Modificazioni del segnale EEG in un compito di memoria visiva con distrattori visivi ‘deboli’ e ‘forti’

La valutazione del segnale elettroencefalografico acquisito durante compiti di Working Memory è utile per indagare regioni e meccanismi cerebrali alla base della capacità di immagazzinare le informazioni provenienti dall’ambiente rilevanti per il task da svolgere e di inibire stimoli irrilevanti/distraenti. In questo lavoro di Tesi è stato condotto uno studio su 13 volontari che hanno svolto un compito di memoria di lavoro visiva, consistente di prove ripetute (trial) ognuna composta di diverse fasi: Encoding (memorizzazione del memory set), Retention (mantenimento in memoria) in cui si mostra un distrattore, che può essere weak (poco interferente) o strong (maggiormente interferente). Ciascun trial termina con la comparsa della Probe, a cui il soggetto deve rispondere indicando se apparteneva o meno al memory set. Durante il task è stato acquisito il segnale EEG da 64 elettrodi, ed analizzato per indagare i potenziali evocati (ERPs) e la sincronizzazione/desincronizzazione in banda alpha (8-12 Hz) e theta (4-8 Hz) correlata agli stimoli visivi; è stata svolta anche un’analisi preliminare ricostruendo l’attività delle sorgenti corticali dal segnale EEG. Dalle analisi emerge che gli ERPs sono visibili principalmente nelle fasi di Encoding e Distractor, e nelle regioni fronto-centrali e parieto-occipitali, e che nella fase di Distractor sono maggiori per distrattore weak rispetto a strong. Si conferma la natura inibitoria del ritmo alpha e il ruolo del ritmo theta nei processi cognitivi; infatti la potenza in banda alpha aumenta nella fase pre-distrattore (sia weak che strong) e la potenza in banda theta è sostenuta durante l’intero task. Non si osservano differenze in banda alpha e theta tra i due distrattori nella fase pre-distrattore, mentre si osserva una modulazione durante la presentazione del distrattore.

Effetto di distrattori acustici rispetto a distrattori visivi in un compito di memoria visiva: analisi del segnale EEG

Studi recenti hanno evidenziato cambiamenti nei ritmi alpha (8-12 Hz) e theta (4-8 Hz) in vari processi modulatori top-down e di controllo cognitivo come la memoria di lavoro (WM, working memory) e la soppressione di distrattori. I compiti di WM richiedono attenzione interna sostenuta per dare priorità alle informazioni rilevanti a discapito di quelle interferenti che distraggono dall’obiettivo. I meccanismi di attenzione in tali compiti sono associati ad aumento di potenza alpha, che riflette la funzione inibitoria di tale ritmo, in regioni che elaborano informazioni distraenti, e ad aumento di potenza theta, soprattutto in regioni frontali, che riflette funzioni di controllo cognitivo per raggiungere l’obiettivo pur in presenza di interferenze. Questo lavoro è volto ad indagare gli effetti di distrattori acustici rispetto a distrattori visivi in un compito di visual WM. A tale scopo sono stati acquisiti ed elaborati i segnali EEG di 12 soggetti volontari mentre eseguivano un compito di visual WM, in cui la fase di retention (mantenimento in memoria delle informazioni codificate) veniva interrotta con la presentazione di distrattori di due modalità sensoriali differenti (visiva e acustica), per valutare le variazioni dell’attività cerebrale in termini di ritmi alpha e theta e le regioni coinvolte. Si è osservato un aumento maggiore di potenza alpha (principalmente posteriore) in presenza del distrattore acustico rispetto al visivo sia nella fase pre-distrattore che nella fase distrattore, statisticamente significativo nella fase distrattore. Si è osservato un aumento maggiore di potenza theta (principalmente frontale) in presenza del distrattore acustico rispetto al visivo in tutte le fasi del task, statisticamente significativo nella fase iniziale di retention e nella fase del distrattore. I risultati potrebbero indicare una maggiore necessità di controllo cognitivo e di protezione da stimoli interferenti in caso di distrattore acustico rispetto al visivo.

