Evidence map›Paper›PMID 26445383›Full record

ArticleJournal of orthopaedic research : official publication of the Orthopaedic Research Society2016

Effect of adipose-derived stromal cells and BMP12 on intrasynovial tendon repair: A biomechanical, biochemical, and proteomics study.

Richard H Gelberman, Hua Shen, Ioannis Kormpakis, Benjamin Rothrauff, Guang Yang, Rocky S Tuan, Younan Xia, Shelly Sakiyama-Elbert, Matthew J Silva, Stavros Thomopoulos

Open access · bronzeAbstract readEvaluation Study
In one paragraph

Article in Journal of orthopaedic research : official publication of the Orthopaedic Research Society, 2016. 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
3.5field-weighted citation impact, top 8% 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, 40 citations in OpenAlex.

  1. Review
  2. Article
  3. Review
  4. Review
  5. Review
  6. Growth Differentiation Factor 7 Prevents Sepsis-Induced Acute Lung Injury in Mice.Evidence-based complementary and alternative medicine : eCAM · 2022
    Article
  7. Review
  8. Article
  9. Review
  10. Tendon and Ligament Healing and Current Approaches to Tendon and Ligament Regeneration.Journal of orthopaedic research : official publication of the Orthopaedic Research Society · 2020
    Review
  11. Stem cell-derived extracellular vesicles attenuate the early inflammatory response after tendon injury and repair.Journal of orthopaedic research : official publication of the Orthopaedic Research Society · 2020
    Article
  12. CTGF induces tenogenic differentiation and proliferation of adipose-derived stromal cells.Journal of orthopaedic research : official publication of the Orthopaedic Research Society · 2019
    Article
  13. Article
  14. Article
  15. Article
  16. Article
  17. Effect of connective tissue growth factor delivered via porous sutures on the proliferative stage of intrasynovial tendon repair.Journal of orthopaedic research : official publication of the Orthopaedic Research Society · 2018
    Article
  18. 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

10 authors at 4 institutions in 1 country.

Richard H GelbermanDepartment of Orthopaedic Surgery, Washington University, St. Louis, Missouri.
Hua ShenDepartment of Orthopaedic Surgery, Washington University, St. Louis, Missouri.
Ioannis KormpakisDepartment of Orthopaedic Surgery, Washington University, St. Louis, Missouri.
Benjamin RothrauffDepartment of Orthopaedic Surgery, Center for Cellular and Molecular Engineering, University of Pittsburgh School of Medicine, Pittsburgh, Pennsylvania.
Guang YangDepartment of Orthopaedic Surgery, Center for Cellular and Molecular Engineering, University of Pittsburgh School of Medicine, Pittsburgh, Pennsylvania.
Rocky S TuanDepartment of Orthopaedic Surgery, Center for Cellular and Molecular Engineering, University of Pittsburgh School of Medicine, Pittsburgh, Pennsylvania.
Younan XiaThe Wallace H. Coulter Department of Biomedical Engineering, School of Chemistry and Biochemistry, School of Chemical and Biomolecular Eng., Georgia Inst. of Tech., Atlanta, Georgia.
Shelly Sakiyama-ElbertDepartment of Biomedical Engineering, Washington University, St. Louis, Missouri.
Matthew J SilvaDepartment of Orthopaedic Surgery, Washington University, St. Louis, Missouri.
Stavros ThomopoulosDepartment of Orthopedic Surgery, Columbia University, New York, New York.
Washington University in St. Louis · USUniversity of Pittsburgh · USColumbia University · USThe Wallace H. Coulter Department of Biomedical Engineering · US

Funding

Washington University Center for Cellular ImagingP30CA091842 · NCI · WASHINGTON UNIVERSITY · PI AIMEE S JAMES · 2001 to 2026
$128.0M
The Role of the Osteoblast Secretome in Bone FormationP30AR057235 · NIAMS · WASHINGTON UNIVERSITY · PI SILVA, MATTHEW J · 2009 to 2018
$5.7M
Enhanced Tendon Healing Through Growth Factor and Cell TherapiesR01AR062947 · NIAMS · WASHINGTON UNIVERSITY · PI GELBERMAN, RICHARD H, THOMOPOULOS, STAVROS · 2012 to 2022
$5.5M
NCI NIH HHS P30 CA091842NCI NIH HHS P30 CA91842NIAMS NIH HHS P30 AR057235NIAMS NIH HHS R01 AR06294NIAMS NIH HHS R01 AR062947
6 · The paper itself

Abstract

The outcomes of flexor tendon repair are highly variable. As recent efforts to improve healing have demonstrated promise for growth factor- and cell-based therapies, the objective of the current study was to enhance repair via application of autologous adipose derived stromal cells (ASCs) and the tenogenic growth factor bone morphogenetic protein (BMP) 12. Controlled delivery of cells and growth factor was achieved in a clinically relevant canine model using a nanofiber/fibrin-based scaffold. Control groups consisted of repair-only (no scaffold) and acellular scaffold. Repairs were evaluated after 28 days of healing using biomechanical, biochemical, and proteomics analyses. Range of motion was reduced in the groups that received scaffolds compared to normal. There was no effect of ASC + BMP12 treatment for range of motion or tensile properties outcomes versus repair-only. Biochemical assays demonstrated increased DNA, glycosaminoglycans, and crosslink concentration in all repair groups compared to normal, but no effect of ASC + BMP12. Total collagen was significantly decreased in the acellular scaffold group compared to normal and significantly increased in the ASC + BMP12 group compared to the acellular scaffold group. Proteomics analysis comparing healing tendons to uninjured tendons revealed significant increases in proteins associated with inflammation, stress response, and matrix degradation. Treatment with ASC + BMP12 amplified these unfavorable changes. In summary, the treatment approach used in this study induced a negative inflammatory reaction at the repair site leading to poor healing. Future approaches should consider cell and growth factor delivery methods that do not incite negative local reactions.

Indexed as

Adipose TissueAnimalsBiomechanical PhenomenaBone Morphogenetic ProteinsDogsExtracellular MatrixProteomeProteomicsStromal CellsTendon InjuriesTendonsTreatment FailureBone Morphogenetic ProteinsProteomegrowth factorproteomicsstem celltendon

Identifiers

PMID26445383
PMCPMC4814315
OpenAlexW2177906449

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.