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1.
Eur J Hum Genet ; 31(9): 1017-1022, 2023 09.
Artículo en Inglés | MEDLINE | ID: mdl-37280359

RESUMEN

De novo variants (DNVs) analysis has proven to be a powerful approach to gene discovery in Autism Spectrum Disorder (ASD), which has not yet been shown in a Brazilian ASD cohort. The relevance of inherited rare variants has also been suggested, particularly in oligogenic models. We hypothesized that three-generation analyses of DNVs could provide new insights into the relevance of de novo and inherited variants across generations. To accomplish this goal, we performed whole-exome sequencing of 33 septet families composed of probands, parents, and grandparents (n = 231 individuals) and compared DNV rates (DNVr) between generations and those from two control cohorts. The DNVr in the probands (DNVr = 1.16) was marginally higher than in parents (DNVr = 0.60; p = 0.054), and in controls (DNVr = 0.68; p = 0.035, congenital heart disorder and DNVr = 0.70; p = 0.047, unaffected ASD siblings from Simons Simplex Collection). Moreover, most of the DNVs were found to have paternal origin in both generations (84.6%). Finally, we observed that 40% (6/15) of the DNVs in parents transmitted for probands are in ASD or ASD candidate genes, representing recently emerged risk variants to ASD in their families and suggest ZNF536, MSL2 and HDAC9 as ASD candidate genes. We did not observe an enrichment of risk variants nor sex bias of transmitted variants in the three generations, that can be due to sample size. These results further reinforce the relevance of de novo variants in ASD.


Asunto(s)
Trastorno del Espectro Autista , Trastorno Autístico , Humanos , Trastorno Autístico/genética , Trastorno del Espectro Autista/genética , Exoma , Predisposición Genética a la Enfermedad , Familia
3.
Clin Genet ; 101(1): 134-141, 2022 01.
Artículo en Inglés | MEDLINE | ID: mdl-34664255

RESUMEN

Prediction of pathogenicity of rare copy number variations (CNVs), a genomic alteration known to contribute to the etiology of autism spectrum disorder (ASD), represents a serious limitation to interpreting genetic tests, particularly for genetic counseling purposes. Chromosomal microarray analysis (CMA) was conducted in a unique collection of 144 Brazilian individuals with ASD of strong European and African ancestries. Rare CNVs were detected in 39 patients: 41 of unknown significance (VUS), four pathogenic and one likely pathogenic CNVs (clinical yield of 4.1%; 5/122). Based on gene content and recurrence in three large cohorts [a Brazilian neurodevelopmental disorder cohort, the autism MSSNG cohort, and the Canadian-based Centre for Applied Genomics microarray database], this work strengthened the pathogenicity of 14 genes (FAT1, CAMK4, BIRC6, DPP6, CSMD1, CTNNA3, CDH8/CDH11, CDH13, OR1C1, CNTN6, CNTNAP4, FGF2 and PTPRN2) within 14 CNVs. Notably, enrichment of cell adhesion proteins to ASD etiology was identified (p < 0.05), highlighting the importance of these gene families in the etiology of ASD.


Asunto(s)
Alelos , Trastorno del Espectro Autista/diagnóstico , Trastorno del Espectro Autista/genética , Adhesión Celular/genética , Variaciones en el Número de Copia de ADN , Predisposición Genética a la Enfermedad , Adolescente , Adulto , Brasil , Niño , Preescolar , Mapeo Cromosómico , Hibridación Genómica Comparativa , Femenino , Estudios de Asociación Genética , Humanos , Lactante , Masculino , Fenotipo , Adulto Joven
4.
Front Cell Neurosci ; 15: 803302, 2021.
Artículo en Inglés | MEDLINE | ID: mdl-35095425

