Evidence map›Paper›PMID 22236028›Full record

ReviewEndocrine, metabolic & immune disorders drug targets2012

Emerging therapy for diabetic neuropathy: cell therapy targeting vessels and nerves.

Hyongbum Kim, Julie J Kim, Young-sup Yoon

Open access · bronzeAbstract readReview
In one paragraph

Review in Endocrine, metabolic & immune disorders drug targets, 2012. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 23 papers.

0numbers the graph read from it
0cells of the map it votes in
23citing papers in PubMed
1.4field-weighted citation impact, top 22% 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

23 citing papers in PubMed, 55 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Review
  5. Review
  6. Review
  7. Review
  8. Obstetric Neuropathy in Diabetic Patients: The "Double Hit Hypothesis".International journal of molecular sciences · 2023
    Review
  9. Blockage of MLKL prevents myelin damage in experimental diabetic neuropathy.Proceedings of the National Academy of Sciences of the United States of America · 2022
    Article
  10. Review
  11. Review
  12. Review
  13. Review
  14. Diabetic neuropathy.Nature reviews. Disease primers · 2019
    Article
  15. Article
  16. Advances in bone marrow stem cell therapy for retinal dysfunction.Progress in retinal and eye research · 2017
    Review
  17. Article
  18. Alternatives to the Streptozotocin-Diabetic Rodent.International review of neurobiology · 2016
    Review
  19. Review
  20. 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

3 authors at 2 institutions in 2 countries.

Hyongbum KimGraduate School of Biomedical Science and Engineering/College of Medicine, Hanyang University, Seoul, Korea.
Julie J Kim
Young-sup Yoon
Emory University · USHanyang University · KR

Funding

Cell therapy for diabetic peripheral neurovascular complicationsDP3DK094346 · NIDDK · EMORY UNIVERSITY · PI CHENG, XIAODONG, YOON, YOUNG-SUP · 2011 to 2011
$6.1M
Generation of Induced Pluripotent Stem Cells with Novel Small Molecule RegulatorRC1GM092035 · NIGMS · EMORY UNIVERSITY · PI CHENG, XIAODONG, YOON, YOUNG-SUP · 2010 to 2010
$1.0M
NHLBI NIH HHS HHSN268201000043CNIDDK NIH HHS DP3 DK094346NIDDK NIH HHS DP3DK094346NIGMS NIH HHS RC1 GM092035NIGMS NIH HHS RC1GM092035
6 · The paper itself

Abstract

Diabetic neuropathy (DN), the most common complication of diabetes, frequently leads to foot ulcers and may progress to limb amputations. Despite continuous increase in incidence, there is no clinical therapy to effectively treat DN. Pathogenetically, DN is characterized by reduced vascularity in peripheral nerves and deficiency in angiogenic and neurotrophic factors. We will briefly review the pathogenetic mechanism of DN and address the effects and the mechanisms of cell therapies for DN. To reverse the changes of DN, studies have attempted to deliver neurotrophic or angiogenic factors for treatment in the form of protein or gene therapy; however, the effects turned out to be very modest if not ineffective. Recent studies have demonstrated that bone marrow (BM)-derived cells such as mononuclear cells or endothelial progenitor cells (EPCs) can effectively treat various cardiovascular diseases through their paracrine effects. As BM-derived cells include multiple angiogenic and neurotrophic cytokines, these cells were used for treating experimental DN and found to reverse manifestations of DN. Particularly, EPCs were shown to exert favorable therapeutic effects through enhanced neural neovascularization and neuro-protective effects. These findings clearly indicate that DN is a complex disorder with pathogenetic involvement of both vascular and neural components. Studies have shown that cell therapies targeting both vascular and neural elements are shown to be advantageous in treating DN.

Indexed as

Stem Cell TransplantationAnimalsDiabetic AngiopathiesDiabetic NeuropathiesEndothelial CellsGenetic TherapyHumansMiceMonocytesNeovascularization, PhysiologicNerve Growth FactorsNervous SystemRatsNerve Growth Factors

Identifiers

PMID22236028
PMCPMC4598945
OpenAlexW2041587811

What OpenQuestion holds

Textmetadata
LicenceTDM
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 OpenQuestion graph.