ABSTRACT
Diffusion tensor imaging (DTI) studies showed that microstructural alterations are correlated to reading skills. In this study, we aim to investigate white matter microstructure of a group of Portuguese speakers with poor reading level, using different parameters of DTI. To perform this analysis, we selected children ranging from 8 to 12 years of age, poor readers (n = 17) and good readers (n = 23), evaluated in the word-level ability based on a Latent Class Analysis (LCA) of Academic Performance Test (TDE). Poor readers exhibited significant fractional anisotropy (FA) reductions in many tracts of both hemispheres, but small and restricted clusters of increased radial diffusivity (RD) in the left hemisphere. Spatial coherence of fibers might be the main source of differences, as changes in FA were not similarly accompanied in terms of extension by changes in RD. Widespread structural alterations in the white matter could prevent good reading ability at word level, which is consistent with recent studies demonstrating the involvement of multiple cortical regions and white matter tracts in reading disabilities.
Subject(s)
Brain/anatomy & histology , Reading , White Matter/anatomy & histology , Anisotropy , Aptitude , Aptitude Tests , Child , Diffusion Tensor Imaging , Female , Humans , MaleABSTRACT
The objective of this study is to present the rationale, methods, design and preliminary results from the High Risk Cohort Study for the Development of Childhood Psychiatric Disorders. We describe the sample selection and the components of each phases of the study, its instruments, tasks and procedures. Preliminary results are limited to the baseline phase and encompass: (i) the efficacy of the oversampling procedure used to increase the frequency of both child and family psychopathology; (ii) interrater reliability and (iii) the role of differential participation rate. A total of 9937 children from 57 schools participated in the screening procedures. From those 2512 (random = 958; high risk = 1554) were further evaluated with diagnostic instruments. The prevalence of any child mental disorder in the random strata and high-risk strata was 19.9% and 29.7%. The oversampling procedure was successful in selecting a sample with higher family rates of any mental disorders according to diagnostic instruments. Interrater reliability (kappa) for the main diagnostic instrument range from 0.72 (hyperkinetic disorders) to 0.84 (emotional disorders). The screening instrument was successful in selecting a sub-sample with "high risk" for developing mental disorders. This study may help advance the field of child psychiatry and ultimately provide useful clinical information.
Subject(s)
Developmental Disabilities/diagnosis , Mental Disorders/epidemiology , Mental Disorders/psychology , Brazil/epidemiology , Child , Cohort Studies , Family/psychology , Female , Health Surveys , Humans , Male , Mass Screening , Mental Disorders/diagnosis , Neuroimaging , Neuropsychological Tests , Prevalence , Psychiatric Status Rating Scales , Reproducibility of Results , Risk Factors , Surveys and QuestionnairesABSTRACT
OBJECTIVE: This systematic review sought to conduct a general analysis of the Brazilian scientific output on autism spectrum disorders (ASD) published between 2002 and 2009. METHODS: A literature search was conducted in the scientific databases PubMed, SciELO, and LILACS and in the CAPES portal, using keywords such as "autism" and "pervasive developmental disorders". RESULTS: A total of 93 articles were identified, most of which were authored by researchers from Southeast Brazil and affiliated with public universities. Approximately one-third of all articles were published in journals with an impact factor ranging from 0.441 to 3.211; most were based on small sample sizes. Furthermore, 140 theses and dissertations were identified, 82.1% of which were master's theses. Interventions for ASD were the predominant research topic. CONCLUSION: Brazilian researchers are clearly interested in the topic of ASD; however, a substantial portion of their scientific output is limited to doctoral dissertations or master's theses. A minority of articles was published in journals with a high impact factor. These findings suggest the need for studies with larger sample sizes, which could produce higher-impact findings and thus increase visibility of the Brazilian scientific output in the field of ASD research.
