Evidence map›Paper›PMID 36829637›Full record

ArticleBioengineering (Basel, Switzerland)2023

A New Osteogenic Membrane to Enhance Bone Healing: At the Crossroads between the Periosteum, the Induced Membrane, and the Diamond Concept.

Julie Manon, Robin Evrard, Lies Fievé, Caroline Bouzin, Delphine Magnin, Daela Xhema, Tom Darius, Eliano Bonaccorsi-Riani, Pierre Gianello, Pierre-Louis Docquier and 4 more

Open access · goldAbstract read
In one paragraph

Article in Bioengineering (Basel, Switzerland), 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing papers in PubMed
3.8field-weighted citation impact, top 7% 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

6 citing papers in PubMed, 12 citations in OpenAlex.

  1. Article
  2. Article
  3. Advances in Fracture Healing Research.Bioengineering (Basel, Switzerland) · 2024
    Article
  4. Article
  5. Article
  6. 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

14 authors at 3 institutions in 1 country.

Julie ManonMorphology Lab (MORF), Institut de Recherche Expérimentale et Clinique (IREC), UCLouvain, 1200 Brussels, Belgium.ORCID 0000-0002-2558-8723
Robin EvrardMorphology Lab (MORF), Institut de Recherche Expérimentale et Clinique (IREC), UCLouvain, 1200 Brussels, Belgium.
Lies FievéMorphology Lab (MORF), Institut de Recherche Expérimentale et Clinique (IREC), UCLouvain, 1200 Brussels, Belgium.
Caroline BouzinImaging Platform (2IP), IREC, UCLouvain, 1200 Brussels, Belgium.ORCID 0000-0003-0694-1947
Delphine MagninBio & Soft Matter (BSMA), Institute of Condensed Matter and Nanosciences (IMCN), UCLouvain, 1348 Louvain-la-Neuve, Belgium.ORCID 0000-0002-9244-245X
Daela XhemaTransplantation and Experimental Surgery Lab (CHEX), IREC, UCLouvain, 1200 Brussels, Belgium.
Tom DariusTransplantation and Experimental Surgery Lab (CHEX), IREC, UCLouvain, 1200 Brussels, Belgium.ORCID 0000-0002-8151-4286
Eliano Bonaccorsi-RianiTransplantation and Experimental Surgery Lab (CHEX), IREC, UCLouvain, 1200 Brussels, Belgium.
Pierre GianelloTransplantation and Experimental Surgery Lab (CHEX), IREC, UCLouvain, 1200 Brussels, Belgium.
Pierre-Louis DocquierNeuromusculoskeletal Lab (NMSK), IREC, UCLouvain, 1200 Brussels, Belgium.
Thomas SchubertNeuromusculoskeletal Lab (NMSK), IREC, UCLouvain, 1200 Brussels, Belgium.ORCID 0000-0001-6670-886X
Benoît LengeléMorphology Lab (MORF), Institut de Recherche Expérimentale et Clinique (IREC), UCLouvain, 1200 Brussels, Belgium.
Catherine BehetsMorphology Lab (MORF), Institut de Recherche Expérimentale et Clinique (IREC), UCLouvain, 1200 Brussels, Belgium.ORCID 0000-0003-0468-7076
Olivier CornuNeuromusculoskeletal Lab (NMSK), IREC, UCLouvain, 1200 Brussels, Belgium.ORCID 0000-0003-3033-7408
Cliniques Universitaires Saint-Luc · BEDirectorate-General Joint Research Centre · BEUCLouvain · BE

Funding

F.N.R.S. (« Fonds National de la Recherche Scientifique ») - Aspirant Fund ID 40004991
6 · The paper itself

Abstract

The lack of viability of massive bone allografts for critical-size bone defect treatment remains a challenge in orthopedic surgery. The literature has reviewed the advantages of a multi-combined treatment with the synergy of an osteoconductive extracellular matrix (ECM), osteogenic stem cells, and growth factors (GFs). Questions are still open about the need for ECM components, the influence of the decellularization process on the latter, the related potential loss of function, and the necessity of using pre-differentiated cells. In order to fill in this gap, a bone allograft surrounded by an osteogenic membrane made of a decellularized collagen matrix from human fascia lata and seeded with periosteal mesenchymal stem cells (PMSCs) was analyzed in terms of de-/recellularization, osteogenic properties, PMSC self-differentiation, and angiogenic potential. While the decellularization processes altered the ECM content differently, the main GF content was decreased in soft tissues but relatively increased in hard bone tissues. The spontaneous osteogenic differentiation was necessarily obtained through contact with a mineralized bone matrix. Trying to deepen the knowledge on the complex matrix-cell interplay could further propel these tissue engineering concepts and lead us to provide the biological elements that allow bone integration in vivo.

Indexed as

bone allograftcell–matrix interplaydecellularizationin vitro model for bone regenerationosteogenic membraneperiosteal mesenchymal stem cells

Identifiers

PMID36829637
PMCPMC9952848
OpenAlexW4317812142

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.