Literature DB >> 15255284

Effects of ospemifene, a novel SERM, on biochemical markers of bone turnover in healthy postmenopausal women.

J Komi1, J Heikkinen, E M Rutanen, K Halonen, R Lammintausta, O Ylikorkala.   

Abstract

Ospemifene is a novel selective estrogen receptor modulator (SERM). Here we studied the effects of ospemifene on bone turnover in postmenopausal women. This was a randomized, double-blind study in which 159 healthy postmenopausal women received 30 (n = 40), 60 (n = 40) or 90 mg (n = 40) of ospemifene or placebo (n = 39) for 3 months. Bone resorption was assessed by measuring the urinary outputs of N- and C-terminal crosslinking telopeptides of type I collagen (NTX and CTX, respectively). Bone formation was assessed by measuring the levels of procollagen type I N propeptide (PINP), procollagen type I C propeptide (PICP), and bone-specific alkaline phosphatase (bone ALP) in serum. All markers were studied at baseline, 3 months, and 2-4 weeks after cessation of the medication. Ospemifene decreased bone resorption dose-dependently, as seen from falls in NTX by 6.1, 9.4 and 12.9% in the 30, 60 and 90 mg ospemifene groups, respectively (p < 0.05 for all dose levels when compared to placebo). CTX values decreased in the 90 mg ospemifene group by 4.8% (p < 0.05). A dose-dependent decrease was also observed in the bone formation markers: PINP values decreased by 9.8 (p < 0.05) and 15.3% (p < 0.01), and PICP values by 12.0 and 11.9% in the 60 and 90 mg ospemifene groups, respectively. Bone ALP decreased in 60 and 90 mg ospemifene groups by 1.9 and 2.6%, respectively (p < 0.05 for both dose levels when compared to placebo). These results show that ospemifene is effective in reducing bone turnover in postmenopausal women.

Entities:  

Mesh:

Substances:

Year:  2004        PMID: 15255284     DOI: 10.1080/09513590410001672197

Source DB:  PubMed          Journal:  Gynecol Endocrinol        ISSN: 0951-3590            Impact factor:   2.260


  17 in total

Review 1.  Current, new and future treatments of osteoporosis.

Authors:  Pooneh Salari Sharif; Mohammad Abdollahi; Bagher Larijani
Journal:  Rheumatol Int       Date:  2010-07-30       Impact factor: 2.631

Review 2.  SERMs in the prevention and treatment of postmenopausal osteoporosis: an update.

Authors:  Jaime Kulak Júnior; Carolina Aguiar Moreira Kulak; Hugh S Taylor
Journal:  Arq Bras Endocrinol Metabol       Date:  2010-03

3.  Ospemifene and 4-hydroxyospemifene effectively prevent and treat breast cancer in the MTag.Tg transgenic mouse model.

Authors:  Rebekah A Burich; Neelima Rakesh Mehta; Gregory T Wurz; Jamie Lee McCall; Brittany E Greenberg; Katie E Bell; Stephen M Griffey; Michael W DeGregorio
Journal:  Menopause       Date:  2012-01       Impact factor: 2.953

Review 4.  Emerging selective estrogen receptor modulators: special focus on effects on coronary heart disease in postmenopausal women.

Authors:  Tatjana Elène Vogelvang; Marius Jan van der Mooren; Velja Mijatovic; Peter Kenemans
Journal:  Drugs       Date:  2006       Impact factor: 9.546

5.  Designing the ideal selective estrogen receptor modulator--an achievable goal?

Authors:  Hugh S Taylor
Journal:  Menopause       Date:  2009 May-Jun       Impact factor: 2.953

6.  From empirical to mechanism-based discovery of clinically useful Selective Estrogen Receptor Modulators (SERMs).

Authors:  Suzanne E Wardell; Erik R Nelson; Donald P McDonnell
Journal:  Steroids       Date:  2014-07-30       Impact factor: 2.668

Review 7.  Ospemifene: first global approval.

Authors:  Shelley Elkinson; Lily P H Yang
Journal:  Drugs       Date:  2013-05       Impact factor: 9.546

8.  Differential effects of selective oestrogen receptor modulators (SERMs) tamoxifen, ospemifene and raloxifene on human osteoclasts in vitro.

Authors:  H Michael; P L Härkönen; L Kangas; H K Väänänen; T A Hentunen
Journal:  Br J Pharmacol       Date:  2007-04-10       Impact factor: 8.739

Review 9.  Selective estrogen receptor modulators for postmenopausal osteoporosis: current state of development.

Authors:  Luigi Gennari; Daniela Merlotti; Fabrizio Valleggi; Giuseppe Martini; Ranuccio Nuti
Journal:  Drugs Aging       Date:  2007       Impact factor: 3.923

10.  Tamoxifen Derivatives Alter Retromer-Dependent Endosomal Tubulation and Sorting to Block Retrograde Trafficking of Shiga Toxins.

Authors:  Andrey S Selyunin; Karinel Nieves-Merced; Danyang Li; Stanton F McHardy; Somshuvra Mukhopadhyay
Journal:  Toxins (Basel)       Date:  2021-06-15       Impact factor: 4.546

View more

北京卡尤迪生物科技股份有限公司 © 2022-2023.