“Event-Related Spectral Perturbations” nel segnale EEG durante un compito di reaching

Questo elaborato ha analizzato le Event Related Spectral Perturbation (ERSP), cioè le variazioni nella potenza del segnale in corrispondenza di una frequenza o una banda di frequenze, suddivisi in Event Related Synchronization (ERS) nel caso di incremento di potenza e Event Related Desynchronization (ERD) nel caso di decremento di potenza, relative a movimenti di reaching eseguiti con l’arto superiore. In particolare, sono state prese in considerazione le potenze nel ritmo alpha (8-12 Hz) e ritmo beta (12-30 Hz), in quanto ritmi associati alla preparazione ed esecuzione del movimento. I segnali EEG analizzati (60 canali) sono relativi a 14 soggetti a cui è stato chiesto di compiere movimenti di reaching verso una posizione target, secondo una tempistica definita dall’accensione di uno stimolo visivo informativo (CUE, corrispondente al led nella posizione target) e un secondo stimolo visivo imperativo (GO) che dà il via libera all’esecuzione del movimento verso il target. Sono codificate 5 posizioni discrete, a 0°, 45°, 90°, 135° e 180°, su una semicirconferenza il cui centro rappresenta il punto di partenza e ritorno, chiamato base. I segnali preventivamente preprocessati, sono stati decomposti tramite trasformata wavelet ed elaborati con la tecnica dell’averaging, con lo scopo di evidenziare ERS e ERD in banda alpha e beta associati a eventi visivi e motori. È stata presentata l’evoluzione nel tempo della distribuzione topologica delle ERSP a livello dello scalpo e sono state svolte analisi suddividendo i dati secondo la direzione (destra, centro, sinistra) del target e secondo la profondità (vicino, medio, lontano) del target. I risultati mostrano una desincronizzazione (ERD) nella fase di preparazione del movimento (immediatamente prima dello stimolo GO), sia in banda alpha che beta e suggeriscono una modulazione dell’ERD in funzione della direzione/profondità del target.

Il segnale EEG in un compito di ’center-out reaching’: analisi e decodifica a livello di scalpo e di corteccia

Nellâ analisi del segnale EEG, sono di particolare interesse i potenziali evento correlato (ERP), che descrivono la risposta cerebrale in seguito alla presentazione di stimoli o eventi esterni o interni. Questi potenziali non sono immediatamente visibili sul tracciato EEG grezzo, ed è necessario, oltre ad unâ��accurata fase di preprocessing, mediare (averaging) i segnali di molti trial ripetuti per visualizzare tali risposte nel tempo. Questo studio ha posto l' attenzione sugli ERP visuomotori generati in un compito di center-out reaching, che prevede il raggiungimento di uno tra cinque target, ognuno associato ad un LED, mediante il braccio dominante, con una tempistica scandita dalla presentazione di due stimoli visivi: lo stimolo preparatorio ¸ (che indica il target) e lo stimolo imperativo (che dà il via libera al movimento). I segnali ERP, ottenuti mediante la tecnica dellâ averaging, sono stati analizzati sia a livello di scalpo, considerando i segnali di elettrodo, sia a livello di corteccia, dopo risoluzione del problema inverso, e considerando rappresentazioni prima a livello di singoli dipoli corticali e quindi di intere regioni corticali (ROI). Inoltre, è stata applicato un metodo di deep learning (rete neurale convoluzionale) per decodificare il segnale EEG a livello di singolo trial, ovvero classificare il target coinvolto nello specifico trial. La decodifica è stata applicata sia ai segnali di scalpo sia ai segnali delle ROI corticali. Complessivamente i risultati mostrano ERP ben visibili a livello di scalpo e legati sia a processing visivo che motorio. Gli ERP a livello di ROI corticali sono più rumorosi e sembrano cogliere meno processing motorio rispetto al visivo, presumibilmente anche in conseguenza di alcune scelte metodologiche nella ricostruzione di segnali di ROI. In linea con questo, le performance di decodifica sono migliori a livello di scalpo che di ROI corticali.

Longitudinal Analysis Of Hippocampal T2 Relaxometry In Fmtle.

