INTRODUCTION: Age-related functional declines in the body and brain pose significant challenges to mobility and postural control. Older individuals are at increased risk for injury from a fall. Declines in gait and balance control make older adults more likely to suffer a fall or recurrent falls. According to the Centers for Disease Control and Prevention (CDC), falls are the leading cause of injury related death among adults age 65 years and older. (Important Facts about Falls | Home and Recreational Safety | CDC Injury Center, 2019) One out of three older adults falls annually and the likelihood of falling increases with age. (Stevens et al., 2008). In the US alone, the number of individuals living aged 65 and older is estimated at 46 million persons and is expected to reach 74 million by 2030. (Healthy Aging in Action: Advancing the National Prevention Strategy, 2019) Fall death rates in the United States increased by 30% from 2007 to 2016, and if this trend continues, it is expected that by 2030 there will be 7 deaths due to falls every hour. (Important Facts about Falls | Home and Recreational Safety | CDC Injury Center, 2019) Interventions designed to improve gait and balance control in the geriatric population can mitigate fall risk and positively impact these trends. OBJECTIVE: Gait and balance control, traditionally regarded as automatic motor processes, have since been determined to be complex motor functions reliant on executive function. (Hausdorff et al., 2005; Woollacott & Shumway-Cook, 2002) Normal walking and balance control are attentionally demanding and require shifting of attentional resources to frontal brain regions in order to maintain upright stance. This ability to dual-task is impaired in older adults. A single session of transcranial direct current stimulation (tDCS), a form of noninvasive brain stimulation, targeting the excitability of the left dorsolateral prefrontal cortex (l-dlPFC) has been found to reduce dual-task costs to gait and balance in both young and healthy older adults. (Manor et al., 2016; Zhou et al., 2014) However, little is known about how tDCS influences electroencephalogram (EEG) patterns and if changes in EEG are associated with functional outcomes. The specific aims of this study were to determine whether 1, 20-minute session tDCS targeting the l-dlPFC reduces the slow-wave/fast-wave frequency power ratio in EEG and absolute EEG power and whether these reductions are associated with changes in measures of postural control. METHODS: The data from this study was analyzed as part of a larger clinical trial testing multiple tDCS stimulation montages in combination with batteries of cognitive, gait, and balance assessments. Twenty-two older adults (median age=71 years) who were free of overt illness or disease were included in the analysis. Participants were outfitted with wireless movement sensors and a wireless 32-electrode EEG cap configured according to the 10-20 system. Participants completed a dual-task of serial subtraction by 3’s from a randomized three-digit number while standing for 60 seconds. EEG was simultaneously recorded during the 60 second trials. One, 20-minute tDCS stimulation targeting the l-dlPFC followed the balance assessment. EEG and dual-task assessments were repeated following the stimulation. EEG was not recorded simultaneously with tDCS. EEG data was processed and analyzed with Cartool EEG software. (Brunet et al., 2011) Spectral analysis of the EEG power values pre and post stimulation was conducted using a paired t-test. Power ratios of slow wave (4-8Hz) to fast wave (12-30Hz) were calculated for pre and post stimulation and analyzed for significant changes. Additionally, absolute power values in theta and beta frequency range were calculated. Postural sway velocity and postural sway area were also assessed and analyzed for changes following stimulation. RESULTS: Spectral analysis showed significant reductions in absolute power values across low theta frequency ranges following stimulation. This significant reduction in power was localized, but not exclusive, to frontal electrodes measuring activity of the l-dlPFC in the 4-8Hz frequency range. Most notably electrode F3, which has been found to correspond to the location and activity of the l-dlPFC using both the 10-20 electrode placement system and MRI guided neuronavigation. (Beam et al., 2009; De Witte et al., 2018) In addition to a significant reduction in power values, there was a reduction in slow-fast EEG ratios following stimulation. The percent reduction in EEG ratio was associated with a reduction in postural sway area (m2/s4) and sway velocity (m/s). CONCLUSION: tDCS is used to facilitate the excitability of cortical neurons. The l-dLPFC is a critical component of executive function. Due to the role of executive function in mediating attentional requirements of gait and balance, the l-dlPFC was chosen as a target to enhance dual-tasking capabilities, and thereby improve gait and postural control. The reduction in the slow wave-fast wave ratio and theta power indicates that participants had higher power in the fast wave relative to the slow wave after tDCS administration. The reduction in slow wave power may be indicative of less cognitive attentional effort required to complete a simultaneous dual-task involving postural control. This is supported by the associated reductions in postural sway following tDCS stimulation. These results further current research of tDCS as a viable intervention for improving balance and cognition in older adults and offers additional information about optimizing the efficacy of noninvasive brain stimulation to improve functional outcomes in this population.