RESUMEN

Biallelic pathogenic variants in TBCK cause encephaloneuropathy, infantile hypotonia with psychomotor retardation, and characteristic facies 3 (IHPRF3). The molecular mechanisms underlying its neuronal phenotype are largely unexplored. In this study, we reported two sisters, who harbored biallelic variants in TBCK and met diagnostic criteria for IHPRF3. We provided evidence that TBCK may play an important role in the early secretory pathway in neuroprogenitor cells (iNPC) differentiated from induced pluripotent stem cells (iPSC). Lack of functional TBCK protein in iNPC is associated with impaired endoplasmic reticulum-to-Golgi vesicle transport and autophagosome biogenesis, as well as altered cell cycle progression and severe impairment in the capacity of migration. Alteration in these processes, which are crucial for neurogenesis, neuronal migration, and cytoarchitecture organization, may represent an important causative mechanism of both neurodevelopmental and neurodegenerative phenotypes observed in IHPRF3. Whether reduced mechanistic target of rapamycin (mTOR) signaling is secondary to impaired TBCK function over other secretory transport regulators still needs further investigation.

5.
Autism Res ; 13(2): 199-206, 2020 02.
Artículo en Inglés | MEDLINE | ID: mdl-31696658

RESUMEN

Large genomic databases of neurodevelopmental disorders (NDD) are helpful resources of genomic variations in complex and heterogeneous conditions, as Autism Spectrum Disorder (ASD). We evaluated the role of rare copy number variations (CNVs) and exonic de novo variants, in a molecularly unexplored Brazilian cohort of 30 ASD trios (n = 90), by performing a meta-analysis of our findings in more than 20,000 patients from NDD cohorts. We identified three pathogenic CNVs: two duplications on 1q21 and 17p13, and one deletion on 4q35. CNVs meta-analysis (n = 8,688 cases and n = 3,591 controls) confirmed 1q21 relevance by identifying duplications in other 16 ASD patients. Exome analysis led the identification of seven de novo variants in ASD genes (SFARI list): three loss-of-function pathogenic variants in CUL3, CACNA1H, and SHANK3; one missense pathogenic variant in KCNB1; and three deleterious missense variants in ATP10A, ANKS1B, and DOCK1. From the remaining 12 de novo variants in non-previous ASD genes, we prioritized PRPF8 and RBM14. Meta-analysis (n = 13,754 probands; n = 2,299 controls) identified six and two additional patients with validated de novo variants in PRPF8 and RBM14, respectively. By comparing the de novo variants with a previously established mutational rate model, PRPF8 showed nominal significance before multiple test correction (P = 0.039, P-value adjusted = 0.079, binomial test), suggesting its relevance to ASD. Approximately 60% of our patients presented comorbidities, and the diagnostic yield was estimated in 23% (7/30: three pathogenic CNVs and four pathogenic de novo variants). Our uncharacterized Brazilian cohort with tetra-hybrid ethnic composition was a valuable resource to validate and identify possible novel candidate loci. Autism Res 2020, 13: 199-206. © 2019 International Society for Autism Research, Wiley Periodicals, Inc. LAY SUMMARY: We believed that to study an unexplored autistic population, such as the Brazilian, could help to find novel genes for autism. In order to test this idea, with our limited budget, we compared candidate genes obtained from genomic analyses of 30 children and their parents, with those of more than 20,000 individuals from international studies. Happily, we identified a genetic cause in 23% of our patients and suggest a possible novel candidate gene for autism (PRPF8).


Asunto(s)
Trastorno del Espectro Autista/genética , Adolescente , Adulto , Brasil , Niño , Preescolar , Deleción Cromosómica , Estudios de Cohortes , Variaciones en el Número de Copia de ADN/genética , Exoma/genética , Exones/genética , Femenino , Predisposición Genética a la Enfermedad/genética , Humanos , Masculino , Adulto Joven
6.
Sci Rep ; 8(1): 11138, 2018 07 24.
Artículo en Inglés | MEDLINE | ID: mdl-30042445

