Objectifs : Le bruxisme survenant au cours du sommeil est un trouble du mouvement caractérisé par du grincement de dents et l’activité rythmique des muscles masticateurs (ARMM). Le bruxisme/ARMM est souvent associé à des mouvements du corps et des à éveils corticaux. Une séquence d’activation précède le ARMM/bruxisme. Ces événements incluent une augmentation des variables suivants : l’activité sympathique (-4 minutes), les activités encéphalographique (-4 second), le fréquence cardiaque, l’amplitude de la respiration (-1 second) et l’activité des muscle suprahyoïdiens (-0.8 second). La présente étude a examiné l’association entre le bruxisme et les changements de la pression artérielle. Méthodes: Dix sujets avec le bruxisme (5 hommes, 5 femmes, âge moyen = 26 ± 1,8) ont complétés 3 nuits de polysomnographie qui comprenait l'enregistrement non invasive de la pression artérielle. La première nuit a servi de dépistage et d’habituation au laboratoire. L'analyse a été réalisée sur les deuxièmes et troisièmes nuits enregistrements. Seuls les épisodes de bruxisme isolés survenant au cours du stade 2 du sommeil ont été utilisés pour l’analyse, pour un total de 65 épisodes. Les mesures des pressions systolique et diastolique ont été prises 20 battements avant et 23 battements après l'apparition de chaque épisode bruxisme lors du sommeil. Les épisodes de bruxisme ont été classés comme suit: 1) bruxisme avec éveil cortical; 2) bruxisme avec mouvement du corps (MC), 3) bruxisme avec éveil cortical et MC. Une quatrième catégorie, bruxisme seul, a également été analysée, mais utilisée comme donnée préliminaire puisque la catégorie se composait de seulement 4 épisodes de bruxisme. Résultats: Les deux pressions systolique et diastolique ont augmenté avec les épisodes de bruxisme. Cette augmentation a été statistiquement significative pour la pression systolique et diastolique pour les épisodes de bruxisme avec éveil cortical et/ou MC (p ≤ 0,05). L’augmentation moyenne de la pression (systolique / diastolique ± SE) a été : 28,4 ± 2,4/13,2 ± 1,5 mm Hg pour le bruxisme avec éveil cortical; 30,7 ± 1,6/19.4 ± 2.3 mm Hg pour bruxisme avec MC; 26.4 ± 2,8 / 14,6 ± 2.0mm Hg pour bruxisme avec éveil cortical et MC; 22,9 ± 5,2/12,4 ± 3,3mm Hg pour les épisodes de bruxisme seuls. Conclusion: Le bruxisme du sommeil est associé à des hausses de la pression artérielle pendant le sommeil. Cette hausse est supérieure dans les épisodes de bruxisme associés à un éveil cortical et / ou MC, qui sont souvent associés avec les événements bruxisme. Ces résultats sont en accord avec nos observations antérieures, où le bruxisme est précédé par une augmentation de l'activité sympathique et de la tachycardie sinusale. / Objectives: Sleep Bruxism (SB) is a movement disorder identified by tooth grinding and rhythmic masticatory muscle activity (RMMA). It is often associated with body movements and sleep arousals. Increases in autonomic sympathetic activities that characterize sleep arousal precede SB. These events include an augmentation of the following variables: sympathetic cardiac activity (-4 minutes), electroencephalography frequencies (-4 seconds), heart rate and respiratory amplitude (-1 seconds), and suprahyoid muscle activity (-0.8 seconds). This study examined whether these sympathetic activities are associated with significant changes in arterial blood pressure (BP). Methods: Ten subjects with SB (5 male; 5 female; mean age ± standard error = 26 ± 1.8) underwent 3 nights of full polysomnography that included non-invasive beat to beat BP recording. The first night served as a screening and habituation night. Analysis was performed on second and third night recordings. Overall analysis was based on single SB episodes occurring in stage 2 sleep only, for a total of 65 episodes. Systolic and diastolic BP measurements were taken from a window of 20 beats before and 23 beats after onset of each SB episode. SB episodes were categorized as: 1) SB + cortical arousal; 2) SB + body movement (BM); 3) SB + cortical arousal + BM. A fourth category, SB alone, was also analysed but used as preliminary data since the category consisted of only 4 episodes. Results: Both systolic and diastolic BP increased with SB episodes. This increase was significant for both systolic and diastolic BP for SB events with cortical arousal and/or BM (p≤0.05). The average BP surges (systolic/diastolic ± SE) were: 28.4 ± 2.4/13.2 ± 1.5mm Hg for SB + cortical arousal; 30.7 ± 1.6/19.4 ± 2.3mm Hg for SB + BM; 26.5 ± 2.8/14.6 ± 2.0mm Hg for SB + cortical arousal + BM; 22.9 ± 5.2/12.4 ± 3.3mm Hg for SB episodes occurring alone. Conclusion: Sleep bruxism is associated with blood pressure fluctuations during sleep. This BP surge is greater in SB episodes associated with cortical arousal and/or BM, which often co-occur with SB events. These results are congruent with our previous observations, where SB is preceded by a rise in sympathetic activity and sinus tachycardia.

Mémoire numérisé par la Division de la gestion de documents et des archives de l'Université de Montréal.

