Evidence map›Paper›PMID 37932515›Full record

ArticleScientific reports2023

Chondrocytes supplemented to bone graft-containing scaffolds expedite cranial defect repair.

Idan Carmon, Anna Zobrab, Michael Alterman, Rami Tabib, Adir Cohen, Leonid Kandel, Alexander Greenberg, Eli Reich, Nardi Casap, Mona Dvir-Ginzberg

Open access · goldAbstract read
In one paragraph

Article in Scientific reports, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
0.4field-weighted citation impact, top 32% 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

2 citing papers in PubMed, 2 citations in OpenAlex.

  1. Review
  2. 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 2 institutions in 1 country.

Idan Carmon *Laboratory of Cartilage Biology, Institute of Bio-Medical and Oral Research, Faculty of Dental Medicine, Hebrew University of Jerusalem, Jerusalem, Israel.
Anna Zobrab *Laboratory of Cartilage Biology, Institute of Bio-Medical and Oral Research, Faculty of Dental Medicine, Hebrew University of Jerusalem, Jerusalem, Israel.
Michael AltermanDepartment of Maxillofacial Surgery, Faculty of Dental Medicine, Hadassah-Hebrew University, P. O. Box 12272, 9112102, Jerusalem, Israel.
Rami TabibDepartment of Maxillofacial Surgery, Faculty of Dental Medicine, Hadassah-Hebrew University, P. O. Box 12272, 9112102, Jerusalem, Israel.
Adir CohenDepartment of Maxillofacial Surgery, Faculty of Dental Medicine, Hadassah-Hebrew University, P. O. Box 12272, 9112102, Jerusalem, Israel.
Leonid KandelJoint Replacement and Reconstruction Unit, Orthopedic Surgery Complex, Hadassah-Hebrew University Medical Center at Mount Scopus, Jerusalem, Israel.
Alexander GreenbergJoint Replacement and Reconstruction Unit, Orthopedic Surgery Complex, Hadassah-Hebrew University Medical Center at Mount Scopus, Jerusalem, Israel.
Eli ReichLaboratory of Cartilage Biology, Institute of Bio-Medical and Oral Research, Faculty of Dental Medicine, Hebrew University of Jerusalem, Jerusalem, Israel.
Nardi CasapDepartment of Maxillofacial Surgery, Faculty of Dental Medicine, Hadassah-Hebrew University, P. O. Box 12272, 9112102, Jerusalem, Israel. Nard@cc.huji.ac.il.
Mona Dvir-GinzbergLaboratory of Cartilage Biology, Institute of Bio-Medical and Oral Research, Faculty of Dental Medicine, Hebrew University of Jerusalem, Jerusalem, Israel. Mona.Dvir-Ginzberg@mail.huji.ac.il.ORCID 0000-0003-3089-6875
Hebrew University of Jerusalem · ILHadassah Medical Center · IL

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Critical maxillofacial bone fractures do not heal spontaneously, thus, often there is a need to facilitate repair via surgical intervention. Gold standard approaches, include the use of autologous bone graft, or devices supplemented with osteogenic growth factors and bone substitutes. This research aimed to employ a critical size calvaria defect model, to determine if the addition of chondrocytes to collagen-containing bone graft substitute, may expedite bone repair. As such, using a critical size rat calvaria defect, we implanted a collagen scaffold containing bone graft substitute (i.e., Bone graft scaffold, BG) or BG supplemented with costal chondrocytes (cBG). The rats were subjected to live CT imaging at 1, 6, 9, and 12 weeks following the surgical procedure and sacrificed for microCT imaging of the defect site. Moreover, serum markers and histological evaluation were assessed to determine osseous tissue regeneration and turnover. Live CT and microCT indicated cBG implants displayed expedited bone repair vs, BG alone, already at 6 weeks post defect induction. cBG also displayed a shorter distance between the defect edges and greater mineral apposition distance compared to BG. Summerizing, the data support the addition of chondrocytes to bone substitute, accelerates the formation of new bone within a critical size defect.

Indexed as

Bone SubstitutesChondrocytesAnimalsBone RegenerationCollagenOsteogenesisRatsSkullTissue ScaffoldsBone SubstitutesCollagen

Identifiers

PMID37932515
PMCPMC10628268
OpenAlexW4388424303

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.