RESUMEN

Several lines of indirect evidence, such as mutations or dysregulated expression of genes related to cytoskeleton, have suggested that cytoskeletal dynamics, a process essential for axons and dendrites development, is compromised in autism spectrum disorders (ASD). However, no study has yet examined whether cytoskeleton dynamics is functionally altered in cells from ASD patients. Here we investigated the regulation of actin cytoskeleton dynamics in stem cells from human exfoliated deciduous teeth (SHEDs) of 13 ASD patients and 8 control individuals by inducing actin filament depolymerization and then measuing their reconstruction upon activation of the RhoGTPases Rac, Cdc42 or RhoA. We observed that stem cells from seven ASD individuals (53%) presented altered dymanics of filament reconstruction, including a patient recently studied by our group whose iPSC-derived neuronal cells show shorten and less arborized neurites. We also report potentially pathogenic genetic variants that might be related to the alterations in actin repolymerization dynamics observed in some patient-derived cells. Our results suggest that, at least for a subgroup of ASD patients, the dynamics of actin polymerization is impaired, which might be ultimately leading to neuronal abnormalities.


Asunto(s)
Citoesqueleto de Actina/química , Actinas/química , Trastorno del Espectro Autista/genética , Neuronas/química , Citoesqueleto de Actina/genética , Actinas/genética , Animales , Trastorno del Espectro Autista/metabolismo , Trastorno del Espectro Autista/patología , Regulación de la Expresión Génica/genética , Humanos , Células Madre Pluripotentes Inducidas/química , Células Madre Pluripotentes Inducidas/metabolismo , Neuronas/metabolismo , Neuronas/patología , Exfoliación Dental , Proteína de Unión al GTP cdc42/genética , Proteínas de Unión al GTP rac/genética , Proteína de Unión al GTP rhoA/genética
7.
Braz J Otorhinolaryngol ; 80(3): 231-6, 2014.
Artículo en Inglés, Portugués | MEDLINE | ID: mdl-25153108

RESUMEN

INTRODUCTION: It is crucial to understand the complex processing of acoustic stimuli along the auditory pathway; comprehension of this complex processing can facilitate our understanding of the processes that underlie normal and altered human communication. AIM: To investigate the performance and lateralization effects on auditory processing assessment in children with specific language impairment (SLI), relating these findings to those obtained in children with auditory processing disorder (APD) and typical development (TD). MATERIAL AND METHODS: Prospective study. Seventy-five children, aged 6-12 years, were separated in three groups: 25 children with SLI, 25 children with APD, and 25 children with TD. All went through the following tests: speech-in-noise test, Dichotic Digit test and Pitch Pattern Sequencing test. RESULTS: The effects of lateralization were observed only in the SLI group, with the left ear presenting much lower scores than those presented to the right ear. The inter-group analysis has shown that in all tests children from APD and SLI groups had significantly poorer performance compared to TD group. Moreover, SLI group presented worse results than APD group. CONCLUSION: This study has shown, in children with SLI, an inefficient processing of essential sound components and an effect of lateralization. These findings may indicate that neural processes (required for auditory processing) are different between auditory processing and speech disorders.


Asunto(s)
Trastornos de la Percepción Auditiva/complicaciones , Desarrollo del Lenguaje , Trastornos del Lenguaje/etiología , Estimulación Acústica , Trastornos de la Percepción Auditiva/fisiopatología , Estudios de Casos y Controles , Niño , Femenino , Lateralidad Funcional , Humanos , Trastornos del Lenguaje/fisiopatología , Masculino , Estudios Prospectivos , Pruebas de Discriminación del Habla
8.
Codas ; 26(2): 105-11, 2014.
Artículo en Inglés, Portugués | MEDLINE | ID: mdl-24918502

