Dopamine receptor D2 and ankyrin repeat domain containing one in temporomandibular disorder of adolescents

Background Temporomandibular disorder (TMD) is a multifactorial condition that combines environmental and genetic factors and its prevalence increases during adolescence. Aim To investigate the association between TMD and genetic polymorphisms in the DRD2 and ANKK1 in a population of Brazilian adole...

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Published inInternational journal of paediatric dentistry Vol. 29; no. 6; pp. 748 - 755
Main Authors Franco, Gizele Batista, Faturri, Aluhe Lopes, Meger, Michelle Nascimento, Paiva Bertoli, Fernanda Mara, Wambier, Letícia Maira, Scariot, Rafaela, Souza, Juliana Feltrin, Küchler, Erika Calvano, Brancher, João Armando
Format Journal Article
LanguageEnglish
Published England Blackwell Publishing Ltd 01.11.2019
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Abstract Background Temporomandibular disorder (TMD) is a multifactorial condition that combines environmental and genetic factors and its prevalence increases during adolescence. Aim To investigate the association between TMD and genetic polymorphisms in the DRD2 and ANKK1 in a population of Brazilian adolescents. Design The TMD group included adolescents diagnosed with any of the following TMD subgroups according to the RDC/TMD criteria: myofascial pain, arthralgia and disc displacement and painful TMD. Genomic DNA for molecular analysis was extracted from buccal cells, and genetic polymorphism rs6275 in DRD2 and rs1800497 in ANKK1 were genotyped by real‐time polymerase chain reactions using the TaqMan assay. Data were analysed using the Epi Info 3.5.7 and Stata software, with significance level of 0.05. Results Two hundred fifty‐one individuals were included in this study, 148 subjects presented TMD. For disc displacement, the genetic polymorphisms rs6275 was associated in a recessive model (P = 0.04), whereas the rs6276 and rs1800497 presented only a borderline association in a recessive and dominant models, respectively (P = 0.07 and P = 0.06). Conclusion The genetic polymorphism rs6275 in DRD2 was associated with disc displacement in Brazilian adolescents.
AbstractList BackgroundTemporomandibular disorder (TMD) is a multifactorial condition that combines environmental and genetic factors and its prevalence increases during adolescence.AimTo investigate the association between TMD and genetic polymorphisms in the DRD2 and ANKK1 in a population of Brazilian adolescents.DesignThe TMD group included adolescents diagnosed with any of the following TMD subgroups according to the RDC/TMD criteria: myofascial pain, arthralgia and disc displacement and painful TMD. Genomic DNA for molecular analysis was extracted from buccal cells, and genetic polymorphism rs6275 in DRD2 and rs1800497 in ANKK1 were genotyped by real‐time polymerase chain reactions using the TaqMan assay. Data were analysed using the Epi Info 3.5.7 and Stata software, with significance level of 0.05.ResultsTwo hundred fifty‐one individuals were included in this study, 148 subjects presented TMD. For disc displacement, the genetic polymorphisms rs6275 was associated in a recessive model (P = 0.04), whereas the rs6276 and rs1800497 presented only a borderline association in a recessive and dominant models, respectively (P = 0.07 and P = 0.06).ConclusionThe genetic polymorphism rs6275 in DRD2 was associated with disc displacement in Brazilian adolescents.
Temporomandibular disorder (TMD) is a multifactorial condition that combines environmental and genetic factors and its prevalence increases during adolescence.BACKGROUNDTemporomandibular disorder (TMD) is a multifactorial condition that combines environmental and genetic factors and its prevalence increases during adolescence.To investigate the association between TMD and genetic polymorphisms in the DRD2 and ANKK1 in a population of Brazilian adolescents.AIMTo investigate the association between TMD and genetic polymorphisms in the DRD2 and ANKK1 in a population of Brazilian adolescents.The TMD group included adolescents diagnosed with any of the following TMD subgroups according to the RDC/TMD criteria: myofascial pain, arthralgia and disc displacement and painful TMD. Genomic DNA for molecular analysis was extracted from buccal cells, and genetic polymorphism rs6275 in DRD2 and rs1800497 in ANKK1 were genotyped by real-time polymerase chain reactions using the TaqMan assay. Data were analysed using the Epi Info 3.5.7 and Stata software, with significance level of 0.05.DESIGNThe TMD group included adolescents diagnosed with any of the following TMD subgroups according to the RDC/TMD criteria: myofascial pain, arthralgia and disc displacement and painful TMD. Genomic DNA for molecular analysis was extracted from buccal cells, and genetic polymorphism rs6275 in DRD2 and rs1800497 in ANKK1 were genotyped by real-time polymerase chain reactions using the TaqMan assay. Data were analysed using the Epi Info 3.5.7 and Stata software, with significance level of 0.05.Two hundred fifty-one individuals were included in this study, 148 subjects presented TMD. For disc displacement, the genetic polymorphisms rs6275 was associated in a recessive model (P = 0.04), whereas the rs6276 and rs1800497 presented only a borderline association in a recessive and dominant models, respectively (P = 0.07 and P = 0.06).RESULTSTwo hundred fifty-one individuals were included in this study, 148 subjects presented TMD. For disc displacement, the genetic polymorphisms rs6275 was associated in a recessive model (P = 0.04), whereas the rs6276 and rs1800497 presented only a borderline association in a recessive and dominant models, respectively (P = 0.07 and P = 0.06).The genetic polymorphism rs6275 in DRD2 was associated with disc displacement in Brazilian adolescents.CONCLUSIONThe genetic polymorphism rs6275 in DRD2 was associated with disc displacement in Brazilian adolescents.
