New therapeutic options for bone diseases

被引:4
|
作者
Kocijan, Roland [1 ,2 ,3 ,4 ,5 ]
Haschka, Judith [1 ,2 ,3 ,4 ]
Feurstein, Julia [1 ,2 ,3 ,4 ]
Zwerina, Jochen [1 ,2 ,3 ,4 ]
机构
[1] Hanusch Hosp OEGK, Ludwig Boltzmann Inst Osteol, Heinrich Collin Str 30, A-1140 Vienna, Austria
[2] AUVA Trauma Ctr Meidling, Heinrich Collin Str 30, A-1140 Vienna, Austria
[3] Hanusch Hosp OEGK, Hanusch Hosp, Med Dept 1, Vienna, Austria
[4] Vienna Bone & Growth Ctr, Vienna, Austria
[5] Sigmund Freud Univ, Med Fac Bone Dis, Vienna, Austria
关键词
Sclerostin antibody; Romosozumab; Burosumab; Asfotase alfa; Rare bone diseases; SCLEROSTIN ANTIBODY TREATMENT; X-LINKED HYPOPHOSPHATEMIA; BRTL/+ MOUSE MODEL; ASFOTASE ALPHA; POSTMENOPAUSAL WOMEN; ADULT PATIENTS; ROMOSOZUMAB; BPS804; MASS;
D O I
10.1007/s10354-020-00810-w
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
In recent years, new treatment options for both common and rare bone diseases have become available. The sclerostin antibody romosozumab is the most recently approved drug for the therapy of postmenopausal osteoporosis. Its anabolic capacity makes it a promising treatment option for severe osteoporosis. Other sclerostin antibodies for the treatment of rare bone diseases such as osteogenesis imperfecta are currently being investigated. For rare bone diseases such as X-linked hypophosphatemia (XLH) and hypophosphatasia (HPP), specific therapies are now also available, showing promising data in children and adults with a severe disease course. However, long-term data are needed to assess a sustained benefit for patients.
引用
收藏
页码:120 / 125
页数:6
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