Evidence map›Paper›PMID 28381371›Full record

ArticleJournal of cranio-maxillo-facial surgery : official publication of the European Association for Cranio-Maxillo-Facial Surgery2017

Condylar geometry variation is associated with ENPP1 variant in a population of patients with dento-facial deformities.

Marion Constant, Romain Nicot, Alexandre R Vieira, Gwenael Raoul, James J Sciote, Joel Ferri

Abstract read
In one paragraph

Article in Journal of cranio-maxillo-facial surgery : official publication of the European Association for Cranio-Maxillo-Facial Surgery, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
1.3field-weighted citation impact, top 20% 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

3 citing papers in PubMed, 11 citations in OpenAlex.

  1. Article
  2. Article
  3. Orthodontics and Genetics.Dental press journal of orthodontics · 2019
    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

6 authors at 4 institutions in 2 countries.

Marion ConstantUniv. Lille, Oral and Maxillofacial Department, Roger Salengro Hospital, CHU Lille, F-59000 Lille, France. Electronic address: constant.marion@hotmail.fr.
Romain NicotUniv. Lille, Oral and Maxillofacial Department, Roger Salengro Hospital, CHU Lille, F-59000 Lille, France. Electronic address: romain.nicot@gmail.com.
Alexandre R VieiraDepartment of Oral Biology, University of Pittsburgh School of Dental Medicine, 3501 Terrace St, Pittsburgh PA 15261, USA. Electronic address: alexandre_vieira@pitt.edu.
Gwenael RaoulUniv. Lille, Oral and Maxillofacial Department, Roger Salengro Hospital, CHU Lille, INSERM U 1008, Controlled Drug Delivery Systems and Biomaterials, F-59000 Lille, France. Electronic address: gwenael.raoul@gmail.com.
James J ScioteKornberg School of Dentistry, Temple University, USA. Electronic address: jjs6@temple.edu.
Joel FerriUniv. Lille, Oral and Maxillofacial Department, Roger Salengro Hospital, CHU Lille, INSERM U 1008, Controlled Drug Delivery Systems and Biomaterials, F-59000 Lille, France. Electronic address: ferri.joel@gmail.com.
Inserm · FRUniversité de Lille · FRTemple College · USUniversity of Pittsburgh · US

Funding

Musculoskeletal Heritable Influences on MalocclusionR21DE022427 · NIDCR · TEMPLE UNIV OF THE COMMONWEALTH · PI SCIOTE, JAMES J · 2012 to 2013
$415k
NIDCR NIH HHS R21 DE022427
6 · The paper itself

Abstract

purposeBone remodeling is essential in maintaining bone health. Considering that ENPP1 contributes to bone geometry and bone mineralization, the aim of our study was to analyze the association between single-nucleotide polymorphisms (SNPs) of ENPP1 and condylar remodeling. MATERIALS AND

methodsA total of 156 patients undergoing orthodontic and maxillofacial surgery treatment for correction of malocclusion were included in this prospective study. Saliva samples from all subjects were used for DNA extraction and genotyping. Four ENPP1 SNPs were selected and tested to determine whether specific allelic variants are correlated with condylar remodeling. The criteria of condylar remodeling chosen were the ratio between each side of condylar height or surface differences on a dental panoramic of each patient. A diagnostic threshold was set at 15% difference between both sides.

resultsThe ENPP1 SNP rs9373000 showed a statistically significant association with condylar height ratio >15% (p = 0.012). The GG genotype was found to be a protective factor against condylar height decrease (p = 0.003).

conclusionThis study identifies the genetic variant rs9373000 as a potentially causal variant for mandibular condyle geometry variation for patients presenting with dento-facial deformities.

Indexed as

Anatomic VariationPolymorphism, Single NucleotideAdultAllelesBone RemodelingFemaleGenotypeHumansMaleMandibular CondyleMaxillofacial AbnormalitiesPhosphoric Diester HydrolasesProspective StudiesPyrophosphatasesectonucleotide pyrophosphatase phosphodiesterase 1Phosphoric Diester HydrolasesPyrophosphatasesEctonucleotide pyrophosphatase phosphodiesterase 1MalocclusionMandibular condyleTemporomandibular joint

Identifiers

PMID28381371
PMCPMC5452077
OpenAlexW2592688618

What OpenQuestion holds

Textmetadata
LicenceTDM
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.