Evidence map›Paper›PMID 33937646›Full record

ArticleOTA international : the open access journal of orthopaedic trauma2018

Atrophic nonunion stromal cells form bone and recreate the bone marrow environment in vivo.

Frederico C Vallim, João Antonio Matheus Guimarães, Rhayra B Dias, Rafaela C Sartore, Amanda Dos S Cavalcanti, Ana C Leal, Maria Eugenia L Duarte, Danielle C Bonfim

Open access · goldAbstract read
In one paragraph

Article in OTA international : the open access journal of orthopaedic trauma, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
8citing papers in PubMed, 1 pooled it
0.1field-weighted citation impact, top 42% 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

8 citing papers in PubMed, 1 synthesis or guideline pooled it, 9 citations in OpenAlex.

  1. Pooled it
  2. Review
  3. Article
  4. Review
  5. Article
  6. Review
  7. Article
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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 1 country.

Frederico C VallimMaster Program in Musculoskeletal Sciences.
João Antonio Matheus GuimarãesTrauma Center.
Rhayra B DiasMaster Program in Musculoskeletal Sciences.
Rafaela C SartoreResearch Division, National Institute of Traumatology and Orthopedics, Rio de Janeiro, RJ, Brazil.
Amanda Dos S CavalcantiResearch Division, National Institute of Traumatology and Orthopedics, Rio de Janeiro, RJ, Brazil.
Ana C LealResearch Division, National Institute of Traumatology and Orthopedics, Rio de Janeiro, RJ, Brazil.
Maria Eugenia L DuarteResearch Division, National Institute of Traumatology and Orthopedics, Rio de Janeiro, RJ, Brazil.
Danielle C BonfimResearch Division, National Institute of Traumatology and Orthopedics, Rio de Janeiro, RJ, Brazil.
Instituto Nacional de Traumatologia e Ortopedia · BR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

introductionNonunion is a challenging condition in orthopaedics as its etiology is not fully understood. Clinical interventions currently aim to stimulate both the biological and mechanical aspects of the bone healing process by using bone autografts and surgical fixation. However, recent observations showed that atrophic nonunion tissues contain putative osteoprogenitors, raising the hypothesis that its reactivation could be explored to achieve bone repair.

methodsHere we characterized atrophic nonunion stromal cells (NUSC) in vitro, using bone marrow stromal cells (BMSC) and osteoblasts as controls cells of the osteoblastic lineage, and evaluated its ability to form bone in vivo.

resultsNUSC had proliferative and senescence rates comparable to BMSC and osteoblasts, and homogeneously expressed the osteolineage markers CD90 and CD73. Regarding CD105 and CD146 expression, NUSC were closely related to osteoblasts, both with an inferior percentage of CD105

conclusionsThis study demonstrates that NUSC are osteogenically competent, supporting the hypothesis that their endogenous reactivation could be a strategy to stimulate the bone formation while reducing the amount of bone autograft requirements.

Indexed as

atrophic nonunionbonefracturenonunion stromal cellosteogenic potential

Identifiers

PMID33937646
PMCPMC7953495
OpenAlexW3122004627

What OpenQuestion holds

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LicenceCC BY-ND
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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.