Subject(s)
Academic Dissertations as Topic , Biomedical Research/statistics & numerical data , Child Development Disorders, Pervasive , Periodicals as Topic/statistics & numerical data , Publishing/statistics & numerical data , Brazil , Child , Humans , Journal Impact FactorSubject(s)
Autistic Disorder/diagnosis , Autistic Disorder/epidemiology , Down Syndrome/diagnosis , Down Syndrome/epidemiology , Mass Screening/methods , Surveys and Questionnaires/standards , Brazil/epidemiology , Child , Child, Preschool , Comorbidity , Evaluation Studies as Topic , Female , Humans , Male , Prevalence , Sensitivity and SpecificityABSTRACT
OBJETIVOS: O presente estudo refere-se a uma revisão sistemática, cujo objetivo foi conduzir uma análise da produção científica de autores brasileiros sobre Transtornos do espectro autista (TEA), no período de 2002 a 2009. MÉTODOS: A busca bibliográfica foi realizada nas bases de dados: PUBMED, SciELO, LILACS e portal CAPES, incluindo diversos descritores, tais como autismo e transtorno invasivo do desenvolvimento. RESULTADOS: Um total de 93 artigos foi identificado, tendo sido publicados, sobretudo por autores da região Sudeste e de universidades públicas. Aproximadamente um terço dos artigos foi publicado em revistas com algum fator de impacto variando entre 0,441 e 3,211; sendo a maioria dos artigos baseada em amostras pequenas. Foram identificadas 140 dissertações e teses; 82,1 por cento eram dissertações de mestrado. O principal tema de pesquisa abordado neste material relacionou-se a programas de intervenção para TEA. CONCLUSÃO: Esta revisão mostra o interesse de pesquisadores brasileiros na temática dos TEA, entretanto, uma parte considerável dessa produção científica se concentra em dissertações/teses e a minoria em artigos científicos publicados em revistas com elevado fator de impacto. Os resultados desta revisão sistemática mostram a necessidade de novos estudos com amostras maiores que levariam a um maior impacto e visibilidade da produção científica brasileira relativa aos TEA.
OBJECTIVE: This study is a systematic review aiming to conduct a general analysis of the scientific production covering publications of Brazilian authors about ASD in the period from 2002 to 2009. METHODS: The bibliographic search was conducted in the following scientific databases: PUBMED, SciELO, LILACS and portal CAPES, by using keywords such as autism and pervasive developmental disorders. RESULTS: A total of 93 papers were identified mainly produced by authors from tSoutheast Brazil and from public universities. Approximately one third of the papers was published in journals with a level of impact factor that ranged from 0.441 to 3.211; most of them were based on small sample sizes. Identified were 140 dissertations/theses; 82.1 percent were masters theses. The major research topic was related to intervention programs addressing ASD. CONCLUSION: This review shows that Brazilian researchers are interested in the ASD theme, however, a large part of this scientific production is concentrated in dissertation/masters theses and the minority of papers was published in journals with a high impact factor. Results of this systematic review suggest the need for studies with larger sample sizes which would produce greater impact and visibility in the Brazilian scientific production in the field of the ASD.
Subject(s)
Child , Humans , Biomedical Research/statistics & numerical data , Child Development Disorders, Pervasive , Academic Dissertations as Topic , Periodicals as Topic/statistics & numerical data , Publishing/statistics & numerical data , Brazil , Journal Impact FactorABSTRACT
OBJECTIVE: To translate into Portuguese, back-translate, culturally adapt and validate a screening instrument for pervasive developmental disorder, the Autism Screening Questionnaire, for use in Brazil. METHOD: A sample of 120 patients was selected based on three groups of 40: patients with a clinical diagnosis of pervasive developmental disorder, Down syndrome, or other psychiatric disorders. The self-administered questionnaire was applied to the patients' legal guardians. Psychometric measures of the final version of the translated questionnaire were tested. RESULTS: The score of 15 had sensitivity of 92.5% and specificity of 95.5% as a cut-off point for the diagnosis of pervasive developmental disorder. Internal validity for a total of 40 questions was 0.895 for alpha and 0.896 for KR-20, ranging from 0.6 to 0.8 for both coefficients. Test and retest reliability values showed strong agreement for most questions. CONCLUSIONS: The final version of this instrument, translated into Portuguese and adapted to the Brazilian culture, had satisfactory measurement properties, suggesting preliminary validation proprieties. It was an easy-to-apply, useful tool for the diagnostic screening of individuals with pervasive developmental disorder.