To investigate the degree of T2 relaxometry changes over time in groups of patients with familial mesial temporal lobe epilepsy (FMTLE) and asymptomatic relatives. We conducted both cross-sectional and longitudinal analyses of T2 relaxometry with Aftervoxel, an in-house software for medical image visualization. The cross-sectional study included 35 subjects (26 with FMTLE and 9 asymptomatic relatives) and 40 controls; the longitudinal study was composed of 30 subjects (21 with FMTLE and 9 asymptomatic relatives; the mean time interval of MRIs was 4.4 ± 1.5 years) and 16 controls. To increase the size of our groups of patients and relatives, we combined data acquired in 2 scanners (2T and 3T) and obtained z-scores using their respective controls. General linear model on SPSS21® was used for statistical analysis. In the cross-sectional analysis, elevated T2 relaxometry was identified for subjects with seizures and intermediate values for asymptomatic relatives compared to controls. Subjects with MRI signs of hippocampal sclerosis presented elevated T2 relaxometry in the ipsilateral hippocampus, while patients and asymptomatic relatives with normal MRI presented elevated T2 values in the right hippocampus. The longitudinal analysis revealed a significant increase in T2 relaxometry for the ipsilateral hippocampus exclusively in patients with seizures. The longitudinal increase of T2 signal in patients with seizures suggests the existence of an interaction between ongoing seizures and the underlying pathology, causing progressive damage to the hippocampus. The identification of elevated T2 relaxometry in asymptomatic relatives and in patients with normal MRI suggests that genetic factors may be involved in the development of some mild hippocampal abnormalities in FMTLE.

Rolandic Epilepsy And Dyslexia.

Although benign epilepsy with centrotemporal spikes (BECTS) is an idiopathic, age-related epilepsy syndrome with favorable outcome, recent studies have shown impairment in specific neuropsychological tests. The objective of this study was to analyze the comorbidity between dyslexia and BECTS. Thirty-one patients with clinical and electroencephalographic diagnosis of BECTS (group A) and 31 paired children (group B) underwent a language and neuropsychological assessment performed with several standardized protocols. Our findings were categorized as: a) dyslexia; b) other difficulties; c) without difficulties. Our results were compared and statistically analyzed. Our data showed that dyslexia occurred in 19.4% and other difficulties in 74.2% of our patients. This was highly significant when compared with the control group (p<0.001). Phonological awareness, writing, reading, arithmetic, and memory tests showed a statistically significant difference when comparing both groups. Our findings show significant evidence of the occurrence of dyslexia in patients with BECTS.

Estudo vídeo-polissonográfico em recém-nascidos de termo pequenos para a idade gestacional

Video-polygraphic-EEG studies were performed in the first 24 life-hours of 26 healthy full-term newborns without perinatal injuries. The neurological examination and cranial ultrasonography were normal. The newborns were divided into two groups: one, with full-term appropriate - birth weight 11 newborns (control group ) and the other with full-term low-birth weight 15 newborns. Thirteen newborns of the second group had video-polygraphic-EEG study abnormalities. The most frequent abnormalities were found in 11 cases, as far as sleep architecture is concerned. Also, when compared with the control group, 8 cases of an excessive amount of startles and 2 cases of low behavior activities were found. The results demonstrate the usefulness of video-polygraphic-EEG study in the full-term newborns with intra-uterine growth retard. This examination was sensitive to detect behavior, sleep architecture and EEG standard differences in the low birth-weight newborns as to the control group.

