Actn3 genotype influences masseter muscle ...
Type de document :
Article dans une revue scientifique: Article original
DOI :
PMID :
URL permanente :
Titre :
Actn3 genotype influences masseter muscle characteristics and self-reported bruxism
Auteur(s) :
Nicot, Romain [Auteur]
Advanced Drug Delivery Systems (ADDS) - U1008
Raoul, Gwénaël [Auteur]
Advanced Drug Delivery Systems (ADDS) - U1008
Vieira, Alexandre R. [Auteur]
University of Pittsburgh School of Medicine
Ferri, Joel [Auteur]
Advanced Drug Delivery Systems (ADDS) - U1008
Sciote, James J. [Auteur]

Advanced Drug Delivery Systems (ADDS) - U1008
Raoul, Gwénaël [Auteur]

Advanced Drug Delivery Systems (ADDS) - U1008
Vieira, Alexandre R. [Auteur]
University of Pittsburgh School of Medicine
Ferri, Joel [Auteur]

Advanced Drug Delivery Systems (ADDS) - U1008
Sciote, James J. [Auteur]
Titre de la revue :
Oral Diseases
Nom court de la revue :
Oral Dis
Date de publication :
2021-11-13
ISSN :
1601-0825
Mot(s)-clé(s) :
masseter muscle
sleep bruxism
malocclusion
bruxism
human
ACTN3 protein
temporomandibular joint disorders
sleep bruxism
malocclusion
bruxism
human
ACTN3 protein
temporomandibular joint disorders
Discipline(s) HAL :
Sciences du Vivant [q-bio]
Résumé en anglais : [en]
OBJECTIVE: Main aim of the study was to explore the association between genetic polymorphisms in ACTN3 and bruxism. Secondary objectives included masseter muscle phenotypes assessment between bruxers and non-bruxers and ...
Lire la suite >OBJECTIVE: Main aim of the study was to explore the association between genetic polymorphisms in ACTN3 and bruxism. Secondary objectives included masseter muscle phenotypes assessment between bruxers and non-bruxers and according to genetic polymorphisms in ACTN3. METHODS: Fifty-four patients undergoing orthognathic surgery for correction of their malocclusion were enrolled. Self-reported bruxism and temporomandibular disorders status were preoperatively recorded. Saliva samples were used for ACTN3 genotyping. Masseter muscle samples were collected bilaterally at the time of orthognathic surgery to explore the muscle fiber characteristics. RESULTS: There were significant differences in genotypes for rs1815739 (R577X nonsense) (p = 0.001), rs1671064 (Q523R missense) (p = 0.005), and rs678397 (intronic variant) (p = 0.001) between bruxers and non-bruxers. Patients with self-reported bruxism presented a larger mean fiber area for types IIA (p = 0.035). The mean fiber areas in individuals with the wild-type CC genotype for rs1815739 (R577X) were significantly larger for type IIA fibers (1394.33 μm222222 CONCLUSIONS: ACTN3 genotypes influence self-reported bruxism in patients with dentofacial deformity through specific masseter muscle fiber characteristics.Lire moins >
Lire la suite >OBJECTIVE: Main aim of the study was to explore the association between genetic polymorphisms in ACTN3 and bruxism. Secondary objectives included masseter muscle phenotypes assessment between bruxers and non-bruxers and according to genetic polymorphisms in ACTN3. METHODS: Fifty-four patients undergoing orthognathic surgery for correction of their malocclusion were enrolled. Self-reported bruxism and temporomandibular disorders status were preoperatively recorded. Saliva samples were used for ACTN3 genotyping. Masseter muscle samples were collected bilaterally at the time of orthognathic surgery to explore the muscle fiber characteristics. RESULTS: There were significant differences in genotypes for rs1815739 (R577X nonsense) (p = 0.001), rs1671064 (Q523R missense) (p = 0.005), and rs678397 (intronic variant) (p = 0.001) between bruxers and non-bruxers. Patients with self-reported bruxism presented a larger mean fiber area for types IIA (p = 0.035). The mean fiber areas in individuals with the wild-type CC genotype for rs1815739 (R577X) were significantly larger for type IIA fibers (1394.33 μm222222 CONCLUSIONS: ACTN3 genotypes influence self-reported bruxism in patients with dentofacial deformity through specific masseter muscle fiber characteristics.Lire moins >
Langue :
Anglais
Comité de lecture :
Oui
Audience :
Internationale
Vulgarisation :
Non
Établissement(s) :
CHU Lille
Inserm
Université de Lille
Inserm
Université de Lille
Collections :
Équipe(s) de recherche :
U1008
Date de dépôt :
2022-04-13T07:12:16Z
2024-01-22T14:19:25Z
2024-01-22T14:19:25Z