L’activité rythmique des muscles masticateurs (ARMM) pendant le sommeil se retrouve chez environ 60% de la population générale adulte. L'étiologie de ce mouvement n'est pas encore complètement élucidée. Il est cependant démontré que l’augmentation de la fréquence des ARMM peut avoir des conséquences négatives sur le système masticatoire. Dans ce cas, l'ARMM est considérée en tant que manifestation d'un trouble moteur du sommeil connue sous le nom de bruxisme. Selon la Classification Internationale des Troubles du Sommeil, le bruxisme est décrit comme le serrement et grincement des dents pendant le sommeil. La survenue des épisodes d’ARMM est associée à une augmentation du tonus du système nerveux sympathique, du rythme cardiaque, de la pression artérielle et elle est souvent en association avec une amplitude respiratoire accrue. Tous ces événements peuvent être décrits dans le contexte d’un micro-éveil du sommeil. Cette thèse comprend quatre articles de recherche visant à étudier i) l'étiologie de l’ARMM pendant le sommeil en relation aux micro-éveils, et à évaluer ii) les aspects cliniques du bruxisme du sommeil, du point de vue diagnostique et thérapeutique. Pour approfondir l'étiologie de l’ARMM et son association avec la fluctuation des micro-éveils, nous avons analysé le patron cyclique alternant (ou cyclic alternating pattern (CAP) en anglais), qui est une méthode d’analyse qui permet d’évaluer l'instabilité du sommeil et de décrire la puissance des micro-éveils. Le CAP a été étudié chez des sujets bruxeurs et des sujets contrôles qui ont participé à deux protocoles expérimentaux, dans lesquels la structure et la stabilité du sommeil ont été modifiées par l'administration d'un médicament (la clonidine), ou avec l'application de stimulations sensorielles (de type vibratoire/auditif) pendant le sommeil. Dans ces deux conditions expérimentales caractérisées par une instabilité accrue du sommeil, nous étions en mesure de démontrer que les micro-éveils ne sont pas la cause ou le déclencheur de l’ARMM, mais ils représentent plutôt la «fenêtre permissive» qui facilite l'apparition de ces mouvements rythmiques au cours du sommeil. Pour évaluer la pertinence clinique du bruxisme, la prévalence et les facteurs de risque, nous avons effectué une étude épidémiologique dans une population pédiatrique (7-17 ans) qui était vue en consultation en orthodontie. Nous avons constaté que le bruxisme est un trouble du sommeil très fréquent chez les enfants (avec une prévalence de 15%), et il est un facteur de risque pour l'usure des dents (risque relatif rapproché, RRR 8,8), la fatigue des muscles masticateurs (RRR 10,5), les maux de tête fréquents (RRR 4,3), la respiration bruyante pendant le sommeil (RRR 3,1), et divers symptômes liés au sommeil, tels que la somnolence diurne (RRR 7,4). Ces résultats nous ont amenés à développer une étude expérimentale pour évaluer l'efficacité d'un appareil d'avancement mandibulaire (AAM) chez un groupe d'adolescents qui présentaient à la fois du bruxisme, du ronflement et des maux de tête fréquents. L'hypothèse est que dans la pathogenèse de ces comorbidités, il y a un mécanisme commun, probablement lié à la respiration pendant le sommeil, et que l'utilisation d'un AAM peut donc agir sur plusieurs aspects liés. À court terme, le traitement avec un AAM semble diminuer l'ARMM (jusqu'à 60% de diminution), et améliorer le ronflement et les maux de tête chez les adolescents. Cependant, le mécanisme d'action exact des AAM demeure incertain; leur efficacité peut être liée à l'amélioration de la respiration pendant le sommeil, mais aussi à l'influence que ces appareils pourraient avoir sur le système masticatoire. Les interactions entre le bruxisme du sommeil, la respiration et les maux de tête, ainsi que l'efficacité et la sécurité à long terme des AAM chez les adolescents, nécessitent des études plus approfondies. / Approximately 60% of the general adult population experiences rhythmic masticatory muscle activity (RMMA) during sleep. The etiology of this movement is not yet understood. However, it has been demonstrated that an increased frequency of RMMA may have detrimental consequences on the stomatognathic system. In this case, RMMA is considered the manifestation of a sleep-related motor disorder known as sleep bruxism (SB). According to the definition of the International Classification of Sleep Disorders, SB is the activity of tooth grinding and clenching during sleep. The occurrence of SB-related activity, i.e., RMMA, is associated with rises of sympathetic tone, heart rate, blood pressure, and it is frequently concomitant with larger respiratory breaths. All these events can be described within a sleep arousal. The present thesis includes four research articles aimed to study i) the etiology of RMMA during sleep in relation to sleep arousal; and ii) the clinical perspectives of SB assessment and management. To further investigate the etiology of RMMA and its association with sleep arousal fluctuations we analyzed the cyclic alternating pattern (CAP), a scoring method to assess sleep instability and describe sleep arousal pressure. CAP was scored in SB subjects and controls that participated in two experimental protocols in which sleep architecture and stability were altered by either a medication (i.e., clonidine), or sensory stimulations (i.e., vibratory/auditory). Under these experimental conditions known to increase sleep instability, we were able to show that sleep arousal is not the trigger or cause of RMMA, rather the “permissive window” that facilitates the occurrence of RMMA during sleep. To evaluate the clinical relevance of SB, we conducted a survey on a 7-17 year old orthodontic population to investigate the