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1.
Int J Psychophysiol ; 98(3 Pt 1): 413-25, 2015 Dec.
Artigo em Inglês | MEDLINE | ID: mdl-26342552

RESUMO

The brain's ability to recognize different acoustic cues (e.g., frequency changes in rapid temporal succession) is important for speech perception and thus for successful language development. Here we report on distinct event-related potentials (ERPs) in 5-6-year-old children recorded in a passive oddball paradigm to repeated tone pair stimuli with a frequency change in the second tone in the pair, replicating earlier findings. An occasional insertion of a third tone within the tone pair generated a more merged pattern, which has not been reported previously in 5-6-year-old children. Both types of deviations elicited pre-attentive discriminative mismatch negativity (MMN) and late discriminative negativity (LDN) responses. Temporal principal component analysis (tPCA) showed a similar topographical pattern with fronto-central negativity for MMN and LDN. We also found a previously unreported discriminative response complex (P340-N440) at the temporal electrode sites at about 140 ms and 240 ms after the frequency deviance, which we suggest reflects a discriminative processing of frequency change. The P340 response was positive with a clear radial distribution preceding the fronto-central frequency MMN by about 30 ms. The results indicate that 5-6-year-old children can detect frequency change and the occasional insertion of an additional tone in sound pairs as reflected by MMN and LDN, even with quite short within-stimulus intervals (150 ms and 50 ms). Furthermore, MMN for these changes is preceded by another response to deviancy, temporal P340, which seems to reflect a parallel but earlier discriminatory process.


Assuntos
Percepção Auditiva/fisiologia , Mapeamento Encefálico , Encéfalo/fisiologia , Variação Contingente Negativa/fisiologia , Potenciais Evocados Auditivos/fisiologia , Som , Estimulação Acústica , Análise de Variância , Criança , Pré-Escolar , Eletroencefalografia , Feminino , Humanos , Masculino , Tempo de Reação/fisiologia
2.
Int J Psychophysiol ; 94(3): 298-310, 2014 Dec.
Artigo em Inglês | MEDLINE | ID: mdl-25312203

RESUMO

Specific reading disability, dyslexia, is a prevalent and heritable disorder impairing reading acquisition characterized by a phonological deficit. However, the underlying mechanism of how the impaired phonological processing mediates resulting dyslexia or reading disabilities remains still unclear. Using ERPs we studied speech sound processing of 30 dyslexic children with familial risk for dyslexia, 51 typically reading children with familial risk for dyslexia, and 58 typically reading control children. We found enhanced brain responses to shortening of a phonemic length in pseudo-words (/at:a/ vs. /ata/) in dyslexic children with familial risk as compared to other groups. The enhanced brain responses were associated with better performance in behavioral phonemic length discrimination task, as well as with better reading and writing accuracy. Source analyses revealed that the brain responses of sub-group of dyslexic children with largest responses originated from a more posterior area of the right temporal cortex as compared to the responses of the other participants. This is the first electrophysiological evidence for a possible compensatory speech perception mechanism in dyslexia. The best readers within the dyslexic group have probably developed alternative strategies which employ compensatory mechanisms substituting their possible earlier deficit in phonological processing and might therefore be able to perform better in phonemic length discrimination and reading and writing accuracy tasks. However, we speculate that for reading fluency compensatory mechanisms are not that easily built and dyslexic children remain slow readers during their adult life.


Assuntos
Estimulação Acústica/métodos , Encéfalo/fisiopatologia , Dislexia/fisiopatologia , Potenciais Evocados Auditivos/fisiologia , Leitura , Percepção da Fala/fisiologia , Mapeamento Encefálico/métodos , Criança , Dislexia/diagnóstico , Feminino , Humanos , Masculino , Fatores de Risco
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