Publication:
EFFECTS OF OP-1 DEVICE ON A POSTEROLATERAL INTER-TRANSVERSE SPINAL FUSION MODEL IN OSTEOPOROTIC RATS

dc.contributor.author Lu, J. en_US
dc.contributor.author Wei, A-Q en_US
dc.contributor.author Bhargav, D. en_US
dc.contributor.author Diwan, Ashish en_US
dc.date.accessioned 2021-11-25T15:31:45Z
dc.date.available 2021-11-25T15:31:45Z
dc.date.issued 2006 en_US
dc.description.abstract Introduction The present experiment is undertaken to determine if a single dose addition of OP-1 device (rhBMP-7 and TCP-CMC) will enhance posterolateral spinal fusion in an osteoporotic rat mode (estrogen deficiency). Posterolateral intertransverse process spinal fusion using recombinant human osteogenic protein (rhBMP-7) was performed in ovariectomised female rats. OP-1 can be manipulated to enhance fusion rates and fracture healing with or without osteoporosis. Osteoporosis is characterised by low bone mass and micro-architectural deterioration of bone structure, resulting in bone fragility and an increase in susceptibility to fracture. Ovariectomised rats have been used as an osteoporotic model for posterolateral intertransverse process fusion in BMP experimental studies. Many studies have shown rhBMP-7 promotes spinal fusions in posterolateral fusion animal models. Not only is OP-1 able to promote spinal fusion in a standard animal model, but also it has been shown to overcome the inhibitory effects of nicotine in a rabbit posterolateral spinal fusion model. OP-1 Putty (Stryker) is an osteoinductive and osteoconductive bone graft material which consists of the recombinant human Osteogenic Protein (rhBMP-7), and TCP putty containing carboxymethylcellulose sodium (CMC) and tricalcium phosphate. This standard OP-1 device is somewhat different from the one Moazzaz et al used (1). The implication of OP-1 in osteoporotic model will open a new therapeutic window for osteoporotic or osteopaenial patients for the requirements of spinal fusion. Methods In present study, a total of 42 ovariectomised Sprague-Dawley female rats were randomly assigned to groups receiving 30 µg lactose + 400mg TCP-CMC, 90 µg lactose + 400 mg TCP-CMC, 30 µg rhBMP-7 + 400 mg TCP-CMC and 90 µg rhBMP-7 + 400 mg TCP-CMC. There was a group of rats receiving 400 mg TCP-CMC alone. Spinal fusion was evaluated by manual motion testing at each lumbar segment, Faxitron digital X-ray evaluation using the Lenke grading system, CT scans, DEXA scans and histology. Results Ovariectomized rats receiving 30 µg lactose + 400mg TCP-CMC, 90 µg lactose + 400 mg TCP-CMC, and 400 mg TCP-CMC alone did not show spinal fusion. OVX rats receiving 90 µg rhBMP-7 + 400 mg TCP-CMC showed significantly higher fusion rates than other groups (P <0.0001). However, the rats receiving 30 µg rhBMP-7 + 400 mg TCP-CMC did not show solid fusion either radiologically and histologically. Discussion Therefore rhBMP-7, in dose of 90 µg, is able to overcome the inhibitory effects of estrogen deficiency on posterolateral spinal fusion and generate a relatively robust fusion. The effect of the OP-1 on osteoporotic spine is dose-dependent with/without carrier-dependent. en_US
dc.description.uri http://www.spinesociety.org.au/ en_US
dc.identifier.uri http://hdl.handle.net/1959.4/44679
dc.language English
dc.language.iso EN en_US
dc.rights CC BY-NC-ND 3.0 en_US
dc.rights.uri https://creativecommons.org/licenses/by-nc-nd/3.0/au/ en_US
dc.source Legacy MARC en_US
dc.title EFFECTS OF OP-1 DEVICE ON A POSTEROLATERAL INTER-TRANSVERSE SPINAL FUSION MODEL IN OSTEOPOROTIC RATS en_US
dc.type Conference Paper en
dcterms.accessRights open access
dspace.entity.type Publication en_US
unsw.accessRights.uri https://purl.org/coar/access_right/c_abf2
unsw.description.publisherStatement Conference abstract en_US
unsw.identifier.doi https://doi.org/10.26190/unsworks/753
unsw.relation.faculty Medicine & Health
unsw.relation.ispartofconferenceLocation Sydney, Australia en_US
unsw.relation.ispartofconferenceName 2006 SPINE SOCIETY OF AUSTRALIA CONFERENCE en_US
unsw.relation.originalPublicationAffiliation Lu, J. en_US
unsw.relation.originalPublicationAffiliation Wei, A-Q en_US
unsw.relation.originalPublicationAffiliation Bhargav, D. en_US
unsw.relation.originalPublicationAffiliation Diwan, Ashish, Clinical School - St George Hospital, Faculty of Medicine, UNSW en_US
unsw.relation.school Clinical School St George Hospital *
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