Treatment needs and current options for postmenopausal osteoporosis

被引:123
作者
Gennari, Luigi [1 ]
Rotatori, Stefano [1 ]
Bianciardi, Simone [1 ]
Nuti, Ranuccio [1 ]
Merlotti, Daniela [1 ,2 ]
机构
[1] Univ Siena, Dept Med Surg & Neurosci, I-53100 Siena, Italy
[2] Ist Sci San Raffaele, Age Related Dis, Div Genet & Cell Biol, I-20132 Milan, Italy
关键词
Osteoporosis; bisphosphonates; denosumab; cathepsin K; teriparatide; SERMS; sclerostin; odanacatib; romosozumab; abaloparatide; BONE-MINERAL DENSITY; HUMAN PARATHYROID-HORMONE; RANDOMIZED CONTROLLED-TRIAL; PLACEBO-CONTROLLED TRIAL; FRACTURE RISK REDUCTION; ESTROGEN PLUS PROGESTIN; CATHEPSIN-K INHIBITOR; BISPHOSPHONATE THERAPY; SCLEROSTIN ANTIBODY; FUTURE PERSPECTIVES;
D O I
10.1080/14656566.2016.1176147
中图分类号
R9 [药学];
学科分类号
100702 [药剂学];
摘要
Introduction: Osteoporosis is a chronic, skeletal disorder characterized by compromised bone strength and increased risk of fractures, affecting up to 50% of postmenopausal women worldwide. Over the past 2 decades there have been consistent developments in the pharmacotherapy of osteoporosis with the availability of potent inhibitors of bone resorption (bisphosphonates, and denosumab) or stimulators of bone formation (PTH analogs) with substantial improvements over calcitonin or estrogen replacement. Areas covered: In this review we summarize the effects of existing treatment options for postmenopausal osteoporosis along with the unmet clinical needs and we discuss about the potential benefits of new compounds under development. Expert opinion: Despite the recent progresses, there are still limitations and unmeet needs with all the available drugs, mainly concerning treatment adherence, efficacy on the prevention of nonvertebral fractures and the long-term adverse events of antiresorptive regimens. Moreover, PTH analogs are the only available compounds able to stimulate bone formation, but with a restricted anabolic window of no more than 2 years. Of interest, the more recent advances in bone biology identified new targets for the development of drugs with a more potent and selective activity on either osteoclasts or osteoblasts, thus making possible to uncouple bone formation from bone resorption.
引用
收藏
页码:1141 / 1152
页数:12
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