No description available.

No description available.

People who suffer from amyotrophic lateral sclerosis (ALS) eventually lose all voluntary muscle control. In the late stages of the disease, traditional augmentative and alternative communication (AAC) devices fail to provide adequate levels of communication. Brain-computer interface (BCI) technology has provided effective communication after all other AAC devices have failed. Nonetheless, EEG-based BCI devices may also fail for people with late-stage ALS due to loss of voluntary eye movement. Specifically, some people may suffer from random eye movement (nystagmus) and/or drooping of the eyelids (ptosis). Presently, it is unclear in the literature whether BCI operation requires voluntary control of eye movement. The current study attempts to simulate involuntary random eye movement in able-bodied individuals employing the P300-based BCI. To simulate involuntary random eye movement, the stimuli shift in the X and Y dimensions. Stimulus movement ‘Jitter’ occurs between each stimulus presentation in increments of 1-5 pixels (Jitter 1), 5-10 pixels (Jitter 2), 10-15 pixels-(Jitter 3), or a no movement control condition. Data collected from a previous study using 22 participants compared the control condition to Jitter 1 and Jitter 2 indicated higher accuracy for control and Jitter 1 than Jitter 2. No significant differences were found in accuracy, selections per minute, or bitrate. Waveform analysis indicated significantly higher P300 amplitude for the control condition and Jitter 1 than Jitter 2. Preference survey scores showed a preference for Jitter 1 as compared to control and Jitter 2. This finding was unexpected and may be due to the slight movement of Jitter 1 forcing participants to be vigilant, but not distracted. Based on our finding in this study, the current study examines the amount of pixel movement that could lead to reductions in performance. Participants completed a control condition and the three levels of Jitter in a counter-balanced design. Preliminary data for the current study was collected from 15 participants. No significant differences were observed between the three conditions in measures of BCI accuracy, selections per minute, and bitrate. Furthermore, preference survey scores indicated no significant difference in condition preference. Based on the findings of the first study, as well as the data collected so far in the current study, it appears that random movement does not have a significant impact on the ability of healthy participants to operate the BCI system. This could indicate that individuals with random eye movement should be able to operate the system with high rates of accuracy.

O potencial visual evocado (PVE) é um sinal elétrico de baixa intensidade originado no córtex visual em resposta a uma estimulação visual periódica. O potencial visual evocado de varredura é um procedimento de PVE modificado para medir acuidade visual de grades em pacientes pré-verbais e não-verbais. Este biopotencial está imerso em uma grande quantidade de ruído eletroencefalográfico e artefato relacionado ao movimento. A relação sinal-ruído tem um papel dominante na determinação de erros sistemáticos e estatísticos. O propósito deste estudo é apresentar um método baseado na transformada wavelet para filtrar e extrair o potencial evocado visual de varredura. Grades de luminância de onda senoidal moduladas em 6 Hertz foram usadas como estímulo para se determinar os limiares de acuidade. A amplitude e a fase da 2ª. harmônica (12 Hertz) do padrão de resposta foram analisadas usando-se a transformada rápida de Fourier após a filtragem por wavelet. O método da transformada wavelet discreta foi usado para decompor o PVE em coeficientes wavelet, determinando-se quais destes representavam uma atividade significativa. Em um passo seguinte somente os coeficientes relevantes foram considerados, zerando-se os demais e reconstruindo-se, assim, o sinal PVE. Isto resultou na filtragem das demais freqüências que foram consideradas ruído. Simulações numéricas e análises com dados de PVE humanos mostraram que este método forneceu maior relação sinal-ruído quando comparado com o método clássico dos mínimos quadrados recursivo (RLS) e ainda uma análise de fase mais apropriada / Visually evoked potential (VEP) is a very small electrical signal originated in the visual cortex in response to periodic visual stimulation. Sweep-VEP is a modified VEP procedure used to measure grating visual acuity in non-verbal and preverbal patients. This biopotential is buried in a large amount of electroencephalographic noise and movement related artifact. The signal-to-noise ratio (SNR) plays a dominant role in determining both systematic and statistic errors. The purpose of this study is to present a method based on wavelet transform technique for filtering and extracting steady-state sweep-VEP. Counter-phase sine-wave luminance gratings modulated at 6 Hertz were used as stimuli to determine sweep-VEP grating acuity thresholds. The amplitude and phase of the second-harmonic (12 Hertz) pattern reversal response were analyzed using the fast Fourier transform after the wavelet filtering. The wavelet transform method was used to decompose the VEP signal into wavelet coefficients by a discrete wavelet analysis to determine which coefficients yield significant activity at the corresponding frequency. In a subsequent step only significant coefficients were considered and the remaining was set to zero allowing a reconstruction of the VEP signal. This procedure resulted in filtering out other frequencies that were considered noise. Numerical simulations and analyses of human VEP data showed that this method has provided higher SNR when compared with the classical recursive least squares (RLS) method. An additional advantage was a more appropriate phase analysis showing more realistic second-harmonic amplitude value during phase brake