prevalence and risk factors associated with SB. It appeared that SB is a highly prevalent sleep disorders in children (15% of prevalence), and is a risk factor for tooth wear (odds ratio, OR 8.8), jaw muscle fatigue (OR 10.5), frequent headache (OR 4.3), loud breathing during sleep (OR 3.1), and several sleep complaints, such as daytime sleepiness (OR 7.4). These findings led us to design an experimental trial using a mandibular advancement appliance (MAA) in adolescents in order to investigate the possible relationship between SB, snoring, and headache. We hypothesized that a common underlying mechanism related to breathing during sleep may be responsible for all concomitant conditions. The short-term use of an MAA appeared to reduce SB (up to 60%), and improve snoring and headache complaints in adolescents. However, the precise mechanism of action of MAA remains under debate; its effectiveness can be either related to the improvement of breathing during sleep, or its influence on the masticatory system. The interactions between SB, breathing, and headache as well as the long-term effectiveness and safety of the MAA in adolescents need further investigations. / L’attività ritmica dei muscoli masticatori (ARMM) durante il sonno si osserva in circa il 60% della popolazione generale adulta. L'eziologia di questo movimento non è stata ancora del tutto compresa. Tuttavia, è dimostrato che un’aumentata frequenza di ARMM può avere conseguenze negative sul sistema stomatognatico. In questo caso, l’ARMM è considerato la manifestazione di un disturbo motorio del sonno noto come bruxismo. Secondo la Classificazione Internazionale dei Disturbi del Sonno, il bruxismo è l'attività di digrignamento e serramento dei denti durante il sonno. La comparsa di episodi di ARMM durante il sonno è associata a un aumento del tono del sistema nervoso simpatico, della frequenza cardiaca, della pressione arteriosa, ed è spesso in concomitanza con un aumentato volume inspiratorio. Le variazioni di questi parametri fisiologici sono compresi nel contesto di un arousal (micro risveglio) del sonno. Questa tesi comprende quattro articoli di ricerca volti a studiare i) l'eziologia dell’ARMM durante il sonno in relazione all’arousal, ed a valutare ii) l’inquadramento clinico del bruxismo nel sonno. Per approfondire l'eziologia dell’ARMM e l’associazione con l’arousal nel sonno, abbiamo analizzato il cyclic alternating pattern (CAP), che permette di valutare l'instabilità del sonno e descrivere la potenza degli arousals. Il CAP è stato esaminato in soggetti con bruxismo e soggetti controllo che hanno partecipato in due protocolli sperimentali, in cui la struttura e la stabilità del sonno sono stati modificati con la somministrazione di un farmaco (la clonidina), o con l’applicazione di stimolazioni sensoriali (di tipo vibratorio/uditivo) durante il sonno. In queste condizioni sperimentali caratterizzate da un’aumentata instabilità del sonno, siamo stati in grado di dimostrare che l’arousal non è la causa o il generatore dell’ARMM, ma piuttosto la "finestra permissiva" che facilita il verificarsi di questi movimenti ritmici durante il sonno. Per valutare la rilevanza clinica del bruxismo, abbiamo condotto uno studio epidemiologico in una popolazione pediatrica afferente alla clinica di ortodonzia per studiare la prevalenza e i fattori di rischio associati al bruxismo. Questa ricerca ha evidenziato che il bruxismo è un comune disturbo del sonno nei bambini (con una prevalenza del 15%), ed è un fattore di rischio per usura dentale (odds ratio, OR 8.8), fatica dei muscoli masticatori (OR 10.5), mal di testa frequenti (OR 4.3), respirazione rumorosa durante il sonno (OR 3.1), e diversi sintomi legati al sonno, quali la sonnolenza diurna (OR 7.4). Questi risultati ci hanno portato a progettare uno studio sperimentale per valutare l’efficacia di un apparecchio di avanzamento mandibolare (AAM) in un gruppo di adolescenti che presentavano al contempo bruxismo, russamento e frequenti cefalee. L’ipotesi è che nella patogenesi di tali comorbidità, vi sia un meccanismo comune, probabilmente legato alla respirazione durante il sonno, e che l’utilizzo di un AAM possa quindi avere un beneficio multiplo. Il trattamento a breve termine con un AAM sembra diminuire l’ARMM (fino al 60%) e migliorare il russamento e i mal di testa negli adolescenti. Tuttavia, l'esatto meccanismo di azione degli AAM rimane incerto; la loro efficacia può essere correlata sia al miglioramento della respirazione durante il sonno, ma anche all’influenza che questi apparecchi svolgono sul sistema masticatorio. Le interazioni tra il bruxismo nel sonno, la respirazione, e le cefalee, così come l'efficacia e la sicurezza a lungo termine degli AAM negli adolescenti, necessitano di ulteriori studi clinici.

Dentre os fatores etiológicos das Disfunções Temporomandibulares (DTMs) merecem destaque os hábitos parafuncionais, que muitas vezes são responsáveis pela manutenção da dor, perda de estrutura dental, como as facetas de desgaste, abfrações e por alterações na mucosa jugal e língua. Uma das terapêuticas mais utilizadas para o tratamento da DTM, está relacionada ao uso da placa estabilizadora oclusal (PEO). Apesar de seu uso ser estudado em vários artigos, não são encontrados relatos sobre as marcas encontradas nesse dispositivo devido ao atrito sofrido pelos dentes tampouco quais são os parâmetros e variáveis que poderiam estar relacionados à estas marcas. O presente estudo procurou reproduzir as marcas observadas na PEO, em 36 corpos de prova de resina acrílica ativada quimicamente, em ambiente controlado e analisou os parâmetros e variáveis para avaliação entre marcas fracas e fortes. Para reprodução das marcas nas amostras, foram