Influence of psychosocial factors, sleep disturbances and genetic factors on pain sensitivity and temporomandibular disorder

Detalhes bibliográficos
Ano de defesa: 2014
Autor(a) principal: Fiamengui, Livia Maria Sales Pinto
Orientador(a): Não Informado pela instituição
Banca de defesa: Não Informado pela instituição
Tipo de documento: Tese
Tipo de acesso: Acesso aberto
Idioma: eng
Instituição de defesa: Biblioteca Digitais de Teses e Dissertações da USP
Programa de Pós-Graduação: Não Informado pela instituição
Departamento: Não Informado pela instituição
País: Não Informado pela instituição
Palavras-chave em Português:
Link de acesso: https://www.teses.usp.br/teses/disponiveis/25/25146/tde-09122021-103657/
Resumo: The present study aimed to evaluate the influence of psychosocial factors depression and anxiety, sleep disturbances poor sleep and bruxism, and single nucleotide polymorphisms of COMT Val158Met (rs4680), IL-1(3954 (rs:1143634), IL6-174 (rs:1800795), IL10-592 (rs:1800872), MMP1-1607 (rs:1799750) and TNF-308 (rs:1800629) as contributors to pain sensitivity and Temporomandibular Disorders. The sample comprised 291 subjects of both genders, with ages ranging from 18 to 65. Psychosocial factors were assessed using Beck Depression Inventory and Beck Anxiety Inventory. Pittsburg Sleep Questionnaire Index Sleep was used to determine sleep quality. Sleep bruxism was diagnosed in accordance with validated clinical diagnostic criteria proposed by American Academy of Sleep Medicine. The saliva samples for the DNA analysis were collected with the Oragene DNA self-collection kit. The single nucleotide polymorphisms analysis was performed using PCR. An algometer was used to record the Pressure Pain Threshold (PPT) value for the TMJ, masseter muscle and anterior temporalis. Linear multiple regression was performed to evaluate the influence of the variables on the PPT. The level of significance was set at p<0.05. In order to evaluate the influence of the above mentioned variables as contributors to TMD, all subjects were examined according to the American Academy of Orofacial Pain Guidelines for assessment, diagnosis and management of TMD and divided into two groups: group 1 (n=143) subjects without TMD and group 2 (n=148) subjects with TMD myofascial pain. Pearson chi-square test followed by a stepwise multivariate logistic regression was used for statistical analysis. The level of significance was set at p<0.05. According to the first analysis, the PPT of TMJ was negatively influenced by SNPs of COMT Val158Met (p=0.013) and IL6- 174 (p=0.006). No genetic influence was found for PPT of masticatory muscles, which were significantly influenced by poor sleep (p=0.003) and sleep bruxism (p=0.000). After the second analysis, sleep bruxism (p=0.000), poor sleep (p=0.000) and anxiety (p=0.003) were found to be associated with TMD. No association between TMD and the genetic profiles evaluated was found. The results provide evidence that pain sensitivity of TMJ is related to decreased COMT activity, and increased IL-6 activity, while pain sensitivity of masticatory muscles is influenced by sleep disturbances. On the other hand, sleep disturbances and anxiety were pointed as contributing factors for TMD.
