Rosen C J, Bilezikian J P
St. Joseph Hospital, Bangor, Maine 04401, USA.
J Clin Endocrinol Metab. 2001 Mar;86(3):957-64. doi: 10.1210/jcem.86.3.7366.
All currently available, approved therapies for osteoporosis inhibit bone resorption. By acting at this site in the bone remodeling cycle, estrogens, selective estrogen receptor modulators, calcitonin, and the bisphosphonates all have the capacity to increase bone mineral density and to reduce the risk of new fractures. There can be no doubt that these agents have had an enormous impact on our diagnostic and therapeutic approach to osteoporosis. Despite their great value, the antiresorptives are generally not associated with dramatic increases in bone mass, and their action to reduce fracture risk, although highly significant, is rarely more than 50% of the baseline risk. Another approach is anabolic therapy, in which bone formation is directly stimulated. In this review we will summarize the anabolic agents that have been studied and present a current view of their current standing. Fluoride, GH, insulin-like growth factor I, the statins, and PTH will be reviewed. Although still in development, approaches to combination therapy with antiresorptives and anabolic agents are also promising.
目前所有已获批的骨质疏松症治疗方法均抑制骨吸收。通过作用于骨重塑周期的这一环节,雌激素、选择性雌激素受体调节剂、降钙素和双膦酸盐都有能力增加骨矿物质密度并降低新发骨折的风险。毫无疑问,这些药物对我们诊断和治疗骨质疏松症的方法产生了巨大影响。尽管它们具有很高的价值,但抗吸收药物通常不会使骨量显著增加,而且它们降低骨折风险的作用虽然非常显著,但很少超过基线风险的50%。另一种方法是促合成代谢疗法,即直接刺激骨形成。在这篇综述中,我们将总结已研究的促合成代谢药物,并阐述它们目前的现状。将对氟化物、生长激素、胰岛素样生长因子I、他汀类药物和甲状旁腺激素进行综述。尽管仍在研发中,但抗吸收药物与促合成代谢药物联合治疗的方法也很有前景。