Epilepsias parciais familiares

OBJECTIVE: To investigate the clinical and genetic characteristics of familial partial epilepsies. METHOD: Family history of seizures was questioned in all patients followed in our epilepsy clinics, from October 1997 to December 1998. Those with positive family history were further investigated and detailed pedigrees were obtained. All possibly affected individuals available underwent clinical evaluation. Seizures and epilepsy syndromes were classified according to the ILAE recommendations. Whenever possible, EEG and MRI were performed. RESULTS: Positive family history was identified in 32 unrelated patients. A total of 213 possibly affected individuals were identified, 161 of whom have been evaluated. The number of affected subjects per family ranged from two to 23. Temporal lobe epilepsy (TLE) was identified in 22 families (68%), frontal lobe epilepsy in one family (3%), partial epilepsy with centrotemporal spikes in five families (15%), and other benign partial epilepsies of childhood in four families (12%). Most of the affected individuals in the TLE families (69%) had clinical and/or EEG characteristics of typical TLE. However, the severity of epilepsy was variable, with 76% of patients with spontaneous seizure remission or good control with medication and 24% with refractory seizures, including 7 patients that underwent surgical treatment. In the other 10 families, we identified 39 possibly affected subjects, 23 of whom were evaluated. All had good seizure control (with or without medication) except for one patient with frontal lobe epilepsy. Pedigree analysis suggested autosomal dominant inheritance with incomplete penetrance in all families. CONCLUSION: Family history of seizures is frequent among patients with partial epilepsies. The majority of our families had TLE and its expression was not different from that observed in sporadic cases. The identification of genes involved in partial epilepsies may be usefull in classification of syndromes, to stablish prognosis and optimal treatment.

Modelos estatísticos indicadores de comportamentos associados a bem-estar térmico para matrizes pesadas

The study of female broiler breeders is of great importance for the country as poultry production is one of the largest export items, and Brazil is the second largest broiler meat exporter. Animal behavior is known as a response to the effect of several interaction factors among them the environment. In this way the internal housing environment is an element that gives hints regarding to the bird s thermal comfort. Female broiler breeder behavior, expresses in form of specific pattern the bird s health and welfare. This research had the objective of applying predictive statistical models through the use of simulation, presenting animal comfort scenarios facing distinct environmental conditions. The research was developed with data collected in a controlled environment using Hybro - PG® breeding submitted to distinct levels of temperature, three distinct types of standard ration and age. Descriptive and exploratory analysis were proceeded, and afterwards the modeling process using the Generalized Estimation Equation (GEE). The research allowed the development of the thermal comfort indicators by statistical model equations of predicting female broiler breeder behavior under distinct studied scenarios.

Benign focal seizures of adolescence and neuropsychological findings in patients from community

RATIONALE: Benign focal seizures of adolescence (BFSA) described by Loiseau et al in 1972, is considered a rare entity, but maybe underdiagnosed. Although mild neuropsychological deficits have been reported in patients with benign epilepsies of childhood, these evaluations have not so far been described in BFSA. The aim of this study is to evaluate neuropsychological functions in BFSA with new onset seizures (<12 months). METHODS: Eight patients with BFSA (according to Loiseau et al, 1972, focal or secondarily tonic clonic generalized seizures between the ages of 10-18 yrs., normal neurologic examination, normal EEG or with mild focal abnormalities) initiated in the last 12 months were studied between July 2008 to May 2009. They were referred from the Pediatric Emergency Section of the Hospital Universitário of the University of Sao Paulo, a secondary care regionalized facility located in a district of middle-low income in Sao Paulo city, Brazil. The study was approved by the Ethics Committee of the Institution. All patients performed neurological, EEG, brain CT and neuropsychological evaluation which consisted of Raven's Special Progressive Matrices - General and Special Scale (according to different ages), Wechsler Children Intelligence Scale-WISC III with ACID Profile, Trail Making Test A/B, Stroop Test, Bender Visuo-Motor Test, Rey Complex Figure, Rey Auditory Verbal Learning Test-RAVLT, Boston Naming Test, Fluency Verbal for phonological and also conceptual patterns - FAS/Animals and Hooper Visual Organization Test. For academic achievement, we used a Brazilian test for named "Teste do Desempenho Escolar", which evaluates abilities to read, write and calculate according to school grade. RESULTS: There were 2 boys and 6 girls, with ages ranging from 10 yrs. 9 m to 14 yrs. 3 m. Most (7/8) of the patients presented one to two seizures and only three of them received antiepileptic drugs (AEDs). Six had mild EEG focal abnormalities and all had normal brain CT. All were literate, attended regular public schools and scored in a median range for IQ, and seven showed discrete higher scores for the verbal subtests. There were low scores for attention in different modalities in six patients, mainly in alternated attention as well as inhibitory subtests (Stroop test and Trail Making Test part B). Four of the latter cases who showed impairment both in alternated and inhibitory attention were not taking AEDs. Visual memory was impaired in five patients (Rey Complex Figure). Executive functions analysis showed deficits in working memory in five, mostly observed in Digits Indirect Order and Arithmetic tests (WISC III). Reading and writing skills were below the expected average for school grade in six patients according to the achievement scholar performance test utilized. One patient of this series who had the best scores in all tests was taking phenobarbital. CONCLUSIONS: Neuropsychological imbalance between normal IQ and mild dysfunctions such as in attention domain and in some executive abilities like working memory and planning, as well as difficulties in visual memory and in reading and writing, were described in this group of patients with BFSA from community. This may reflect mild higher level neurological dysfunctions in adolescence idiopathic focal seizures probably caused by an underlying dysmaturative epileptogenic process. Although academic problems often have multiple causes, a specific educational approach may be necessary in these adolescents, in order to improve their scholastic achievements, helping in this way, to decrease the stigma associated to epileptic seizures in the community.

