Anabolic therapy for osteoporosis: Parathyroid hormone

被引:14
作者
Cosman F. [1 ]
机构
[1] Regional Bone Center, Helen Hayes Hospital, New York, NY 10993, Route 9W, West Haverstraw
关键词
Osteoporosis; Vertebral Fracture; Alendronate; Raloxifene; Teriparatide;
D O I
10.1007/s11926-006-0028-0
中图分类号
学科分类号
摘要
Recombinant human parathyroid hormone (PTH 1-34) is the only anabolic agent currently approved for the treatment of osteoporosis. The term anabolic is based on mechanism of action. PTH stimulates bone formation, in contrast to antiresorptive agents, which reduce bone resorption and formation. Recent investigations involving the PTH(1-34) and PTH(1-84) peptides, alone and in combination or sequential regimens with antiresorptive agents, have provided a greater understanding of the place of PTH in the armamentarium against osteoporosis. These studies indicate that adding a bisphosphonate to PTH in previously untreated individuals does not produce additional bone benefit; however, sequential use of PTH followed-up by an antiresorptive agent is highly effective at increasing bone mineral density. Adding PTH after an antiresorptive agent also produces substantial bone density increments, though the magnitude of bone density increase may differ for different antiresorptive agents. PTH can repair underlying micro-architectural defects in bone, improve bone mass substantially, and perhaps change macro-architecture and geometry of bone. There are still many unanswered questions regarding PTH treatment of osteoporosis, including the optimal duration of treatment, optimal dosing regimen, mechanism of resistance to its effect after 18-24 months, and the effect of subsequent rechallenge. Copyright © 2006 by Current Science Inc.
引用
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页码:63 / 69
页数:6
相关论文
共 44 条
[1]  
McClung M.R., San Martin J., Miller P.D., Et al., Opposite bone remodeling effects of teriparatide and alendronate in increasing bone mass, Arch Intern Med, 165, pp. 1762-1768, (2005)
[2]  
Arlot M., Meunier P.J., Boivin G., Et al., Differential effects of teriparatide and alendronate on bone remodeling in postmenopausal women assessed by histomorphometric parameters, J Bone Miner Res, 20, pp. 1244-1253, (2005)
[3]  
Chavassieux P.M., Arot M.E., Reda C., Et al., Histomorphometric assessment of the long-term effects of alendronate on bone quality and remodeling in patients with osteoporosis, J Clin Invest, 100, pp. 1475-1480, (1997)
[4]  
Boivin G.Y., Chavassieux P.M., Santora A.C., Et al., Alendronate increases bone strength by increasing the mean degree of mineralization of bone tissue in osteoporotic women, Bone, 27, pp. 687-694, (2000)
[5]  
Roschger P., Rinnerthaler S., Yates J., Et al., Alendronate increases degree and uniformity of mineralization in cancellous bone and decreases the porosity in cortical bone of osteoporotic women, Bone, 29, pp. 185-191, (2001)
[6]  
Hang 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)
[7]  
Dempster D.W., Cosman F., Kurland E.S., Et al., Effects of daily treatment with parathyroid hormone on bone microarchitecture and turnover in patients with osteoporosis: A paired biopsy study, J Bone Miner Res, 16, pp. 1846-1853, (2001)
[8]  
Parfitt A.M., PTH and periosteal bone expansion, J Bone Miner Res, 17, pp. 1741-1743, (2002)
[9]  
Burr D., Does early PTH treatment compromise bone strength? the balance between remodeling, porosity, bone mineral, and bone size, Curr Osteoporos Rep, 3, pp. 19-24, (2005)
[10]  
Rehman Q., Lang T.F., Arnaud C.D., Et al., Daily treatment with parathyroid hormone is associated with an increase in vertebral cross-sectional area in postmenopausal women with glucocorticoid-induced osteoporosis, Osteoporos Int, 14, pp. 77-81, (2003)