Background: Dimensional models of psychopathology demonstrate that two correlated factors of fear and distress account for the covariation among depressive and anxiety disorders. Nevertheless, these models tend to exclude variables relevant to psychopathology, such as temperament traits. This study examined the joint structure of DSM-IV-based major depression and anxiety disorders along with trait negative affect in a representative sample of adult individuals residing in the cities of São Paulo and Rio de Janeiro, Brazil. Methods: The sample consisted of 3,728 individuals who were administered sections D (phobic, anxiety and panic disorders) and E (depressive disorders) of the Composite International Diagnostic Interview (CIDI) 2.1 and a validated version of the Positive and Negative Affect Schedule. Data were analyzed using correlational and structural equation modeling. Results: Lifetime prevalence ranged from 2.4% for panic disorder to 23.2% for major depression. Most target variables were moderately correlated. A two-factor model specifying correlated fear and distress factors was retained and confirmed for models including only diagnostic variables and diagnostic variables along with trait negative affect. Conclusions: This study provides support for characterization of internalizing psychopathology and trait negative affect in terms of correlated dimensions of distress and fear. These results have potential implications for psychiatric taxonomy and for understanding the relationship between temperament and psychopathology.

Objetivos:Avaliar a relação entre o polimorfismo 3111 T/C do gene CLOCK (rs1801260) e a presença de obesidade, bem como a duração do sono, em crianças de 6 a 13 anos. Em adultos, essa variante genética foi associada à duração do sono, níveis de grelina, peso e padrão alimentar. Embora, em crianças, a curta duração do sono tenha sido relacionada à obesidade, até o momento nenhum estudo foi direcionado no sentido de identificar possíveis mecanismos moleculares dessa associação.Métodos:Peso, altura e circunferências foram transformados em escores-Z para idade e sexo. A genotipagem foi realizada pela metodologia Taqman. Um questionário sobre horas de sono foi entregue aos pais. Testes estatísticos apropriados foram realizados.Resultados:Foram avaliadas 370 crianças (45% meninos, 55% meninas, idade média 8,5±1,5 anos). A prevalência de excesso de peso foi de 18%. A duração do sono foi, em média, 9,7 horas, sendo inversamente relacionada à idade (p < 0,001). A distribuição genotípica foi: 4% CC, 31% TC e 65% TT. Houve uma tendência de maior prevalência de excesso de peso em crianças que dormiam menos de 9 h (23%), quando comparadas às que dormiam mais de 10 h (16%, p = 0,06). O genótipo não se correlacionou significativamente a nenhum dos desfechos avaliados.Conclusões:O polimorfismo CLOCK 3111 T/C não está significativamente associado ao excesso de peso ou à duração do sono em crianças desta localidade.

Objectives:To evaluate the association between 3111T/C polymorphism of the CLOCK gene and the presence of obesity and sleep duration in children aged 6-13 years. In adults, this genetic variant has been associated with duration of sleep, ghrelin levels, weight, and eating habits. Although short sleep duration has been linked to obesity in children, no study has aimed to identify the possible molecular mechanisms of this association to date.Methods:Weight, height, and circumferences were transformed into Z-scores for age and gender. Genotyping was performed using TaqMan methodology. A questionnaire regarding hours of sleep was provided to parents. The appropriate statistical tests were performed.Results:This study evaluated 370 children (45% males, 55% females, mean age 8.5 ± 1.5 years). The prevalence of overweight was 18%. The duration of sleep was, on average, 9.7 hours, and was inversely related to age (p < 0.001). Genotype distribution was: 4% CC, 31% CT, and 65% TT. There was a trend toward higher prevalence of overweight in children who slept less than nine hours (23%) when compared to those who slept more than ten hours (16%, p = 0.06). Genotype was not significantly correlated to any of the assessed outcomes.Conclusions:The CLOCK 3111T/C polymorphism was not significantly associated with overweight or sleep duration in children in this city.

Objective: Positive and negative affect are the two psychobiological-dispositional dimensions reflecting proneness to positive and negative activation that influence the extent to which individuals experience life events as joyful or as distressful. The Positive and Negative Affect Schedule (PANAS) is a structured questionnaire that provides independent indexes of positive and negative affect. This study aimed to validate a Brazilian interview-version of the PANAS by means of factor and internal consistency analysis. Methods: A representative community sample of 3,728 individuals residing in the cities of São Paulo and Rio de Janeiro, Brazil, voluntarily completed the PANAS. Exploratory structural equation model analysis was based on maximum likelihood estimation and reliability was calculated via Cronbach's alpha coefficient. Results: Our results provide support for the hypothesis that the PANAS reliably measures two distinct dimensions of positive and negative affect. Conclusion: The structure and reliability of the Brazilian version of the PANAS are consistent with those of its original version. Taken together, these results attest the validity of the Brazilian adaptation of the instrument.