Antinociceptive effect of stimulating the occipital or retrosplenial cortex in rats

A role for the occipital or retrosplenial cortex in nociceptive processing has not been demonstrated yet, but connections from these cortices to brain structures involved in descending pain-inhibitory mechanisms were already demonstrated. This study demonstrated that the electrical stimulation of the occipital or retrosplenial cortex produces antinociception in the rat tail-flick and formalin tests. Bilateral lesions of the dorsolateral funiculus abolished the effect of cortical stimulation in the tail-flick test. Injection of glutamate into the same targets was also antinociceptive in the tail-flick test. No rats stimulated in the occipital or retrosplenial cortex showed any change in motor performance on the Rota-rod test, or had epileptiform changes in the EEG recording during or up to 3 hours after stimulation. The antinociception induced by occipital cortex stimulation persisted after neural block of the retrosplenial cortex. The effect of retrosplenial cortex stimulation also persisted after neural block of the occipital cortex. We conclude that stimulation of the occipital or retrosplenial cortex in rats leads to antinociception activating distinct descending pain-inhibitory mechanisms, and this is unlikely to result from a reduced motor performance or a postictal phenomenon. Perspective: This study presents evidence that stimulation of the retrosplenial or occipital cortex produces antinociception in rat models of acute pain. These findings enhance our understanding of the role of the cerebral cortex in control of pain. (C) 2010 by the American Pain Society

Frequency Domain Connectivity Identification: An Application of Partial Directed Coherence in fMRI

Functional magnetic resonance imaging (fMRI) has become an important tool in Neuroscience due to its noninvasive and high spatial resolution properties compared to other methods like PET or EEG. Characterization of the neural connectivity has been the aim of several cognitive researches, as the interactions among cortical areas lie at the heart of many brain dysfunctions and mental disorders. Several methods like correlation analysis, structural equation modeling, and dynamic causal models have been proposed to quantify connectivity strength. An important concept related to connectivity modeling is Granger causality, which is one of the most popular definitions for the measure of directional dependence between time series. In this article, we propose the application of the partial directed coherence (PDC) for the connectivity analysis of multisubject fMRI data using multivariate bootstrap. PDC is a frequency domain counterpart of Granger causality and has become a very prominent tool in EEG studies. The achieved frequency decomposition of connectivity is useful in separating interactions from neural modules from those originating in scanner noise, breath, and heart beating. Real fMRI dataset of six subjects executing a language processing protocol was used for the analysis of connectivity. Hum Brain Mapp 30:452-461, 2009. (C) 2007 Wiley-Liss, Inc.

