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Cranio ; 40(2): 152-159, 2022 Mar.
Artigo em Inglês | MEDLINE | ID: mdl-31868570

RESUMO

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.


Assuntos
Bruxismo , Polimorfismo de Nucleotídeo Único , Receptores de Dopamina D2/genética , Bruxismo/genética , Catecol O-Metiltransferase , Genótipo , Humanos , Fenótipo , Proteínas Serina-Treonina Quinases
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