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1.
Ear Hear ; 40(5): 1197-1209, 2019.
Artigo em Inglês | MEDLINE | ID: mdl-30762600

RESUMO

OBJECTIVE: Cochlear implants (CIs) restore a sense of hearing in deaf individuals. However, they do not transmit the acoustic signal with sufficient fidelity, leading to difficulties in recognizing emotions in voice and in music. The study aimed to explore the neurophysiological bases of these limitations. DESIGN: Twenty-two adults (18 to 70 years old) with CIs and 22 age-matched controls with normal hearing participated. Event-related potentials (ERPs) were recorded in response to emotional bursts (happy, sad, or neutral) produced in each modality (voice or music) that were for the most part correctly identified behaviorally. RESULTS: Compared to controls, the N1 and P2 components were attenuated and prolonged in CI users. To a smaller degree, N1 and P2 were also attenuated and prolonged in music compared to voice, in both populations. The N1-P2 complex was emotion-dependent (e.g., reduced and prolonged response to sadness), but this was also true in both populations. In contrast, the later portion of the response, between 600 and 850 ms, differentiated happy and sad from neutral stimuli in normal hearing but not in CI listeners. CONCLUSIONS: The early portion of the ERP waveform reflected primarily the general reduction in sensory encoding by CI users (largely due to CI processing itself), whereas altered emotional processing (by CI users) could be found in the later portion of the ERP and extended beyond the realm of speech.


Assuntos
Surdez/reabilitação , Emoções , Potenciais Evocados Auditivos/fisiologia , Música , Percepção da Fala , Adolescente , Adulto , Idoso , Implantes Cocleares , Surdez/fisiopatologia , Surdez/psicologia , Eletroencefalografia , Potenciais Evocados , Feminino , Humanos , Masculino , Pessoa de Meia-Idade , Percepção , Voz , Adulto Jovem
2.
Ann N Y Acad Sci ; 1517(1): 279-285, 2022 11.
Artigo em Inglês | MEDLINE | ID: mdl-35980667

RESUMO

Congenital amusia is a lifelong disorder that compromises the normal development of musical abilities in 1.5-4% of the general population. There is a substantial genetic contribution to congenital amusia, and it bears similarities to neurodevelopmental disorders of language. Here, we examine the extent to which variants in the forkhead box P2 gene (FOXP2)-the first gene to be identified as causal in developmental speech deficits-are associated with the amusic trait. Using a cohort of 49 individuals with amusia, of which 27 were unrelated, the role of FOXP2 variants in amusia was evaluated. Fourteen variants were examined in the cohort. None segregated with the amusic trait among participants for whom family information was available; nor were they predicted to be deleterious to protein function. Thus, variants in FOXP2 are not likely to cause amusia. Implications for ongoing debates about the distinction between musicality and language are discussed.


Assuntos
Transtornos da Percepção Auditiva , Humanos , Transtornos da Percepção Auditiva/genética , Distúrbios da Fala/genética , Idioma , Fatores de Transcrição Forkhead/genética
3.
Prog Neuropsychopharmacol Biol Psychiatry ; 32(3): 803-15, 2008 Apr 01.
Artigo em Inglês | MEDLINE | ID: mdl-18280023

RESUMO

Approximately 30 to 50% of people suffering from Gilles de la Tourette Syndrome (GTS) also fulfill diagnostic criteria for obsessive-compulsive disorder (OCD). Despite this high degree of comorbidity, very few studies have addressed the question of obsessive-compulsive symptoms (OCS) in GTS patients using specific brain event-related potentials (ERP) responses. The aim of the current study was to quantify neurocognitive aspects of comorbidity, using ERPs. Fourteen adults with GTS (without OCD) were compared to a group of 12 participants with GTS and comorbid obsessive-compulsive symptoms (GTS+OCS), to a group of 15 participants with OCD and to a group of 14 control participants without neurological or psychiatric problems. The P200 and P300 components were recorded during a visual counting oddball task. Results showed intact P200 amplitude in all groups, whilst the P300 amplitude was affected differentially across groups. The P300 oddball effect was reduced in participants in both OCD and GTS+OCS groups in the anterior region. However, the P300 oddball effect was significantly larger in participants of the GTS group compared to all other groups, mostly in the parietal region. These findings suggest that adults with GTS are characterized by enhanced working memory updating processes and that the superimposition of OCS can lead to a reduction of these processes. The discrepancy between our findings and results obtained in previous studies on GTS could reflect the modulating effect of OCS on late ERP components.


Assuntos
Encéfalo/fisiopatologia , Potenciais Evocados/fisiologia , Transtorno Obsessivo-Compulsivo , Síndrome de Tourette , Adulto , Análise de Variância , Mapeamento Encefálico , Comorbidade , Eletroencefalografia/métodos , Feminino , Lateralidade Funcional , Humanos , Masculino , Pessoa de Meia-Idade , Transtorno Obsessivo-Compulsivo/epidemiologia , Transtorno Obsessivo-Compulsivo/etiologia , Transtorno Obsessivo-Compulsivo/patologia , Estimulação Luminosa/métodos , Índice de Gravidade de Doença , Síndrome de Tourette/complicações , Síndrome de Tourette/epidemiologia , Síndrome de Tourette/patologia
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