RESUMEN

PURPOSE: To investigate the existence of correlations between the performance of children in auditory temporal tests (Frequency Pattern and Gaps in Noise--GIN) and IQ, attention, memory and age measurements. METHOD: Fifteen typically developing individuals between the ages of 7 to 12 years and normal hearing participated in the study. Auditory temporal processing tests (GIN and Frequency Pattern), as well as a Memory test (Digit Span), Attention tests (auditory and visual modality) and intelligence tests (RAVEN test of Progressive Matrices) were applied. RESULTS: Significant and positive correlation between the Frequency Pattern test and age variable were found, which was considered good (p<0.01, 75.6%). There were no significant correlations between the GIN test and the variables tested. CONCLUSIONS: Auditory temporal skills seem to be influenced by different factors: while the performance in temporal ordering skill seems to be influenced by maturational processes, the performance in temporal resolution was not influenced by any of the aspects investigated.


Asunto(s)
Atención/fisiología , Inteligencia/fisiología , Memoria/fisiología , Percepción del Habla/fisiología , Estimulación Acústica/métodos , Niño , Femenino , Pruebas Auditivas/métodos , Humanos , Masculino
9.
Braz. j. otorhinolaryngol. (Impr.) ; 80(3): 231-236, May-June/2014. tab
Artículo en Inglés | LILACS | ID: lil-712981

RESUMEN

INTRODUCTION: It is crucial to understand the complex processing of acoustic stimuli along the auditory pathway ;comprehension of this complex processing can facilitate our understanding of the processes that underlie normal and altered human communication. AIM: To investigate the performance and lateralization effects on auditory processing assessment in children with specific language impairment (SLI), relating these findings to those obtained in children with auditory processing disorder (APD) and typical development (TD). MATERIAL AND METHODS: Prospective study. Seventy-five children, aged 6-12 years, were separated in three groups: 25 children with SLI, 25 children with APD, and 25 children with TD. All went through the following tests: speech-in-noise test, Dichotic Digit test and Pitch Pattern Sequencing test. RESULTS: The effects of lateralization were observed only in the SLI group, with the left ear presenting much lower scores than those presented to the right ear. The inter-group analysis has shown that in all tests children from APD and SLI groups had significantly poorer performance compared to TD group. Moreover, SLI group presented worse results than APD group. CONCLUSION: This study has shown, in children with SLI, an inefficient processing of essential sound components and an effect of lateralization. These findings may indicate that neural processes (required for auditory processing) are different between auditory processing and speech disorders. .


INTRODUÇÃO: Entender como os estímulos acústicos são processados ao longo da via auditiva é fundamental para compreender os processos que subjazem à comunicação humana normal e alterada. OBJETIVO: Investigar o desempenho e efeitos de lateralidade na avaliação do processamento auditivo em crianças com distúrbio específico de linguagem (DEL), comparando os resultados obtidos aos encontrados em crianças com transtorno de processamento auditivo (TPA) e desenvolvimento típico (DT). MATERIAL E MÉTODO: Estudo Prospectivo. 75 crianças (6-12 anos), divididas em três grupos (25 crianças com DEL, 25 crianças com TPA e 25 crianças em DT), foram submetidas aos seguintes testes: Teste de Figura com Ruído, Teste Dicótico de Dígitos e Teste de Padrão de Frequência. RESULTADO: Os efeitos de lateralidade foram observados apenas no grupo DEL, sendo o desempenho na orelha esquerda inferior ao apresentado na orelha direita. Na comparação intergrupos, o desempenho dos grupos TPA e DEL foi significativamente inferior ao observado no grupo DT para todos os testes. Além disso, observamos nas crianças do grupo DEL um desempenho inferior às do grupo TPA. CONCLUSÃO: Este estudo constatou o processamento ineficiente de componentes cruciais de sons e o efeito de lateralidade em crianças com DEL. Esses achados evidenciam que os processos neurais que subjazem ao processamento auditivo são diferentes entre alterações de processamento auditivo e alterações de fala. .