Subject(s)
Autistic Disorder/diagnosis , Child Development Disorders, Pervasive/diagnosis , Cross-Cultural Comparison , Mass Screening , Surveys and Questionnaires/standards , Analysis of Variance , Autistic Disorder/psychology , Brazil , Child , Child Development Disorders, Pervasive/psychology , Diagnostic and Statistical Manual of Mental Disorders , Epidemiologic Methods , Female , Humans , Language , Male , Psychometrics , TranslatingABSTRACT
OBJECTIVE: To translate into Portuguese, back-translate, culturally adapt and validate a screening instrument for pervasive developmental disorder, the Autism Screening Questionnaire, for use in Brazil. METHOD: A sample of 120 patients was selected based on three groups of 40: patients with a clinical diagnosis of pervasive developmental disorder, Down syndrome, or other psychiatric disorders. The self-administered questionnaire was applied to the patients' legal guardians. Psychometric measures of the final version of the translated questionnaire were tested. RESULTS: The score of 15 had sensitivity of 92.5 percent and specificity of 95.5 percent as a cut-off point for the diagnosis of pervasive developmental disorder. Internal validity for a total of 40 questions was 0.895 for alpha and 0.896 for KR-20, ranging from 0.6 to 0.8 for both coefficients. Test and retest reliability values showed strong agreement for most questions. CONCLUSIONS: The final version of this instrument, translated into Portuguese and adapted to the Brazilian culture, had satisfactory measurement properties, suggesting preliminary validation proprieties. It was an easy-to-apply, useful tool for the diagnostic screening of individuals with pervasive developmental disorder.
OBJETIVO: Tradução, retro-versão, adaptação cultural e validação do Autism Screening Questionnaire para a língua portuguesa e para o seu uso no Brasil. MÉTODO: Foi selecionada uma amostra inicial de 120 pacientes, encaminhados de duas clínicas privadas e uma pública, divida em três grupos de 40 pacientes distintos: pacientes com diagnóstico clínico de transtornos globais do desenvolvimento ou transtornos invasivos do desenvolvimento; de síndrome de Down e de outros transtornos psiquiátricos. O questionário foi aplicado aos responsáveis legais dos pacientes seguindo os padrões de um questionário auto-aplicável. As medidas psicométricas do questionário traduzido, na sua versão final, foram testadas. RESULTADOS: Valores de sensibilidade de 92,5 por cento e especificidade de 95,5 por cento foram encontrados para uma pontuação de 15, como sendo um valor discriminativo para os sujeitos com características de transtornos globais do desenvolvimento/transtornos invasivos do desenvolvimento. A validade interna para o total das 40 questões foi de 0,895, com uma variação entre 0,6 a 0,8. Os valores de confiabilidade obtidos pelo teste e re-teste demonstraram que a maioria das questões obteve alta concordância. CONCLUSÕES: A versão final do instrumento de pesquisa, traduzido e adaptado à cultura brasileira, apresentou propriedades de medida satisfatórias, sugerindo adequadas propriedades preliminares de validação. É um instrumento de fácil aplicação e uma ferramenta útil para a realização de um screening diagnóstico em indivíduos com transtornos globais do desenvolvimento/transtornos invasivos do desenvolvimento.
Subject(s)
Child , Female , Humans , Male , Autistic Disorder/diagnosis , Child Development Disorders, Pervasive/diagnosis , Cross-Cultural Comparison , Mass Screening , Surveys and Questionnaires/standards , Analysis of Variance , Autistic Disorder/psychology , Brazil , Child Development Disorders, Pervasive/psychology , Diagnostic and Statistical Manual of Mental Disorders , Epidemiologic Methods , Language , Psychometrics , TranslatingABSTRACT
Neurogenesis studies had an increased development after BrdU (5-bromo-3'-deoxyuridine), a marker of cell proliferation. Today, several studies have showed the relevance of neurogenesis in the hippocampal formation. Notwithstanding, other brains areas have been described presenting neurogenesis, including the amygdala. This key structure is a complex cerebral region which has been associated with social behaviors and the emotional significance of the daily experiences. Several studies have associated the amygdala to the autism, a severe neurodevelopmental disorder. In this paper, we discuss the hypothesis of neurogenesis in the amygdala as a contributing cause of autism. The social skills require competent new neuronal connections, including efficient plasticity synaptic rearranging. Interestingly, emotional context cannot be imprinting in mature neurons in the presence of GABA, a neurotransmitter release during new environments experiences. However, it is known that new neurons are not well responsive to GABA stimulation, allowing the long-term potentiation necessary for the learning process. Based on these evidence it is tantalizing to hypothesize that the sociability impairment seen in some individuals with autism may partly be assigned to impaired regulation of the GABAergic system and to the impact of this impairment on the adequate functioning of the amygdala and on its capacity to store new experiences and to modulate the plasticity of the corticostriatal connections.
