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Influence of Statins locally applied from orthopedic implants on osseous integration

BACKGROUND: Simvastatin increases the expression of bone morphogenetic protein 2 (BMP-2) in osteoblasts, therefore it is important to investigate the influence of statins on bone formation, fracture healing and implant integration. The aim of the present study was to investigate the effect of Simvas...

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Autores principales: Pauly, Stephan, Back, David A, Kaeppler, Kathrin, Haas, Norbert P, Schmidmaier, Gerhard, Wildemann, Britt
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2012
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3495199/
https://www.ncbi.nlm.nih.gov/pubmed/23102098
http://dx.doi.org/10.1186/1471-2474-13-208
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author Pauly, Stephan
Back, David A
Kaeppler, Kathrin
Haas, Norbert P
Schmidmaier, Gerhard
Wildemann, Britt
author_facet Pauly, Stephan
Back, David A
Kaeppler, Kathrin
Haas, Norbert P
Schmidmaier, Gerhard
Wildemann, Britt
author_sort Pauly, Stephan
collection PubMed
description BACKGROUND: Simvastatin increases the expression of bone morphogenetic protein 2 (BMP-2) in osteoblasts, therefore it is important to investigate the influence of statins on bone formation, fracture healing and implant integration. The aim of the present study was to investigate the effect of Simvastatin, locally applied from intramedullary coated and bioactive implants, on bone integration using biomechanical and histomorphometrical analyses. METHODS: Eighty rats received retrograde nailing of the femur with titanium implants: uncoated vs. polymer-only (poly(D,L-lactide)) vs. polymer plus drug coated (either Simvastatin low- or high dosed; “SIM low/ high”). Femurs were harvested after 56 days for radiographic and histomorphometric or biomechanical analysis (push-out). RESULTS: Radiographic analysis revealed no pathological findings for animals of the control and SIM low dose group. However, n=2/10 animals of the SIM high group showed osteolysis next to the implant without evidence of bacterial infection determined by microbiological analysis. Biomechanical results showed a significant decrease in fixation strength for SIM high coated implants vs. the control groups (uncoated and PDLLA). Histomorphometry revealed a significantly reduced total as well as direct bone/implant contact for SIM high- implants vs. controls (uncoated and PDLLA-groups). Total contact was reduced for SIM low vs. uncoated controls. Significantly reduced new bone formation was measured around SIM high coated implants vs. both control groups. CONCLUSIONS: This animal study suggests impaired implant integration with local application of Simvastatin from intramedullary titanium implants after 8 weeks when compared to uncoated or carrier-only coated controls.
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spelling pubmed-34951992012-11-12 Influence of Statins locally applied from orthopedic implants on osseous integration Pauly, Stephan Back, David A Kaeppler, Kathrin Haas, Norbert P Schmidmaier, Gerhard Wildemann, Britt BMC Musculoskelet Disord Research Article BACKGROUND: Simvastatin increases the expression of bone morphogenetic protein 2 (BMP-2) in osteoblasts, therefore it is important to investigate the influence of statins on bone formation, fracture healing and implant integration. The aim of the present study was to investigate the effect of Simvastatin, locally applied from intramedullary coated and bioactive implants, on bone integration using biomechanical and histomorphometrical analyses. METHODS: Eighty rats received retrograde nailing of the femur with titanium implants: uncoated vs. polymer-only (poly(D,L-lactide)) vs. polymer plus drug coated (either Simvastatin low- or high dosed; “SIM low/ high”). Femurs were harvested after 56 days for radiographic and histomorphometric or biomechanical analysis (push-out). RESULTS: Radiographic analysis revealed no pathological findings for animals of the control and SIM low dose group. However, n=2/10 animals of the SIM high group showed osteolysis next to the implant without evidence of bacterial infection determined by microbiological analysis. Biomechanical results showed a significant decrease in fixation strength for SIM high coated implants vs. the control groups (uncoated and PDLLA). Histomorphometry revealed a significantly reduced total as well as direct bone/implant contact for SIM high- implants vs. controls (uncoated and PDLLA-groups). Total contact was reduced for SIM low vs. uncoated controls. Significantly reduced new bone formation was measured around SIM high coated implants vs. both control groups. CONCLUSIONS: This animal study suggests impaired implant integration with local application of Simvastatin from intramedullary titanium implants after 8 weeks when compared to uncoated or carrier-only coated controls. BioMed Central 2012-10-26 /pmc/articles/PMC3495199/ /pubmed/23102098 http://dx.doi.org/10.1186/1471-2474-13-208 Text en Copyright ©2012 Pauly et al.; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License ( http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research Article
Pauly, Stephan
Back, David A
Kaeppler, Kathrin
Haas, Norbert P
Schmidmaier, Gerhard
Wildemann, Britt
Influence of Statins locally applied from orthopedic implants on osseous integration
title Influence of Statins locally applied from orthopedic implants on osseous integration
title_full Influence of Statins locally applied from orthopedic implants on osseous integration
title_fullStr Influence of Statins locally applied from orthopedic implants on osseous integration
title_full_unstemmed Influence of Statins locally applied from orthopedic implants on osseous integration
title_short Influence of Statins locally applied from orthopedic implants on osseous integration
title_sort influence of statins locally applied from orthopedic implants on osseous integration
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3495199/
https://www.ncbi.nlm.nih.gov/pubmed/23102098
http://dx.doi.org/10.1186/1471-2474-13-208
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