Vários estudos têm apontado que falhas nas habilidades do processamento fonológico (consciência fonológica, memória fonológica e acesso ao léxico) estão relacionadas com distúrbios de leitura e escrita. Programas terapêuticos baseados na estimulação da consciência fonológica têm sido propostos, porém poucos se propõem a estimular as três habilidades do processamento fonológico. A efetividade dos programas terapêuticos é evidenciada por testes comportamentais e, na busca por biomarcadores da evolução terapêutica, o potencial evocado auditivo de longa latência (P300) tem sido estudado. O P300 é um potencial endógeno que avalia a resposta do sujeito a estímulos acústicos, envolvidos nas regiões cerebrais corticais e subcorticais relacionados com atenção, discriminação auditiva e memória. O presente estudo teve por objetivo investigar a eficácia de um programa de estimulação do processamento fonológico em escolares com Distúrbios de Leitura e Escrita por meio da análise dos testes comportamentais e P300 pré e pós-estimulação. Participaram deste estudo 10 escolares, que frequentavam regularmente o 4º, 5º, 6º ou 7º ano do Ensino Fundamental, com Distúrbio de Leitura e Escrita. Os escolares foram submetidos às avaliações de aritmética, consciência fonológica, memória fonológica, nomeação automática rápida, leitura e escrita, e submetidos ao exame P300, em seguida iniciaram uma intervenção baseada na estimulação das habilidades do processamento fonológico. A intervenção foi realizada em 20 sessões (semanais de 45 minutos). A proposta de intervenção foi baseada em exercícios de estimulação dos três componentes do processamento fonológico. Após a intervenção, foram novamente submetidos às mesmas avaliações comportamentais e avaliação do P300. Os resultados pré e pós-estimulação foram comparados por meio do Wilcoxon-test para amostras pareadas com o nível de significância de 0,05. Observou-se melhora no desempenho em todas as tarefas do Processamento Fonológico (p<0,05). A melhora também foi observada na leitura de palavras e pseudopalavras e compreensão de texto (p<0,05), além de diminuição de erros ortográficos no ditado e escrita espontânea (p<0,05). O P300 não apresentou diferença no período pós-estimulação, mostrando que o programa foi efetivo e que o P300 não foi um biomarcador eficiente de evolução terapêutica. / Several studies have pointed out that failures in phonological processing skills (phonological awareness, phonological memory and lexical retrieval) are related to reading and writing disorders. Therapeutic programs based on phonological awareness have been proposed, but few are meant to stimulate the three phonological processing skills. The effectiveness of therapeutic programs is evidenced by behavioral tests, however, in the search for biomarkers of therapeutic evolution, the long-latency auditory evoked potential (P300) has been studied. The P300 is an endogenous potential that evaluates the response of the subject to acoustic stimuli involved in cortical and subcortical brain regions related to attention, auditory discrimination and memory. This study aimed to investigate the effectiveness of a stimulation program of phonological processing in children with reading and writing disorders by analyzing the behavioral tests and the P300 pre and post-stimulation. The participants of this study were 10 students who regularly attended the 4th, 5th, 6th or 7th year of elementary school and have reading and writing disorder. The students were submitted to arithmetic reviews, phonological awareness, phonological memory, rapid automatized naming, reading and writing, and submitted to the P300 examination, then began an intervention based on the stimulation of phonological processing skills. This intervention was performed in 20 sessions (45 minutes weekly). The proposed intervention was based on the stimulation exercises of the three components of phonological processing. After the intervention, they were again subjected to the same behavioral assessments and evaluation of P300. The pre and post-stimulation were compared using the Wilcoxon-test for paired samples with the 0.05 significance level. There was an improved performance in all tasks of Phonological Processing (p <0.05). The improvement was also observed in reading words and pseudo words and reading comprehension (p <0.05), and a reduction of spelling errors in dictation and spontaneous writing (p <0.05). The P300 showed no difference in post-stimulation period, showing that the program was effective and P300 cannot be considered a biomarker of therapeutic evolution.

