Curr Med Res Opin. 2011 Sep;27(9):1705-7. doi: 10.1185/03007995.2011.599837. Epub 2011 Jul 11.
Osteoanabolic therapy is theoretically and practically an appealing therapeutic option for men and postmenopausal women with osteoporosis because bone formation is directly stimulated, an action that is not shared by any antiresorptive agent. Parathyroid hormone (PTH), in the form of the full-length molecule (PTH[1-84]) and its fully active but truncated amino-terminal fragment teriparatide (PTH[1-34]), belong to this osteoanabolic class. Both formulations of PTH increase bone mineral density, increase biochemical markers of bone turnover, and reduce fracture incidence. They improve skeletal microstructure. While antiresorptive agents are considered by most to be first line for the treatment of osteoporosis, there are situations when anabolic therapy could be reasonably considered as first line. In most situations, however, treatment with PTH follows a course of antiresorptive therapy. Simultaneous combination therapy with PTH and an antiresorptive drug does not appear to provide any advantages over monotherapy. After the recommended 2-year period of PTH treatment, an antiresorptive should be used to maintain densitometric gains. The drugs are well tolerated. Early safety concerns about osteosarcoma in rats have not been borne out after almost 9 years experience with human subjects.
骨合成治疗在理论上和实际上对于男性和绝经后骨质疏松症妇女都是一种有吸引力的治疗选择,因为它直接刺激骨形成,而这一作用是任何抗吸收药物都不具备的。甲状旁腺激素(PTH)有全长分子(PTH[1-84])和其完全活性但截短的氨基末端片段特立帕肽(PTH[1-34])两种形式,属于这一类骨合成药物。这两种 PTH 制剂都能增加骨矿物质密度、增加骨转换的生化标志物、减少骨折发生率。它们还能改善骨骼微结构。虽然大多数人认为抗吸收药物是骨质疏松症治疗的一线药物,但在某些情况下,合成治疗可以合理地被视为一线治疗。然而,在大多数情况下,PTH 的治疗需要先进行抗吸收治疗。同时联合使用 PTH 和抗吸收药物似乎并没有比单独使用药物更有优势。在推荐的 2 年 PTH 治疗期后,应该使用抗吸收药物来维持密度计增益。这些药物的耐受性良好。近 9 年的人体研究后,关于大鼠骨肉瘤的早期安全担忧并没有得到证实。