Indiana University-Purdue University Indianapolis (IUPUI) / Non-invasive brain stimulation is valuable for studying neural circuits and treating various neurological disorders in human. However, current technologies of noninvasive brain stimulation usually have low spatial and temporal precision and poor brain penetration, which greatly limit their application. A new class of nanoparticles known as magneto-electric nanoparticles (MENs) is highly efficient in coupling an externally applied magnetics wave with generating local electric fields for neuronal activity modulation. Here, a new type of MENs was developed that consisted of CoFe2O4- BaTiO3 and had excellent magneto-electrical coupling properties. Calcium imaging technique was used to demonstrate their efficacy in evoking neuronal activity in organotyic and acute cortical slices that expressed GCaMP6 protein. For in vivo noninvasive delivery of MENs to brain, fluorescently labeled MENs were intravenously injected and attracted to pass through blood brain barrier to a targeted brain region by applying a focal magnet field. Magnetic wave (~450 G at 10 Hz) applied to mouse brain was able to activate cortical network activity, as revealed by in vivo two-photon and mesoscopic imaging of calcium signals at both cellular and global network levels. The effect was further confirmed by the increased number of c-Fos expressing cells after magnetic stimulation. Histological analysis indicated that neither brain delivery of MENs nor the subsequent magnetic stimulation caused any significant increases in the numbers of GFAP and IBA1 positive astrocytes and microglia in the brain. MENs stimulation also show high efficacy in short-term pain relieve when tested with a tibial nerve injury mouse model. The study demonstrates the feasibility of using MENs as a novel efficient and non-invasive technique of brain stimulation, which may have great potential for translation.

Anodal transcranial direct current stimulation (tDCS) is an intervention which is thought to enhance motor learning in healthy and stroke-injured states, when applied adjunctively during skill learning. We set out to investigate whether anodal tDCS might enhance functional rehabilitation from incomplete tetraplegic SCI. To address current limitations in the measurement of task-dependent skill, a novel integrated skill training and measurement task, the Motor Skill Rehabilitation Task (MSRT) was designed and developed. Measures of performance from this task delivered the functional measure of spatial motor skill learning, Task Productivity Rate (TPR). TPR was analysed and validated as a univariate dependent outcome, which is of potential importance to the future development of clinical measures measuring goal-directed motor skills. The MSRT was included alongside conventional behavioural measures in a repeated-measures RCT pilot study, the first to investigate the effect of anodal tDCS on rehabilitation of motor skill from chronic spinal cord injury. Adjunctive application of anodal tDCS had a statistically significant benefit upon retention of skill in the incomplete spinal cord injured population, but only when the independent factor of sensory acuity was included in the analysis. Differences between the development of task-dependent skill and generic dexterity over time suggested that spatial skill development was subject to an interaction of short-term and lasting effects. A larger study in healthy persons further investigated these phenomena, also applying Transcranial Magnetic Stimulation (TMS)–evoked measurements to investigate intervention-dependent effects upon the excitability of projections between the primary motor cortex and muscles involved in the prehension task. The findings revealed that active tDCS did not enhance skill learning at 7 days beyond the training period, but did significantly alter the development of motor skill following a period of learning and subsequent skill consolidation which was associated with underlying perturbation of motor control strategy. Significant and divergent patterns of cortical plasticity were evoked in projections to muscles necessary for reaching and grasping. The main findings of this thesis do not support anodal tDCS as an effective adjunctive means of enhancing spatial motor skill in rehabilitation from incomplete tetraplegic SCI. If applied in patient populations, the clinical benefits of anodal tDCS may be contingent both on the nature of the sensorimotor deficit affecting upper limb function and the spatial demands of the behavioural task. The findings of this project serve to inform further research in relation to the effect of anodal tDCS on the brain and behavioural outcomes, the potential for efficacy in target patient groups and the sensitivity of outcome measures to spatial and temporal dimensions of practical motor skills.

