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Mesenchymal stem cell implantation in atrophic nonunion of the long bones: A translational study

OBJECTIVES: To explore the therapeutic potential of combining bone marrow-derived mesenchymal stem cells (BM-MSCs) and hydroxyapatite (HA) granules to treat nonunion of the long bone. METHODS: Ten patients with an atrophic nonunion of a long bone fracture were selectively divided into two groups. Fi...

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Autores principales: Ismail, H.D., Phedy, P., Kholinne, E., Djaja, Y. P., Kusnadi, Y., Merlina, M., Yulisa, N. D.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4957179/
https://www.ncbi.nlm.nih.gov/pubmed/27412657
http://dx.doi.org/10.1302/2046-3758.57.2000587
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author Ismail, H.D.
Phedy, P.
Kholinne, E.
Djaja, Y. P.
Kusnadi, Y.
Merlina, M.
Yulisa, N. D.
author_facet Ismail, H.D.
Phedy, P.
Kholinne, E.
Djaja, Y. P.
Kusnadi, Y.
Merlina, M.
Yulisa, N. D.
author_sort Ismail, H.D.
collection PubMed
description OBJECTIVES: To explore the therapeutic potential of combining bone marrow-derived mesenchymal stem cells (BM-MSCs) and hydroxyapatite (HA) granules to treat nonunion of the long bone. METHODS: Ten patients with an atrophic nonunion of a long bone fracture were selectively divided into two groups. Five subjects in the treatment group were treated with the combination of 15 million autologous BM-MSCs, 5g/cm(3) (HA) granules and internal fixation. Control subjects were treated with iliac crest autograft, 5g/cm(3) HA granules and internal fixation. The outcomes measured were post-operative pain (visual analogue scale), level of functionality (LEFS and DASH), and radiograph assessment. RESULTS: Post-operative pain evaluation showed no significant differences between the two groups. The treatment group demonstrated faster initial radiographic and functional improvements. Statistically significant differences in functional scores were present during the first (p = 0.002), second (p = 0.005) and third (p = 0.01) month. Both groups achieved similar outcomes by the end of one-year follow-up. No immunologic or neoplastic side effects were reported. CONCLUSIONS: All cases of nonunion of a long bone presented in this study were successfully treated using autologous BM-MSCs. The combination of autologous BM-MSCs and HA granules is a safe method for treating nonunion. Patients treated with BM-MSCs had faster initial radiographic and functional improvements. By the end of 12 months, both groups had similar outcomes. Cite this article: H.D. Ismail, P. Phedy, E. Kholinne, Y. P. Djaja, Y. Kusnadi, M. Merlina, N. D. Yulisa. Mesenchymal stem cell implantation in atrophic nonunion of the long bones: A translational study. Bone Joint Res 2016;5:287–293. DOI: 10.1302/2046-3758.57.2000587.
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spelling pubmed-49571792016-08-03 Mesenchymal stem cell implantation in atrophic nonunion of the long bones: A translational study Ismail, H.D. Phedy, P. Kholinne, E. Djaja, Y. P. Kusnadi, Y. Merlina, M. Yulisa, N. D. Bone Joint Res Research OBJECTIVES: To explore the therapeutic potential of combining bone marrow-derived mesenchymal stem cells (BM-MSCs) and hydroxyapatite (HA) granules to treat nonunion of the long bone. METHODS: Ten patients with an atrophic nonunion of a long bone fracture were selectively divided into two groups. Five subjects in the treatment group were treated with the combination of 15 million autologous BM-MSCs, 5g/cm(3) (HA) granules and internal fixation. Control subjects were treated with iliac crest autograft, 5g/cm(3) HA granules and internal fixation. The outcomes measured were post-operative pain (visual analogue scale), level of functionality (LEFS and DASH), and radiograph assessment. RESULTS: Post-operative pain evaluation showed no significant differences between the two groups. The treatment group demonstrated faster initial radiographic and functional improvements. Statistically significant differences in functional scores were present during the first (p = 0.002), second (p = 0.005) and third (p = 0.01) month. Both groups achieved similar outcomes by the end of one-year follow-up. No immunologic or neoplastic side effects were reported. CONCLUSIONS: All cases of nonunion of a long bone presented in this study were successfully treated using autologous BM-MSCs. The combination of autologous BM-MSCs and HA granules is a safe method for treating nonunion. Patients treated with BM-MSCs had faster initial radiographic and functional improvements. By the end of 12 months, both groups had similar outcomes. Cite this article: H.D. Ismail, P. Phedy, E. Kholinne, Y. P. Djaja, Y. Kusnadi, M. Merlina, N. D. Yulisa. Mesenchymal stem cell implantation in atrophic nonunion of the long bones: A translational study. Bone Joint Res 2016;5:287–293. DOI: 10.1302/2046-3758.57.2000587. 2016-07-22 /pmc/articles/PMC4957179/ /pubmed/27412657 http://dx.doi.org/10.1302/2046-3758.57.2000587 Text en © 2016 Ismail et al. This is an open-access article distributed under the terms of the Creative Commons Attributions licence (CC-BY-NC), which permits unrestricted use, distribution, and reproduction in any medium, but not for commercial gain, provided the original author and source are credited.
spellingShingle Research
Ismail, H.D.
Phedy, P.
Kholinne, E.
Djaja, Y. P.
Kusnadi, Y.
Merlina, M.
Yulisa, N. D.
Mesenchymal stem cell implantation in atrophic nonunion of the long bones: A translational study
title Mesenchymal stem cell implantation in atrophic nonunion of the long bones: A translational study
title_full Mesenchymal stem cell implantation in atrophic nonunion of the long bones: A translational study
title_fullStr Mesenchymal stem cell implantation in atrophic nonunion of the long bones: A translational study
title_full_unstemmed Mesenchymal stem cell implantation in atrophic nonunion of the long bones: A translational study
title_short Mesenchymal stem cell implantation in atrophic nonunion of the long bones: A translational study
title_sort mesenchymal stem cell implantation in atrophic nonunion of the long bones: a translational study
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4957179/
https://www.ncbi.nlm.nih.gov/pubmed/27412657
http://dx.doi.org/10.1302/2046-3758.57.2000587
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