Asunto(s)
Niño , Femenino , Humanos , Masculino , Trastornos de la Percepción Auditiva/complicaciones , Desarrollo del Lenguaje , Trastornos del Lenguaje/etiología , Estimulación Acústica , Trastornos de la Percepción Auditiva/fisiopatología , Estudios de Casos y Controles , Lateralidad Funcional , Trastornos del Lenguaje/fisiopatología , Estudios Prospectivos , Pruebas de Discriminación del Habla
10.
CoDAS ; 26(2): 105-111, Mar-Apr/2014. tab
Artículo en Inglés | LILACS | ID: lil-711133

RESUMEN

PURPOSE: To investigate the existence of correlations between the performance of children in auditory temporal tests (Frequency Pattern and Gaps in Noise - GIN) and IQ, attention, memory and age measurements. METHOD: Fifteen typically developing individuals between the ages of 7 to 12 years and normal hearing participated in the study. Auditory temporal processing tests (GIN and Frequency Pattern), as well as a Memory test (Digit Span), Attention tests (auditory and visual modality) and intelligence tests (RAVEN test of Progressive Matrices) were applied. RESULTS: Significant and positive correlation between the Frequency Pattern test and age variable were found, which was considered good (p<0.01, 75.6%). There were no significant correlations between the GIN test and the variables tested. CONCLUSIONS: Auditory temporal skills seem to be influenced by different factors: while the performance in temporal ordering skill seems to be influenced by maturational processes, the performance in temporal resolution was not influenced by any of the aspects investigated. .


OBJETIVO: Investigar a existência de correlações entre o desempenho de crianças com desenvolvimento típico em testes temporais auditivos (Padrão de Frequência e Gaps in Noise - GIN) e medidas de memória, atenção, quociente intelectual e a idade. MÉTODO: Quinze participantes, com idades entre 7 e 12 anos, sem queixas envolvendo audição e desenvolvimento cognitivo, foram submetidos aos testes de processamento temporal auditivo (GIN e Padrão de Frequência), teste de Memória (Span de Dígitos), Atenção (auditiva e visual) e testes de inteligência (Matrizes Progressivas de Raven). RESULTADOS: Foram encontradas correlações significantes e positivas entre o teste Padrão de Frequência e a variável idade, sendo essa considerada boa (p<0,01, 75,6%). Não foram verificadas correlações significantes entre o teste GIN e as variáveis testadas. CONCLUSÃO: As habilidades temporais consideradas parecem ser influenciadas por diferentes fatores: enquanto a habilidade de ordenação temporal parece ser influenciada por processos maturacionais, o desempenho para a habilidade de resolução temporal não foi influenciado por nenhum dos aspectos investigados. .


Asunto(s)
Niño , Femenino , Humanos , Masculino , Atención/fisiología , Inteligencia/fisiología , Memoria/fisiología , Percepción del Habla/fisiología , Estimulación Acústica/métodos , Pruebas Auditivas/métodos
11.
Estud. psicol. (Natal) ; 17(1): 179-186, Jan.-Apr. 2012. tab
Artículo en Portugués | LILACS | ID: lil-643708

RESUMEN

A distrofia muscular de Duchenne é uma doença genética caracterizada por enfraquecimento muscular progressivo e degeneração irreversível, acompanhados por danos sensoriais e neuropsicológicos. Os objetivos do estudo consistiram em avaliar o perfil comportamental de crianças/adolescentes com DMD e a influência do prejuízo motor, da idade no início do uso de cadeira de rodas e da idade no diagnóstico. Participaram 34 pacientes e 20 controles. Os pacientes formaram dois grupos conforme o quociente de inteligência (QI). Os pais responderam ao Inventário de Comportamentos da Infância e da Adolescência. Pacientes com DMD obtiveram escores mais baixos em Atividades e Sociabilidade (p < 0,01; ANCOVA). Os pacientes com QI < 80 apresentaram menores índices de Escolaridade. O prejuízo motor e as idades referentes à cadeira e ao diagnóstico correlacionaram-se com sintomas psiquiátricos/somáticos e problemas escolares. Os achados enfatizam a necessidade de programas educacionais acerca da doença como base para o desenvolvimento de estratégias de inclusão social.