Producing speech is a highly complex task, involving the integration of sensory and linguistic information, with the precise, high-speed, co-ordination of muscles controlling breathing and the movement of the vocal folds and articulators. In spite of this complexity, producing fluent speech - moving smoothly from one speech sound to the next - can appear effortless. Speech fluency is highly socially valued, and the personal and societal costs of living with a disorder of fluency, such as developmental stuttering, are considerable. The outcomes of behavioural therapies to increase fluency are limited, however, especially for those seeking treatment in adulthood. The overarching aim of this thesis was to investigate how anodal transcranial direct current stimulation (A-TDCS) can be used to increase speech fluency, with a particular focus on the potential application to developmental stuttering. A-TDCS is a noninvasive brain stimulation technique that can enhance the effects of motor, speech, and language training. First, in a series of single-session experiments in typically fluent speakers, I demonstrated that applying A-TDCS over the left IFC increased speech motor learning relative to a sham control, but did not improve consolidation of this learning (chapter 2). Furthermore, I found that neither increasing stimulation intensity from 1 mA to 2 mA, nor changing from a unihemispheric to a bihemispheric configuration, had an additional effect on learning. Next, in single-session study with adults who stutter, I assessed the feasibility of using A-TDCS to improve fluency (chapter 3). Fluency was temporarily induced, by speaking in unison with another person, but the concurrent application of 1-mA unihemispheric A-TDCS over left inferior frontal cortex did not significantly prolong this fluency. Nevertheless, a trend towards stuttering reduction gave some indication that fluency might be increased using a multiple-session approach. Furthermore, I gained a number of important insights from these single-session studies, which I used to inform the design of the final multiple-session trial. In this final study, I completed a randomised controlled trial in 30 adult males with moderate to severe stuttering. Participants were randomized to receive either 1-mA A-TDCS or sham stimulation over left inferior frontal cortex combined with temporary fluency inducing behavioural techniques, for 20 minutes a day over 5 days (chapter 4). A-TDCS significantly reduced disfluency for at least 5 weeks following this intervention. The effect was specific to the speech impairment of development stuttering, as measures of the psycho-social consequences of stuttering were not modulated by A-TDCS. The findings of these studies offer significant promise for the future application of non-invasive stimulation as an adjunctive therapy for adults who stutter. In the concluding chapter, I discuss the important implications of my findings for the future use of this technique.

Deficits in executive functions, specifically in response inhibition (RI), have been reported in antisocial behavior, conduct disorder, attention-deficit/hyperactivity disorder (ADHD), etc. Individuals with deficits in RI have a high probability to show non-adapted social behavior that can lead to crime. Many studies have shown that transcranial direct current stimulation (tDCS), a noninvasive brain stimulation (NIBS) technique, modulate the activity of the prefrontal cortex and the functions involved in executive control and RI. This article aims to review the literature on the effect of tDCS on RI and executive control and to highlight research avenues to develop therapeutic alternatives to prevent onset and recidivism of crime. A systematic review of the literature was performed in the Libsearch database following PRISMA method. Ten studies were selected showing tDCS modulation of RI measured with the Stop Signal and the Go-NoGo task. Eight of the studies showed gains on RI with tDCS versus sham. The data led to consideration of tDCS as a new therapeutic alternative to improve RI and hence prevention of onset and recidivism on crime. Individual differences, targeted brain areas, the polarity of electrodes and long-term learning effects are further discussed as crucial considerations for future studies.

