Oelzner Peter, Eidner T, Pfeil A
Funktionsbereich Rheumatologie und Osteologie, Klinik für Innere Medizin III, Universitätsklinikum Jena, Am Klinikum 1, 07740, Jena, Deutschland.
Z Rheumatol. 2022 Mar;81(2):125-133. doi: 10.1007/s00393-021-01128-7. Epub 2022 Jan 10.
The following substances are approved for the treatment of glucocorticoid-induced osteoporosis: the oral bisphosphonates alendronate and risedronate, the intravenous bisphosphonate zoledronate, the RANKL antibody denosumab as antiresorptive substances and teriparatide as osteoanabolic substance. In comparison to placebo a reduction of vertebral fractures is proven for all mentioned substances. Thereby, teriparatide is more effective than alendronate and risedronate with respect to the reduction of vertebral fractures. The severity of osteoporosis, especially the presence of osteoporotic fractures, the approach of treatment (preventive or curative) and contraindications are factors that are important for the differentiated application of the mentioned substances. Furthermore, it must be noted that the effect of osteoanabolic treatment must be stabilized by a subsequent antiresorptive treatment and that after termination of antiresorptive treatment with denosumab a temporary bisphosphonate treatment is required to prevent a rebound phenomenon.
口服双膦酸盐阿仑膦酸钠和利塞膦酸钠、静脉注射双膦酸盐唑来膦酸、作为抗吸收物质的RANKL抗体地诺单抗以及作为骨合成代谢物质的特立帕肽。与安慰剂相比,所有上述物质均已证实可减少椎体骨折。因此,在减少椎体骨折方面,特立帕肽比阿仑膦酸钠和利塞膦酸钠更有效。骨质疏松症的严重程度,尤其是骨质疏松性骨折的存在、治疗方法(预防性或治疗性)和禁忌症是对上述物质进行差异化应用的重要因素。此外,必须注意的是,骨合成代谢治疗的效果必须通过后续的抗吸收治疗来稳定,并且在停用抗吸收药物地诺单抗后,需要进行临时双膦酸盐治疗以防止反弹现象。