Evidence map›Paper›PMID 26446403›Full record

ArticleEuropean journal of orthodontics2016

Critical roles of periostin in the process of orthodontic tooth movement.

Afsaneh Rangiani, Yan Jing, Yinshi Ren, Sumit Yadav, Reginald Taylor, Jian Q Feng

Abstract read
In one paragraph

Article in European journal of orthodontics, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 19 papers.

0numbers the graph read from it
0cells of the map it votes in
19citing papers in PubMed
1.9field-weighted citation impact, top 13% 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

19 citing papers in PubMed, 34 citations in OpenAlex.

  1. The NLRP3 Inflammasome Regulates Orthodontic Tooth Movement.Orthodontics & craniofacial research · 2026
    Article
  2. Review
  3. Temporal and spatial expression analysis of periostin in mice periodontitis model.Hua xi kou qiang yi xue za zhi = Huaxi kouqiang yixue zazhi = West China journal of stomatology · 2024
    Article
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  18. Expression ofJournal of dental sciences · 2016
    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

6 authors at 2 institutions in 1 country.

Afsaneh RangianiDepartment of Biomedical Sciences, Texas A&M Baylor College of Dentistry, Dallas, TX, USA, Division of Orthodontics, University of Connecticut Health Center, Farmington, CT, USA, and.
Yan JingDepartment of Biomedical Sciences, Texas A&M Baylor College of Dentistry, Dallas, TX, USA.
Yinshi RenDepartment of Biomedical Sciences, Texas A&M Baylor College of Dentistry, Dallas, TX, USA.
Sumit YadavDivision of Orthodontics, University of Connecticut Health Center, Farmington, CT, USA, and.
Reginald TaylorDepartment of Orthodontics, Texas A&M Baylor College of Dentistry, Dallas, TX, USA.
Jian Q FengDepartment of Biomedical Sciences, Texas A&M Baylor College of Dentistry, Dallas, TX, USA, jfeng@bcd.tamhsc.edu.
Baylor University · USUConn Health · US

Funding

Biphasic Roles of OSX-WNT-B-Catenin Signaling Pathway in Tooth Root FormationR01DE025014 · NIDCR · TEXAS A&M UNIVERSITY HEALTH SCIENCE CTR · PI FENG, JIAN Q. · 2015 to 2019
$1.8M
NIDCR NIH HHS R01 DE025014
6 · The paper itself

Abstract

aimThe process of orthodontic tooth movement (OTM) involves multiple mechanisms of action including bone and extracellular matrix remodelling, although the role of periodontal ligament (PDL) in this process is largely unknown. Periostin, which is highly expressed in the PDL, is known to be responsible for mechanical stimulation in maintaining the integrity of periodontal tissues. We hypothesize that this protein plays an important role during OTM. MATERIAL AND

methodsBy using spring in 4-week-old wild-type (WT) and periostin null mice, the rate of tooth movement and mineralization were evaluated. For the evaluation, double labelling, expression of sclerostin (SOST), number of TRAP-positive cells, and quality of collagen fibrils by Sirius red were analysed and compared between these two groups.

resultsOur findings showed that the distance of the tooth movement and mineral deposition rates were significantly reduced in periostin null mice (P < 0.05), with a lack of expression changes in SOST as observed in the WT group. The arrangement, digestion, and integrity of collagen fibrils were impaired in periostin null mice. The number of osteoclasts reflected by expressions of TRAP (tartrate-resistant acid phosphatase) in the null mice was also significantly lower than the WT control (P < 0.05).

conclusionPeriostin plays a stimulatory role in both SOST and TRAP responses to OTM in the compassion site, although it is not clear if this role is direct or indirect during orthodontic loading.

Indexed as

Adaptor Proteins, Signal TransducingAnimalsBone RemodelingCell Adhesion MoleculesCollagenGlycoproteinsIntercellular Signaling Peptides and ProteinsMiceMice, KnockoutOsteoclastsPeriodontal LigamentTartrate-Resistant Acid PhosphataseTooth Movement TechniquesAcp5 protein, mouseAdaptor Proteins, Signal TransducingCell Adhesion MoleculesCollagenGlycoproteinsIntercellular Signaling Peptides and ProteinsPostn protein, mouseSost protein, mouseTartrate-Resistant Acid Phosphatase

Identifiers

PMID26446403
PMCPMC4964749
OpenAlexW2284367398

What OpenQuestion holds

Textmetadata
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.