O potencial visual evocado (PVE) é um sinal elétrico de baixa intensidade originado no córtex visual em resposta a uma estimulação visual periódica. O potencial visual evocado de varredura é um procedimento de PVE modificado para medir acuidade visual de grades em pacientes pré-verbais e não-verbais. Este biopotencial está imerso em uma grande quantidade de ruído eletroencefalográfico e artefato relacionado ao movimento. A relação sinal-ruído tem um papel dominante na determinação de erros sistemáticos e estatísticos. O propósito deste estudo é apresentar um método baseado na transformada wavelet para filtrar e extrair o potencial evocado visual de varredura. Grades de luminância de onda senoidal moduladas em 6 Hertz foram usadas como estímulo para se determinar os limiares de acuidade. A amplitude e a fase da 2ª. harmônica (12 Hertz) do padrão de resposta foram analisadas usando-se a transformada rápida de Fourier após a filtragem por wavelet. O método da transformada wavelet discreta foi usado para decompor o PVE em coeficientes wavelet, determinando-se quais destes representavam uma atividade significativa. Em um passo seguinte somente os coeficientes relevantes foram considerados, zerando-se os demais e reconstruindo-se, assim, o sinal PVE. Isto resultou na filtragem das demais freqüências que foram consideradas ruído. Simulações numéricas e análises com dados de PVE humanos mostraram que este método forneceu maior relação sinal-ruído quando comparado com o método clássico dos mínimos quadrados recursivo (RLS) e ainda uma análise de fase mais apropriada / Visually evoked potential (VEP) is a very small electrical signal originated in the visual cortex in response to periodic visual stimulation. Sweep-VEP is a modified VEP procedure used to measure grating visual acuity in non-verbal and preverbal patients. This biopotential is buried in a large amount of electroencephalographic noise and movement related artifact. The signal-to-noise ratio (SNR) plays a dominant role in determining both systematic and statistic errors. The purpose of this study is to present a method based on wavelet transform technique for filtering and extracting steady-state sweep-VEP. Counter-phase sine-wave luminance gratings modulated at 6 Hertz were used as stimuli to determine sweep-VEP grating acuity thresholds. The amplitude and phase of the second-harmonic (12 Hertz) pattern reversal response were analyzed using the fast Fourier transform after the wavelet filtering. The wavelet transform method was used to decompose the VEP signal into wavelet coefficients by a discrete wavelet analysis to determine which coefficients yield significant activity at the corresponding frequency. In a subsequent step only significant coefficients were considered and the remaining was set to zero allowing a reconstruction of the VEP signal. This procedure resulted in filtering out other frequencies that were considered noise. Numerical simulations and analyses of human VEP data showed that this method has provided higher SNR when compared with the classical recursive least squares (RLS) method. An additional advantage was a more appropriate phase analysis showing more realistic second-harmonic amplitude value during phase brake

No description available.

Transkranijinė magnetinė stimuliacija (TMS) – tai modernus neinvazinis vaistams rezistentiškų psichiatrinių sutrikimų gydymo būdas. Fiziologiniai TMS tyrimai pasižymi įvairiais, dažnai prieštaringais rezultatais, daugeliu atvejų didžiausias dėmesys skiriamas betarpiškiems poveikiams po vienos TMS procedūros, bet ne po pilno terapinio kurso. Manoma, kad rezultatų įvairovę TMS praktikoje įtakoja skirtingi stimuliacijos parametrai ir netikslumai parenkant stimuliuojamą zoną smegenyse. Nors TMS terapija dažnai traktuojama kaip švelnesnė alternatyva elektros impulsų terapijai (EIT), palyginamųjų fiziologinių šių metodikų tyrimų labai trūksta. Darbo tikslas buvo įvertinti TMS terapijos kurso poveikį bioelektriniam galvos smegenų aktyvumui ir palyginti jį su EIT terapijos poveikiu. Buvo tirta aukšto ir žemo dažnių (10 Hz ir 1 Hz) TMS terapijos įtaka EEG dažnių galios spektrui bei sukeltiniam klausos potencialui P300, naudojant standartinį ir neuronavigacinį taikinio pozicionavimą. TMS sukelti EEG pokyčiai palyginti su EIT terapijos sukeltais EEG pokyčiais, išmatuota TMS terapijos sąlygotų pokyčių dinamika kelių mėnesių bėgyje. Rezultatai parodė, kad TMS terapijos pasekoje smegenyse ryškiausiai padidėja delta dažnio galia. Naudojant standartinį pozicionavimą 10 Hz TMS sukėlė įvairesnius ir intensyvesnius EEG galios spektro pokyčius nei 1 Hz TMS. Pritaikius neuronavigacinę sistemą 10 Hz TMS atveju sumažėjo teta ir alfa dažnių galios pokyčiai. Praėjus keliems mėnesiams nuo TMS... [toliau žr. visą tekstą] / Transcranial magnetic stimulation (TMS) is a modern non invasive method of drug resistant psychiatric disorder treatment. TMS physiology research is hindered by variable, often controversial results. In most studies main attention is being focused on immediate effects after single TMS procedure rather than the influence of a complete therapy course. It is considered that variability of results in TMS practice is caused by different stimulation parameters and imprecision of stimulated area placement in the brain. Although TMS therapy is often viewed as a milder alternative to electroconvulsive therapy (ECT), comparative physiological studies of these two methods are very rare. The aim of this study was to evaluate the effect of rTMS therapy course on bioelectrical brain activity and compare it to an ECT effect. Research included the effect of high and low frequency (10 Hz and 1 Hz) TMS on EEG band power spectrum and auditory evoked potential P300, using both standard and neuronavigated target positioning. TMS evoked EEG changes were also compared to the changes of ECT. Change dynamics after several months of TMS therapy were also measured. Results showed that after TMS therapy the most notable change in the brain occurs in the form of delta power increase. When using standard positioning 10 Hz TMS evokes more diverse and intense EEG band power spectrum changes than the 1 Hz TMS. Application of neuronavigation system decreases theta and alpha band power changes in 10 Hz TMS... [to full text]

