PAX7 gene polymorphism in muscular temporomandibular disorders as potentially related to muscle stem cells

Abstract Background Temporomandibular disorders (TMD) are a group of painful and debilitating disorders, involving the masticatory muscles and/or the temporomandibular joint (TMJ). Chronic TMD pain can be associated with genetic changes in the key muscle development genes. Objective To evaluate the...

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Autores principales: Valquiria Quinelato, Letícia Ladeira Bonato, Alexandre Rezende Vieira, José Mauro Granjeiro, Karla Menezes, Radovan Borojevic, Priscila Ladeira Casado, Jose Albuquerque Calasans-Maia, Ricardo Tesch
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Publicado: BMC 2021
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spelling oai:doaj.org-article:26e7b9c3bfa54e99b18b46b4ff19ae9d2021-11-21T12:27:36ZPAX7 gene polymorphism in muscular temporomandibular disorders as potentially related to muscle stem cells10.1186/s12891-021-04846-w1471-2474https://doaj.org/article/26e7b9c3bfa54e99b18b46b4ff19ae9d2021-11-01T00:00:00Zhttps://doi.org/10.1186/s12891-021-04846-whttps://doaj.org/toc/1471-2474Abstract Background Temporomandibular disorders (TMD) are a group of painful and debilitating disorders, involving the masticatory muscles and/or the temporomandibular joint (TMJ). Chronic TMD pain can be associated with genetic changes in the key muscle development genes. Objective To evaluate the association between polymorphisms in the PAX7 (paired box 7) gene and masticatory myalgia in patients with temporomandibular disorders (TMD). Materials and methods This is a case-control study. Patients with TMD were divided into two groups: (a) presence of muscular TMD (n = 122) and (b) absence of muscular TMD (n = 49). Genomic DNA was obtained from saliva samples from all participants to allow for genotyping single nucleotide polymorphisms in PAX7 (rs766325 and rs6659735). Over-representation of alleles was tested using chi-square or Fisher’s exact tests. Values of p < 0.05 were considered to be statistically significant. Results Individuals without muscular TMD were less likely to have the PAX7 rs6659735 GG genotype (p = 0.03). No associations were found for PAX7 rs766325. Conclusions Alterations in PAX7 may influence muscular pathophysiology and individuals with TMD and the rs6659735 homozygous genotype (GG) are seemingly associated with muscular involvement of the disorder. No associations were found in the region rs766325.Valquiria QuinelatoLetícia Ladeira BonatoAlexandre Rezende VieiraJosé Mauro GranjeiroKarla MenezesRadovan BorojevicPriscila Ladeira CasadoJose Albuquerque Calasans-MaiaRicardo TeschBMCarticleChronic painTemporomandibular joint dysfunction syndromeMyalgiaPolymorphism geneticDiseases of the musculoskeletal systemRC925-935ENBMC Musculoskeletal Disorders, Vol 22, Iss 1, Pp 1-7 (2021)
institution DOAJ
collection DOAJ
language EN
topic Chronic pain
Temporomandibular joint dysfunction syndrome
Myalgia
Polymorphism genetic
Diseases of the musculoskeletal system
RC925-935
spellingShingle Chronic pain
Temporomandibular joint dysfunction syndrome
Myalgia
Polymorphism genetic
Diseases of the musculoskeletal system
RC925-935
Valquiria Quinelato
Letícia Ladeira Bonato
Alexandre Rezende Vieira
José Mauro Granjeiro
Karla Menezes
Radovan Borojevic
Priscila Ladeira Casado
Jose Albuquerque Calasans-Maia
Ricardo Tesch
PAX7 gene polymorphism in muscular temporomandibular disorders as potentially related to muscle stem cells
description Abstract Background Temporomandibular disorders (TMD) are a group of painful and debilitating disorders, involving the masticatory muscles and/or the temporomandibular joint (TMJ). Chronic TMD pain can be associated with genetic changes in the key muscle development genes. Objective To evaluate the association between polymorphisms in the PAX7 (paired box 7) gene and masticatory myalgia in patients with temporomandibular disorders (TMD). Materials and methods This is a case-control study. Patients with TMD were divided into two groups: (a) presence of muscular TMD (n = 122) and (b) absence of muscular TMD (n = 49). Genomic DNA was obtained from saliva samples from all participants to allow for genotyping single nucleotide polymorphisms in PAX7 (rs766325 and rs6659735). Over-representation of alleles was tested using chi-square or Fisher’s exact tests. Values of p < 0.05 were considered to be statistically significant. Results Individuals without muscular TMD were less likely to have the PAX7 rs6659735 GG genotype (p = 0.03). No associations were found for PAX7 rs766325. Conclusions Alterations in PAX7 may influence muscular pathophysiology and individuals with TMD and the rs6659735 homozygous genotype (GG) are seemingly associated with muscular involvement of the disorder. No associations were found in the region rs766325.
format article
author Valquiria Quinelato
Letícia Ladeira Bonato
Alexandre Rezende Vieira
José Mauro Granjeiro
Karla Menezes
Radovan Borojevic
Priscila Ladeira Casado
Jose Albuquerque Calasans-Maia
Ricardo Tesch
author_facet Valquiria Quinelato
Letícia Ladeira Bonato
Alexandre Rezende Vieira
José Mauro Granjeiro
Karla Menezes
Radovan Borojevic
Priscila Ladeira Casado
Jose Albuquerque Calasans-Maia
Ricardo Tesch
author_sort Valquiria Quinelato
title PAX7 gene polymorphism in muscular temporomandibular disorders as potentially related to muscle stem cells
title_short PAX7 gene polymorphism in muscular temporomandibular disorders as potentially related to muscle stem cells
title_full PAX7 gene polymorphism in muscular temporomandibular disorders as potentially related to muscle stem cells
title_fullStr PAX7 gene polymorphism in muscular temporomandibular disorders as potentially related to muscle stem cells
title_full_unstemmed PAX7 gene polymorphism in muscular temporomandibular disorders as potentially related to muscle stem cells
title_sort pax7 gene polymorphism in muscular temporomandibular disorders as potentially related to muscle stem cells
publisher BMC
publishDate 2021
url https://doaj.org/article/26e7b9c3bfa54e99b18b46b4ff19ae9d
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