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1.
J Autism Dev Disord ; 45(2): 473-80, 2015 Feb.
Artigo em Inglês | MEDLINE | ID: mdl-23989937

RESUMO

An emerging focus of research on autism spectrum disorder (ASD) targets the identification of early-developing ASD endophenotypes using infant siblings of affected children. One potential neural endophenotype is resting frontal electroencephalogram (EEG) alpha asymmetry, a metric of hemispheric organization. Here, we examined the development of frontal EEG alpha asymmetry in ASD high-risk and low-risk infant populations. Our findings demonstrate that low and high-risk infants show different patterns of alpha asymmetry at 6 months of age and opposite growth trajectories in asymmetry over the following 12 months. These results support the candidacy of alpha asymmetry as an early neural ASD endophenotype.


Assuntos
Ritmo alfa/fisiologia , Transtornos Globais do Desenvolvimento Infantil/fisiopatologia , Dominância Cerebral/fisiologia , Endofenótipos , Lobo Frontal/fisiopatologia , Sintomas Prodrômicos , Fatores Etários , Eletroencefalografia , Feminino , Humanos , Lactente , Masculino , Irmãos/psicologia
2.
PLoS One ; 9(8): e105176, 2014.
Artigo em Inglês | MEDLINE | ID: mdl-25140874

RESUMO

In the field of autism research, recent work has been devoted to studying both behavioral and neural markers that may aide in early identification of autism spectrum disorder (ASD). These studies have often tested infants who have a significant family history of autism spectrum disorder, given the increased prevalence observed among such infants. In the present study we tested infants at high- and low-risk for ASD (based on having an older sibling diagnosed with the disorder or not) at 6- and 12-months-of-age. We computed intrahemispheric linear coherence between anterior and posterior sites as a measure of neural functional connectivity derived from electroencephalography while the infants were listening to speech sounds. We found that by 12-months-of-age infants at risk for ASD showed reduced functional connectivity compared to low risk infants. Moreover, by 12-months-of-age infants later diagnosed with ASD showed reduced functional connectivity, compared to both infants at low risk for the disorder and infants at high risk who were not later diagnosed with ASD. Significant differences in functional connectivity were also found between low-risk infants and high-risk infants who did not go onto develop ASD. These results demonstrate that reduced functional connectivity appears to be related to genetic vulnerability for ASD. Moreover, they provide further evidence that ASD is broadly characterized by differences in neural integration that emerge during the first year of life.


Assuntos
Transtorno do Espectro Autista/diagnóstico , Transtorno do Espectro Autista/fisiopatologia , Transtorno do Espectro Autista/metabolismo , Transtorno Autístico/diagnóstico , Transtorno Autístico/fisiopatologia , Biomarcadores/metabolismo , Eletroencefalografia/métodos , Humanos , Lactente , Risco
3.
PLoS One ; 7(6): e39127, 2012.
Artigo em Inglês | MEDLINE | ID: mdl-22745707

RESUMO

Current research suggests that autism spectrum disorder (ASD) is characterized by asynchronous neural oscillations. However, it is unclear whether changes in neural oscillations represent an index of the disorder or are shared more broadly among both affected and unaffected family members. Additionally, it remains unclear how early these differences emerge in development and whether they remain constant or change over time. In this study we examined developmental trajectories in spectral power in infants at high- or low-risk for ASD. Spectral power was extracted from resting EEG recorded over frontal regions of the scalp when infants were 6, 9, 12, 18 and 24 months of age. We used multilevel modeling to assess change over time between risk groups in the delta, theta, low alpha, high alpha, beta, and gamma frequency bands. The results indicated that across all bands, spectral power was lower in high-risk infants as compared to low-risk infants at 6-months of age. Furthermore high-risk infants showed different trajectories of change in spectral power in the subsequent developmental window indicating that not only are the patterns of change different, but that group differences are dynamic within the first two years of life. These findings remained the same after removing data from a subset of participants who displayed ASD related behaviors at 24 or 36 months. These differences in the nature of the trajectories of EEG power represent important endophenotypes of ASD.


Assuntos
Transtornos Globais do Desenvolvimento Infantil/fisiopatologia , Eletroencefalografia/métodos , Pré-Escolar , Cognição/fisiologia , Endofenótipos , Feminino , Humanos , Lactente , Masculino
4.
Zero Three ; 30(2): 9-13, 2009 Nov 01.
Artigo em Inglês | MEDLINE | ID: mdl-23894221

RESUMO

Research over the past several decades has provided insight into the processes that govern early brain development and how those processes contribute to behavior. In the following article, we provide an overview of early brain development beginning with a summary of the prenatal period. We then turn to postnatal development and examine how brain functions are built and how experience mediates this process. Specifically, we discuss findings from research on speech and on face processing. The results of this research highlight how the first few years of life are a particularly important period of development of the brain.

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