Abstract: Randomized and self-controlled study with anterior lumbar interbody fusion in a porcine model. Objective: To determine the osteoinductive potential of an equine bone protein extract in anterior interbody spinal fusion. Background: Interbody spinal fusion with bone graft transplantation is a common spine procedure. Complications related to bone graft harvesting are still a major concern. Equine demineralized bone matrix has been reported to be osteoinductive. However, the application of equine bone protein extract in spine fusion has not been documented. In this experiment, we evaluated equine bone protein extract in a porcine spinal fusion model. Methods: Due to their size and availability, we chose 12 normal Danish landrace pigs, each weighing 50 kg, as our experimental animals. Lumbar spine interbody fusion of L3/4, L4/5 using titanium alloy cages and pedicle screws instrumentation was performed on each pig. Cages packed with either autograft or equine bone protein extract (COLLOSS E; OSSACUR AG, Oberstenfeld, Germany) were randomly assigned to the 2 levels anteriorly. The pigs were followed for 3 months. After sacrifice, radiograph, microcomputed tomography, and histomorphometry were used to evaluate the spine segments. Results: All pigs went through the observation without major complications. Radiograph examination after 12 weeks revealed no implant breakage, loosening, or spinal deformity. Microcomputed tomography scanning showed that cages with COLLOSS E had the same fusion rate (11/12) as those with autograft. Three-dimensional evaluation from microcomputed tomography found a significant difference only in trabecular thickness; trabeculae from COLLOSS E-filled cages were much thinner (P = 0.04). Histologic evaluations demonstrated longitudinally formed bone trabeculae in both autograft and COLLOSS E-filled cages. Bone volume calculation from histomorphometry correlates well with that from microcomputed tomography results (R = 0.5; P = 0.01). Conclusions: In this porcine model, COLLOSS E is as effective as autograft for anterior spinal fusion.
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The research study uses a pig model to evaluate the use of equine bone protein extract for spinal fusion surgery. The results indicate that the equine bone protein, known as COLLOSS E, is as effective as traditional bone grafts in these procedures.
Objective and Background of the Study
The study seeks to analyze the osteoinductive (bone formation-enhancing) potential of an equine bone protein extract in anterior interbody spinal fusion surgery on a porcine (pig) model.
Existing surgical methods involve bone graft transplantation, which can have complications. The researchers theorize that using equine demineralized bone matrix, reported to be osteoinductive, may reduce these complications.
Research Methodology
Twelve normal Danish landrace pigs, each weighing 50 kg, were chosen for the study due to their size and availability.
Every pig underwent a lumbar spine interbody fusion involving levels L3/4 and L4/5 using titanium alloy cages and pedicle screws. The cages were packed with either an autograft or the equine bone protein extract (COLLOSS E), assigned randomly.
The pigs were monitored for three months before being sacrificed for evaluation. Their spine segments were analyzed through radiographs, microcomputed tomography, and histomorphometry (a method of measuring properties of bone).
Key Research Findings
No major complications were observed in any of the pigs. Radiographs recorded no implant breakage, loosening, or spinal deformity.
Microcomputed tomography scans showed that the fusion rate of cages filled with COLLOSS E was the same as those filled with autografts.
A statistically significant difference was noted in trabecular thickness with the COLLOSS E-filled cages containing much thinner trabeculae (bone structure).
Conclusion
Based on the experimental results from the study, the researchers concluded that the use of COLLOSS E (equine bone protein extract) is as effective as an autograft in anterior spinal fusion surgeries, shown in the porcine model. This opens up potential avenues for the mitigation of complications related to bone graft harvesting.
Cite This Article
APA
Li H, Zou X, Springer M, Briest A, Lind M, Bünger C.
(2007).
Instrumented anterior lumbar interbody fusion with equine bone protein extract.
Spine (Phila Pa 1976), 32(4), E126-E129.
https://doi.org/10.1097/01.brs.0000255210.67616.2b
Orthopaedic Research Laboratory, Orthopaedic Department E, Aarhus University Hospital, Aarhus, Denmark. haisheng.li@ki.au.dk
Zou, Xuenong
Springer, Marco
Briest, Arne
Lind, Martin
Bünger, Cody
MeSH Terms
Animals
Bone Morphogenetic Proteins / physiology
Bone Morphogenetic Proteins / therapeutic use
Bone Screws
Bone Transplantation / methods
Collagen / physiology
Collagen / therapeutic use
Female
Horses
Lumbar Vertebrae / diagnostic imaging
Lumbar Vertebrae / surgery
Models, Animal
Osteogenesis / physiology
Random Allocation
Spinal Fusion / methods
Swine
Tomography, X-Ray Computed
Transplantation, Autologous
Citations
This article has been cited 2 times.
Jensen J, Foldager CB, Jakobsen TV, Søballe K, Bünger C, Baas J. Use of carboxymethyl cellulose and collagen carrier with equine bone lyophilisate suggests late onset bone regenerative effect in a humerus drill defect - a pilot study in six sheep. Open Orthop J 2010 May 11;4:181-7.
Yoshizato H, Morimoto T, Nonaka T, Otani K, Kobayashi T, Nakashima T, Hirata H, Tsukamoto M, Mawatari M. Animal Model for Anterior Lumbar Interbody Fusion: A Literature Review. Spine Surg Relat Res 2024 Jul 27;8(4):373-382.