Introdução: Níveis elevados de ansiedade têm sido associados com intensidade e comportamento da dor em pacientes com dores aguda e crônica. Foi observado, em indíviduos com síndrome dolorosa miofascial (SDM), que o estresse e a ansiedade aumentam a predisposição para o desenvolvimento de pontos-gatilhos miofasciais. Adicionalmente a isto, existe a tendência do indivíduo experimentar emoções negativas em situações de estresse (neuroticismo), característica de personalidade associada ao traço de personalidade, que pode influenciar negativamente na experiência de dor. Indivíduos com alta ansiedade-traço são geralmente hipersensíveis a estímulos e psicologicamente mais reativos. É concebível supôr a coexistência de alteração na excitabilidade cortical, entre dor crônica e ansiedade nestes pacientes. Para melhorar a compreensão dos mecanismos centrais relacionados à ansiedade e à dor crônica, avaliou-se os parâmetros de excitabilidade cortical, usando estimulação magnética transcraniana (EMT), pulso único e pareado. Nossa hipótese é que a excitabilidade corticoespinhal seja modulada pela ansiedade favorecendo a perda de influxo inibitório descendente. Objetivos: O presente estudo teve como objetivo responder a três perguntas relacionadas à síndrome dolorosa miofascial (SDM): 1) A excitabilidade do córtex motor está relacionada com a ansiedade-traço? 2) A ansiedade-traço modula alterações da excitabilidade corticoespinhal, após dor evocada pelo Quantitative Sensory Testing (QST)? 3) A ansiedade-traço prevê resposta à dor evocada pelo QST, se receber simultaneamente um estímulo heterotópico [Conditioned Pain Modulation (CPM)]? Pacientes e métodos: Foram incluídas mulheres com SDM (n = 47) e controles saudáveis (n = 11), com idade entre 19 e 65 anos. A excitabilidade do córtex motor foi avaliada pela EMT, e a ansiedade foi avaliada com base no Inventário de Ansiedade Traço-Estado (IDATE). A incapacidade relacionada à dor foi avaliada pelo perfil da escala de dor crônica para a população brasileira (B:PCP:S), e as medidas psicofísicas da dor foram medidas pelo QST e CPM. Resultados: Nas pacientes, a ansiedade-traço foi positivamente correlacionada com a facilitação intracortical (FIC) no baseline e após a dor evocada pelo QST (β = 0,05 e β = 0,04, respectivamente) e negativamente relacionada com o período de silêncio cortical (PSC) no baseline e após a dor evocada pelo QST (β = -1,17 e β = -1,23, respectivamente) (P <0,05 para todas as comparações). Após dor evocada pelo QST, a incapacidade relacionada à dor crônica foi positivamente correlacionada com a FIC (β = 0,02) (P <0,05). Os escores de dor durante o CPM foram positivamente correlacionados com a ansiedadetraço, quando a incapacidade relacionada à dor crônica foi igualmente alta (β = 0,39, P = 0,02). A excitabilidade cortical das controles saudáveis permaneceu inalterada após o QST. Conclusões: Estes resultados sugerem que, na SDM, o desequilíbrio entre os sistemas excitatórios e inibitórios descendentes do trato corticoespinhal está associado concomitantemente a maiores níveis de ansiedade-traço e maiores níveis de incapacidade funcional ocasionados pela dor crônica. / Background: High levels of anxiety have been associated with the intensity and pain behavior in patients with acute and chronic pain. It was observed that in subjects with myofascial pain (SDM), stress and anxiety syndrome increase the predisposition for the development of myofascial trigger points. In addition to this, there is a tendency of individuals to experience negative emotions in stressful situations (neuroticism), personality characteristic associated with trait personality that may negatively influence in the experience of pain. Individuals with higher trait anxiety are usually hypersensitive to stimuli and more psychologically reactive. It is conceivable to assume the co-existence of change in cortical excitability, chronic pain and anxiety, in these patients. To improve the understanding of the central mechanisms related to anxiety and chronic pain, we assessed cortical excitability parameters by single and paired pulse transcranial magnetic stimulation (TMS). We hypothesize that corticospinal excitability is modulated by anxiety favoring loss of descendent inhibitory influx. Objectives: This study aimed to answer three questions related to chronic myofascial pain syndrome (MPS): 1) Is the motor cortex excitability, as assessed by transcranial magnetic stimulation parameters (TMS), related to state-trait anxiety? 