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Single nucleotide polymorphisms in dopamine receptor D2 are associated with bruxism and its circadian phenotypes in children.

Authors :
Scariot, Rafaela
Brunet, Leonardo
Olsson, Bernardo
Palinkas, Marcelo
Regalo, Simone Cecilio Hallak
Rebellato, Nelson Luis Barbosa
Brancher, João Armando
Torres, Carolina Paes
Diaz-Serrano, Kranya Victoria
Küchler, Erika Calvano
Zielak, João Cesar
Source :
CRANIO: The Journal of Craniomandibular & Sleep Practice; Mar2022, Vol. 40 Issue 2, p152-159, 8p
Publication Year :
2022

Abstract

Objective: To evaluate the association of bruxism phenotypes with single nucleotide polymorphisms in FKBP5, DRD2, ANKK1, and COMT.Methods: Clinical oral examination was performed to diagnose bruxism phenotypes in 150 children. DNA was collected from saliva. Logistic univariate regression, Chi-square, and Fisher's exact tests were performed (p < 0.05).Results: Bruxism was associated with DRD2 (p = 0.02). Tooth grinding while awake was associated with ANKK1 (p < 0.001), and tooth grinding while asleep was associated with DRD2 in the additive (p = 0.030) and dominant (p = 0.008) model. Tooth clenching while awake was associated with ANKK1 in the additive (p = 0.005) and dominant (p = 0.008) models, whereas tooth clenching while asleep was associated with ANKK1 (p < 0.001) and with COMT in the additive (p = 0.001) and dominant (p = 0.003) models.Discussion: Polymorphisms in DRD2, ANKK1, and COMT are associated with bruxism phenotypes. [ABSTRACT FROM AUTHOR]

Details

Language :
English
ISSN :
08869634
Volume :
40
Issue :
2
Database :
Supplemental Index
Journal :
CRANIO: The Journal of Craniomandibular & Sleep Practice
Publication Type :
Academic Journal
Accession number :
155550465
Full Text :
https://doi.org/10.1080/08869634.2019.1705629