Literature DB >> 25432357

Future directions for new medical entities in osteoporosis.

Serge Ferrari1.   

Abstract

Odanacatib, a selective cathepsin K inhibitor, decreases bone resorption, whereas osteoclast number increases and bone formation is maintained, perhaps even increased on some cortical surfaces. In a phase 2 clinical trial, post-menopausal women receiving odanacatib presented a sustained reduction of bone resorption markers, whereas procollagen type 1 N-terminal propeptide returned to normal. In turn areal bone mineral density increased continuously at both spine and hip for up to 5 years. Blosozumab and romosozumab are sclerostin neutralizing antibodies that exert potent anabolic effects on both trabecular and cortical compartments. A phase 2 clinical trial has reported areal bone mineral density gains at spine and hip that were greater with romosozumab compared with placebo, but also with teriparatide. It also showed that antagonizing sclerostin results in a transient stimulation of bone formation but progressive inhibition of bone resorption. Other new medical entities that are promising for the treatment of osteoporosis include abaloparatide, a parathyroid hormone-related analogue with improved bone formation-resorption ratio.
Copyright © 2014 Elsevier Ltd. All rights reserved.

Entities:  

Keywords:  PTHrP; blosozumab; cathepsin K; denosumab; fractures; odanacatib; osteoporosis; romosozumab; sclerostin; teriparatide

Mesh:

Substances:

Year:  2014        PMID: 25432357     DOI: 10.1016/j.beem.2014.08.002

Source DB:  PubMed          Journal:  Best Pract Res Clin Endocrinol Metab        ISSN: 1521-690X            Impact factor:   4.690


  6 in total

Review 1.  Current Status of Bone-Forming Therapies for the Management of Osteoporosis.

Authors:  Anne Sophie Koldkjær Sølling; Torben Harsløf; Bente Langdahl
Journal:  Drugs Aging       Date:  2019-07       Impact factor: 3.923

Review 2.  The clinical potential of romosozumab for the prevention of fractures in postmenopausal women with osteoporosis.

Authors:  Anne Sophie Koldkjær Sølling; Torben Harsløf; Bente Langdahl
Journal:  Ther Adv Musculoskelet Dis       Date:  2018-06-07       Impact factor: 5.346

3.  The role of biochemical of bone turnover markers in osteoporosis and metabolic bone disease: a consensus paper of the Belgian Bone Club.

Authors:  E Cavalier; P Bergmann; O Bruyère; P Delanaye; A Durnez; J-P Devogelaer; S L Ferrari; E Gielen; S Goemaere; J-M Kaufman; A Nzeusseu Toukap; J-Y Reginster; A-F Rousseau; S Rozenberg; A J Scheen; J-J Body
Journal:  Osteoporos Int       Date:  2016-03-30       Impact factor: 4.507

4.  Niclosamide and its derivative DK-520 inhibit RANKL-induced osteoclastogenesis.

Authors:  Yurui Jiao; Chenglong Chen; Xijian Hu; Xu Feng; Zhenqi Shi; Jie Cao; Qing Li; Yikun Zhu
Journal:  FEBS Open Bio       Date:  2020-07-22       Impact factor: 2.693

Review 5.  Treatment of Osteoporosis: Unmet Needs and Emerging Solutions.

Authors:  Bente Lomholt Langdahl; Jane Dahl Andersen
Journal:  J Bone Metab       Date:  2018-08-31

6.  Small molecule inhibitors of the Dishevelled-CXXC5 interaction are new drug candidates for bone anabolic osteoporosis therapy.

Authors:  Hyun-Yi Kim; Sehee Choi; Ji-Hye Yoon; Hwan Jung Lim; Hyuk Lee; Jiwon Choi; Eun Ji Ro; Jung-Nyoung Heo; Weontae Lee; Kyoung Tai No; Kang-Yell Choi
Journal:  EMBO Mol Med       Date:  2016-04-01       Impact factor: 12.137

  6 in total

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