X-linked myoclonic epilepsy with spasticity and intellectual disability - Mutation in the homeobox gene ARX

Objective: To describe a new syndrome of X-linked myoclonic epilepsy with generalized spasticity and intellectual disability (XMESID) and identify the gene defect underlying this disorder. Methods: The authors studied a family in which six boys over two generations had intractable seizures using a validated seizure questionnaire, clinical examination, and EEG studies. Previous records and investigations were obtained. Information on seizure disorders was obtained on 271 members of the extended family. Molecular genetic analysis included linkage studies and mutational analysis using a positional candidate gene approach. Results: All six affected boys had myoclonic seizures and TCS; two had infantile spasms, but only one had hypsarrhythmia. EEG studies show diffuse background slowing with slow generalized spike wave activity. All affected boys had moderate to profound intellectual disability. Hyperreflexia was observed in obligate carrier women. A late-onset progressive spastic ataxia in the matriarch raises the possibility of late clinical manifestations in obligate carriers. The disorder was mapped to Xp11.2-22.2 with a maximum lod score of 1.8. As recently reported, a missense mutation (1058C>T/P353L) was identified within the homeodomain of the novel human Aristaless related homeobox gene (ARX). Conclusions: XMESID is a rare X-linked recessive myoclonic epilepsy with spasticity and intellectual disability in boys. Hyperreflexia is found in carrier women. XMESID is associated with a missense mutation in ARX. This disorder is allelic with X-linked infantile spasms (ISSX; MIM 308350) where polyalanine tract expansions are the commonly observed molecular defect. Mutations of ARX are associated with a wide range of phenotypes; functional studies in the future may lend insights to the neurobiology of myoclonic seizures and infantile spasms.

A medial to lateral shift in premovement cortical activity in hemi-Parkinson's disease: Studies of event-related potentials and whole-scalp magneto encephalography

Cortical activity associated with voluntary movement is shifted from medial to lateral premotor areas in Parkinson's disease. This occurs bilaterally, even for unilateral movements. We have used both EEG and MEG to further investigate medial and lateral premotor activity in patients with hemi-Parkinson's disease, in whom basal ganglia impairment is most pronounced in one hemisphere. The CNV, recorded from 21 scalp positions in a Go/NoGo task, was maximal over central medial regions in control subjects. For hemi-Parkinson's disease subjects, activity was shifted more frontally, reduced in the midline and lateralised towards the side of greatest basal ganglia impairment. With 143 channel whole-scalp magneto encephalography (MEG) we are further examining asymmetries in supplementary motor/premotor cortical activity prior to self-paced voluntary movement. In preliminary results, one hemi-Parkinson's disease patient with predominantly left-side symptoms showed strong medial activity consistent with a dominant source in the left supplementary motor area (SMA). Three patients showed little medial activity, but early bilateral sources within lateral premotor cortex. Results suggest greater involvement of lateral premotor rather than the SMA prior to movement in Parkinson's disease and provide evidence for asymmetric function of the SMA in hemi- Parkinson's disease, with reduced activity on the side of greatest basal ganglia deficit.

Prevalence of Epilepsy in Children From a Brazilian Area of High Deprivation

This study assessed the prevalence rate of epilepsy and its causes in children and adolescents in one area of high deprivation in Sao Paulo, Sao Paulo, in Southeast Brazil. Between July 2005 and June 2006, 4947 families from a population of 22,013 inhabitants (including 10,405 children and adolescents between the ages of 0 and 16 years) living in the shantytown of Paraisopolis, were interviewed. In the first phase, a validated questionnaire was administered, to identify the occurrence of seizures. In the second phase, clinical history, neurologic examination, electroencephalography, and structural neuroimaging were performed. The diagnosis of epilepsy, including etiology, seizure types, and epileptic syndrome classification, was according to criteria of the International League Against Epilepsy. The screening phase identified 353 presumptive cases. In the second phase, 101 of these cases (33.8%) received the diagnosis of epilepsy. Crude prevalence of epilepsy was 9.7/1000 and prevalence of active epilepsy was 8.7/1000. Partial seizures were the most frequent seizure type (62/101). Symptomatic focal epilepsy was the most common form, and hypoxic-ischemic encephalopathy the most common etiology, reflecting the socioeconomic conditions of this specific population. Adequate public policies regarding perinatal assistance could help reduce the prevalence of epilepsy. (C) 2010 by Elsevier Inc. All rights reserved.