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

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          Summary

          Purpose

          Bone 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 Methods

          A 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 SNP s 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.

          Results

          The 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).

          Conclusion

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

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          Author and article information

          Contributors
          Role: Resident
          Role: Chief Resident
          Role: Associate Professor
          Role: Professor
          Role: Professor of Orthodontics
          Role: Professor
          Journal
          8704309
          4648
          J Craniomaxillofac Surg
          J Craniomaxillofac Surg
          Journal of cranio-maxillo-facial surgery : official publication of the European Association for Cranio-Maxillo-Facial Surgery
          1010-5182
          1878-4119
          10 April 2017
          08 March 2017
          June 2017
          01 June 2018
          : 45
          : 6
          : 826-830
          Affiliations
          Univ. Lille, Oral and Maxillofacial Department, Roger Salengro Hospital, CHU Lille, F-59000 Lille, France
          Univ. Lille, Oral and Maxillofacial Department, Roger Salengro Hospital, CHU Lille, F-59000 Lille, France
          Department of Oral Biology, University of Pittsburgh School of Dental Medicine, 3501 Terrace St, Pittsburgh PA 15261
          Univ. Lille, Oral and Maxillofacial Department, Roger Salengro Hospital, CHU Lille, INSERM U 1008, Controlled Drug Delivery Systems and Biomaterials, F-59000 Lille, France
          Professor of Orthodontics, Kornberg School of Dentistry, Temple University
          Univ. Lille, Oral and Maxillofacial Department, Roger Salengro Hospital, CHU Lille, INSERM U 1008, Controlled Drug Delivery Systems and Biomaterials, F-59000 Lille, France
          Author notes
          Corresponding author: Dr. Romain Nicot, Service de Chirurgie Maxillo Faciale et Stomatologie Hôpital Roger Salengro - Bd du Prof Emile Laine - 59037-Lille-Cedex - FRANCE; romain.nicot@ 123456gmail.com
          Article
          PMC5452077 PMC5452077 5452077 nihpa858389
          10.1016/j.jcms.2017.02.020
          5452077
          28381371
          f3bba255-e2df-4b3e-a697-d74296363571
          History
          Categories
          Article

          ectonucleotide pyrophosphatase phosphodiesterase 1,mandibular condyle,temporomandibular joint,malocclusion

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