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Clinical Efficacy of Stem Cell Therapy for Diabetes Mellitus: A Meta-Analysis
BACKGROUND: Stem cell therapy is a promising therapeutic modality for advanced diabetes mellitus (DM). This study presents a meta-analysis of relevant clinical trials to determine the efficacy of stem cell therapy in DM. We aim to critically evaluate and synthesize clinical evidence on the safety an...
Autores principales: | , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Public Library of Science
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4830527/ https://www.ncbi.nlm.nih.gov/pubmed/27073927 http://dx.doi.org/10.1371/journal.pone.0151938 |
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author | El-Badawy, Ahmed El-Badri, Nagwa |
author_facet | El-Badawy, Ahmed El-Badri, Nagwa |
author_sort | El-Badawy, Ahmed |
collection | PubMed |
description | BACKGROUND: Stem cell therapy is a promising therapeutic modality for advanced diabetes mellitus (DM). This study presents a meta-analysis of relevant clinical trials to determine the efficacy of stem cell therapy in DM. We aim to critically evaluate and synthesize clinical evidence on the safety and efficiency of different types of stem cell therapy for both T1DM and T2DM. METHODS AND FINDINGS: We pooled participant-level data from twenty-two eligible clinical trials that satisfied our inclusion criteria, with a total of 524 patients. There were significant differences in the outcome based on the type and source of the infused cells. Out of all T1DM patients who received CD34(+) hematopoietic stem cell (HSC) infusion, 58.9% became insulin independent for a mean period of 16 months, whereas the results were uniformly negative in patients who received umbilical cord blood (UCB). Infusion of umbilical cord mesenchymal stem cells (UC-MSCs) provided significantly beneficial outcome in T1DM, when compared to bone-marrow mesenchymal stem cells (BM-MSCs) (P<0.0001 and P = 0.1557). Administration of stem cell therapy early after DM diagnosis was more effective than intervention at later stages (relative risk = 2.0, P = 0.0008). Adverse effects were observed in only 21.72% of both T1DM and T2DM stem cell recipients with no reported mortality. Out of all poor responders, 79.5% were diagnosed with diabetic ketoacidosis. CONCLUSIONS: Stem cell transplantation can represent a safe and effective treatment for selected patients with DM. In this cohort of trials, the best therapeutic outcome was achieved with CD34(+) HSC therapy for T1DM, while the poorest outcome was observed with HUCB for T1DM. Diabetic ketoacidosis impedes therapeutic efficacy. |
format | Online Article Text |
id | pubmed-4830527 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | Public Library of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-48305272016-04-22 Clinical Efficacy of Stem Cell Therapy for Diabetes Mellitus: A Meta-Analysis El-Badawy, Ahmed El-Badri, Nagwa PLoS One Research Article BACKGROUND: Stem cell therapy is a promising therapeutic modality for advanced diabetes mellitus (DM). This study presents a meta-analysis of relevant clinical trials to determine the efficacy of stem cell therapy in DM. We aim to critically evaluate and synthesize clinical evidence on the safety and efficiency of different types of stem cell therapy for both T1DM and T2DM. METHODS AND FINDINGS: We pooled participant-level data from twenty-two eligible clinical trials that satisfied our inclusion criteria, with a total of 524 patients. There were significant differences in the outcome based on the type and source of the infused cells. Out of all T1DM patients who received CD34(+) hematopoietic stem cell (HSC) infusion, 58.9% became insulin independent for a mean period of 16 months, whereas the results were uniformly negative in patients who received umbilical cord blood (UCB). Infusion of umbilical cord mesenchymal stem cells (UC-MSCs) provided significantly beneficial outcome in T1DM, when compared to bone-marrow mesenchymal stem cells (BM-MSCs) (P<0.0001 and P = 0.1557). Administration of stem cell therapy early after DM diagnosis was more effective than intervention at later stages (relative risk = 2.0, P = 0.0008). Adverse effects were observed in only 21.72% of both T1DM and T2DM stem cell recipients with no reported mortality. Out of all poor responders, 79.5% were diagnosed with diabetic ketoacidosis. CONCLUSIONS: Stem cell transplantation can represent a safe and effective treatment for selected patients with DM. In this cohort of trials, the best therapeutic outcome was achieved with CD34(+) HSC therapy for T1DM, while the poorest outcome was observed with HUCB for T1DM. Diabetic ketoacidosis impedes therapeutic efficacy. Public Library of Science 2016-04-13 /pmc/articles/PMC4830527/ /pubmed/27073927 http://dx.doi.org/10.1371/journal.pone.0151938 Text en © 2016 El-Badawy, El-Badri http://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited. |
spellingShingle | Research Article El-Badawy, Ahmed El-Badri, Nagwa Clinical Efficacy of Stem Cell Therapy for Diabetes Mellitus: A Meta-Analysis |
title | Clinical Efficacy of Stem Cell Therapy for Diabetes Mellitus: A Meta-Analysis |
title_full | Clinical Efficacy of Stem Cell Therapy for Diabetes Mellitus: A Meta-Analysis |
title_fullStr | Clinical Efficacy of Stem Cell Therapy for Diabetes Mellitus: A Meta-Analysis |
title_full_unstemmed | Clinical Efficacy of Stem Cell Therapy for Diabetes Mellitus: A Meta-Analysis |
title_short | Clinical Efficacy of Stem Cell Therapy for Diabetes Mellitus: A Meta-Analysis |
title_sort | clinical efficacy of stem cell therapy for diabetes mellitus: a meta-analysis |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4830527/ https://www.ncbi.nlm.nih.gov/pubmed/27073927 http://dx.doi.org/10.1371/journal.pone.0151938 |
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