Evidence map›Paper›PMID 38639414›Full record

ArticleJournal of orthopaedic research : official publication of the Orthopaedic Research Society2024

Cell-based tissue engineered flexor tendon allograft: A canine in vivo study.

Subin Lin, Ramona Reisdorf, Chun Kuan Lu, Zhanwen Wang, Kai-Nan An, Steven L Moran, Peter C Amadio, Chunfeng Zhao

Open access · bronzeAbstract read
In one paragraph

Article in Journal of orthopaedic research : official publication of the Orthopaedic Research Society, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
–field-weighted citation impact, top 93% 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

1 citing paper in PubMed, 0 citations in OpenAlex.

  1. Review
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

8 authors at 1 institution in 2 countries.

Subin LinDepartment of Orthopedic Surgery, Mayo Clinic, Rochester, Minnesota, USA.
Ramona ReisdorfDepartment of Orthopedic Surgery, Mayo Clinic, Rochester, Minnesota, USA.
Chun Kuan LuDepartment of Orthopedic Surgery, Mayo Clinic, Rochester, Minnesota, USA.
Zhanwen WangDepartment of Orthopedic Surgery, Mayo Clinic, Rochester, Minnesota, USA.
Kai-Nan AnDepartment of Orthopedic Surgery, Mayo Clinic, Rochester, Minnesota, USA.
Steven L MoranDepartment of Orthopedic Surgery, Mayo Clinic, Rochester, Minnesota, USA.
Peter C AmadioDepartment of Orthopedic Surgery, Mayo Clinic, Rochester, Minnesota, USA.ORCID 0000-0002-2206-4772
Chunfeng ZhaoDepartment of Orthopedic Surgery, Mayo Clinic, Rochester, Minnesota, USA.ORCID 0000-0002-8737-4587
Mayo Clinic · US

Funding

Engineering Tendon Grafts for Better OutcomesR01AR057745 · NIAMS · MAYO CLINIC ROCHESTER · PI ZHAO, CHUNFENG · 2010 to 2018
$3.5M
Flexor tendon intrinsic healing and intervention strategy developmentR01AR076339 · NIAMS · MAYO CLINIC ROCHESTER · PI ZHAO, CHUNFENG · 2021 to 2025
$2.5M
NIAMS NIH HHS R01 AR057745NIAMS NIH HHS R01 AR076339
6 · The paper itself

Abstract

This study aimed to compare the clinically established autologous extrasynovial tendon graft to a newly developed tissue-engineered allograft (Eng-allograft) in terms of functional outcomes following flexor tendon reconstruction in a canine model. The second and fifth flexor digitorum profundus (FDP) tendons from 16 dogs were transected and repaired in Zone II. After 6 weeks of cage activity, the repaired tendons were intentionally ruptured, creating a clinically relevant model for reconstruction. The re-ruptured FDP tendons were then reconstructed using either the clinically standard autologous extrasynovial tendon graft or the Eng-allograft, which had been revitalized with autologous bone marrow-derived mesenchymal stem cells (BMSCs) and synovialized using carbodiimide derivatized synovial fluid (cd-SYN). Following 12 weeks of postoperative rehabilitation, the functional outcomes of the surgical digits were evaluated. The Eng-allograft group exhibited improved digital function, including lower digit work of flexion and reduced adhesion status, while maintaining similar tendon gliding resistance compared to the autograft group. However, the failure load of both the distal and proximal host/graft conjunctions in the Eng-allograft group was significantly lower than that of the autograft group with higher graft rupture at the host-graft junction. In conclusion, the decellularized allogenic intrasynovial tendon, when revitalized BMSCs and synovialized with cd-SYN, demonstrates positive effects on digital function improvement and adhesion reduction. However, the healing at both proximal and distal graft/host junctions is far lower than the autograft. Further research is needed to enhance the healing capacity of allograft conjunctions, aiming to achieve a comparable level of healing seen with autografts.

Indexed as

AllograftsTendonsTissue EngineeringAnimalsDogsFemaleMaleMesenchymal Stem Cell TransplantationTendon Injuriesallograftflexor tendon reconstructionrevitalizationstem cellsynovialization

Identifiers

PMID38639414
PMCPMC11293999
OpenAlexW4394962541

What OpenQuestion holds

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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.