Comparable outcomes in fracture reduction and bone properties with RANKL inhibition and alendronate treatment in a mouse model of osteogenesis imperfecta

被引:37
|
作者
Bargman, R. [1 ]
Posham, R. [2 ]
Boskey, A. L. [2 ]
DiCarlo, E. [2 ]
Raggio, C. [2 ]
Pleshko, N. [2 ,3 ]
机构
[1] NYPH Weill Cornell Med Ctr, New York, NY USA
[2] Hosp Special Surg, New York, NY 10021 USA
[3] Temple Univ, Philadelphia, PA 19122 USA
关键词
Alendronate; Mouse; oim/oim; Osteogenesis imperfecta; RANK/RANKL; RANK-Fc; 2 RAT MODELS; RECEPTOR ACTIVATOR; POSTMENOPAUSAL WOMEN; INDUCED ARTHRITIS; ZOLEDRONIC ACID; OSTEOPROTEGERIN; CHILDREN; PAMIDRONATE; RESORPTION; DENOSUMAB;
D O I
10.1007/s00198-011-1742-7
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
We report a direct comparison of receptor activator of nuclear factor kappa B ligand (RANKL) inhibition (RANK-Fc) with bisphosphonate treatment (alendronate, ALN) from infancy through early adulthood in a mouse model of osteogenesis imperfecta. Both ALN and RANK-Fc decreased fracture incidence to the same degree with increases in metaphyseal bone volume via increased number of thinner trabeculae. The potential therapeutic benefit of RANKL inhibitors in osteogenesis imperfecta (OI) is under investigation. We report a direct comparison of RANKL inhibition (RANK-Fc) with bisphosphonate treatment (ALN) from infancy through early adulthood in a model of OI, the oim/oim mouse. Two-week-old oim/oim, oim/+, and wildtype (+/+) mice were treated with RANK-Fc 1.5 mg/kg twice per week, ALN 0.21 mg/kg/week or saline (n = 12-20 per group) for 12 weeks. ALN and RANK-Fc both decreased fracture incidence (9.0 +/- 3.0 saline 4.4 +/- 2.7 ALN, 4.3 +/- 3.0 RANK-Fc fractures per mouse). Serum TRACP-5b activity decreased to 65% after 1 month in all treated mice, but increased sacrifice with RANK-Fc to 130-200% at sacrifice. Metaphyseal density was significantly increased with ALN in +/+ and oim/oim mice (p < 0.05) and tended to increase with RANK-Fc in +/+ mice. No changes in oim/oim femur biomechanical parameters occurred with treatment. Both ALN and RANK-Fc significantly increased trabecular number (3.73 +/- 0.77 1/mm for oim/oim saline vs 7.93 +/- 0.67 ALN and 7.34 +/- 1.38 RANK-Fc) and decreased trabecular thickness (0.045 mm +/- 0.003 for oim/oim saline vs 0.034 +/- 0.003 ALN and 0.032 +/- 0.002 RANK-Fc) and separation in all genotypes (0.28 +/- 0.08 mm for oim/oim saline vs 0.12 +/- 0.010 ALN and 13 +/- 0.03 RANK-Fc)., with significant increase in bone volume fraction (BVF) with ALN, and a trend towards increased BVF in RANK-Fc. Treatment of oim/oim mice with either a bisphosphonate or a RANK-Fc causes similar decreases in fracture incidence with increases in metaphyseal bone volume via increased number of thinner trabeculae.
引用
收藏
页码:1141 / 1150
页数:10
相关论文
共 50 条
  • [1] Comparable outcomes in fracture reduction and bone properties with RANKL inhibition and alendronate treatment in a mouse model of osteogenesis imperfecta
    R. Bargman
    R. Posham
    A. L. Boskey
    E. DiCarlo
    C. Raggio
    N. Pleshko
    Osteoporosis International, 2012, 23 : 1141 - 1150
  • [2] Comparable Effects of Strontium Ranelate and Alendronate Treatment on Fracture Reduction in a Mouse Model of Osteogenesis Imperfecta
    Shi, Changgui
    Sun, Bin
    Ma, Chao
    Wu, Huiqiao
    Chen, Rui
    He, Hailong
    Zhang, Ying
    BIOMED RESEARCH INTERNATIONAL, 2021, 2021
  • [3] RANKL Inhibition Improves Bone Properties in a Mouse Model of Osteogenesis Imperfecta
    Bargman, Renee
    Huang, Alice
    Boskey, Adele L.
    Raggio, Cathleen
    Pleshko, Nancy
    CONNECTIVE TISSUE RESEARCH, 2010, 51 (02) : 123 - 131
  • [4] The effects of RANKL inhibition on fracture healing and bone strength in a mouse model of osteogenesis imperfecta
    Delos, Demetris
    Yang, Xu
    Ricciardi, Benjamin F.
    Myers, Elizabeth R.
    Bostrom, Mathias P. G.
    Camacho, Nancy Pleshko
    JOURNAL OF ORTHOPAEDIC RESEARCH, 2008, 26 (02) : 153 - 164
  • [5] Fracture healing with alendronate treatment in the Brtl/ plus mouse model of osteogenesis imperfecta
    Meganck, J. A.
    Begun, D. L.
    McElderry, J. D.
    Swick, A.
    Kozloff, K. M.
    Goldstein, S. A.
    Morris, M. D.
    Marini, J. C.
    Caird, M. S.
    BONE, 2013, 56 (01) : 204 - 212
  • [6] Alendronate treatment for infants with osteogenesis imperfecta: Demonstration of efficacy in a mouse model
    McCarthy E.A.
    Raggio C.L.
    Hossack M.D.
    Miller E.A.
    Jain S.
    Boskey A.L.
    Camacho N.P.
    Pediatric Research, 2002, 52 (5) : 660 - 670
  • [7] Alendronate treatment for infants with osteogenesis imperfecta: Demonstration of efficacy in a mouse model
    McCarthy, EA
    Raggio, CL
    Hossack, MD
    Miller, EA
    Jain, S
    Boskey, AL
    Camacho, NP
    PEDIATRIC RESEARCH, 2002, 52 (05) : 660 - 670
  • [8] Osteogenesis imperfecta: The effect of alendronate treatment on the oim mouse model.
    Lau, ST
    Martin, RB
    Oberbauer, AM
    JOURNAL OF INVESTIGATIVE MEDICINE, 1998, 46 (01) : 93A - 93A
  • [9] BONE FRACTURE TREATMENT IN OSTEOGENESIS IMPERFECTA
    SCHWEIKE.CH
    WESSINGH.D
    RAHMANZA.R
    MONATSSCHRIFT FUR UKNFALLHEILKUNDE VERISCHERUNGS-VERSORUNGS-UND VERKEHRSMEDIZIN, 1969, 72 (09): : 371 - &
  • [10] The effect of alendronate on long bone growth and growth plate in the OIM mouse model for osteogenesis imperfecta
    Evans, KD
    Martin, RB
    Lau, ST
    Oberbauer, AM
    BONE, 2001, 28 (05) : S114 - S115