Recent non-placebo-control led 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 (similar to2 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 versus 1.6 +/- 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 ail 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 of should prove to be effective.
机构:
Univ Michigan, Dept Orthopaed Surg, Orthopaed Res Labs, Ann Arbor, MI 48109 USA
Univ Michigan, Dept Biomed Engn, Ann Arbor, MI 48109 USAUniv Michigan, Dept Orthopaed Surg, Orthopaed Res Labs, Ann Arbor, MI 48109 USA
Meganck, J. A.
Begun, D. L.
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Univ Michigan, Dept Orthopaed Surg, Orthopaed Res Labs, Ann Arbor, MI 48109 USA
Univ Michigan, Dept Biomed Engn, Ann Arbor, MI 48109 USAUniv Michigan, Dept Orthopaed Surg, Orthopaed Res Labs, Ann Arbor, MI 48109 USA
Begun, D. L.
McElderry, J. D.
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Univ Michigan, Dept Chem, Ann Arbor, MI 48109 USAUniv Michigan, Dept Orthopaed Surg, Orthopaed Res Labs, Ann Arbor, MI 48109 USA
McElderry, J. D.
Swick, A.
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Univ Michigan, Dept Orthopaed Surg, Orthopaed Res Labs, Ann Arbor, MI 48109 USA
Univ Michigan, Dept Biomed Engn, Ann Arbor, MI 48109 USAUniv Michigan, Dept Orthopaed Surg, Orthopaed Res Labs, Ann Arbor, MI 48109 USA
Swick, A.
Kozloff, K. M.
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Univ Michigan, Dept Orthopaed Surg, Orthopaed Res Labs, Ann Arbor, MI 48109 USA
Univ Michigan, Dept Biomed Engn, Ann Arbor, MI 48109 USAUniv Michigan, Dept Orthopaed Surg, Orthopaed Res Labs, Ann Arbor, MI 48109 USA
Kozloff, K. M.
Goldstein, S. A.
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Univ Michigan, Dept Orthopaed Surg, Orthopaed Res Labs, Ann Arbor, MI 48109 USA
Univ Michigan, Dept Biomed Engn, Ann Arbor, MI 48109 USAUniv Michigan, Dept Orthopaed Surg, Orthopaed Res Labs, Ann Arbor, MI 48109 USA
Goldstein, S. A.
Morris, M. D.
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Univ Michigan, Dept Chem, Ann Arbor, MI 48109 USAUniv Michigan, Dept Orthopaed Surg, Orthopaed Res Labs, Ann Arbor, MI 48109 USA
Morris, M. D.
Marini, J. C.
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NICHHD, Bone & Extracellular Matrix Branch, NIH, Bethesda, MD 20892 USAUniv Michigan, Dept Orthopaed Surg, Orthopaed Res Labs, Ann Arbor, MI 48109 USA
Marini, J. C.
Caird, M. S.
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Univ Michigan, Dept Orthopaed Surg, Orthopaed Res Labs, Ann Arbor, MI 48109 USAUniv Michigan, Dept Orthopaed Surg, Orthopaed Res Labs, Ann Arbor, MI 48109 USA
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Peking Union Med Coll Hosp CAMS & PUMC, Dept Endocrinol & Radiol, Beijing, Peoples R ChinaPeking Union Med Coll Hosp CAMS & PUMC, Dept Endocrinol & Radiol, Beijing, Peoples R China
Li, Mei
Xia, Wei-bo
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Peking Union Med Coll Hosp CAMS & PUMC, Dept Endocrinol & Radiol, Beijing, Peoples R ChinaPeking Union Med Coll Hosp CAMS & PUMC, Dept Endocrinol & Radiol, Beijing, Peoples R China
Xia, Wei-bo
Xing, Xiao-ping
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Peking Union Med Coll Hosp CAMS & PUMC, Dept Endocrinol & Radiol, Beijing, Peoples R ChinaPeking Union Med Coll Hosp CAMS & PUMC, Dept Endocrinol & Radiol, Beijing, Peoples R China
Xing, Xiao-ping
Yu, Wei
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Peking Union Med Coll Hosp CAMS & PUMC, Dept Endocrinol & Radiol, Beijing, Peoples R ChinaPeking Union Med Coll Hosp CAMS & PUMC, Dept Endocrinol & Radiol, Beijing, Peoples R China
Yu, Wei
Jiang, Yan
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Peking Union Med Coll Hosp CAMS & PUMC, Dept Endocrinol & Radiol, Beijing, Peoples R ChinaPeking Union Med Coll Hosp CAMS & PUMC, Dept Endocrinol & Radiol, Beijing, Peoples R China
Jiang, Yan
Wang, Ou
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Peking Union Med Coll Hosp CAMS & PUMC, Dept Endocrinol & Radiol, Beijing, Peoples R ChinaPeking Union Med Coll Hosp CAMS & PUMC, Dept Endocrinol & Radiol, Beijing, Peoples R China
Wang, Ou
Liu, Hai-juan
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Peking Union Med Coll Hosp CAMS & PUMC, Dept Endocrinol & Radiol, Beijing, Peoples R ChinaPeking Union Med Coll Hosp CAMS & PUMC, Dept Endocrinol & Radiol, Beijing, Peoples R China
Liu, Hai-juan
Han, Lan-wen
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Peking Union Med Coll Hosp CAMS & PUMC, Dept Endocrinol & Radiol, Beijing, Peoples R ChinaPeking Union Med Coll Hosp CAMS & PUMC, Dept Endocrinol & Radiol, Beijing, Peoples R China
Han, Lan-wen
Hu, Ying-ying
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Peking Union Med Coll Hosp CAMS & PUMC, Dept Endocrinol & Radiol, Beijing, Peoples R ChinaPeking Union Med Coll Hosp CAMS & PUMC, Dept Endocrinol & Radiol, Beijing, Peoples R China
Hu, Ying-ying
Meng, Xun-wu
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Peking Union Med Coll Hosp CAMS & PUMC, Dept Endocrinol & Radiol, Beijing, Peoples R ChinaPeking Union Med Coll Hosp CAMS & PUMC, Dept Endocrinol & Radiol, Beijing, Peoples R China