Transcranial magnetic stimulation (TMS) is a modern non invasive method of drug resistant psychiatric disorder treatment. TMS physiology research is hindered by variable, often controversial results. In most studies main attention is being focused on immediate effects after single TMS procedure rather than the influence of a complete therapy course. It is considered that variability of results in TMS practice is caused by different stimulation parameters and imprecision of stimulated area placement in the brain. Although TMS therapy is often viewed as a milder alternative to electroconvulsive therapy (ECT), comparative physiological studies of these two methods are very rare. The aim of this study was to evaluate the effect of rTMS therapy course on bioelectrical brain activity and compare it to an ECT effect. Research included the effect of high and low frequency (10 Hz and 1 Hz) TMS on EEG band power spectrum and auditory evoked potential P300, using both standard and neuronavigated target positioning. TMS evoked EEG changes were also compared to the changes of ECT. Change dynamics after several months of TMS therapy were also measured. Results showed that after TMS therapy the most notable change in the brain occurs in the form of delta power increase. When using standard positioning 10 Hz TMS evokes more diverse and intense EEG band power spectrum changes than the 1 Hz TMS. Application of neuronavigation system decreases theta and alpha band power changes in 10 Hz TMS... [to full text] / Transkranijinė magnetinė stimuliacija (TMS) – tai modernus neinvazinis vaistams rezistentiškų psichiatrinių sutrikimų gydymo būdas. Fiziologiniai TMS tyrimai pasižymi įvairiais, dažnai prieštaringais rezultatais, daugeliu atvejų didžiausias dėmesys skiriamas betarpiškiems poveikiams po vienos TMS procedūros, bet ne po pilno terapinio kurso. Manoma, kad rezultatų įvairovę TMS praktikoje įtakoja skirtingi stimuliacijos parametrai ir netikslumai parenkant stimuliuojamą zoną smegenyse. Nors TMS terapija dažnai traktuojama kaip švelnesnė alternatyva elektros impulsų terapijai (EIT), palyginamųjų fiziologinių šių metodikų tyrimų labai trūksta. Darbo tikslas buvo įvertinti TMS terapijos kurso poveikį bioelektriniam galvos smegenų aktyvumui ir palyginti jį su EIT terapijos poveikiu. Buvo tirta aukšto ir žemo dažnių (10 Hz ir 1 Hz) TMS terapijos įtaka EEG dažnių galios spektrui bei sukeltiniam klausos potencialui P300, naudojant standartinį ir neuronavigacinį taikinio pozicionavimą. TMS sukelti EEG pokyčiai palyginti su EIT terapijos sukeltais EEG pokyčiais, išmatuota TMS terapijos sąlygotų pokyčių dinamika kelių mėnesių bėgyje. Rezultatai parodė, kad TMS terapijos pasekoje smegenyse ryškiausiai padidėja delta dažnio galia. Naudojant standartinį pozicionavimą 10 Hz TMS sukėlė įvairesnius ir intensyvesnius EEG galios spektro pokyčius nei 1 Hz TMS. Pritaikius neuronavigacinę sistemą 10 Hz TMS atveju sumažėjo teta ir alfa dažnių galios pokyčiai. Praėjus keliems mėnesiams nuo TMS... [toliau žr. visą tekstą]

