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Stem cell therapies for periodontal tissue regeneration: A meta-analysis of clinical trials

OBJECTIVE: Stem cell therapy in periodontal tissue regeneration has reported optimistic regenerative results; evidence supporting its superiority over conventional methods is still ambiguous. Therefore, this meta-analysis aims to evaluate the therapeutic effects of stem cells in human periodontal re...

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Autores principales: Nguyen-Thi, Thuy-Duong, Nguyen-Huynh, Bao-Hung, Vo-Hoang, Thuy-Tien, Nguyen-Thanh, Tung
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10415796/
https://www.ncbi.nlm.nih.gov/pubmed/37576801
http://dx.doi.org/10.1016/j.jobcr.2023.07.001
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author Nguyen-Thi, Thuy-Duong
Nguyen-Huynh, Bao-Hung
Vo-Hoang, Thuy-Tien
Nguyen-Thanh, Tung
author_facet Nguyen-Thi, Thuy-Duong
Nguyen-Huynh, Bao-Hung
Vo-Hoang, Thuy-Tien
Nguyen-Thanh, Tung
author_sort Nguyen-Thi, Thuy-Duong
collection PubMed
description OBJECTIVE: Stem cell therapy in periodontal tissue regeneration has reported optimistic regenerative results; evidence supporting its superiority over conventional methods is still ambiguous. Therefore, this meta-analysis aims to evaluate the therapeutic effects of stem cells in human periodontal regeneration. DESIGN: A literature search was conducted to retrieve relevant articles on periodontal regeneration in stem cell therapy. A meta-analysis of the studies was conducted using the Stata software. RESULTS: Fifteen studies that examined the effect of stem cell therapies on periodontal tissue regeneration in 369 patients were selected from databases. Regardless of the various types of cells, both odontogenic (periodontal ligament, dental pulp, gingiva stem cell) and non-odontogenic (bone marrow, periosteum-derived, and umbilical cord stem cells), the cell therapies witnessed significant improvements in terms of clinical attachment level (SMD, −0.67; 95CI, −0.90 to −0.43), probing depth (SMD, −0.76; 95% CI, −1.21 to - 0.31), radiographic intrabony defect depth (SMD, −0.87; 95% CI, −1.52 to −0.23), and histomorphometric analysis of mineralized bone (SMD, 0.80; 95% CI, 0.42 to 1.19) when compared to traditional without-cell treatment in patients. However, evidence on gingival recession, alveolar thickness gain, bone mineral density of bone core, and bone volume fraction of bone core outcomes did not reach statistical significance. CONCLUSIONS: Evidence suggests that the implementation of stem cell therapies in reconstructing compromised gingiva and alveolar bone tissue produces positive outcomes compared with conventional approaches. However, further well-designed investigations are needed to comprehensively identify the most effective source of cells and biomaterials for each case.
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spelling pubmed-104157962023-08-12 Stem cell therapies for periodontal tissue regeneration: A meta-analysis of clinical trials Nguyen-Thi, Thuy-Duong Nguyen-Huynh, Bao-Hung Vo-Hoang, Thuy-Tien Nguyen-Thanh, Tung J Oral Biol Craniofac Res Article OBJECTIVE: Stem cell therapy in periodontal tissue regeneration has reported optimistic regenerative results; evidence supporting its superiority over conventional methods is still ambiguous. Therefore, this meta-analysis aims to evaluate the therapeutic effects of stem cells in human periodontal regeneration. DESIGN: A literature search was conducted to retrieve relevant articles on periodontal regeneration in stem cell therapy. A meta-analysis of the studies was conducted using the Stata software. RESULTS: Fifteen studies that examined the effect of stem cell therapies on periodontal tissue regeneration in 369 patients were selected from databases. Regardless of the various types of cells, both odontogenic (periodontal ligament, dental pulp, gingiva stem cell) and non-odontogenic (bone marrow, periosteum-derived, and umbilical cord stem cells), the cell therapies witnessed significant improvements in terms of clinical attachment level (SMD, −0.67; 95CI, −0.90 to −0.43), probing depth (SMD, −0.76; 95% CI, −1.21 to - 0.31), radiographic intrabony defect depth (SMD, −0.87; 95% CI, −1.52 to −0.23), and histomorphometric analysis of mineralized bone (SMD, 0.80; 95% CI, 0.42 to 1.19) when compared to traditional without-cell treatment in patients. However, evidence on gingival recession, alveolar thickness gain, bone mineral density of bone core, and bone volume fraction of bone core outcomes did not reach statistical significance. CONCLUSIONS: Evidence suggests that the implementation of stem cell therapies in reconstructing compromised gingiva and alveolar bone tissue produces positive outcomes compared with conventional approaches. However, further well-designed investigations are needed to comprehensively identify the most effective source of cells and biomaterials for each case. Elsevier 2023 2023-07-31 /pmc/articles/PMC10415796/ /pubmed/37576801 http://dx.doi.org/10.1016/j.jobcr.2023.07.001 Text en © 2023 The Authors https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).
spellingShingle Article
Nguyen-Thi, Thuy-Duong
Nguyen-Huynh, Bao-Hung
Vo-Hoang, Thuy-Tien
Nguyen-Thanh, Tung
Stem cell therapies for periodontal tissue regeneration: A meta-analysis of clinical trials
title Stem cell therapies for periodontal tissue regeneration: A meta-analysis of clinical trials
title_full Stem cell therapies for periodontal tissue regeneration: A meta-analysis of clinical trials
title_fullStr Stem cell therapies for periodontal tissue regeneration: A meta-analysis of clinical trials
title_full_unstemmed Stem cell therapies for periodontal tissue regeneration: A meta-analysis of clinical trials
title_short Stem cell therapies for periodontal tissue regeneration: A meta-analysis of clinical trials
title_sort stem cell therapies for periodontal tissue regeneration: a meta-analysis of clinical trials
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10415796/
https://www.ncbi.nlm.nih.gov/pubmed/37576801
http://dx.doi.org/10.1016/j.jobcr.2023.07.001
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