Literature DB >> 32355628

A Comparative Evaluation of Commercially Available Cell-Based Allografts in a Rat Spinal Fusion Model.

Brian Johnstone1, Nianli Zhang2, Erik I Waldorff2, Eric Semler3, Anouska Dasgupta3, Marcel Betsch1, Paolo Punsalan1, Holly Cho1, James T Ryaby2, Jung Yoo1.   

Abstract

BACKGROUND: To evaluate the comparative abilities of commercially available, viable, cellular bone allografts to promote posterolateral spinal fusion.
METHODS: Human allografts containing live cells were implanted in the athymic rat model of posterolateral spine fusion. Three commercially available allogeneic cellular bone matrices (Trinity Evolution, Trinity ELITE and Osteocel Plus) were compared with syngeneic iliac crest bone as the control. All spines underwent radiographs, manual palpation, and micro-computed tomography (CT) analysis after excision at 6 weeks. Histological sections of randomly selected spines were subjected to semiquantitative histopathological scoring for bone formation.
RESULTS: By manual palpation, posterolateral fusion was detected in 40% (6/15) of spines implanted with syngeneic bone, whereas spines implanted with Trinity Evolution and Trinity ELITE allografts yielded 71% (10/14) and 77% (10/13) fusion, respectively. Only 7% (1/14) of spines implanted with Osteocel Plus allografts were judged fused by manual palpation (statistically significantly less than ELITE, P < .0007, and Evolution, P < .0013). The mineralized cancellous bone component of the allografts confounded radiographic analysis, but Trinity Evolution (0.452 ± 0.064) and Trinity ELITE (0.536 ± 0.109) allografts produced statistically significantly higher bone fusion mass volumes measured by quantitative micro-CT than did syngeneic bone (0.292 ± 0.109, P < .0001 for ELITE and P < .003 for Evolution) and Osteocel Plus (0.258 ± 0.103, P < .0001). Semiquantitative histopathological scores supported these findings because the total bone and bone marrow scores reflected significantly better new bone and marrow formation in the Trinity groups than in the Osteocel Plus group.
CONCLUSIONS: The Trinity Evolution and Trinity ELITE cellular bone allografts were more effective at creating posterolateral fusion than either the Osteocel Plus allografts or syngeneic bone in this animal model. CLINICAL RELEVANCE: The superior fusion rate of Trinity cellular bone allografts may lead to better clinical outcome of spinal fusion surgeries. ©International Society for the Advancement of Spine Surgery 2020.

Entities:  

Keywords:  Osteocel Plus; Posterolateral spine fusion; Trinity ELITE; Trinity Evolution; allograft; athymic rat; stem cells

Year:  2020        PMID: 32355628      PMCID: PMC7188100          DOI: 10.14444/7026

Source DB:  PubMed          Journal:  Int J Spine Surg        ISSN: 2211-4599


  17 in total

1.  A comparison of commercially available demineralized bone matrix for spinal fusion.

Authors:  Jeffrey C Wang; A Alanay; Davies Mark; Linda E A Kanim; Pat A Campbell; Edgar G Dawson; Jay R Lieberman
Journal:  Eur Spine J       Date:  2007-01-05       Impact factor: 3.134

2.  Harvesting autogenous iliac bone grafts. A review of complications and techniques.

Authors:  L T Kurz; S R Garfin; R E Booth
Journal:  Spine (Phila Pa 1976)       Date:  1989-12       Impact factor: 3.468

Review 3.  Graft options in posterolateral and posterior interbody lumbar fusion.

Authors:  Jeffrey A Rihn; Kelly Kirkpatrick; Todd J Albert
Journal:  Spine (Phila Pa 1976)       Date:  2010-08-01       Impact factor: 3.468

Review 4.  Cellular bone matrices: viable stem cell-containing bone graft substitutes.

Authors:  Branko Skovrlj; Javier Z Guzman; Motasem Al Maaieh; Samuel K Cho; James C Iatridis; Sheeraz A Qureshi
Journal:  Spine J       Date:  2014-06-11       Impact factor: 4.166

5.  Augmentation of spinal arthrodesis with autologous bone marrow in a rabbit posterolateral spine fusion model.

Authors:  L J Curylo; B Johnstone; C A Petersilge; J A Janicki; J U Yoo
Journal:  Spine (Phila Pa 1976)       Date:  1999-03-01       Impact factor: 3.468

6.  Lumbar spine fusion by local gene therapy with a cDNA encoding a novel osteoinductive protein (LMP-1).

Authors:  S D Boden; L Titus; G Hair; Y Liu; M Viggeswarapu; M S Nanes; C Baranowski
Journal:  Spine (Phila Pa 1976)       Date:  1998-12-01       Impact factor: 3.468

7.  Accuracy and interobserver agreement for determinations of rabbit posterolateral spinal fusion.

Authors:  Albert Juang Ming Yee; Hyun W Bae; Darin Friess; Mark Robbin; Brian Johnstone; Jung U Yoo
Journal:  Spine (Phila Pa 1976)       Date:  2004-06-15       Impact factor: 3.468

8.  The role of Osteocel Plus as a fusion substrate in minimally invasive instrumented transforaminal lumbar interbody fusion.

Authors:  Joshua M Ammerman; Joseph Libricz; Matthew D Ammerman
Journal:  Clin Neurol Neurosurg       Date:  2012-11-20       Impact factor: 1.876

9.  Allograft cellular bone matrix in extreme lateral interbody fusion: preliminary radiographic and clinical outcomes.

Authors:  Antoine G Tohmeh; Blake Watson; Mirna Tohmeh; Xavier J Zielinski
Journal:  ScientificWorldJournal       Date:  2012-12-02

10.  Determining a clinically relevant strategy for bone tissue engineering: an "all-in-one" study in nude mice.

Authors:  Pierre Corre; Christophe Merceron; Caroline Vignes; Sophie Sourice; Martial Masson; Nicolas Durand; Florent Espitalier; Paul Pilet; Thomas Cordonnier; Jacques Mercier; Séverine Remy; Ignacio Anegon; Pierre Weiss; Jérôme Guicheux
Journal:  PLoS One       Date:  2013-12-11       Impact factor: 3.240

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