17 research outputs found

    Associations of cognitive reserve and psychological resilience with cognitive functioning in subjects with cerebral white matter hyperintensities

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    Background and purpose Cerebral small vessel disease is characterized by progressive white matter hyperintensities (WMH) and cognitive decline. However, variability exists in how individuals maintain cognitive capabilities despite significant neuropathology. The relationships between individual cognitive reserve, psychological resilience and cognitive functioning were examined in subjects with varying degrees of WMH. Methods In the Helsinki Small Vessel Disease Study, 152 subjects (aged 65-75 years) underwent a comprehensive neuropsychological assessment, evaluation of subjective cognitive complaints and brain magnetic resonance imaging with volumetric WMH evaluation. Cognitive reserve was determined by education (years) and the modified Cognitive Reserve Scale (mCRS). Psychological resilience was evaluated with the Resilience Scale 14. Results The mCRS total score correlated significantly with years of education (r = 0.23, p < 0.01), but it was not related to age, sex or WMH volume. Together, mCRS score and education were associated with performance in a wide range of cognitive domains including processing speed, executive functions, working memory, verbal memory, visuospatial perception and verbal reasoning. Independently of education, the mCRS score had incremental predictive value on delayed verbal recall and subjective cognitive complaints. Psychological resilience was not significantly related to age, education, sex, WMH severity or cognitive test scores, but it was associated with subjective cognitive complaints. Conclusions Cognitive reserve has strong and consistent associations with cognitive functioning in subjects with WMH. Education is widely associated with objective cognitive functioning, whereas lifetime engagement in cognitively stimulating leisure activities (mCRS) has independent predictive value on memory performance and subjective cognitive complaints. Psychological resilience is strongly associated with subjective, but not objective, cognitive functioning.Peer reviewe

    Sornatosensory evoked potential and EEG in children with focal idiopathic epilepsies with and without evoked spikes by tapping of the feet or hands

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    The characteristics of SEP cortical components were studied in 40 children with focal idiopathic epilepsies of childhood. Twenty children had focal idiopathic epilepsies and evoked spikes (FIE-ES) on the EEG and 20 had benign focal epilepsy of childhood with centrotemporal spikes (CTE) but without evoked spikes (ES). These data were compared with those of a control group of 20 normal children. N35 high-amplitude component was more frequent in the CTE group than in the control group (p<0.001). P98 showed high amplitude in 50% of the children of FIE-ES group, and in none of the CTE and control groups (p<0.001). The P98 high amplitude component was more common in the FIE-ES group than in the other groups, and so was the N35 high amplitude component in the CTE group. Lateralization of high-amplitude components of N35 in the CTE group and of P98 in FIE group was not correlated with lateralization of epileptiform activity and evoked spikes. Based on our findings, there are SEPs cortical component differences in childhood focal idiopathic epilepsies according to occurrence or absence of ES.36319419

    Epilepsia occipital benigna da infùncia de início precoce (tipo Panayiotopoulos): aspectos clínicos e eletrencefalogråficos evolutivos em 14 crianças Early-onset benign childhood occipital epilepsy (Panayiotopoulos type): clinical and electroencephalographic features in 14 children

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    Foram estudadas as caracterĂ­sticas evolutivas clĂ­nico-eletrencefalogrĂĄficas de 14 crianças com epilepsia occipital benigna da infĂąncia de inĂ­cio precoce (tipo Panayiotopoulos). O tempo mĂ©dio de segmento foi 50,5 meses. A idade mĂ©dia na primeira crise foi 3,7 anos. O nĂșmero total de crises foi atĂ© 3 crises em 11 casos, numerosas em 3; o perĂ­odo mĂ©dio entre a primeira e a Ășltima crise foi 14,5 meses. Em 4 casos as crises tiveram duração prolongada, constituindo estado de mal parcial. Atividade epileptiforme (AE) occipital foi observada em todos os casos no primeiro EEG e, foi tambĂ©m, extra-occipital, em 3 casos. Houve bloqueio da AE occipital, pela abertura dos olhos, em 4 casos; em 3 casos foram observadas, tambĂ©m, pontas evocadas. O EEG normalizou-se em 9 casos, em um perĂ­odo mĂ©dio de 29 meses.<br>We studied clinical and electroencephalographic features of 14 children, age range of 2 -8 years, with no neurological or neuroradiological evidence of brain damage and with occipital epileptiform activity in the EEG. Seizures were numerous in 3 cases. Age at onset was between 1-7 years. In 4 cases the seizures last for more than 20 min. Spikes were observed in 6 cases and spike and slow-wave complex in 8. Discharges blocking by eyes opening were confirmed in 4 cases. Somatosensory evoked spikes by foot stimulation were observed in 2 cases. Autonomic and versive seizures are the main clinical manifestations of Panayiotopoulos syndrome. Discharges blocking by eyes opening are a less frequent feature

    Calcificação nos nĂșcleos da base na tomografia computadorizada: correlação clĂ­nica em 25 pacientes consecutivos Basal ganglia calcification on computed tomography: clinical characteristics in 25 patients

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    Analisamos os aspectos clĂ­nicos de 25 pacientes consecutivos que apresentaram calcificação nos nĂșcleos da base na tomografia computadorizada (TC) de crĂąnio. Esta ocorreu em 0,68% de todos os exames realizados no perĂ­odo. Vinte e trĂȘs pacientes apresentavam condiçÔes clĂ­nicas diversas, a saber: cefalĂ©ia em 7 casos, acidente vascular cerebral em 5, sĂ­ndrome extrapiramidal em 2, processo expansivo cerebral em 2, epilepsia, retardo do desenvolvimento neuropsicomotor, demĂȘncia e trauma de crĂąnio em um caso cada ou outras condiçÔes neurolĂłgicas em 3. NĂŁo havia sintomas neurolĂłgicos em 2 casos. Em 15 pacientes (60,0%) havia, alĂ©m da calcificação dos nĂșcleos da base, outras alteraçÔes na TC. Correlação clĂ­nica foi observada apenas com as outras alteraçÔes da TC e nĂŁo com a calcificação dos nĂșcleos da base, corroborando a hipĂłtese de que esta possa ser um achado incidental.<br>Twenty-five patients presenting basal ganglia calcification were assessed. This finding comprised 0.68% of all skull CT scan carried out during the period. Two patients were neurologically asymptomatic and 23 presented a variety neurological disorders - headache (7 patients), stroke (5 patients), extrapyramidal syndromes (2 patients), tumor (2 patients), epilepsy (1 patient), mental retardation (1 patient), dementia (1 patient), cranial trauma (1 patient), other neurological conditions (3 patients) - or were asymptomatic from the neurological point of view (2 patients). Findings in the CT scan other than the basal ganglia calcification were observed in 15 (60%) patients. There was a clinical-CT scan correlation in these cases but not in those in which the basal ganglia calcification was an isolated finding. This study highlights the fact that basal ganglia calcification is often a nonspecific finding on CT scan and that it may not be possible to establish a clinical-pathological correlation between them
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