Subject(s)
Amygdala/physiopathology , Autistic Disorder/etiology , Amygdala/growth & development , Amygdala/pathology , Animals , Autistic Disorder/pathology , Autistic Disorder/physiopathology , Autistic Disorder/psychology , Humans , Models, Neurological , Neuronal Plasticity , Social Behavior , gamma-Aminobutyric Acid/physiologyABSTRACT
The frequencies of pervasive developmental disorder (PDD) in Down's syndrome (DS) have been reported from 1% to 11%. However, it is not clear if the frequency of this co-occurrence is higher or lower than in other mental retardations. We study a large sample of DS population, finding a PDD frequency of 15.6%, with 5.58% of autism (eight males and two females) and 10.05% of PDD non autism (nine males and nine females. The meaning of this frequency is discussed.
Subject(s)
Child Development Disorders, Pervasive/epidemiology , Down Syndrome/epidemiology , Adult , Child , Female , Humans , Male , PrevalenceABSTRACT
BACKGROUND: Obsessive-compulsive spectrum disorders (OCSDs) are more frequent in patients with active or prior rheumatic fever (RF), suggesting that OCSD and RF may share underlying etiologic mechanisms. Our objective was to estimate the frequency of OCSD in first-degree relatives (FDRs) of RF patients and controls to determine whether there is a familial relationship between OCSD and RF. METHODS: This is a case-control family study. Of the 98 probands included in this study, 31 had RF without Sydenham's chorea (SC) and had 131 relatives, 28 had RF with SC and had 120 relatives, and 39 were controls without RF. All probands, 87.9% of the RF FDRs and 93.7% of the control FDRs were assessed directly with structured psychiatric interviews and best-estimate diagnoses were assigned. Odds ratios of morbid risks were estimated using logistic regression by the generalized estimating equations (GEE) method and compared between groups. RESULTS: The rate of OCSDs was significantly higher among FDRs of RF probands than among FDRs of controls (n=37; 14.7% vs. n=10; 7.3%, i=.0279). A diagnosis of OCSDs in an RF proband was associated with a higher rate of OCSDs among FDRs when compared to control FDRs (p-GEE=.02). There was a trend for a higher rate of OCSDs among FDRs of RF probands presenting no OCSD, although the difference was not significant (p-GEE=.09). CONCLUSION: The results are consistent with the hypothesis that a familial relationship exists between OCSD and RF, since an OCSD in the RF proband was found to increase the risk of OCSDs among FDRs. Additional neuroimmunological and genetic studies involving larger samples are needed to further elucidate this apparent familial relationship between RF and OCSD.
Subject(s)
Obsessive-Compulsive Disorder/epidemiology , Rheumatic Fever/epidemiology , Adolescent , Adult , Bacterial Proteins/immunology , Case-Control Studies , Child , Data Interpretation, Statistical , Family , Female , Humans , Interview, Psychological , Logistic Models , Male , Observer Variation , Obsessive-Compulsive Disorder/diagnosis , Obsessive-Compulsive Disorder/genetics , Odds Ratio , Psychiatric Status Rating Scales , Rheumatic Fever/genetics , Risk , Streptococcal Infections/diagnosis , Streptococcal Infections/epidemiology , Streptolysins/immunologyABSTRACT
Revisar as evidências da relação entre epilepsia, transtorno obsessivo-compulsivo (TOC) e transtornos de tiques. Revisão dos estudos mais relevantes investigando possíveis associações entre estes transtornos. Os transtornos psiquiátricos são frequentes em pacientes com epilepsia. Entretanto, a associação entre sintomas obsessivo-compulsivos, tiques e epilepsia ainda é pouco explorada na literatura. Os realtos de caso mais frequentes descrevem TOC e tiques em pacientes com epilepsia do lobo temporal e também após o tratamento cirúrgico da epilepsia. Considerando o quanto a presença desses transtornos pode afetar a qualidade de vida dos pacientes com epilepsia, é importante investigar a presença dos mesmos em pacientes com epilepsia e faz-se necessário que todo paciente candidato a cirurgia de epilepsia tenha uma avaliação psiquiátrica no pré-operatório e que seja acompanhado no pós-operatório
