Evidence map›Paper›PMID 24164629›Full record

ArticleJournal of clinical periodontology2014

Improving oral implant osseointegration in a murine model via Wnt signal amplification.

Sylvain Mouraret, Daniel J Hunter, Claire Bardet, Antoine Popelut, John B Brunski, Catherine Chaussain, Philippe Bouchard, Jill A Helms

Abstract read
In one paragraph

Article in Journal of clinical periodontology, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 16 papers.

0numbers the graph read from it
0cells of the map it votes in
16citing papers in PubMed
–field-weighted citation impact
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

16 citing papers in PubMed.

  1. Article
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  12. Biophysical regulation of osteotomy healing: An animal study.Clinical implant dentistry and related research · 2017
    Article
  13. Article
  14. Article
  15. Review
  16. Rescuing failed oral implants via Wnt activation.Journal of clinical periodontology · 2016
    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

8 authors.

Sylvain MouraretDivision of Plastic and Reconstructive Surgery, Department of Surgery, Stanford School of Medicine, Stanford, CA, USA; Department of Periodontology, Service of Odontology, Rothschild Hospital, AP-HP, Paris 7 - Denis, Diderot University, U.F.R. of Odontology, Paris, France.
Daniel J Hunter
Claire Bardet
Antoine Popelut
John B Brunski
Catherine Chaussain
Philippe Bouchard
Jill A Helms

Funding

Mechanobiology at Healing Bone-Implant InterfacesR01EB000504 · NIBIB · STANFORD UNIVERSITY · PI BRUNSKI, JOHN BEYER, HELMS, JILL A · 2003 to 2011
$4.4M
Mechanobiology at Healing Bone-Implant InterfacesR01DE024000 · NIDCR · STANFORD UNIVERSITY · PI BRUNSKI, JOHN BEYER, HELMS, JILL A · 2014 to 2018
$3.4M
NIBIB NIH HHS R01 EB000504NIDCR NIH HHS R01 DE024000
6 · The paper itself

Abstract

aimTo determine the key biological events occurring during implant failure and then we use this knowledge to develop new biology-based strategies that improve osseointegration. MATERIALS AND

methodsWild-type and Axin2(LacZ/LacZ) adult male mice underwent oral implant placement, with and without primary stability. Peri-implant tissues were evaluated using histology, alkaline phosphatase (ALP) activity, tartrate resistant acid phosphatase (TRAP) activity and TUNEL staining. In addition, mineralization sites, collagenous matrix organization and the expression of bone markers in the peri-implant tissues were assessed.

resultsMaxillary implants lacking primary stability show histological evidence of persistent fibrous encapsulation and mobility, which recapitulates the clinical problems of implant failure. Despite histological and molecular evidence of fibrous encapsulation, osteoblasts in the gap interface exhibit robust ALP activity. This mineralization activity is counteracted by osteoclast activity that resorbs any new bony matrix and consequently, the fibrous encapsulation remains. Using a genetic mouse model, we show that implants lacking primary stability undergo osseointegration, provided that Wnt signalling is amplified.

conclusionsIn a mouse model of oral implant failure caused by a lack of primary stability, we find evidence of active mineralization. This mineralization, however, is outpaced by robust bone resorption, which culminates in persistent fibrous encapsulation of the implant. Fibrous encapsulation can be prevented and osseointegration assured if Wnt signalling is elevated at the time of implant placement.

Indexed as

Dental ImplantsAcid PhosphataseAlkaline PhosphataseAlveolar ProcessAnimalsAxin ProteinBone MatrixBone ResorptionCalcification, PhysiologicCollagenConnective TissueDental Implantation, EndosseousDental Restoration FailureFibrosisIsoenzymesMaleAcid PhosphataseAcp5 protein, mouseAlkaline PhosphataseAxin2 protein, mouseAxin ProteinCollagenDental ImplantsIsoenzymesTartrate-Resistant Acid PhosphataseAxin2bonedentalfibrointegrationfibrous encapsulationhistologyin vivomaxillamicemodeloral cavityWnt

Identifiers

PMID24164629
PMCPMC4993043

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.