Literature DB >> 12409511

Alendronate treatment for infants with osteogenesis imperfecta: demonstration of efficacy in a mouse model.

Edith A McCarthy1, Cathleen L Raggio, Michael D Hossack, Elizabeth A Miller, Sargam Jain, Adele L Boskey, Nancy P Camacho.   

Abstract

Recent non-placebo-controlled studies of the bisphosphonate pamidronate have shown it to be effective in reducing fractures and improving bone density in infants and children with osteogenesis imperfecta (OI). To evaluate the effects of bisphosphonate treatment in a controlled study, the oim/oim mouse model of OI was studied. Nursing infant mouse pups (approximately 2 wk old) with moderate to severe OI (oim/oim mouse) and age- and background-matched control mice (+/+) were treated either with the third-generation bisphosphonate alendronate (ALN), or with saline. Fracture risk, bone quality, and growth were evaluated over a 12-wk treatment period. ALN at a dose of 0.03 mg/kg/d or saline was administered via s.c. injection to infant oim/oim and wild-type (+/+) mice from 2 to 14 wk of age (n = 20 per subgroup). The average number of fractures sustained by the ALN-treated oim/oim mice was reduced significantly compared with the untreated oim/oim mice (0.7 +/- 0.7 fractures/mouse versus 2.0 +/- 0.2 fractures/mouse). Bone density increased significantly in the femur and the spine with treatment (2.0 +/- 0.5 versus 1.2 +/- 0.5 in femur and 2.1 +/- 0.5 versus1.6 +/- 0.5 in spine). Histologic evaluation revealed the percentage of metaphyseal tibial bone increased significantly with treatment in both +/+ and oim/oim mice. Mechanical testing revealed an increase in structural stiffness for both treated +/+ and oim/oim mice compared with untreated animals. None of the material properties examined were significantly altered with treatment, nor was spinal curvature affected. Weight gain and long bone growth were comparable in the treated and untreated oim/oim mice. In wild-type mice, femur lengths were significantly shorter in the treated mice compared with untreated counterparts. This animal study demonstrates that treatment of OI in mice as early as 2 wk of age with ALN appears to be effective in reducing fractures and increasing bone properties. Based on the data from this study, ALN therapy in infants with OI should prove to be effective.

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Year:  2002        PMID: 12409511     DOI: 10.1203/00006450-200211000-00010

Source DB:  PubMed          Journal:  Pediatr Res        ISSN: 0031-3998            Impact factor:   3.756


  28 in total

1.  Disruption of bone development and homeostasis by trisomy in Ts65Dn Down syndrome mice.

Authors:  Joshua D Blazek; Anna Gaddy; Rachel Meyer; Randall J Roper; Jiliang Li
Journal:  Bone       Date:  2010-09-24       Impact factor: 4.398

2.  Are Changes in Composition in Response to Treatment of a Mouse Model of Osteogenesis Imperfecta Sex-dependent?

Authors:  Adele L Boskey; Josephine Marino; Lyudmila Spevak; Nancy Pleshko; Stephen Doty; Erin M Carter; Cathleen L Raggio
Journal:  Clin Orthop Relat Res       Date:  2015-08       Impact factor: 4.176

3.  Bisphosphonate Withdrawal: Effects on Bone Formation and Bone Resorption in Maturing Male Mice.

Authors:  Frank C Ko; Lamya Karim; Daniel J Brooks; Mary L Bouxsein; Marie B Demay
Journal:  J Bone Miner Res       Date:  2017-01-17       Impact factor: 6.741

4.  Single dose of bisphosphonate preserves gains in bone mass following cessation of sclerostin antibody in Brtl/+ osteogenesis imperfecta model.

Authors:  Joseph E Perosky; Basma M Khoury; Terese N Jenks; Ferrous S Ward; Kai Cortright; Bethany Meyer; David K Barton; Benjamin P Sinder; Joan C Marini; Michelle S Caird; Kenneth M Kozloff
Journal:  Bone       Date:  2016-09-15       Impact factor: 4.398

5.  Low Dose of Bisphosphonate Enhances Sclerostin Antibody-Induced Trabecular Bone Mass Gains in Brtl/+ Osteogenesis Imperfecta Mouse Model.

Authors:  Diana Olvera; Rachel Stolzenfeld; Joan C Marini; Michelle S Caird; Kenneth M Kozloff
Journal:  J Bone Miner Res       Date:  2018-05-07       Impact factor: 6.741

6.  Gender-dependence of bone structure and properties in adult osteogenesis imperfecta murine model.

Authors:  Xiaomei Yao; Stephanie M Carleton; Arin D Kettle; Jennifer Melander; Charlotte L Phillips; Yong Wang
Journal:  Ann Biomed Eng       Date:  2013-03-28       Impact factor: 3.934

7.  RANKL inhibition improves bone properties in a mouse model of osteogenesis imperfecta.

Authors:  Renee Bargman; Alice Huang; Adele L Boskey; Cathleen Raggio; Nancy Pleshko
Journal:  Connect Tissue Res       Date:  2010-04       Impact factor: 3.417

8.  Quantitative second harmonic generation imaging of the diseased state osteogenesis imperfecta: experiment and simulation.

Authors:  Ronald Lacomb; Oleg Nadiarnykh; Paul J Campagnola
Journal:  Biophys J       Date:  2008-02-15       Impact factor: 4.033

9.  Effect of bisphosphonates on the rapidly growing male murine skeleton.

Authors:  Eric D Zhu; Leeann Louis; Daniel J Brooks; Mary L Bouxsein; Marie B Demay
Journal:  Endocrinology       Date:  2014-01-14       Impact factor: 4.736

10.  Alendronate treatment promotes bone formation with a less anisotropic microstructure during intramembranous ossification in rats.

Authors:  Masafumi Kashii; Jun Hashimoto; Takayoshi Nakano; Yukichi Umakoshi; Hideki Yoshikawa
Journal:  J Bone Miner Metab       Date:  2008-01-10       Impact factor: 2.626

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