Evidence mapPaperPMID 37817652Full record

ReviewCurrent stem cell research & therapy2024

Mesenchymal Stem Cell Transplantation in Type 1 Diabetes Treatment: Current Advances and Future Opportunity.

Jie Liu, Xin-Xing Wan, Sheng-Yuan Zheng, Md Asaduzzaman Khan, Hui-Hong He, Yu-Xing Feng, Jing-Ge Xiao, Yu Chen, Xi-Min Hu, Qi Zhang and 1 more

Abstract readReview
PubMed Publisher
In one paragraph

Review in Current stem cell research & therapy, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed
1.6field-weighted citation impact, top 16% 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.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

4 citing papers in PubMed, 5 citations in OpenAlex.

  1. Review
  2. Review
  3. Article
  4. Article
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

11 authors at 2 institutions in 2 countries.

Jie LiuDepartment of Endocrinology, Third Xiangya Hospital, Central South University, Changsha, 410013, China.ORCID 0009-0000-3138-4025
Xin-Xing WanDepartment of Endocrinology, Third Xiangya Hospital, Central South University, Changsha, 410013, China.
Sheng-Yuan ZhengClinical Medicine Eight-year Program, 19 Grade, Xiangya School of Medicine, Central South University, Changsha, 410013, China.
Md Asaduzzaman KhanNature Study Society of Bangladesh, Dhaka, 1000, Bangladesh.
Hui-Hong HeDepartment of Endocrinology, Third Xiangya Hospital, Central South University, Changsha, 410013, China.
Yu-Xing FengClinical Medicine Eight-year Program, 19 Grade, Xiangya School of Medicine, Central South University, Changsha, 410013, China.
Jing-Ge XiaoClinical Medicine Eight-year Program, 19 Grade, Xiangya School of Medicine, Central South University, Changsha, 410013, China.
Yu ChenClinical Medicine Eight-year Program, 19 Grade, Xiangya School of Medicine, Central South University, Changsha, 410013, China.
Xi-Min HuClinical Medicine Eight-year Program, 17 Grade, Xiangya School of Medicine, Central South University, Changsha, 410013, China.
Qi ZhangDepartment of Anatomy and Neurobiology, School of Basic Medical Science, Central South University, Changsha, 410013, China.
Kun XiongDepartment of Anatomy and Neurobiology, School of Basic Medical Science, Central South University, Changsha, 410013, China.
Central South University · CNBangladesh Academy of Sciences · BD

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Type 1 Diabetes (T1D) is characterized by hyperglycemia, and caused by a lack of insulin secretion. At present there is no cure for T1D and patients are dependent on exogenous insulin for lifelong, which seriously affects their lives. Mesenchymal stem cells (MSCs) can be differentiated to β cell-like cells to rescue the secretion of insulin and reconstruct immunotolerance to preserve the function of islet β cells. Due to the higher proportion of children and adolescents in T1D patients, the efficacy and safety issue of the application of MSC's transplant in T1D was primarily demonstrated and identified by human clinical trials in this review. Then we clarified the mechanism of MSCs to relieve the symptom of T1D and found out that UC-MSCs have no obvious advantage over the other types of MSCs, the autologous MSCs from BM or menstrual blood with less expanded ex vivo could be the better choice for clinical application to treat with T1D through documentary analysis. Finally, we summarized the advances of MSCs with different interventions such as genetic engineering in the treatment of T1D, and demonstrated the advantages and shortage of MSCs intervened by different treatments in the transplantation, which may enhance the clinical efficacy and overcome the shortcomings in the application of MSCs to T1D in future.

Indexed as

Diabetes Mellitus, Type 1Mesenchymal Stem CellsMesenchymal Stem Cell TransplantationAnimalsCell DifferentiationHumansInsulin-Secreting Cellsgenetic engineeringmenstrual blood.mesenchymal stem cellsMSCsT1Dtransplant

Identifiers

PMID37817652
OpenAlexW4387516141

What Socratic holds

Textmetadata
Read underepoch 390

Registered trials

None linked

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.