Subject(s)
Epilepsy , Obsessive-Compulsive Disorder , Tics , Tourette SyndromeABSTRACT
BACKGROUND: Recent findings suggest that acute-phase rheumatic fever (RF) patients present with higher frequencies of obsessive-compulsive disorder (OCD) and tic disorders. Until now, there have been no such studies in RF in non-acute phases. OBJECTIVE: To verify whether patients with a history of RF with or without Sydenham's chorea (SC) present with higher rates of OCD, tic disorders, and other obsessive-compulsive (OC) spectrum disorders (such as body dysmorphic disorder [BDD]) than controls. METHOD: Between February 1999 and December 2002, 59 consecutive outpatients with non-acute RF (28 with and 31 without SC) from an RF clinic and 39 controls from an orthopedics clinic were blindly assessed for OC spectrum disorders using structured interviews to assign DSM-IV diagnosis. Data were analyzed with Fisher exact and chi(2) tests to compare frequencies of disorders, and Kaplan-Meier survival analyses were used to obtain age-corrected rates. RESULTS: The age-corrected rates of tic disorders were higher in patients with RF without SC (N = 3; 14.39%) (p =.003) when compared with controls. Age-corrected rates for OC spectrum disorders (OCD, tic disorders, and BDD) combined were higher both in RF without SC (N = 4; 20.65%) and RF with SC (N = 5; 19.55%) groups than in controls (N = 1; 2.56%) (p =.048). CONCLUSIONS: RF, even in the non-acute phase, may increase the risk for some OC spectrum disorders, such as OCD, tic disorders, and BDD. These data, although preliminary, reinforce the idea that OC spectrum disorders may share common underlying pathophysiologic mechanisms and vulnerability factors with RF or that RF could trigger central nervous system late manifestations such as OC spectrum disorders.
Subject(s)
Chorea/epidemiology , Obsessive-Compulsive Disorder/epidemiology , Rheumatic Fever/epidemiology , Adolescent , Adult , Age Factors , Age of Onset , Brazil/epidemiology , Child , Chorea/diagnosis , Comorbidity , Diagnostic and Statistical Manual of Mental Disorders , Disease Susceptibility/diagnosis , Disease Susceptibility/epidemiology , Female , Humans , Male , Obsessive-Compulsive Disorder/diagnosis , Prevalence , Psychiatric Status Rating Scales/statistics & numerical data , Rheumatic Fever/diagnosis , Somatoform Disorders/diagnosis , Somatoform Disorders/epidemiology , Survival Analysis , Tic Disorders/diagnosis , Tic Disorders/epidemiologyABSTRACT
Os autores descrevem um caso inedito de transtorno obsessivo-compulsivo (TOC) em paciente com sindrome de Tourette (ST) e febre reumatica (FR) sem coreia de Sydenham (CS), com inicio dos tiques no comeco da infancia. Discutem os possiveis mecanismos fisiopatologicos implicados nessa associacao
Subject(s)
Humans , Male , Adult , Clomipramine/therapeutic use , Obsessive-Compulsive Disorder/therapy , Tourette Syndrome/etiology , Obsessive-Compulsive Disorder/diagnosis , Obsessive-Compulsive Disorder/genetics , Rheumatic Fever/etiologyABSTRACT
Estudos genéticos, imunológicos, neurofisológicos, farmacológicos e fenomenológicos indicam que o Transtorno Obsessivo-Compulsivo (TOC) é um transtorno hetrogêneo, englobando conjuntos de pacientes com características peculiares a cada grupo. Estudos familiares sugerem que algumas formas do TOC podem representar uma forma de expressäo do mesmo substrato genético da Síndrome de Tourette (ST). Trabalhos clínicos e fenomenológicos indicam que pacientes com TOC associado à ST apresentam mais frequentemente compulsöes "tic-like", além de fenômenos sensoriais precedendo seus comportamentos repetitivos, quando comparados com TOC sem ST. O objetivo deste trabalho é analisar características clínicas, fenomenológicas e de comorbidade que possam determinar diferenças entre pacientes com TOC de início precoce (até os dez anos) e após os 17 anos de idade (aqui chamados de início tardio)