id USP_17171de1b74c8b5ec844c57b707aa2f2
oai_identifier_str oai:teses.usp.br:tde-09122021-103657
network_acronym_str USP
network_name_str Biblioteca Digital de Teses e Dissertações da USP
repository_id_str
spelling Influence of psychosocial factors, sleep disturbances and genetic factors on pain sensitivity and temporomandibular disorderInfluência de fatores psicossociais, distúrbios do sono e fatores genéticos na sensibilidade dolorosa e disfunção temporomandibularDor facialFacial PainLimiar da dorPain ThresholdPolimorfismo de nucleotídeo únicoSingle Nucleotide PolymorphismThe present study aimed to evaluate the influence of psychosocial factors depression and anxiety, sleep disturbances poor sleep and bruxism, and single nucleotide polymorphisms of COMT Val158Met (rs4680), IL-1(3954 (rs:1143634), IL6-174 (rs:1800795), IL10-592 (rs:1800872), MMP1-1607 (rs:1799750) and TNF-308 (rs:1800629) as contributors to pain sensitivity and Temporomandibular Disorders. The sample comprised 291 subjects of both genders, with ages ranging from 18 to 65. Psychosocial factors were assessed using Beck Depression Inventory and Beck Anxiety Inventory. Pittsburg Sleep Questionnaire Index Sleep was used to determine sleep quality. Sleep bruxism was diagnosed in accordance with validated clinical diagnostic criteria proposed by American Academy of Sleep Medicine. The saliva samples for the DNA analysis were collected with the Oragene DNA self-collection kit. The single nucleotide polymorphisms analysis was performed using PCR. An algometer was used to record the Pressure Pain Threshold (PPT) value for the TMJ, masseter muscle and anterior temporalis. Linear multiple regression was performed to evaluate the influence of the variables on the PPT. The level of significance was set at p<0.05. In order to evaluate the influence of the above mentioned variables as contributors to TMD, all subjects were examined according to the American Academy of Orofacial Pain Guidelines for assessment, diagnosis and management of TMD and divided into two groups: group 1 (n=143) subjects without TMD and group 2 (n=148) subjects with TMD myofascial pain. Pearson chi-square test followed by a stepwise multivariate logistic regression was used for statistical analysis. The level of significance was set at p<0.05. According to the first analysis, the PPT of TMJ was negatively influenced by SNPs of COMT Val158Met (p=0.013) and IL6- 174 (p=0.006). No genetic influence was found for PPT of masticatory muscles, which were significantly influenced by poor sleep (p=0.003) and sleep bruxism (p=0.000). After the second analysis, sleep bruxism (p=0.000), poor sleep (p=0.000) and anxiety (p=0.003) were found to be associated with TMD. No association between TMD and the genetic profiles evaluated was found. The results provide evidence that pain sensitivity of TMJ is related to decreased COMT activity, and increased IL-6 activity, while pain sensitivity of masticatory muscles is influenced by sleep disturbances. On the other hand, sleep disturbances and anxiety were pointed as contributing factors for TMD.O presente estudo teve como objetivo avaliar a influência de fatores psicossociais depressão e ansiedade; distúrbios do sono má qualidade do sono e bruxismo; e os polimorfismos de nucleotídeo único (SNP) da COMT Val158Met (rs4680), IL-13954 (rs:1143634), IL6-174 (rs:1800795), IL10-592 (rs:1800872), MMP1-1607 (rs:1799750) e TNF-308 (rs:1800629) na sensibilidade dolorosa da Articulação Temporomandibular (ATM) e dos músculos mastigatórios; e como fator contribuinte para Disfunção Temporomandibular (DTM). A amostra foi composta por 291 indivíduos, ambos sexos, com idade entre 18 e 65 anos. Os fatores psicossociais foram avaliados através dos Inventários de Depressão e Ansiedade de Beck. O Índice de Qualidade de Sono de Pittsburg foi utilizado para determinar a qualidade do sono, e o bruxismo do sono foi diagnosticado de acordo com critério de diagnóstico validado proposto pela Academia Americana de Medicina do Sono. Para análise do DNA, utilizou-se amostras de saliva coletadas utilizando-se o kit de autocoleta Oragene® DNA. A análise dos SNPs foi realizada através de PCR. As