Duchenne Muscular Dystrophy is a genetic disease characterized by progressive muscle weakness and degeneration, which are accompanied by sensory and neuropsychological losses. The aims of this study were to evaluate the behavior profile of DMD children and adolescents and examine the influence of motor impairment, age at start using a wheelchair, and age at diagnosis on behavioral characteristics. Thirty-five patients and 20 controls participated. DMD patients formed two different groups according to the intelligence quotient (IQ). Participants' parents completed the Child Behavior Checklist. DMD groups scored lower on the Activities and the Social scales. Patients with QI < 80 presented lower indices in the School scale (p < 0.01, ANCOVA). Motor impairment and age at start using a wheelchair and at diagnosis correlated with psychiatric/somatic symptoms and school problems. The findings highlight the need of educational programs concerning the disease as a basis for the development of social inclusion strategies.


Asunto(s)
Humanos , Masculino , Niño , Adolescente , Aptitud , Conducta , Distrofia Muscular de Duchenne/patología , Inteligencia
12.
Dement. neuropsychol ; 5(2)jun. 2011.
Artículo en Inglés | LILACS | ID: lil-592309

RESUMEN

The neuropsychological tests of spatial span are designed to measure attention and working memory. The version of the spatial span test in the Cambridge Neuropsychological Test Automated Battery (CANTAB) evaluates these functions through the recall of sequences of spatial locations presented to the subject. Objective: The present study investigated how age, gender and educational level might affect the performance of the non-verbal system. Methods: A total of 60 children and adolescents aged 6 to 18 years were assessed (25 males and 35 females). Results: The results showed no gender differences in test performance. Children with six or more years of education showed better performance than children with less than three years of education. Older children had more schooling and thus were able to recall a greater number of items. Span length values proved similar to a previous large normative study which also employed the CANTAB Spatial Span (De Luca et al., 2003). Conclusion: The similarity in performance of the Brazilian children and adolescents studied and the group of Australian participants examined by the cited authors, despite the socio-cultural and economical differences, points to the suitability of the task for the assessment of attention and working memory in Brazilian children.


Testes neuropsicológicos de span visuoespacial são construídos para avaliar amplitude atencional e memória de trabalho. Na versão do teste de span visuoespacial da Cambridge Neuropsychological Test Automated Battery (CANTAB) essa avaliação é feita através de sequências de localização espacial. Objetivo: O presente estudo investiga como a idade, o sexo e a escolaridade podem afetar o desempenho nesse sistema não-verbal. Métodos: Foram avaliadas 60 crianças e adolescentes com idades entre 6 e 18 anos (25 meninos; 35 meninas). Resultados: Os resultados não mostraram diferenças no desempenho do teste entre os sexos. O grupo de crianças com seis ou mais anos de escolaridade foi melhor do que a de crianças menores de três anos de estudo. Nossos resultados sugerem que as crianças mais velhas e, portanto, com maior tempo de escolaridade conseguem se lembrar de um número maior de itens. Os valores de amplitude foram similares aos obtidos em um experimento normativo prévio amplo no qual foi utilizado o teste Spatial Span do CANTAB (De Luca et al., 2003). Conclusão: Estas concordâncias de desempenhos entre crianças e adolescentes brasileiros e o grupo de participantes australianos examinados pelos autores citados nos mostram que apesar das diferenças sócio-culturais e econômicas existentes, a tarefa é adequada para avaliação de atenção e memória de trabalho em crianças brasileiras.