Temporomandibular disorder (TMD) is a multifactorial condition that combines environmental and genetic factors and its prevalence increases during adolescence. To investigate the association between TMD and genetic polymorphisms in the DRD2 and ANKK1 in a population of Brazilian adolescents. The TMD group included adolescents diagnosed with any of the following TMD subgroups according to the RDC/TMD criteria: myofascial pain, arthralgia and disc displacement and painful TMD. Genomic DNA for molecular analysis was extracted from buccal cells, and genetic polymorphism rs6275 in DRD2 and rs1800497 in ANKK1 were genotyped by real-time polymerase chain reactions using the TaqMan assay. Data were analysed using the Epi Info 3.5.7 and Stata software, with significance level of 0.05. Two hundred fifty-one individuals were included in this study, 148 subjects presented TMD. For disc displacement, the genetic polymorphisms rs6275 was associated in a recessive model (P = 0.04), whereas the rs6276 and rs1800497 presented only a borderline association in a recessive and dominant models, respectively (P = 0.07 and P = 0.06). The genetic polymorphism rs6275 in DRD2 was associated with disc displacement in Brazilian adolescents.
Background Temporomandibular disorder (TMD) is a multifactorial condition that combines environmental and genetic factors and its prevalence increases during adolescence. Aim To investigate the association between TMD and genetic polymorphisms in the DRD2 and ANKK1 in a population of Brazilian adolescents. Design The TMD group included adolescents diagnosed with any of the following TMD subgroups according to the RDC/TMD criteria: myofascial pain, arthralgia and disc displacement and painful TMD. Genomic DNA for molecular analysis was extracted from buccal cells, and genetic polymorphism rs6275 in DRD2 and rs1800497 in ANKK1 were genotyped by real‐time polymerase chain reactions using the TaqMan assay. Data were analysed using the Epi Info 3.5.7 and Stata software, with significance level of 0.05. Results Two hundred fifty‐one individuals were included in this study, 148 subjects presented TMD. For disc displacement, the genetic polymorphisms rs6275 was associated in a recessive model (P = 0.04), whereas the rs6276 and rs1800497 presented only a borderline association in a recessive and dominant models, respectively (P = 0.07 and P = 0.06). Conclusion The genetic polymorphism rs6275 in DRD2 was associated with disc displacement in Brazilian adolescents.
Author Souza, Juliana Feltrin
Meger, Michelle Nascimento
Scariot, Rafaela
Küchler, Erika Calvano
Wambier, Letícia Maira
Brancher, João Armando
Faturri, Aluhe Lopes
Franco, Gizele Batista
Paiva Bertoli, Fernanda Mara
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2019 BSPD, IAPD and John Wiley & Sons A/S. Published by John Wiley & Sons Ltd.
International Journal of Paediatric Dentistry © 2019 BSPD, IAPD and John Wiley & Sons A/S. Published by John Wiley & Sons Ltd
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Keywords disc displacement
TMJ diseases
genetic polymorphisms
adolescents
Language English
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Snippet Background Temporomandibular disorder (TMD) is a multifactorial condition that combines environmental and genetic factors and its prevalence increases during...
Temporomandibular disorder (TMD) is a multifactorial condition that combines environmental and genetic factors and its prevalence increases during adolescence....
BackgroundTemporomandibular disorder (TMD) is a multifactorial condition that combines environmental and genetic factors and its prevalence increases during...
Temporomandibular disorder (TMD) is a multifactorial condition that combines environmental and genetic factors and its prevalence increases during...
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SubjectTerms Adolescent
Adolescents
Ankyrin Repeat
Ankyrins
Arthralgia
Brazil
disc displacement
Dopamine D2 receptors
Gene polymorphism
Genetic factors
genetic polymorphisms
Genotype
Humans
Mouth Mucosa
Polymorphism
Teenagers
Temporomandibular Joint Disorders
TMJ diseases
Title Dopamine receptor D2 and ankyrin repeat domain containing one in temporomandibular disorder of adolescents
URI https://onlinelibrary.wiley.com/doi/abs/10.1111%2Fipd.12544
https://www.ncbi.nlm.nih.gov/pubmed/31144779
https://www.proquest.com/docview/2302200955
https://www.proquest.com/docview/2232481424
Volume 29
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