utilizadas esferas de aço com diâmetros de 3 mm, 4 mm e 5 mm. Para cada diâmetro de esfera foram utilizados os seguintes parâmetros: carga de 2 kgf e 65 kgf e ciclos de repetições de 600 e 1200 vezes. As amostras foram randomizadas com números aleatórios e estabelecido padrão entre marcas fracas e fortes para cada diâmetro de esfera, com apenas uma amostra de cada triplicata. Na sequência, 3 observadores cegos fizeram suas classificações para correlação do padrão. Para correlação do padrão vs. observadores e observadores entre observadores, foi realizado o teste kappa de Fleiss. Foram obtidos níveis excelentes em todos os testes, quando não havia mistura de diâmetro de esfera, e nível razoável quando os observadores avaliaram as amostras com os diâmetros de esferas misturados. Relacionado aos resultados, as variáveis consideradas foram, diâmetro da calota impressa e profundidade calculada da calota com a fórmula da dureza Brinell. As variáveis, dureza e diâmetro de calota impressa, não demostraram robustez para estabelecer critério na avalição entre marca forte e fraca. Já a variável \"profundidade calculada de calota\" demostrou que ao passo que aumentava a profundidade calculada da calota, a marca tinha maior tendência a ser classificada como forte. Desta forma, pode-se concluir que o parâmetro carga foi o fator de maior relevância na classificação entre as marcas fracas e fortes. A variável profundidade calculada da calota mostrou relevância na classificação das marcas fortes e fracas e os diâmetros de esferas diferentes, com mesma carga e quantidade de ciclos geraram marcas diferentes. / Among the etiological factors of TMDs is the parafunctional habits, which are often responsible for the loss of dental structure, such as the wear facets and abfraction and changes in the oral mucosa, such as cheeks and tongue. One of the most used therapies for the treatment of TMD is related to the use of the occlusal splint (OS). Although its use is reported in several articles, no reports are found on the marks found in this device due to the friction suffered by the teeth, nor are the parameters and variables that are related to these marks. The present study reproduced the observed marks in the OS in 36 chemically activated acrylic resin samples in a controlled environment and analyzed the parameters and variables for evaluation between weak and strong marks. For the reproduction of the marks in the samples, stainless steel sphere with different diameters of 3 mm, 4 mm and 5 mm were used. For each sphere diameter the following parameters were used: load of 2 kgf and 65 kgf and repetition cycles of 600 and 1200 times. Samples were randomized with random numbers and established pattern between weak and strong marks for each sphere diameter, with only one sample from each triplicate. Subsequently, 3 observers made their classifications for pattern correlation. For correlation of the Standard vs. Observers and Between Observers, the Fleiss kappa test was performed. Excellent levels were obtained in all tests, when there was no sphere diameter crossing, and fair level when observers evaluated the samples with the sphere diameters crossed. Regarding the results, the variables considered were Brinell hardness, diameter of the printed cap and depth of the cap. The variables, hardness and diameter of printed cap, did not demonstrate the robustness to establish standard in the evaluation between weak and Strong marks. The variable depth of printed cap proves that while the depth of the printed cap increased, the mark had a more tendency to be classified as strong. In this way, we can conclude that the load parameter is the factor of greater relevance in the classification between the weak and strong marks. The variable depth of the printed cap demonstrated relevance in the classification of the weak and strong marks, and finally the diameters of different spheres with the same load and number of cycles created different marks.

O núcleo motor do trigêmeo (Mo5) está cercado por um anel de neurônios pré-motores localizados na região h. Estudos demonstram que neurônios que inervam o Mo5 estão distribuídos no tronco encefálico e no prosencéfalo. Após implante de traçador retrógrado no Mo5, verificamos células retrogradamente marcadas no núcleo mesencefálico do trigêmeo (Me5), na região h e em núcleos prosencefálicos como o central da amígdala (CeA), a área hipotalâmica lateral (LH) e o parasubtalâmico (PSTh). Para confirmação, realizamos injeção de traçador anterógrado e investigamos, também, a neuroquímica das projeções. Neurônios do CeA que se projetam para o Mo5 recebem inervação de fibras imunorreativas ao fator liberador de corticotrofina (CFR-ir) e/ou à tirosina hidroxilase (TH-ir); alguns neurônios da LH que se projetam para o Mo5 são imunorreativos à orexina (ORX) e alguns neurônios do PSTh que se projetam para o Mo5 são innervados por fibras TH-ir. O Me5 recebe grande inervação do CeA e moderada da LH e do PSTh, possuindo grande aferência de fibras imunorreativas ao CRF, ORX e TH / The trigeminal motor nucleus (Mo5) is surrounded by a ring of premotor neurons defined as the h region. Studies have shown that neurons innervating the Mo5 are located in brainstem and in forebrain nuclei. Through the injection of the retrograde tracer cholera toxin b subunit/CTb in the Mo5, we found retrograde labeled neurons in the brainstem including the h region and the mesencephalic trigeminal nucleus (Me5), and in forebrain nuclei such as the central nucleus of amygdala (CeA), the lateral hypothalamic area (LH) and the parasubthalamic nucleus (PSTh). As control, we injected the anterograde tracer biotin dextran amine and found that these areas project direct or indirectly via the h region or the Me5 to the Mo5. Some CeA neurons that project to the Mo5 receive corticotrophin releasing factor (CRF) and tyrosine hydroxylase (TH) innervation, some LH neurons that project to Mo5 express orexin, and PSTh neurons that project to the Mo5 receive TH innervation. The Me5 is also innervated by CeA, LH and PSTh neurons and by CRF, orexin and TH immunoreactive fibers

