Literature DB >> 23561959

Efficacy and safety of autologous bone marrow-derived stem cell transplantation in patients with type 2 diabetes mellitus: a randomized placebo-controlled study.

Anil Bhansali, Premkumar Asokumar, Rama Walia, Shobhit Bhansali, Vivek Gupta, Ashish Jain, Naresh Sachdeva, Rati Ram Sharma, Neelam Marwaha, Niranjan Khandelwal.   

Abstract

There is a growing interest in cell-based therapies in T2DM as β-cell failure is progressive and inexorable with the advancing duration of disease. This prospective, randomized, single-blinded placebo-controlled study evaluates the efficacy and safety of autologous bone marrow-derived stem cell transplantation (ABMSCT) in T2DM. Twenty-one patients with triple oral antidiabetic drug failure and requiring insulin ≥0.4 IU per kg per day with HbA1c <7.5% were randomly assigned to an intervention (n = 11) and control group (n = 10) and followed for 12 months. Patients in the intervention group received ABMSCT through a targeted approach, and after 12 weeks, a second dose of stem cells was administered through the antecubital vein after mobilization with G-CSF, while the control group underwent a sham procedure. The primary end point was a reduction in insulin requirement by ≥50% from baseline while maintaining HbA1c <7%. Nine out of the 11 (82%) patients in the intervention group achieved the primary end point, whereas none of the patients in the control group did over the study period (p = 0.002). The insulin requirement decreased by 66.7% in the intervention group from 42.0 (31.0‐64.0) IU per day to 14.0 (0.0‐30.0) IU per day (p = 0.011), while in controls it decreased by 32.1% from 40.5 (31.8‐44.3) IU per day to 27.5 (23.5‐33.3) IU per day (p = 0.008) at 12 months. The reduction in insulin requirement was significantly more in the intervention group compared to controls at both 6 (p = 0.001) and 12 months (p = 0.004). There was a modest but nonsignificant increase in HbA1c (%) in cases from 6.9% (6.4‐7.2%) to 7.1% (6.6‐7.5%) as well as in controls from 6.9% (6.2‐7.0%) to 7.0% (6.9‐7.5%). Ten out of 11 (91%) patients could maintain HbA1c <7% in the intervention group, whereas 6 out of 10 did (60%) in the control group (p = 0.167). The glucagon-stimulated C-peptide significantly increased in treated cases compared to controls (p = 0.036). The decrease in insulin requirement positively correlated with stimulated C-peptide (r = 0.8, p = 0.001). In conclusion, ABMSCT results in a significant decrease in the insulin dose requirement along with an improvement in the stimulated C-peptide levels in T2DM. However, a greater number of patients with a longer duration of follow-up are required to substantiate these observations.

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Year:  2014        PMID: 23561959     DOI: 10.3727/096368913X665576

Source DB:  PubMed          Journal:  Cell Transplant        ISSN: 0963-6897            Impact factor:   4.064


  42 in total

Review 1.  A review of clinical trials: mesenchymal stem cell transplant therapy in type 1 and type 2 diabetes mellitus.

Authors:  Jang Cho; Matthew D'Antuono; Michael Glicksman; Jing Wang; Jacqueline Jonklaas
Journal:  Am J Stem Cells       Date:  2018-10-01

2.  Bone marrow derived stem cell therapy for type 2 diabetes mellitus.

Authors:  Tarek Wehbe; Nassim Abi Chahine; Salam Sissi; Isabelle Abou-Joaude; Louis Chalhoub
Journal:  Stem Cell Investig       Date:  2016-12-06

Review 3.  Current progress of human trials using stem cell therapy as a treatment for diabetes mellitus.

Authors:  Shuk Kei Cheng; Elisse Y Park; Andjela Pehar; Alexandra C Rooney; G Ian Gallicano
Journal:  Am J Stem Cells       Date:  2016-10-20

4.  Cortical bone laminar analysis reveals increased midcortical and periosteal porosity in type 2 diabetic postmenopausal women with history of fragility fractures compared to fracture-free diabetics.

Authors:  U Heilmeier; K Cheng; C Pasco; R Parrish; J Nirody; J M Patsch; C A Zhang; G B Joseph; A J Burghardt; A V Schwartz; T M Link; G Kazakia
Journal:  Osteoporos Int       Date:  2016-05-06       Impact factor: 4.507

5.  IFN-γ and TNF-α Pre-licensing Protects Mesenchymal Stromal Cells from the Pro-inflammatory Effects of Palmitate.

Authors:  Lauren Boland; Anthony J Burand; Alex J Brown; Devlin Boyt; Vitor A Lira; James A Ankrum
Journal:  Mol Ther       Date:  2017-12-19       Impact factor: 11.454

6.  Human placental mesenchymal stromal cell therapy restores the cytokine efflux and insulin signaling in the skeletal muscle of obesity-induced type 2 diabetes rat model.

Authors:  Nagasuryaprasad Kotikalapudi; Samuel Joshua Pragasam Sampath; Sukesh Narayan Sinha; R Bhonde; Sathish Kumar Mungamuri; Vijayalakshmi Venkatesan
Journal:  Hum Cell       Date:  2022-01-29       Impact factor: 4.174

7.  Phenotypic, trophic, and regenerative properties of mesenchymal stem cells from different osseous tissues.

Authors:  Douhong Zou; Marina Vigen; Andrew J Putnam; Chen Cao; Susan A Tarlé; Tyler Guinn; Darnell Kaigler
Journal:  Cell Tissue Res       Date:  2022-01-14       Impact factor: 4.051

Review 8.  Bone Marrow Stromal Stem Cells in Tissue Engineering and Regenerative Medicine.

Authors:  A Polymeri; W V Giannobile; D Kaigler
Journal:  Horm Metab Res       Date:  2016-11-21       Impact factor: 2.788

9.  Stem cell therapy for patients with diabetes: a systematic review and meta-analysis of metabolomics-based risks and benefits.

Authors:  Fakher Rahim; Babak Arjmand; Kiarash Shirbandi; Moloud Payab; Bagher Larijani
Journal:  Stem Cell Investig       Date:  2018-11-14

10.  Impact of Syndecan-2-Selected Mesenchymal Stromal Cells on the Early Onset of Diabetic Cardiomyopathy in Diabetic db/db Mice.

Authors:  Kathleen Pappritz; Fengquan Dong; Kapka Miteva; Arpad Kovacs; Muhammad El-Shafeey; Bahtiyar Kerim; Lisa O'Flynn; Stephen Joseph Elliman; Timothy O'Brien; Nazha Hamdani; Carsten Tschöpe; Sophie Van Linthout
Journal:  Front Cardiovasc Med       Date:  2021-05-21
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