Evidence map›Paper›PMID 34080789›Full record

Trial reportStem cells translational medicine2021

Type 2 diabetes mellitus duration and obesity alter the efficacy of autologously transplanted bone marrow-derived mesenchymal stem/stromal cells.

Liem Thanh Nguyen, Duc M Hoang, Kien T Nguyen, Duc M Bui, Hieu T Nguyen, Hong T A Le, Van T Hoang, Hue T H Bui, Phuong T M Dam, Xuan T A Hoang and 11 more

Registry-linked trialOpen access · goldAbstract readRandomized Controlled Trial
In one paragraph

Trial report in Stem cells translational medicine, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT03343782 (Outcomes of Expanded Autologous Bone Marrow-derived Mesenchymal Stem Cells Therapy in Type 2 Diabetes), which is not on this map. Cited by 44 papers.

0numbers the graph read from it
0cells of the map it votes in
44citing papers in PubMed
5.8field-weighted citation impact, top 3% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

NCT03343782 phase1 / phase2completednot on this map

Outcomes of Expanded Autologous Bone Marrow-derived Mesenchymal Stem Cells Therapy in Type 2 Diabetes

TypeinterventionalSponsorVinmec Research Institute of Stem Cell and Gene TechnologyRan2017 to 2019Enrolled30ConditionsType 2 Diabetes MellitusArmsExpanded autologous bone marrow-derived mesenchymal stem cell
3 · Its place in the literature

Who cites it

44 citing papers in PubMed, 61 citations in OpenAlex.

  1. Trial
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  4. Review
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  8. Utilization of Stem Cells in Medicine: A Narrative Review.International journal of molecular sciences · 2025
    Review
  9. Article
  10. Advancements in diabetes research and stem cell therapy: a concise review.Journal of diabetes and metabolic disorders · 2025
    Review
  11. Article
  12. Article
  13. Review
  14. Review
  15. Article
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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

21 authors at 2 institutions in 2 countries.

Liem Thanh NguyenDepartment of Research and Development (R&D), Vinmec Research Institute of Stem Cell and Gene Technology, Vinmec Healthcare System, Hanoi, Vietnam.ORCID 0000-0002-4036-0161
Duc M HoangDepartment of Research and Development (R&D), Vinmec Research Institute of Stem Cell and Gene Technology, Vinmec Healthcare System, Hanoi, Vietnam.ORCID 0000-0001-5444-561X
Kien T NguyenDepartment of Research and Development (R&D), Vinmec Research Institute of Stem Cell and Gene Technology, Vinmec Healthcare System, Hanoi, Vietnam.
Duc M BuiDepartment of Internal Medicine, Vinmec Times City International Hospital, Hanoi, Vietnam.
Hieu T NguyenDepartment of Research and Development (R&D), Vinmec Research Institute of Stem Cell and Gene Technology, Vinmec Healthcare System, Hanoi, Vietnam.
Hong T A LeDepartment of Research and Development (R&D), Vinmec Research Institute of Stem Cell and Gene Technology, Vinmec Healthcare System, Hanoi, Vietnam.
Van T HoangDepartment of Research and Development (R&D), Vinmec Research Institute of Stem Cell and Gene Technology, Vinmec Healthcare System, Hanoi, Vietnam.
Hue T H BuiDepartment of Cellular Therapy, Vinmec High-Tech Center, Hanoi, Vietnam.
Phuong T M DamDepartment of Cellular Therapy, Vinmec High-Tech Center, Hanoi, Vietnam.
Xuan T A HoangDepartment of Research and Development (R&D), Vinmec Research Institute of Stem Cell and Gene Technology, Vinmec Healthcare System, Hanoi, Vietnam.
Anh T L NgoDepartment of Research and Development (R&D), Vinmec Research Institute of Stem Cell and Gene Technology, Vinmec Healthcare System, Hanoi, Vietnam.
Hang M LeDepartment of Cellular Therapy, Vinmec High-Tech Center, Hanoi, Vietnam.
Nhi Y PhungDepartment of Cellular Therapy, Vinmec High-Tech Center, Hanoi, Vietnam.
Duc M VuDepartment of Research and Development (R&D), Vinmec Research Institute of Stem Cell and Gene Technology, Vinmec Healthcare System, Hanoi, Vietnam.
Trung T DuongDepartment of Research and Development (R&D), Vinmec Research Institute of Stem Cell and Gene Technology, Vinmec Healthcare System, Hanoi, Vietnam.
Tu D NguyenDepartment of Cellular Therapy, Vinmec High-Tech Center, Hanoi, Vietnam.
Lien T HaDepartment of Medical Genetics, Vinmec High-Tech Center, Hanoi, Vietnam.
Hoa T P BuiDepartment of Medical Genetics, Vinmec High-Tech Center, Hanoi, Vietnam.
Hoa K NguyenDepartment of Research and Development (R&D), Vinmec Research Institute of Stem Cell and Gene Technology, Vinmec Healthcare System, Hanoi, Vietnam.
Michael HekeDepartment of Biology, Stanford University, Stanford, California, USA.
Anh V BuiDepartment of Cellular Therapy, Vinmec High-Tech Center, Hanoi, Vietnam.
Vinmec International Hospital · VNStanford University · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Human bone marrow-derived mesenchymal stem/stromal cells (BM-MSCs) represent promising stem cell therapy for the treatment of type 2 diabetes mellitus (T2DM), but the results of autologous BM-MSC administration in T2DM patients are contradictory. The purpose of this study was to test the hypothesis that autologous BM-MSC administration in T2DM patient is safe and that the efficacy of the treatment is dependant on the quality of the autologous BM-MSC population and administration routes. T2DM patients were enrolled, randomly assigned (1:1) by a computer-based system into the intravenous and dorsal pancreatic arterial groups. The safety was assessed in all the treated patients, and the efficacy was evaluated based on the absolute changes in the hemoglobin A1c, fasting blood glucose, and C-peptide levels throughout the 12-month follow-up. Our data indicated that autologous BM-MSC administration was well tolerated in 30 T2DM patients. Short-term therapeutic effects were observed in patients with T2DM duration of <10 years and a body mass index <23, which is in line with the phenotypic analysis of the autologous BM-MSC population. T2DM duration directly altered the proliferation rate of BM-MSCs, abrogated the glycolysis and mitochondria respiration of BM-MSCs, and induced the accumulation of mitochondria DNA mutation. Our data suggest that autologous administration of BM-MSCs in the treatment of T2DM should be performed in patients with T2DM duration <10 years and no obesity. Prior to further confirming the effects of T2DM on BM-MSC biology, future work with a larger cohort focusing on patients with different T2DM history is needed to understand the mechanism underlying our observation.

Indexed as

Diabetes Mellitus, Type 2Mesenchymal Stem CellsMesenchymal Stem Cell TransplantationBone MarrowBone Marrow CellsHumansObesityautologousautologous stem cell transplantationbone marrowdiabetes

Identifiers

PMID34080789
PMCPMC8380443
OpenAlexW3164868598

What Socratic holds

Textmetadata
LicenceCC BY-NC-ND
Read underepoch 390

Registered trials

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the Socratic graph.