Please use this identifier to cite or link to this item: https://dora.health.qld.gov.au/qldresearchjspui/handle/1/2349
Title: Combination treatment with growth hormone and zoledronic acid in a mouse model of Osteogenesis imperfecta
Authors: Cheng, T. L.
Little, D. G.
Munns, C. F.
Biggin, A.
Schindeler, A.
Lee, L. R.
Holman, A. E.
Li, X.
Vasiljevski, E. R.
O'Donohue, A. K.
Issue Date: 2022
Source: 159 , 2022
Journal: Bone
Abstract: Introduction: Osteogenesis imperfecta (OI) or brittle bone disease is a genetic disorder that results in bone fragility. Bisphosphonates such as zoledronic acid (ZA) are used clinically to increase bone mass and reduce fracture risk. Human growth hormone (hGH) has been used to promote long bone growth and forestall short stature in children with OI. The potential for hGH to improve bone quality, particularly in combination with ZA has not been robustly studied. Methods: A preclinical study was performed using n = 80 mice split evenly by genotype (WT, Col1a2+/G610C). Groups of n = 10 were treated with +/−ZA and +/−hGH in a factorial design for each genotype. Outcome measures included bone length, isolated muscle mass, bone parameters assessed by microCT analysis, dynamic histomorphometry, and biomechanical testing. Results: Treatment with hGH alone led to an increase in femur length in WT but not OI mice, however bone length was increased in both genotypes with the combination of hGH/ZA. MicroCT showed that hGH/ZA treatment increased cortical BV in both WT (+15%) and OI mice (+14.3%); hGH/ZA were also found to be synergistic in promoting cortical thickness in OI bone. ZA was found to have a considerably greater positive impact on trabecular bone than hGH. ZA was found to suppress bone turnover, and this was rescued by hGH treatment in terms of cortical periosteal perimeter, but not by dynamic bone remodeling. Statistically significant improvements in long bone by microCT did not translate into improvements in mechanical strength in a 4-point bending test, nor did vertebral strength improve in L4 compression testing in WT/OI bone. Discussion/Conclusion: These data support hGH/ZA combination as a treatment for short stature, however the improvements granted by hGH alone and in combination with ZA on bone quality are modest. Increased periosteal perimeter does show promise in improving bone strength in OI, however a longer treatment time may be required to see effects on bone strength through mechanical testing.L20171501212022-03-11
2022-03-15
DOI: 10.1016/j.bone.2022.116378
Resources: https://www.embase.com/search/results?subaction=viewrecord&id=L2017150121&from=exporthttp://dx.doi.org/10.1016/j.bone.2022.116378 |
Keywords: in vitro study;long bone;male;micro-computed tomography;morphometry;mouse;muscle growth;muscle mass;nonhuman;osteogenesis imperfecta;outcome assessment;periosteum;phenotype;synergistic effect;trabecular bone;bisphosphonic acid derivativehuman growth hormone;zoledronic acid;animal genetics;animal husbandry;article;biomechanics;bone length;bone mineralization;bone quality;bone remodeling;bone strength;bone turnover;cohort analysis;collagen fiber;controlled study;cortical thickness (bone);drug effect;female;femur length;genetic variation;genotype;Gly610Cys gene
Type: Article
Appears in Sites:Children's Health Queensland Publications

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