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Peer-reviewed veterinary case report

rhBMP-7 injection does not repair disc degeneration in dogs

By Willems, Nicole et al.·Published in Arthritis research & therapy·2015·Department of Clinical Sciences of Companion Animals, Netherlands·View original on PubMed

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Original publication title: Intradiscal application of rhBMP-7 does not induce regeneration in a canine model of spontaneous intervertebral disc degeneration.

Species:
dog

Plain-English summary

A group of dogs with early intervertebral disc degeneration received injections of a protein called rhBMP-7 to see if it could help regenerate their damaged discs. Unfortunately, after six months of monitoring, none of the dogs showed any signs of improvement in their disc health. Instead, some dogs developed excessive bone growth outside the discs after receiving higher doses of the treatment. This means that rhBMP-7 injections are not effective for treating intervertebral disc degeneration in dogs.

People also search for: dog back pain treatment · intervertebral disc degeneration in dogs · rhBMP-7 for dogs · dog spinal injury recovery

Abstract

INTRODUCTION: Strategies for biological repair and regeneration of the intervertebral disc (IVD) by cell and tissue engineering are promising, but few have made it into a clinical setting. Recombinant human bone morphogenetic protein 7 (rhBMP-7) has been shown to stimulate matrix production by IVD cells in vitro and in vivo in animal models of induced IVD degeneration. The aim of this study was to determine the most effective dose of an intradiscal injection of rhBMP-7 in a spontaneous canine IVD degeneration model for translation into clinical application for patients with low back pain. METHODS: Canine nucleus pulposus cells (NPCs) were cultured with rhBMP-7 to assess the anabolic effect of rhBMP-7 in vitro, and samples were evaluated for glycosaminoglycan (GAG) and DNA content, histology, and matrix-related gene expression. Three different dosages of rhBMP-7 (2.5 μg, 25 μg, and 250 μg) were injected in vivo into early degenerated IVDs of canines, which were followed up for six months by magnetic resonance imaging (T2-weighted images, T1rho and T2 maps). Post-mortem, the effects of rhBMP-7 were determined by radiography, computed tomography, and macroscopy, and by histological, biochemical (GAG, DNA, and collagen), and biomolecular analyses of IVD tissue. RESULTS: In vitro, rhBMP-7 stimulated matrix production of canine NPCs as GAG deposition was enhanced, DNA content was maintained, and gene expression levels of ACAN and COL2A1 were significantly upregulated. Despite the wide dose range of rhBMP-7 (2.5 to 250 μg) administered in vivo, no regenerative effects were observed at the IVD level. Instead, extensive extradiscal bone formation was noticed after intradiscal injection of 25 μg and 250 μg of rhBMP-7. CONCLUSIONS: An intradiscal bolus injection of 2.5 μg, 25 μg, and 250 μg rhBMP-7 showed no regenerative effects in a spontaneous canine IVD degeneration model. In contrast, intradiscal injection of 250 μg rhBMP-7, and to a lesser extent 25 μg rhBMP-7, resulted in extensive extradiscal bone formation, indicating that a bolus injection of rhBMP-7 alone cannot be used for treatment of IVD degeneration in human or canine patients.

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Original publication on PubMed: https://pubmed.ncbi.nlm.nih.gov/26013758/