaluate the response to therapy.
骨质疏松症的诊断基于低骨矿物质密度(BMD)和/或脆性骨折的发生。然而,大多数患者还存在骨基质矿化异常低的情况。后者表明骨转换率和/或新形成的骨基质内矿物质积累动力学发生了改变。骨质疏松症治疗可根据其对骨转换和/或矿化动力学的作用来改变骨基质矿化。抗吸收药物,包括使用最广泛的双膦酸盐,可降低骨转换率,导致异质性降低,矿化程度朝着正常甚至超过正常值增加。合成代谢药物增加骨体积和新形成骨的量,可能导致矿化平均程度和均匀性暂时降低。因此,骨基质矿化的测量是评估治疗反应的敏感工具。