Objetivos: Comparar o efeito de três intervenções de fisioterapia com tratamento odontológico na dor e sintomas, abertura mandibular, ansiedade, estresse, depressão, qualidade de saúde bucal e sono em indivíduos com bruxismo. Métodos: Noventa e seis indivíduos com dor e bruxismo do sono e vigília entre 18 e 60 anos de idade foram randomizados em quatro grupos: Grupo 1 (n=24) massoterapia e exercícios de alongamento muscular; Grupo 2 (n=24) terapia de relaxamento e imaginação; Grupo 3 (n=24) massoterapia, exercícios, relaxamento e imaginação e Grupo 4 (n=24) tratamento odontológico pela restauração direta. As variáveis primárias foram dor e sintomas, sendo a intensidade avaliada pela escala visual analógica e limiar de dor com dolorímetro; e abertura mandibular com paquímetro digital. As variáveis secundárias foram ansiedade avaliada com Inventário de Ansiedade Traço-Estado; estresse com Escala de Estresse Percebido; depressão com Inventário de Depressão de Beck; qualidade de saúde bucal com Perfil de Impacto de Saúde Bucal e sono com Índice de Qualidade de Sono de Pittsburgh. Todos os participantes foram avaliados antes, após seis semanas e dois meses das intervenções por avaliador cego. As intervenções de fisioterapia foram individualizadas por 40 minutos, duas vezes por semana, por seis semanas; e o tratamento odontológico incluiu duas sessões individuais, com intervalo de uma semana e duração de aproximadamente duas horas. O nível de significância estabelecido foi alfa=5%. Resultados: Após seis semanas, houve melhora com diferença significativa entre os Grupos 1, 2 e 3 e o Grupo 4 na dor muscular do masseter [Média da Diferença=2,3 / 2,7 / 5,5 (IC95%=0,2 a 4,4 / 0,9 a 4,4 / 3,8 a 7,2)], temporal anterior [Média da Diferença=2,6 / 2,1 / 5 (IC95%=0,5 a 4,7 / 0,1 a 4,1 / 3,2 a 6,7)], esternocleidomastóideo [Média da Diferença=3,3 / 4,2 / 6,1 (IC95%=1,6 a 4,9 / 2,6 a 5,8 / 4,6 a 7,5)] e trapézio superior [Média da Diferença=3,8 / 4,1 / 6,6 (IC95% = 2,1 a 5,5 / 2,3 a 5,5 / 5,4 a 7,7)]. Melhora similar foi encontrada nos sintomas de cefaleia, apertamento dentário e dificuldade de dormir, bem como no estado de ansiedade, estresse, depressão e qualidade de sono (p < 0,001). Os Grupos 2 e 3 melhoraram o traço de ansiedade e qualidade de saúde bucal e o Grupo 3 melhorou o limiar de dor do músculo trapézio superior e abertura mandibular, com diferença significativa comparados ao Grupo 4 (p < 0,05). Houve manutenção destas melhoras dois meses após as intervenções (p < 0,05), porém a melhora na qualidade de saúde bucal e aumento na abertura mandibular não se mantiveram nos Grupos 2 e 3 (p > 0,05), respectivamente. Conclusão: Os dados sugerem que as três intervenções de fisioterapia comparadas a tratamento odontológico reduzem a dor e sintomas e indicam melhora da ansiedade, estresse, depressão e qualidade de sono. Os resultados apontam que as intervenções de fisioterapia: isolada (terapia de relaxamento e imaginação) e combinada (massoterapia, exercícios, relaxamento e imaginação) melhoram a qualidade de saúde bucal; e somente a combinada aumenta o limiar de dor no músculo trapézio superior e abertura mandibular em indivíduos com bruxismo / Objectives: To compare the effects of three different physical therapy interventions with dental treatment in the pain and symptoms, mandibular opening, anxiety, stress, depression, oral health and sleep in individuals with bruxism. Methods: Ninety-six individuals with pain and awake and sleep bruxism and 18-60 years old were allocated to the one of four groups: Group 1: massage and stretching exercises (n=24), Group 2: relaxation therapy and imagination (n=24), Group 3: massage, exercises, relaxation and imagination (n=24) or Group 4: dental treatment by the direct restoration (n=24). Primary outcomes included muscle pain and symptoms (intensity measured using a visual analogue scale and pain threshold with algometry) and mandibular opening (measured using a digital pachymeter). Secondary outcomes included anxiety (state-trait anxiety inventory), stress (perceived stress scale), depression (Beck depression inventory), oral health (oral health impact profile-14), and sleep quality (Pittsburgh sleep quality index). Outcomes were evaluated at baseline, 6 weeks and 2 months post-initial intervention by the blinded assessor. Physical therapy interventions included individual sessions that lasted 40 min biweekly for 6 weeks and dental treatment, two 2-h individual sessions conducted a week apart. The level of significance established was alfa=5%. Results: At 6 weeks after, the improvement with difference among Groups 1, 2, 3 and Group 4 was observed in masseter muscle pain [Mean Difference=2.3 / 2.7 / 5.5 (95%CI=0.2 to 4.4 / 0.9 to 4.4 / 3.8 to 7.2)], anterior temporalis [Mean Difference=2.6 / 2.1 / 5 (95%CI=0.5 to 4.7 / 0.1 to 4.1 / 3.2 to 6.7)], sternocleidomastoid [Mean Difference=3.3 / 4.2 / 6.1 (95%CI=1.6 to 4.9 / 2.6 to 5.8 / 4.6 to 7.5)] and upper trapezius [Mean Difference=3.8 / 4.1 /6.6 (95%CI=2.1 to 5.5 / 2.3 to 5.5 / 5.4 to7.7)] as well as in symptoms of headache, teeth clenching and sleep difficulties, anxiety state, stress, depression and sleep quality (p < 0.001). Both Group 2 as Group 3 improved oral health and anxiety trait and the Group 3 increased the pain threshold of upper trapezius muscle and mandibular opening with significant difference relative to Group 4 (p < 0.05). These results were sustained for up to 2 months (p < 0.05), however the improvements of oral health and mandibular opening were not maintained in Groups 2 and 3(p > 0.05), respectively. Conclusions: The results suggest that three physical therapy interventions compared to dental treatment reduce the pain and symptoms and indicate improvement of anxiety, stress, depression and sleep quality. Moreover, the date demonstrate that both combined physical therapy interventions (massage, exercises, relaxation and imagination) as isolated (relaxation therapy and imagination) improve the oral health and only the combined increases the mandibular opening and pain threshold of upper trapezius muscle in individuals with bruxism

