Combination anabolic and antiresorptive therapy for osteoporosis: Opening the anabolic window

被引:88
作者
Bilezikian J.P. [1 ]
机构
[1] Department of Medicine, College of Physicians and Surgeons, Columbia University, New York, NY 10032
关键词
Osteoporosis; Vertebral Fracture; Alendronate; Raloxifene; Teriparatide;
D O I
10.1007/s11914-008-0005-9
中图分类号
学科分类号
摘要
Antiresorptive agents for osteoporosis are a cornerstone of therapy, but anabolic drugs have recently increased our options. By stimulating bone formation, anabolic agents reduce fracture incidence by improving bone qualities in addition to increasing bone mass. The only anabolic agent currently approved for osteoporosis by the US Food and Drug Administration, teriparatide (recombinant human parathyroid hormone [1-34]), has emerged as a major approach to selected patients with osteoporosis. Recombinant human parathyroid hormone (1-84) is also available in Europe. Teriparatide increases bone density and bone turnover, improves microarchitecture, and changes bone size. The incidence of vertebral and nonvertebral fractures is reduced. A current concept in the mechanism of teriparatide action is related to its effect to stimulate processes associated with bone formation before it stimulates processes associated with bone resorption. This sequence of events has led to the concept of the anabolic window, the period of time when teriparatide is maximally anabolic. Newer approaches to the use of teriparatide alone and in combination with antiresorptive agents have led to ways in which the anabolic window can be expanded. © Springer Science+Business Media, LLC 2008.
引用
收藏
页码:24 / 30
页数:6
相关论文
共 50 条
[1]  
Hodsman A.B., Bauer D.C., Dempster D., Et al., Parathyroid hormone and teriparatide for the treatment of osteoporosis: A review of the evidence and suggested guidelines for its use, Endocr Rev, 26, pp. 688-703, (2005)
[2]  
Canalis E., Giustina A., Bilezikian J.P., Mechanisms of anabolic therapies for osteoporosis, N Engl J Med, 357, pp. 905-916, (2007)
[3]  
Dempster D.W., Parisien M., Silverberg S.J., Et al., On the mechanism of cancellous bone preservation in postmenopausal women with mild primary hyperparathyroidism, J Clin Endocrinol Metab, 84, pp. 1562-1566, (1999)
[4]  
Girotra M., Rubin M., Bilezikian J., The use of parathyroid hormone in the treatment of osteoporosis, Rev Endocr Metab Disord, 7, pp. 113-121, (2006)
[5]  
Jiang Y., Zhao J.J., Mitlak B.H., Et al., Recombinant human parathyroid hormone (1-34) [teriparatide] improves both cortical and cancellous bone structure, J Bone Miner Res, 18, pp. 1932-1941, (2003)
[6]  
Sellmeyer D.E., Black D.M., Palermo L., Et al., Heterogeneity in skeletal response to full-length parathyroid hormone (PTH) in the treatment of osteoporosis, Osteoporos Int, 18, pp. 973-979, (2007)
[7]  
Burr D.B., Hirano T., Turner C.H., Et al., Intermittently administered human parathyroid hormone(1-34) treatment increases intracortical bone turnover and porosity without reducing bone strength in the humerus of ovariectomized cynomolgus monkeys, J Bone Miner Res, 16, pp. 157-165, (2001)
[8]  
Keaveny T.M., Hoffman P.E., Kepperdahl, Et al., Comparison of the effects of teriparatide and alendronate on parameters of total hip strength as assessed by finite element analysis, J Bone Miner Res, 22, SUPPL. 1, (2007)
[9]  
Borggrefe J., Graeff C., Nickelsen T.N., Et al., Effects of 2 year teriparatide treatment on 3-D femoral neck bone distribution, geometry, and bone strength: Results from the EUROFORS study, J Bone Miner Res, 22, SUPPL. 1, (2007)
[10]  
Parfitt A.M., Parathyroid hormone and periosteal bone expansion, J Bone Miner Res, 17, pp. 1741-1743, (2002)