2) Does anxiety modulate corticospinal excitability changes after evoked pain by Quantitative Sensory Testing (QST)? 3) Does the state-trait anxiety predict the response to pain evoked by QST if simultaneously receiving a heterotopic stimulus [Conditional Pain Modulation (CPM)]? Patient and methods: We included females with chronic MPS (n=47) and healthy controls (n=11), aged from 19 to 65 years. Motor cortex excitability was assessed by TMS, and anxiety was assessed based on the State-Trait Anxiety Inventory. The disability related to pain (DRP) was assessed by the Profile of Chronic Pain scale for the Brazilian population (B:PCP:S), and the psychophysical pain measurements were measured by the QST and CPM. Results: In patients, trait-anxiety was positively correlated to intracortical facilitation (ICF) at baseline and after QST evoked pain (β= 0.05 and β= 0.04, respectively) and negatively correlated to the cortical silent period (CSP) (β= -1.17 and β= -1.23, respectively) (P <0.05 for all comparisons). After QST evoked pain, the DRP was positively correlated to ICF (β= 0.02) (P<0.05). Pain scores during CPM were positively correlated with trait-anxiety when it was concurrently with high DRP (β= 0.39; P= 0.02). Controls’cortical excitability remained unchanged after QST. Conclusions: These findings suggest that, in chronic MPS, the imbalance between excitatory and inhibitory descending systems of the corticospinal tract is associated with higher trait-anxiety concurrent with higher DRP.

Les hallucinations auditives sont un symptôme fréquent et invalidant de la schizophrénie. Bien qu'habituellement jugulés par des traitements antipsychotiques, ces symptômes sont résistants dans 25 % des cas et leur physiopathologie reste méconnue. Dans ce travail de thèse, nous proposons d'utiliser la stimulation transcrânienne en courant continu (tDCS) dans une série d'études afin de traiter et de caractériser les hallucinations auditives résistantes de la schizophrénie. Dans une première série d'études cliniques, nous avons rapporté que la tDCS fronto-temporale diminuait les hallucinations auditives de la schizophrénie. Dans une autre étude, nous avons montré que la diminution des hallucinations auditives était corrélée à l'amélioration des processus cognitifs de source- monitoring chez les patients. Dans une étude chez des sujets sains, nous avons montré que ces processus cognitifs étaient liés à l'activité de la jonction temporo-pariétale gauche. Enfin, dans une étude d'imagerie, nous avons montré que la tDCS fronto-temporale modulait la connectivité fonctionnelle de la jonction temporo-pariétale gauche avec un large réseau cérébral impliqué dans les hallucinations et le traitement du langage. L'étude des effets cliniques, cognitifs et neurophysiologiques de la tDCS nous a permis de mieux comprendre la physiopathologie des hallucinations auditives et notamment le rôle central de la jonction temporo-pariétale gauche. Ces travaux seront mis en relation et confrontés à la littérature existante, afin de proposer des perspectives de prise en charge des hallucinations auditives / Auditory hallucinations are prominent and disabling features of schizophrenia. For 25%-30% of patients with schizophrenia, such hallucinations are refractory to drug treatment and their physiopathology remains unknown. This thesis aims at using transcranial direct current stimulation (tDCS) in several studies to alleviate and characterize refractory auditory hallucinations in schizophrenia. First, we conducted a clinical study in patients with schizophrenia and we reported that fronto-temporal tDCS reduced auditory hallucinations. ln another study, we reported that the reduced severity of auditory hallucinations was correlated with improved source monitoring performances. ln a study in healthy volunteers, we reported that source-monitoring processes were associated with activity of the left temporo-parietal junction. Finally, using functional magnetic resonance imaging, we observed that tDCS modulates the functional connectivity of the left temporo-parietal junction with a distributed network involved in auditory hallucinations and language processing. The study of clinical, cognitive and neural effects of tDCS allows a better understanding of brain mechanisms involved in auditory hallucinations and of the central role of the left temporo-parietal junction. These works were discussed together in light of available literature to pave the way for valuable alternative approaches to alleviate auditoryhallucinations in schizophrenia