Objectifs : Le bruxisme survenant au cours du sommeil est un trouble du mouvement caractérisé par du grincement de dents et l’activité rythmique des muscles masticateurs (ARMM). Le bruxisme/ARMM est souvent associé à des mouvements du corps et des à éveils corticaux. Une séquence d’activation précède le ARMM/bruxisme. Ces événements incluent une augmentation des variables suivants : l’activité sympathique (-4 minutes), les activités encéphalographique (-4 second), le fréquence cardiaque, l’amplitude de la respiration (-1 second) et l’activité des muscle suprahyoïdiens (-0.8 second). La présente étude a examiné l’association entre le bruxisme et les changements de la pression artérielle. Méthodes: Dix sujets avec le bruxisme (5 hommes, 5 femmes, âge moyen = 26 ± 1,8) ont complétés 3 nuits de polysomnographie qui comprenait l'enregistrement non invasive de la pression artérielle. La première nuit a servi de dépistage et d’habituation au laboratoire. L'analyse a été réalisée sur les deuxièmes et troisièmes nuits enregistrements. Seuls les épisodes de bruxisme isolés survenant au cours du stade 2 du sommeil ont été utilisés pour l’analyse, pour un total de 65 épisodes. Les mesures des pressions systolique et diastolique ont été prises 20 battements avant et 23 battements après l'apparition de chaque épisode bruxisme lors du sommeil. Les épisodes de bruxisme ont été classés comme suit: 1) bruxisme avec éveil cortical; 2) bruxisme avec mouvement du corps (MC), 3) bruxisme avec éveil cortical et MC. Une quatrième catégorie, bruxisme seul, a également été analysée, mais utilisée comme donnée préliminaire puisque la catégorie se composait de seulement 4 épisodes de bruxisme. Résultats: Les deux pressions systolique et diastolique ont augmenté avec les épisodes de bruxisme. Cette augmentation a été statistiquement significative pour la pression systolique et diastolique pour les épisodes de bruxisme avec éveil cortical et/ou MC (p ≤ 0,05). L’augmentation moyenne de la pression (systolique / diastolique ± SE) a été : 28,4 ± 2,4/13,2 ± 1,5 mm Hg pour le bruxisme avec éveil cortical; 30,7 ± 1,6/19.4 ± 2.3 mm Hg pour bruxisme avec MC; 26.4 ± 2,8 / 14,6 ± 2.0mm Hg pour bruxisme avec éveil cortical et MC; 22,9 ± 5,2/12,4 ± 3,3mm Hg pour les épisodes de bruxisme seuls. Conclusion: Le bruxisme du sommeil est associé à des hausses de la pression artérielle pendant le sommeil. Cette hausse est supérieure dans les épisodes de bruxisme associés à un éveil cortical et / ou MC, qui sont souvent associés avec les événements bruxisme. Ces résultats sont en accord avec nos observations antérieures, où le bruxisme est précédé par une augmentation de l'activité sympathique et de la tachycardie sinusale. / Objectives: Sleep Bruxism (SB) is a movement disorder identified by tooth grinding and rhythmic masticatory muscle activity (RMMA). It is often associated with body movements and sleep arousals. Increases in autonomic sympathetic activities that characterize sleep arousal precede SB. These events include an augmentation of the following variables: sympathetic cardiac activity (-4 minutes), electroencephalography frequencies (-4 seconds), heart rate and respiratory amplitude (-1 seconds), and suprahyoid muscle activity (-0.8 seconds). This study examined whether these sympathetic activities are associated with significant changes in arterial blood pressure (BP). Methods: Ten subjects with SB (5 male; 5 female; mean age ± standard error = 26 ± 1.8) underwent 3 nights of full polysomnography that included non-invasive beat to beat BP recording. The first night served as a screening and habituation night. Analysis was performed on second and third night recordings. Overall analysis was based on single SB episodes occurring in stage 2 sleep only, for a total of 65 episodes. Systolic and diastolic BP measurements were taken from a window of 20 beats before and 23 beats after onset of each SB episode. SB episodes were categorized as: 1) SB + cortical arousal; 2) SB + body movement (BM); 3) SB + cortical arousal + BM. A fourth category, SB alone, was also analysed but used as preliminary data since the category consisted of only 4 episodes. Results: Both systolic and diastolic BP increased with SB episodes. This increase was significant for both systolic and diastolic BP for SB events with cortical arousal and/or BM (p≤0.05). The average BP surges (systolic/diastolic ± SE) were: 28.4 ± 2.4/13.2 ± 1.5mm Hg for SB + cortical arousal; 30.7 ± 1.6/19.4 ± 2.3mm Hg for SB + BM; 26.5 ± 2.8/14.6 ± 2.0mm Hg for SB + cortical arousal + BM; 22.9 ± 5.2/12.4 ± 3.3mm Hg for SB episodes occurring alone. Conclusion: Sleep bruxism is associated with blood pressure fluctuations during sleep. This BP surge is greater in SB episodes associated with cortical arousal and/or BM, which often co-occur with SB events. These results are congruent with our previous observations, where SB is preceded by a rise in sympathetic activity and sinus tachycardia.