medições do Limiar de Dor à Pressão (LDP) da ATM, masséter e temporal anterior foram realizadas utilizando-se um algômetro. Regressão múltipla linear foi realizada para avaliar a influência das variáveis no LDP. Com o objetivo de avaliar a influência das variáveis acima mencionadas como contribuintes para DTM, os indivíduos foram examinados de acordo com o guia de avaliação, diagnóstico e tratamento das DTMs da Academia Americana de Dor Orofacial e divididos em dois grupos: grupo 1 (n=143) indivíduos sem DTM e grupo 2 (n=148) indivíduos com DTM. O teste de correlação de Pearson seguido de regressão logística multivariada foi utilizado para análise estatística. O nível de significância foi de 5%. De acordo com a primeira análise, o LDP da ATM foi negativamente influenciado pelos SNPs da COMT Val158Met (p=0,013) e IL6-174 (p=0,006). O LDP da musculatura mastigatória foi negativamente influenciado pela má qualidade de sono (p=0,003) e bruxismo do sono (p=0,000), mas não sofreu influência de nenhum SNP avaliado. Após a segunda análise, bruxismo do sono (p=0,000), má qualidade de sono (p=0,000) e ansiedade (p=0,003) foram associados com a presença de DTM. Nenhuma associação entre DTM e os genótipos avaliados foi encontrada. Os resultados sugerem que a sensibilidade dolorosa da ATM está relacionada com a atividade diminuída da COMT, e com a atividade aumentada da IL-6, enquanto a sensibilidade dos músculos mastigatórios está relacionada com distúrbios do sono. Por outro lado, distúrbios do sono e ansiedade parecem ser fatores contribuintes para DTM, independentemente de fatores genéticos.Biblioteca Digitais de Teses e Dissertações da USPConti, Paulo Cesar RodriguesGarlet, Gustavo PompermaierFiamengui, Livia Maria Sales Pinto2014-12-15info:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/doctoralThesisapplication/pdfhttps://www.teses.usp.br/teses/disponiveis/25/25146/tde-09122021-103657/reponame:Biblioteca Digital de Teses e Dissertações da USPinstname:Universidade de São Paulo (USP)instacron:USPLiberar o conteúdo para acesso público.info:eu-repo/semantics/openAccesseng2021-12-09T20:09:16Zoai:teses.usp.br:tde-09122021-103657Biblioteca Digital de Teses e Dissertaçõeshttp://www.teses.usp.br/PUBhttp://www.teses.usp.br/cgi-bin/mtd2br.plvirginia@if.usp.br|| atendimento@aguia.usp.br||virginia@if.usp.bropendoar:27212021-12-09T20:09:16Biblioteca Digital de Teses e Dissertações da USP - Universidade de São Paulo (USP)false
dc.title.none.fl_str_mv Influence of psychosocial factors, sleep disturbances and genetic factors on pain sensitivity and temporomandibular disorder
Influência de fatores psicossociais, distúrbios do sono e fatores genéticos na sensibilidade dolorosa e disfunção temporomandibular
title Influence of psychosocial factors, sleep disturbances and genetic factors on pain sensitivity and temporomandibular disorder
spellingShingle Influence of psychosocial factors, sleep disturbances and genetic factors on pain sensitivity and temporomandibular disorder
Fiamengui, Livia Maria Sales Pinto
Dor facial
Facial Pain
Limiar da dor
Pain Threshold
Polimorfismo de nucleotídeo único
Single Nucleotide Polymorphism
title_short Influence of psychosocial factors, sleep disturbances and genetic factors on pain sensitivity and temporomandibular disorder
title_full Influence of psychosocial factors, sleep disturbances and genetic factors on pain sensitivity and temporomandibular disorder
title_fullStr Influence of psychosocial factors, sleep disturbances and genetic factors on pain sensitivity and temporomandibular disorder
title_full_unstemmed Influence of psychosocial factors, sleep disturbances and genetic factors on pain sensitivity and temporomandibular disorder
title_sort Influence of psychosocial factors, sleep disturbances and genetic factors on pain sensitivity and temporomandibular disorder
author Fiamengui, Livia Maria Sales Pinto
author_facet Fiamengui, Livia Maria Sales Pinto
author_role author
dc.contributor.none.fl_str_mv Conti, Paulo Cesar Rodrigues
Garlet, Gustavo Pompermaier
dc.contributor.author.fl_str_mv Fiamengui, Livia Maria Sales Pinto
dc.subject.por.fl_str_mv Dor facial
Facial Pain
Limiar da dor
Pain Threshold