Introdução: Níveis elevados de ansiedade têm sido associados com intensidade e comportamento da dor em pacientes com dores aguda e crônica. Foi observado, em indíviduos com síndrome dolorosa miofascial (SDM), que o estresse e a ansiedade aumentam a predisposição para o desenvolvimento de pontos-gatilhos miofasciais. Adicionalmente a isto, existe a tendência do indivíduo experimentar emoções negativas em situações de estresse (neuroticismo), característica de personalidade associada ao traço de personalidade, que pode influenciar negativamente na experiência de dor. Indivíduos com alta ansiedade-traço são geralmente hipersensíveis a estímulos e psicologicamente mais reativos. É concebível supôr a coexistência de alteração na excitabilidade cortical, entre dor crônica e ansiedade nestes pacientes. Para melhorar a compreensão dos mecanismos centrais relacionados à ansiedade e à dor crônica, avaliou-se os parâmetros de excitabilidade cortical, usando estimulação magnética transcraniana (EMT), pulso único e pareado. Nossa hipótese é que a excitabilidade corticoespinhal seja modulada pela ansiedade favorecendo a perda de influxo inibitório descendente. Objetivos: O presente estudo teve como objetivo responder a três perguntas relacionadas à síndrome dolorosa miofascial (SDM): 1) A excitabilidade do córtex motor está relacionada com a ansiedade-traço? 2) A ansiedade-traço modula alterações da excitabilidade corticoespinhal, após dor evocada pelo Quantitative Sensory Testing (QST)? 3) A ansiedade-traço prevê resposta à dor evocada pelo QST, se receber simultaneamente um estímulo heterotópico [Conditioned Pain Modulation (CPM)]? Pacientes e métodos: Foram incluídas mulheres com SDM (n = 47) e controles saudáveis (n = 11), com idade entre 19 e 65 anos. A excitabilidade do córtex motor foi avaliada pela EMT, e a ansiedade foi avaliada com base no Inventário de Ansiedade Traço-Estado (IDATE). A incapacidade relacionada à dor foi avaliada pelo perfil da escala de dor crônica para a população brasileira (B:PCP:S), e as medidas psicofísicas da dor foram medidas pelo QST e CPM. Resultados: Nas pacientes, a ansiedade-traço foi positivamente correlacionada com a facilitação intracortical (FIC) no baseline e após a dor evocada pelo QST (β = 0,05 e β = 0,04, respectivamente) e negativamente relacionada com o período de silêncio cortical (PSC) no baseline e após a dor evocada pelo QST (β = -1,17 e β = -1,23, respectivamente) (P <0,05 para todas as comparações). Após dor evocada pelo QST, a incapacidade relacionada à dor crônica foi positivamente correlacionada com a FIC (β = 0,02) (P <0,05). Os escores de dor durante o CPM foram positivamente correlacionados com a ansiedadetraço, quando a incapacidade relacionada à dor crônica foi igualmente alta (β = 0,39, P = 0,02). A excitabilidade cortical das controles saudáveis permaneceu inalterada após o QST. Conclusões: Estes resultados sugerem que, na SDM, o desequilíbrio entre os sistemas excitatórios e inibitórios descendentes do trato corticoespinhal está associado concomitantemente a maiores níveis de ansiedade-traço e maiores níveis de incapacidade funcional ocasionados pela dor crônica. / Background: High levels of anxiety have been associated with the intensity and pain behavior in patients with acute and chronic pain. It was observed that in subjects with myofascial pain (SDM), stress and anxiety syndrome increase the predisposition for the development of myofascial trigger points. In addition to this, there is a tendency of individuals to experience negative emotions in stressful situations (neuroticism), personality