Mémoire numérisé par la Division de la gestion de documents et des archives de l'Université de Montréal

L’activité rythmique des muscles masticateurs (ARMM) pendant le sommeil se retrouve chez environ 60% de la population générale adulte. L'étiologie de ce mouvement n'est pas encore complètement élucidée. Il est cependant démontré que l’augmentation de la fréquence des ARMM peut avoir des conséquences négatives sur le système masticatoire. Dans ce cas, l'ARMM est considérée en tant que manifestation d'un trouble moteur du sommeil connue sous le nom de bruxisme. Selon la Classification Internationale des Troubles du Sommeil, le bruxisme est décrit comme le serrement et grincement des dents pendant le sommeil. La survenue des épisodes d’ARMM est associée à une augmentation du tonus du système nerveux sympathique, du rythme cardiaque, de la pression artérielle et elle est souvent en association avec une amplitude respiratoire accrue. Tous ces événements peuvent être décrits dans le contexte d’un micro-éveil du sommeil. Cette thèse comprend quatre articles de recherche visant à étudier i) l'étiologie de l’ARMM pendant le sommeil en relation aux micro-éveils, et à évaluer ii) les aspects cliniques du bruxisme du sommeil, du point de vue diagnostique et thérapeutique. Pour approfondir l'étiologie de l’ARMM et son association avec la fluctuation des micro-éveils, nous avons analysé le patron cyclique alternant (ou cyclic alternating pattern (CAP) en anglais), qui est une méthode d’analyse qui permet d’évaluer l'instabilité du sommeil et de décrire la puissance des micro-éveils. Le CAP a été étudié chez des sujets bruxeurs et des sujets contrôles qui ont participé à deux protocoles expérimentaux, dans lesquels la structure et la stabilité du sommeil ont été modifiées par l'administration d'un médicament (la clonidine), ou avec l'application de stimulations sensorielles (de type vibratoire/auditif) pendant le sommeil. Dans ces deux conditions expérimentales caractérisées par une instabilité accrue du sommeil, nous étions en mesure de démontrer que les micro-éveils ne sont pas la cause ou le déclencheur de l’ARMM, mais ils représentent plutôt la «fenêtre permissive» qui facilite l'apparition de ces mouvements rythmiques au cours du sommeil. Pour évaluer la pertinence clinique du bruxisme, la prévalence et les facteurs de risque, nous avons effectué une étude épidémiologique dans une population pédiatrique (7-17 ans) qui était vue en consultation en orthodontie. Nous avons constaté que le bruxisme est un trouble du sommeil très fréquent chez les enfants (avec une prévalence de 15%), et il est un facteur de risque pour l'usure des dents (risque relatif rapproché, RRR 8,8), la fatigue des muscles masticateurs (RRR 10,5), les maux de tête fréquents (RRR 4,3), la respiration bruyante pendant le sommeil (RRR 3,1), et divers symptômes liés au sommeil, tels que la somnolence diurne (RRR 7,4). Ces résultats nous ont amenés à développer une étude expérimentale pour évaluer l'efficacité d'un appareil d'avancement mandibulaire (AAM) chez un groupe d'adolescents qui présentaient à la fois du bruxisme, du ronflement et des maux de tête fréquents. L'hypothèse est que dans la pathogenèse de ces comorbidités, il y a un mécanisme commun, probablement lié à la respiration pendant le sommeil, et que l'utilisation d'un AAM peut donc agir sur plusieurs aspects liés. À court terme, le traitement avec un AAM semble diminuer l'ARMM (jusqu'à 60% de diminution), et améliorer le ronflement et les maux de tête chez les adolescents. Cependant, le mécanisme d'action exact des AAM demeure incertain; leur efficacité peut être liée à l'amélioration de la respiration pendant le sommeil, mais aussi à l'influence que ces appareils pourraient avoir sur le système masticatoire. Les interactions entre le bruxisme du sommeil, la respiration et les maux de tête, ainsi que l'efficacité et la sécurité à long terme des AAM chez les adolescents, nécessitent des études plus approfondies. / Approximately 60% of the general adult population experiences rhythmic masticatory muscle activity (RMMA) during sleep. The etiology of this movement is not yet understood. However, it has been demonstrated that an increased frequency of RMMA may have detrimental consequences on the stomatognathic system. In this case, RMMA is considered the manifestation of a sleep-related motor disorder known as sleep bruxism (SB). According to the definition of the International Classification of Sleep Disorders, SB is the activity of tooth grinding and clenching during sleep. The occurrence of SB-related activity, i.e., RMMA, is associated with rises of sympathetic tone, heart rate, blood pressure, and it is frequently concomitant with larger respiratory breaths. All these events can be described within a sleep arousal. The present thesis includes four research articles aimed to study i) the etiology of RMMA during sleep in relation to sleep arousal; and ii) the clinical perspectives of SB assessment and management. To further investigate the etiology of RMMA and its association with sleep arousal fluctuations we analyzed the cyclic alternating pattern (CAP), a scoring method to assess sleep instability and describe sleep arousal pressure. CAP was scored in SB subjects and controls that participated in two experimental protocols in which sleep architecture and stability were altered by either a medication (i.e., clonidine), or sensory stimulations (i.e., vibratory/auditory). Under these experimental conditions known to increase sleep instability, we were able to show that sleep arousal is not the trigger or cause of RMMA, rather the “permissive window” that facilitates the occurrence of RMMA during sleep. To evaluate the clinical relevance of SB, we conducted a survey on a 7-17 year old orthodontic population to investigate the prevalence and risk factors associated with SB. It appeared that SB is a highly prevalent sleep disorders in children (15% of prevalence), and is a risk factor for tooth wear (odds ratio, OR 8.8), jaw muscle fatigue (OR 10.5), frequent headache (OR 4.3), loud breathing during sleep (OR 3.1), and several sleep complaints, such as daytime sleepiness (OR 7.4). These findings led us to design an experimental trial using a mandibular advancement appliance (MAA) in adolescents in order to investigate the possible relationship between SB, snoring, and