Evidence map›Paper›PMID 24699186›Full record

ArticleInternational journal of oral science2014

Dental and periodontal phenotype in sclerostin knockout mice.

Ulrike Kuchler, Uwe Y Schwarze, Toni Dobsak, Patrick Heimel, Dieter D Bosshardt, Michaela Kneissel, Reinhard Gruber

Open access · goldAbstract read
In one paragraph

Article in International journal of oral science, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 32 papers.

0numbers the graph read from it
0cells of the map it votes in
32citing papers in PubMed
6.9field-weighted citation impact, top 3% 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

32 citing papers in PubMed, 63 citations in OpenAlex.

  1. Article
  2. Review
  3. Review
  4. Article
  5. Review
  6. Article
  7. Article
  8. Article
  9. Review
  10. Article
  11. Article
  12. Review
  13. Article
  14. Article
  15. Review
  16. Article
  17. Review
  18. Review
  19. Article
  20. 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

7 authors at 4 institutions in 2 countries.

Ulrike Kuchler1] Department of Oral Surgery, Medical University of Vienna, Vienna, Austria [2] Austrian Cluster for Tissue Regeneration, Vienna, Austria [3] Department of Oral Surgery and Stomatology, School of Dental Medicine, University of Berne, Berne, Switzerland.
Uwe Y Schwarze1] Department of Oral Surgery, Medical University of Vienna, Vienna, Austria [2] Austrian Cluster for Tissue Regeneration, Vienna, Austria [3] Karl Donath Laboratory for Hard Tissue and Biomaterial Research, University Clinic of Dentistry, Medical University of Vienna, Vienna, Austria.
Toni Dobsak1] Department of Oral Surgery, Medical University of Vienna, Vienna, Austria [2] Austrian Cluster for Tissue Regeneration, Vienna, Austria [3] Karl Donath Laboratory for Hard Tissue and Biomaterial Research, University Clinic of Dentistry, Medical University of Vienna, Vienna, Austria.
Patrick Heimel1] Department of Oral Surgery, Medical University of Vienna, Vienna, Austria [2] Austrian Cluster for Tissue Regeneration, Vienna, Austria [3] Karl Donath Laboratory for Hard Tissue and Biomaterial Research, University Clinic of Dentistry, Medical University of Vienna, Vienna, Austria [4] Ludwig Boltzmann Institute for Experimental and Clinical Traumatology in AUVA Research Center, Vienna, Austria.
Dieter D Bosshardt1] Department of Oral Surgery and Stomatology, School of Dental Medicine, University of Berne, Berne, Switzerland [2] Robert K. Schenk Laboratory of Oral Histology, School of Dental Medicine, University of Berne, Berne, Switzerland.
Michaela KneisselMusculoskeletal Disease Area, Novartis Institutes for BioMedical Research, Basel, Switzerland.
Reinhard Gruber1] Department of Oral Surgery, Medical University of Vienna, Vienna, Austria [2] Austrian Cluster for Tissue Regeneration, Vienna, Austria [3] Laboratory of Oral Cell Biology, School of Dental Medicine, University of Berne, Berne, Switzerland.
Medical University of Vienna · ATAustrian Cluster for Tissue Regeneration · ATNovartis (Switzerland) · CHUniversity of Bern · CH

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Sclerostin is a Wnt signalling antagonist that controls bone metabolism. Sclerostin is expressed by osteocytes and cementocytes; however, its role in the formation of dental structures remains unclear. Here, we analysed the mandibles of sclerostin knockout mice to determine the influence of sclerostin on dental structures and dimensions using histomorphometry and micro-computed tomography (μCT) imaging. μCT and histomorphometric analyses were performed on the first lower molar and its surrounding structures in mice lacking a functional sclerostin gene and in wild-type controls. μCT on six animals in each group revealed that the dimension of the basal bone as well as the coronal and apical part of alveolar part increased in the sclerostin knockout mice. No significant differences were observed for the tooth and pulp chamber volume. Descriptive histomorphometric analyses of four wild-type and three sclerostin knockout mice demonstrated an increased width of the cementum and a concomitant moderate decrease in the periodontal space width. Taken together, these results suggest that the lack of sclerostin mainly alters the bone and cementum phenotypes rather than producing abnormalities in tooth structures such as dentin.

Indexed as

Adaptor Proteins, Signal TransducingAnimalsFemaleGlycoproteinsIntercellular Signaling Peptides and ProteinsMiceMice, KnockoutPeriodontiumPhenotypeToothAdaptor Proteins, Signal TransducingGlycoproteinsIntercellular Signaling Peptides and ProteinsSost protein, mouse

Identifiers

PMID24699186
PMCPMC5130054
OpenAlexW2089307105

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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.