Asunto(s)
Humanos , Niño , Adolescente , Escolaridad , Memoria , Trastornos de la Memoria , Memoria a Corto Plazo , Pruebas Neuropsicológicas
13.
Dement Neuropsychol ; 5(2): 129-134, 2011.
Artículo en Inglés | MEDLINE | ID: mdl-29213735

RESUMEN

The neuropsychological tests of spatial span are designed to measure attention and working memory. The version of the spatial span test in the Cambridge Neuropsychological Test Automated Battery (CANTAB) evaluates these functions through the recall of sequences of spatial locations presented to the subject. OBJECTIVE: The present study investigated how age, gender and educational level might affect the performance of the non-verbal system. METHODS: A total of 60 children and adolescents aged 6 to 18 years were assessed (25 males and 35 females). RESULTS: The results showed no gender differences in test performance. Children with six or more years of education showed better performance than children with less than three years of education. Older children had more schooling and thus were able to recall a greater number of items. Span length values proved similar to a previous large normative study which also employed the CANTAB Spatial Span (De Luca et al., 2003). CONCLUSION: The similarity in performance of the Brazilian children and adolescents studied and the group of Australian participants examined by the cited authors, despite the socio-cultural and economical differences, points to the suitability of the task for the assessment of attention and working memory in Brazilian children.


Testes neuropsicológicos de span visuoespacial são construídos para avaliar amplitude atencional e memória de trabalho. Na versão do teste de span visuoespacial da Cambridge Neuropsychological Test Automated Battery (CANTAB) essa avaliação é feita através de sequências de localização espacial. OBJETIVO: O presente estudo investiga como a idade, o sexo e a escolaridade podem afetar o desempenho nesse sistema não-verbal. MÉTODOS: Foram avaliadas 60 crianças e adolescentes com idades entre 6 e 18 anos (25 meninos; 35 meninas). RESULTADOS: Os resultados não mostraram diferenças no desempenho do teste entre os sexos. O grupo de crianças com seis ou mais anos de escolaridade foi melhor do que a de crianças menores de três anos de estudo. Nossos resultados sugerem que as crianças mais velhas e, portanto, com maior tempo de escolaridade conseguem se lembrar de um número maior de itens. Os valores de amplitude foram similares aos obtidos em um experimento normativo prévio amplo no qual foi utilizado o teste Spatial Span do CANTAB (De Luca et al., 2003). CONCLUSÃO: Estas concordâncias de desempenhos entre crianças e adolescentes brasileiros e o grupo de participantes australianos examinados pelos autores citados nos mostram que apesar das diferenças sócio-culturais e econômicas existentes, a tarefa é adequada para avaliação de atenção e memória de trabalho em crianças brasileiras.

14.
J Occup Environ Med ; 51(12): 1403-12, 2009 Dec.
Artículo en Inglés | MEDLINE | ID: mdl-19952794

RESUMEN

OBJECTIVE: To evaluate whether there are visual and neuropsychological decrements in workers with low exposure to Hg vapor. METHODS: Visual fields, contrast sensitivity, color vision, and neuropsychological functions were measured in 10 workers (32.5 +/- 8.5 years) chronically exposed to Hg vapor (4.3 +/- 2.8 years; urinary Hg concentration 22.3 +/- 9.3 microg/g creatinine). RESULTS: For the worst eyes, we found altered visual field thresholds, lower contrast sensitivity, and color discrimination compared with controls (P <0.05). There were no significant differences between Hg-exposed subjects and controls on neuropsychological tests. Nevertheless, duration of exposure was statistically correlated to verbal memory and depression scores. CONCLUSIONS: Chronic exposure to Hg vapor at currently accepted safety levels was found to be associated with visual losses but not with neuropsychological dysfunctions in the sample of workers studied.


