Evidence map›Paper›PMID 20490372›Full record

ArticleInternational journal of clinical rheumatology2009

Potential implications of cell therapy for osteogenesis imperfecta.

Christopher Niyibizi, Feng Li

Abstract read
In one paragraph

Article in International journal of clinical rheumatology, 2009. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 18 papers.

0numbers the graph read from it
0cells of the map it votes in
18citing papers in PubMed
1.3field-weighted citation impact, top 18% 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

18 citing papers in PubMed, 32 citations in OpenAlex.

  1. Article
  2. Review
  3. Gene-repaired iPS cells as novel approach for patient withFrontiers in bioengineering and biotechnology · 2023
    Article
  4. Current Overview of Osteogenesis Imperfecta.Medicina (Kaunas, Lithuania) · 2021
    Review
  5. Article
  6. Article
  7. Article
  8. Article
  9. Review
  10. Autologous implantation of BMP2-expressing dermal fibroblasts to improve bone mineral density and architecture in rabbit long bones.Journal of orthopaedic research : official publication of the Orthopaedic Research Society · 2015
    Article
  11. Article
  12. Article
  13. Article
  14. Gene delivery to bone.Advanced drug delivery reviews · 2012
    Review
  15. Article
  16. Review
  17. The collagen family.Cold Spring Harbor perspectives in biology · 2011
    Review
  18. 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

2 authors.

Christopher Niyibizi
Feng Li

Funding

STEM CELL THERAPY FOR DISEASES OF BONE IN A MOUSE MODELR01AR049688 · NIAMS · UNIVERSITY OF PITTSBURGH AT PITTSBURGH · PI NIYIBIZI, CHRISTOPHER · 2002 to 2005
$1.3M
NIAMS NIH HHS R01 AR049688
6 · The paper itself

Abstract

Osteogenesis imperfecta (OI) is a brittle-bone disease whose hallmark is bone fragility. Since the disease is genetic, there is currently no available cure. Several pharmacological agents have been tried with not much success, except the recent use of bisphosphonates. Stem cells have been suggested as an alternative OI treatment, but many hurdles remain before this technology can be applied for treating patients with OI. This review summarizes what is known at present regarding the application of stem cells to treat OI using animal models, clinical trials using mesenchymal stem cells to treat patients with OI and the knowledge gained from the clinical trials. Application of gene therapy in combination with stem cells is also discussed. The hurdles to be overcome to bring stem cells close to the clinic and future perspectives are discussed.

Identifiers

PMID20490372
PMCPMC2873227
OpenAlexW1753915842

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.