characteristic associated with trait personality that may negatively influence in the experience of pain. Individuals with higher trait anxiety are usually hypersensitive to stimuli and more psychologically reactive. It is conceivable to assume the co-existence of change in cortical excitability, chronic pain and anxiety, in these patients. To improve the understanding of the central mechanisms related to anxiety and chronic pain, we assessed cortical excitability parameters by single and paired pulse transcranial magnetic stimulation (TMS). We hypothesize that corticospinal excitability is modulated by anxiety favoring loss of descendent inhibitory influx. Objectives: This study aimed to answer three questions related to chronic myofascial pain syndrome (MPS): 1) Is the motor cortex excitability, as assessed by transcranial magnetic stimulation parameters (TMS), related to state-trait anxiety? 2) Does anxiety modulate corticospinal excitability changes after evoked pain by Quantitative Sensory Testing (QST)? 3) Does the state-trait anxiety predict the response to pain evoked by QST if simultaneously receiving a heterotopic stimulus [Conditional Pain Modulation (CPM)]? Patient and methods: We included females with chronic MPS (n=47) and healthy controls (n=11), aged from 19 to 65 years. Motor cortex excitability was assessed by TMS, and anxiety was assessed based on the State-Trait Anxiety Inventory. The disability related to pain (DRP) was assessed by the Profile of Chronic Pain scale for the Brazilian population (B:PCP:S), and the psychophysical pain measurements were measured by the QST and CPM. Results: In patients, trait-anxiety was positively correlated to intracortical facilitation (ICF) at baseline and after QST evoked pain (β= 0.05 and β= 0.04, respectively) and negatively correlated to the cortical silent period (CSP) (β= -1.17 and β= -1.23, respectively) (P <0.05 for all comparisons). After QST evoked pain, the DRP was positively correlated to ICF (β= 0.02) (P<0.05). Pain scores during CPM were positively correlated with trait-anxiety when it was concurrently with high DRP (β= 0.39; P= 0.02). Controls’cortical excitability remained unchanged after QST. Conclusions: These findings suggest that, in chronic MPS, the imbalance between excitatory and inhibitory descending systems of the corticospinal tract is associated with higher trait-anxiety concurrent with higher DRP.

Introdução: Níveis elevados de ansiedade têm sido associados com intensidade e comportamento da dor em pacientes com dores aguda e crônica. Foi observado, em indíviduos com síndrome dolorosa miofascial (SDM), que o estresse e a ansiedade aumentam a predisposição para o desenvolvimento de pontos-gatilhos miofasciais. Adicionalmente a isto, existe a tendência do indivíduo experimentar emoções negativas em situações de estresse (neuroticismo), característica de personalidade associada ao traço de personalidade, que pode influenciar negativamente na experiência de dor. Indivíduos com alta ansiedade-traço são geralmente hipersensíveis a estímulos e psicologicamente mais reativos. É concebível supôr a coexistência de alteração na excitabilidade cortical, entre dor crônica e ansiedade nestes pacientes. Para melhorar a compreensão dos mecanismos centrais relacionados à ansiedade e à dor crônica, avaliou-se os parâmetros de excitabilidade cortical, usando estimulação magnética transcraniana (EMT), pulso único e pareado. Nossa hipótese é que a excitabilidade corticoespinhal seja modulada pela ansiedade favorecendo a perda de influxo inibitório descendente. Objetivos: O presente estudo teve como objetivo responder a três perguntas relacionadas à síndrome dolorosa miofascial (SDM): 1) A excitabilidade do córtex motor está relacionada com a ansiedade-traço? 2) A ansiedade-traço modula alterações da excitabilidade corticoespinhal, após dor evocada pelo Quantitative Sensory Testing (QST)? 