Asunto(s)
Contaminantes Ocupacionales del Aire/efectos adversos , Trastornos Mentales/inducido químicamente , Trastornos Mentales/epidemiología , Exposición Profesional/efectos adversos , Trastornos de la Visión/inducido químicamente , Trastornos de la Visión/epidemiología , Adulto , Contaminantes Ocupacionales del Aire/orina , Brasil/epidemiología , Percepción de Color/efectos de los fármacos , Pruebas de Percepción de Colores , Sensibilidad de Contraste/efectos de los fármacos , Creatinina/orina , Femenino , Humanos , Masculino , Mercurio/orina , Persona de Mediana Edad , Pruebas Neuropsicológicas , Exposición Profesional/análisis , Campos Visuales/efectos de los fármacos , Adulto Joven
15.
Dement Neuropsychol ; 2(2): 91-95, 2008.
Artículo en Inglés | MEDLINE | ID: mdl-29213549

RESUMEN

Elemental mercury is a liquid toxic metal widely used in industry. Occupational exposure occurs mainly via inhalation. Previously, neuropsychological assessment detected deficits in former workers of a fluorescent lamp plant who had been exposed to elemental mercury vapor and were away from exposure for several years at the time of examination. OBJECTIVES: The purpose of this work was to reexamine these functions after 18 months in order to evaluate their progression. METHODS: Thirteen participants completed tests of attention, inhibitory control, verbal/visual memory, psychomotor speed, verbal fluency, visuomotor ability, executive function, semantic knowledge, and depression and anxiety inventories on 2 separate occasions. RESULTS: At baseline, the former workers indicated slower psychomotor and information processing speed, verbal spontaneous recall memory impairment, and increased depression and anxiety symptoms compared to controls (P<0.05). Paired comparisons of neuropsychological functioning within the exposed group at baseline and 1.5 years later showed poorer immediate memory performance (P<0.05). There were no differences on other measures. CONCLUSIONS: Although the literature show signs of recovery of functions, the neuropsychological effects related to mercury exposure are found to persist for many years.


Mercúrio metálico é um metal líquido e tóxico com ampla aplicação industrial. A exposição ocupacional ao metal ocorre principalmente por inalação. Previamente, comprometimento em várias funções neuropsicológicas foi constatado em ex-trabalhadores de fábrica de lâmpadas fluorescentes que haviam sido expostos ao vapor de mercúrio e estavam afastados da fonte de exposição por vários anos no momento do exame. OBJETIVOS: Reexaminar estas funções após 18 meses, com a finalidade de verificar a possível progressão do comprometimento. MÉTODOS: Treze participantes foram submetidos a testes de atenção, controle inibitório, memória verbal e visual, funções executivas, conhecimento semântico e inventários de depressão e ansiedade. RESULTADOS: Na linha de base, os ex-trabalhadores mostraram lentificação psicomotora e no processamento de informações, déficit de memória verbal espontânea, além de maiores sintomas de depressão e ansiedade comparados com controles (P<0,05). Comparações pareadas do grupo exposto na linha de base e 18 meses após indicaram pior desempenho em memória imediata (P<0,05). Não houve diferença nas demais medidas. CONCLUSÕES: Embora a literatura mostre indícios de recuperação das funções, os efeitos neuropsicológicos relacionados ao mercúrio podem persistir por muitos anos.

16.
Psicol. USP ; 17(4): 287-300, 2006.
Artículo en Portugués | LILACS | ID: lil-457264

RESUMEN

O desenvolvimento da neuropsicologia acompanhou a evolução do estudo do cérebro desde os registros mais antigos. A ciência neuropsicológica faz uso de medidas quantitativas de desempenho e tecnologias para produção de neuroimagem que, em conjunto, permitem a observação das relações cérebro-comportamento. No âmbito experimental, a neuropsicologia tem revelado novos conhecimentos na investigação de alterações cognitivas, psicomotoras ou comportamentais associadas a patologias congênitas ou adquiridas. No presente artigo são abordados aspectos históricos da neuropsicologia experimental e apresentados os principais resultados de um estudo referente às alterações neuropsicológicas de pacientes com histórico de intoxicação por vapor de mercúrio, presentes anos após o período de exposição ao metal


Asunto(s)
Intoxicación por Mercurio/psicología , Neuropsicología
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