Polimorfismo de nucleotídeo único
Single Nucleotide Polymorphism
topic Dor facial
Facial Pain
Limiar da dor
Pain Threshold
Polimorfismo de nucleotídeo único
Single Nucleotide Polymorphism
description The present study aimed to evaluate the influence of psychosocial factors depression and anxiety, sleep disturbances poor sleep and bruxism, and single nucleotide polymorphisms of COMT Val158Met (rs4680), IL-1(3954 (rs:1143634), IL6-174 (rs:1800795), IL10-592 (rs:1800872), MMP1-1607 (rs:1799750) and TNF-308 (rs:1800629) as contributors to pain sensitivity and Temporomandibular Disorders. The sample comprised 291 subjects of both genders, with ages ranging from 18 to 65. Psychosocial factors were assessed using Beck Depression Inventory and Beck Anxiety Inventory. Pittsburg Sleep Questionnaire Index Sleep was used to determine sleep quality. Sleep bruxism was diagnosed in accordance with validated clinical diagnostic criteria proposed by American Academy of Sleep Medicine. The saliva samples for the DNA analysis were collected with the Oragene DNA self-collection kit. The single nucleotide polymorphisms analysis was performed using PCR. An algometer was used to record the Pressure Pain Threshold (PPT) value for the TMJ, masseter muscle and anterior temporalis. Linear multiple regression was performed to evaluate the influence of the variables on the PPT. The level of significance was set at p<0.05. In order to evaluate the influence of the above mentioned variables as contributors to TMD, all subjects were examined according to the American Academy of Orofacial Pain Guidelines for assessment, diagnosis and management of TMD and divided into two groups: group 1 (n=143) subjects without TMD and group 2 (n=148) subjects with TMD myofascial pain. Pearson chi-square test followed by a stepwise multivariate logistic regression was used for statistical analysis. The level of significance was set at p<0.05. According to the first analysis, the PPT of TMJ was negatively influenced by SNPs of COMT Val158Met (p=0.013) and IL6- 174 (p=0.006). No genetic influence was found for PPT of masticatory muscles, which were significantly influenced by poor sleep (p=0.003) and sleep bruxism (p=0.000). After the second analysis, sleep bruxism (p=0.000), poor sleep (p=0.000) and anxiety (p=0.003) were found to be associated with TMD. No association between TMD and the genetic profiles evaluated was found. The results provide evidence that pain sensitivity of TMJ is related to decreased COMT activity, and increased IL-6 activity, while pain sensitivity of masticatory muscles is influenced by sleep disturbances. On the other hand, sleep disturbances and anxiety were pointed as contributing factors for TMD.
publishDate 2014
dc.date.none.fl_str_mv 2014-12-15
dc.type.status.fl_str_mv info:eu-repo/semantics/publishedVersion
dc.type.driver.fl_str_mv info:eu-repo/semantics/doctoralThesis
format doctoralThesis
status_str publishedVersion
dc.identifier.uri.fl_str_mv https://www.teses.usp.br/teses/disponiveis/25/25146/tde-09122021-103657/
url https://www.teses.usp.br/teses/disponiveis/25/25146/tde-09122021-103657/
dc.language.iso.fl_str_mv eng
language eng
dc.relation.none.fl_str_mv
dc.rights.driver.fl_str_mv Liberar o conteúdo para acesso público.
info:eu-repo/semantics/openAccess
rights_invalid_str_mv Liberar o conteúdo para acesso público.
eu_rights_str_mv openAccess
dc.format.none.fl_str_mv application/pdf
dc.coverage.none.fl_str_mv
dc.publisher.none.fl_str_mv Biblioteca Digitais de Teses e Dissertações da USP
publisher.none.fl_str_mv Biblioteca Digitais de Teses e Dissertações da USP
dc.source.none.fl_str_mv
reponame:Biblioteca Digital de Teses e Dissertações da USP
instname:Universidade de São Paulo (USP)
instacron:USP
instname_str Universidade de São Paulo (USP)
instacron_str USP
institution USP
reponame_str Biblioteca Digital de Teses e Dissertações da USP
collection Biblioteca Digital de Teses e Dissertações da USP
repository.name.fl_str_mv Biblioteca Digital de Teses e Dissertações da USP - Universidade de São Paulo (USP)
repository.mail.fl_str_mv virginia@if.usp.br|| atendimento@aguia.usp.br||virginia@if.usp.br
_version_ 1815258017306771456