Le p300/CBP acétyltransférase est un co-activateur transcriptionnel très important qui est impliqué dans la régulation d'un grand nombre de processus biologiques, comme la transcription d'ADN, le développement et l'immunité innée. Jusqu'à présent, le rôle de p300/CBP dans la régulation de l'expression des gènes a été largement étudiée, mais les mécanismes qui régulent son activité enzymatique sont encore peu connus. Des études ont montré que le dysfonctionnement de p300/CBP est associé à plusieurs formes de cancer et de maladies neurodégénératives. Dés lors, chaque progrès concernant les mécanismes de régulation de p300/CBP est devenu primordial pour le développement de nouvelles thérapies. Le 'noyau' de p300/CBP contient deux domaines pour la reconnaissance des modifications post-traductionnelles (MPTs), un bromodomaine et un PHD finger (le module BP), adjacent à un domaine HAT (ou domaine histone acétyltransférase). Plusieurs enzymes, modifiant la chromatine, contiennent des domaines de reconnaissance des MPTs. Fréquemment des groupements particuliers de ces domaines sont très conservés et liés, au sein de la même protéine ou du même complexe protéique, suggérant qu'ils réalisent des fonctions coordonnées. Ces domaines adjacents peuvent agir en concertation dans la reconnaissance simultanée de différents MPTs ou peuvent exercer des fonctions différentes de celles qui sont effectuées par ces deux domaines particuliers, tels que les fonctions de régulation enzymatique. Plusieurs études suggèrent que les cycles acétylation/désacétylation dans la boucle d'auto-inhibition, à l'intérieur du domaine HAT, jouent un rôle important dans la régulation de l'activité enzymatique de p300/CBP. La proximité du module BP et du domaine HAT suggère que la spécificité de liaison, appartenant au module BP, peut être intrinsèquement liée à la régulation de l'activité du domaine HAT. L'objectif de ma thèse est de déterminer le rôle du module BP dans la régulation de l'activité du domaine HAT. Je propose que le module BP soit impliqué dans la régulation de p300/CBP de deux façons. La première consiste à établir un lien avec le domaine HAT qui stabilise la conformation auto-inhibée de l'enzyme. La deuxième exige que le module BP joue un rôle dans le choix des substrats de p300/CBP. J'ai été en mesure de montrer que BP peut se lier au domaine HAT et à la chromatine modifiée et qu'il peut reconnaître les modifications effectuées par p300/CBP lui-même. Les données obtenues indiquent que le module BP peut être impliqué dans la régulation de l'activité de p300/CBP et dans son ciblage à la chromatine. / The p300/CBP acetyltransferase is an important transcriptional co-activator which is involved in regulating a wide range of biological processes, such as DNA transcription, development and innate immunity. To date, the role of p300/CBP in gene regulation has been extensively described but little is known about the mechanisms which regulate its activity. Since misregulation of p300/CBP has been associated to the development of several forms of cancers and neurodegenerative diseases, studies directed to decipher the mechanisms of regulation of p300/CBP are of great importance for the development of new therapies. The p300/CBP 'core' contains two post-translational modifications (PTMs) recognition motifs, a bromodomain and a PHD domain (the bromo-PHD module, BP), in close proximity to a histone acetyltransferase domain (HAT). Many chromatin modifying enzymes contain recognition modules for PTMs. Frequently particular groupings of such modules are conserved and linked within the same protein or the same multisubunit complex, suggesting that they perform concerted functions. These linked modules may act combinatorially to allow recognition of multiple PTMs or display new functions that are not possessed by the single modules, such as regulatory properties. Accumulating evidence suggests that acetylation/deacetylation in a conserved autoinhibitory loop of the p300/CBP HAT domain plays an important role in regulation of HAT activity. The close apposition of the BP module and the HAT domain suggests that BP substrate recognition is intrinsically linked to regulation of HAT activity. During my thesis work, I have investigated the role of BP in HAT regulation. I propose that the BP module is involved in p300/CBP regulation by binding to the HAT domain and stabilizing the autoinhibited conformation of the enzyme. I have also investigated substrate specificity of the BP module towards modified chromatin. I could show that the BP module binds histone modifications including those that are p300/CBP dependent. Altogether, the data suggests that the BP module is involved in regulating p300/CBP HAT activity and in targeting of chromatin.