headache. We hypothesized that a common underlying mechanism related to breathing during sleep may be responsible for all concomitant conditions. The short-term use of an MAA appeared to reduce SB (up to 60%), and improve snoring and headache complaints in adolescents. However, the precise mechanism of action of MAA remains under debate; its effectiveness can be either related to the improvement of breathing during sleep, or its influence on the masticatory system. The interactions between SB, breathing, and headache as well as the long-term effectiveness and safety of the MAA in adolescents need further investigations. / L’attività ritmica dei muscoli masticatori (ARMM) durante il sonno si osserva in circa il 60% della popolazione generale adulta. L'eziologia di questo movimento non è stata ancora del tutto compresa. Tuttavia, è dimostrato che un’aumentata frequenza di ARMM può avere conseguenze negative sul sistema stomatognatico. In questo caso, l’ARMM è considerato la manifestazione di un disturbo motorio del sonno noto come bruxismo. Secondo la Classificazione Internazionale dei Disturbi del Sonno, il bruxismo è l'attività di digrignamento e serramento dei denti durante il sonno. La comparsa di episodi di ARMM durante il sonno è associata a un aumento del tono del sistema nervoso simpatico, della frequenza cardiaca, della pressione arteriosa, ed è spesso in concomitanza con un aumentato volume inspiratorio. Le variazioni di questi parametri fisiologici sono compresi nel contesto di un arousal (micro risveglio) del sonno. Questa tesi comprende quattro articoli di ricerca volti a studiare i) l'eziologia dell’ARMM durante il sonno in relazione all’arousal, ed a valutare ii) l’inquadramento clinico del bruxismo nel sonno. Per approfondire l'eziologia dell’ARMM e l’associazione con l’arousal nel sonno, abbiamo analizzato il cyclic alternating pattern (CAP), che permette di valutare l'instabilità del sonno e descrivere la potenza degli arousals. Il CAP è stato esaminato in soggetti con bruxismo e soggetti controllo che hanno partecipato in due protocolli sperimentali, in cui la struttura e la stabilità del sonno sono stati modificati con la somministrazione di un farmaco (la clonidina), o con l’applicazione di stimolazioni sensoriali (di tipo vibratorio/uditivo) durante il sonno. In queste condizioni sperimentali caratterizzate da un’aumentata instabilità del sonno, siamo stati in grado di dimostrare che l’arousal non è la causa o il generatore dell’ARMM, ma piuttosto la "finestra permissiva" che facilita il verificarsi di questi movimenti ritmici durante il sonno. Per valutare la rilevanza clinica del bruxismo, abbiamo condotto uno studio epidemiologico in una popolazione pediatrica afferente alla clinica di ortodonzia per studiare la prevalenza e i fattori di rischio associati al bruxismo. Questa ricerca ha evidenziato che il bruxismo è un comune disturbo del sonno nei bambini (con una prevalenza del 15%), ed è un fattore di rischio per usura dentale (odds ratio, OR 8.8), fatica dei muscoli masticatori (OR 10.5), mal di testa frequenti (OR 4.3), respirazione rumorosa durante il sonno (OR 3.1), e diversi sintomi legati al sonno, quali la sonnolenza diurna (OR 7.4). Questi risultati ci hanno portato a progettare uno studio sperimentale per valutare l’efficacia di un apparecchio di avanzamento mandibolare (AAM) in un gruppo di adolescenti che presentavano al contempo bruxismo, russamento e frequenti cefalee. L’ipotesi è che nella patogenesi di tali comorbidità, vi sia un meccanismo comune, probabilmente legato alla respirazione durante il sonno, e che l’utilizzo di un AAM possa quindi avere un beneficio multiplo. Il trattamento a breve termine con un AAM sembra diminuire l’ARMM (fino al 60%) e migliorare il russamento e i mal di testa negli adolescenti. Tuttavia, l'esatto meccanismo di azione degli AAM rimane incerto; la loro efficacia può essere correlata sia al miglioramento della respirazione durante il sonno, ma anche all’influenza che questi apparecchi svolgono sul sistema masticatorio. Le interazioni tra il bruxismo nel sonno, la respirazione, e le cefalee, così come l'efficacia e la sicurezza a lungo termine degli AAM negli adolescenti, necessitano di ulteriori studi clinici.

O núcleo motor do trigêmeo (Mo5) está cercado por um anel de neurônios pré-motores localizados na região h. Estudos demonstram que neurônios que inervam o Mo5 estão distribuídos no tronco encefálico e no prosencéfalo. Após implante de traçador retrógrado no Mo5, verificamos células retrogradamente marcadas no núcleo mesencefálico do trigêmeo (Me5), na região h e em núcleos prosencefálicos como o central da amígdala (CeA), a área hipotalâmica lateral (LH) e o parasubtalâmico (PSTh). Para confirmação, realizamos injeção de traçador anterógrado e investigamos, também, a neuroquímica das projeções. Neurônios do CeA que se projetam para o Mo5 recebem inervação de fibras imunorreativas ao fator liberador de corticotrofina (CFR-ir) e/ou à tirosina hidroxilase (TH-ir); alguns neurônios da LH que se projetam para o Mo5 são imunorreativos à orexina (ORX) e alguns neurônios do PSTh que se projetam para o Mo5 são innervados por fibras TH-ir. O Me5 recebe grande inervação do CeA e moderada da LH e do PSTh, possuindo grande aferência de fibras imunorreativas ao CRF, ORX e TH / The trigeminal motor nucleus (Mo5) is surrounded by a ring of premotor neurons defined as the h region. Studies have shown that neurons innervating the Mo5 are located in brainstem and in forebrain nuclei. Through the injection of the retrograde tracer cholera toxin b subunit/CTb in the Mo5, we found retrograde labeled neurons in the brainstem including the h region and the mesencephalic trigeminal nucleus (Me5), and in forebrain nuclei such as the central nucleus of amygdala (CeA), the lateral hypothalamic area (LH) and the parasubthalamic nucleus (PSTh). As control, we injected the anterograde tracer biotin dextran amine and found that these areas project direct or indirectly via the h region or the Me5 to the Mo5. Some CeA neurons that project to the Mo5 receive corticotrophin releasing factor (CRF) and tyrosine hydroxylase (TH) innervation, some LH neurons that project to Mo5 express orexin, and PSTh neurons that project to the Mo5 receive TH innervation. The Me5 is also innervated by CeA, LH and PSTh neurons and by CRF, orexin and TH immunoreactive fibers