3) A ansiedade-traço prevê resposta à dor evocada pelo QST, se receber simultaneamente um estímulo heterotópico [Conditioned Pain Modulation (CPM)]? Pacientes e métodos: Foram incluídas mulheres com SDM (n = 47) e controles saudáveis (n = 11), com idade entre 19 e 65 anos. A excitabilidade do córtex motor foi avaliada pela EMT, e a ansiedade foi avaliada com base no Inventário de Ansiedade Traço-Estado (IDATE). A incapacidade relacionada à dor foi avaliada pelo perfil da escala de dor crônica para a população brasileira (B:PCP:S), e as medidas psicofísicas da dor foram medidas pelo QST e CPM. Resultados: Nas pacientes, a ansiedade-traço foi positivamente correlacionada com a facilitação intracortical (FIC) no baseline e após a dor evocada pelo QST (β = 0,05 e β = 0,04, respectivamente) e negativamente relacionada com o período de silêncio cortical (PSC) no baseline e após a dor evocada pelo QST (β = -1,17 e β = -1,23, respectivamente) (P <0,05 para todas as comparações). Após dor evocada pelo QST, a incapacidade relacionada à dor crônica foi positivamente correlacionada com a FIC (β = 0,02) (P <0,05). Os escores de dor durante o CPM foram positivamente correlacionados com a ansiedadetraço, quando a incapacidade relacionada à dor crônica foi igualmente alta (β = 0,39, P = 0,02). A excitabilidade cortical das controles saudáveis permaneceu inalterada após o QST. Conclusões: Estes resultados sugerem que, na SDM, o desequilíbrio entre os sistemas excitatórios e inibitórios descendentes do trato corticoespinhal está associado concomitantemente a maiores níveis de ansiedade-traço e maiores níveis de incapacidade funcional ocasionados pela dor crônica. / Background: High levels of anxiety have been associated with the intensity and pain behavior in patients with acute and chronic pain. It was observed that in subjects with myofascial pain (SDM), stress and anxiety syndrome increase the predisposition for the development of myofascial trigger points. In addition to this, there is a tendency of individuals to experience negative emotions in stressful situations (neuroticism), personality characteristic associated with trait personality that may negatively influence in the experience of pain. Individuals with higher trait anxiety are usually hypersensitive to stimuli and more psychologically reactive. It is conceivable to assume the co-existence of change in cortical excitability, chronic pain and anxiety, in these patients. To improve the understanding of the central mechanisms related to anxiety and chronic pain, we assessed cortical excitability parameters by single and paired pulse transcranial magnetic stimulation (TMS). We hypothesize that corticospinal excitability is modulated by anxiety favoring loss of descendent inhibitory influx. Objectives: This study aimed to answer three questions related to chronic myofascial pain syndrome (MPS): 1) Is the motor cortex excitability, as assessed by transcranial magnetic stimulation parameters (TMS), related to state-trait anxiety? 2) Does anxiety modulate corticospinal excitability changes after evoked pain by Quantitative Sensory Testing (QST)? 3) Does the state-trait anxiety predict the response to pain evoked by QST if simultaneously receiving a heterotopic stimulus [Conditional Pain Modulation (CPM)]? Patient and methods: We included females with chronic MPS (n=47) and healthy controls (n=11), aged from 19 to 65 years. Motor cortex excitability was assessed by TMS, and anxiety was assessed based on the State-Trait Anxiety Inventory. The disability related to pain (DRP) was assessed by the Profile of Chronic Pain scale for the Brazilian population (B:PCP:S), and the psychophysical pain measurements were measured by the QST and CPM. Results: In patients, trait-anxiety was positively correlated to intracortical facilitation (ICF) at baseline and after QST evoked pain (β= 0.05 and β= 0.04, respectively) and negatively correlated to the cortical silent period (CSP) (β= -1.17 and β= -1.23, respectively) (P <0.05 for all comparisons). After QST evoked pain, the DRP was positively correlated to ICF (β= 0.02) (P<0.05). Pain scores during CPM were positively correlated with trait-anxiety when it was concurrently with high DRP (β= 0.39; P= 0.02). Controls’cortical excitability remained unchanged after QST. Conclusions: These findings suggest that, in chronic MPS, the imbalance between excitatory and inhibitory descending systems of the corticospinal tract is associated with higher trait-anxiety concurrent with higher DRP.