OBJETIVO: Investigar a presença de variantes nos genes TAC3 e TACR3, os quais codificam a NKB e seu receptor (NK3R), respectivamente, em uma coorte de pacientes com distúrbios puberais centrais idiopáticos. SUJEITOS E MÉTODOS: Duzentos e trinta e sete pacientes foram estudados: 114 com puberdade precoce central (PPC), 73 com hipogonadismo hipogonadotrófico isolado normósmico (HHI) e 50 com retardo constitucional do crescimento e desenvolvimento (RCCD). O grupo controle consistiu de 150 indivíduos brasileiros que apresentaram desenvolvimento puberal normal. O DNA genômico foi extraído de sangue periférico, e as regiões codificadoras dos genes TAC3 e TACR3 foram amplificadas e sequenciadas automaticamente. RESULTADOS: Uma variante (p.A63P) foi identificada na NKB, e quatro variantes, p.G18D, p.L58L (c.172C>T), p.W275X e p.A449S, foram identificadas no NK3R, as quais foram ausentes no grupo controle. A variante p.A63P foi identificada em uma menina com PPC, e a variante p.A449S, em uma menina com RCCD. As variantes previamente descritas, p.G18D, p.L58L e p.W275X, foram identificadas em três indivíduos com HHI normósmico do sexo masculino não relacionados. CONCLUSÃO: Variantes raras nos genes TAC3 e TACR3 foram identificadas em pacientes com distúrbios puberais centrais idiopáticos. Mutações de perda de função no gene TACR3 foram associadas com o fenótipo de HHI normósmico. Arq Bras Endocrinol Metab. 2012;56(9):646-52

OBJECTIVE: To investigate the presence of variants in the TAC3 and TACR3 genes, which encode NKB and its receptor (NK3R), respectively, in a large cohort of patients with idiopathic central pubertal disorders. SUBJECTS AND METHODS: Two hundred and thirty seven patients were studied: 114 with central precocious puberty (CPP), 73 with normosmic isolated hypogonadotropic hypogonadism (IHH), and 50 with constitutional delay of growth and puberty (CDGP). The control group consisted of 150 Brazilian individuals with normal pubertal development. Genomic DNA was extracted from peripheral blood and the entire coding region of both TAC3 and TACR3 genes were amplified and automatically sequenced. RESULTS: We identified one variant (p.A63P) in NKB and four variants, p.G18D, p.L58L (c.172C>T), p.W275* and p.A449S in NK3R, which were absent in the control group. The p.A63P variant was identified in a girl with CPP, and p.A449S in a girl with CDGP. The known p.G18D, p.L58L, and p.W275* variants were identified in three unrelated males with normosmic IHH. CONCLUSION: Rare variants in the TAC3 and TACR3 genes were identified in patients with central pubertal disorders. Loss-of-function variants of TACR3 were associated with the normosmic IHH phenotype. Arq Bras Endocrinol Metab. 2012;56(9):646-52

As folhas de Myrcia multiflora (Lam.) DC, Myrcia guianensis (Aubl.) Urb. e Eugenia punicifolia (H. B. K.) DC. são anatômica c morfologicamentc descritas. As espécies revelaram diversos elementos histológicos universais para a família, bem como peculiares das mesmas e importantes para orientar a diagnose desses vegetais e para o reconhecimento de fraudes, que ocorrem através de substituições intencionais ou não. Entre os elementos histológicos característicos, destacam-se: ornamentações de cutícula foliar, tipos de estômatos, tipos de contornos celulares das células epidérmicas em vista facial, tipo e abundância relativa de inclusões celulares inorgânicas.

The anatomy and morphology of the leaves of Myrcia multiflora (Lam.) DC, Myrcia guianensis (Aubl) Urb. and of Eugenia punicifolia (H. B. K.) DC. are described. Although these species show the universal characteristics of the Myrtaceae, they also present some peculiarities that allow their identification and the recognition of fraud, intentional or not. The main characteristic histological elements of these species are: ornamentation of the cuticle, stomata types, outline of epidermal cells in surface view and types and comparative abundance of inorganic cellular inclusions.

Foram determinadas as concentrações de cobre e ceruloplasmina em amostras de sangue venoso periférico e pré-hepático de 11 pacientes esquistossomóticos e de 1 paciente com degeneração hepatolenticular, submetidos a anastomose portocava ou esplenorrenal. Nos 11 pacientes não wilsonianos, as diferenças individuais não se revelaram estatisticamente significantes. Os resultados são comentados em relação aos conhecimentos atuais sobre a patogenia da moléstia de Wilson.

Copper and ceruloplasmin contents were determined in samples of peripheral and pre-hepatic venous blood of 11 patients with Manson's schistosomiasis and one patient with hepatolenticular degeneration, all of çhich submitted either to porto-caval or spleno-renal shunt. Individual difference were not significant in any of the non-Wilsonian patients. The results are discussed in regard to the current knowledge on the pathogenesis of Wilson's disease.

As a contribution to the knowledge on inorganic arsenic concentration in peripheral nerves, a study was carried out in 20 nerve fragments (10 from N. ulnaris and 10 from N. tibialis) excised during necropsy from 20 corpses less than 24 hours after death and showing no apparent disease of the nervous system. The samples were ashed in an oven overnight at 550°C. The ashes were dissolved in a known volume of 2N-HC1. In this solution inorganic arsenic was determined by the Kingsley-Schaffert method. The results revealed no significant concentrations (vestiges) of inorganic arsenic in the peripheral nerves.

Estudo da osmolalidade de 22 amostras de LCR e de 22 amostras de sôro. As amostras de LCR foram colhidas de pacientes sem afecções do sistema nervoso central e sem alterações metabólicas gerais e, as de sôro, de pessoas sadias. A osmolalidade foi determinada em osmômetro de Fiske. Os resultados são expressos em mOsm/kg d'água e estão reunidos nas tabelas 1 (LCR) e 2 (sôro); na tabela 3 são apresentadas as estimativas correspondentes. Não foram encontradas diferenças significativas entre a osmolalidade do LCR e do sôro. Êste dado confirma resultados consignados na literatura, obtidos pelo mesmo método, mas baseados na análise de menor número de casos.

The osmolality of the cerebrospinal fluid (CSF) in normal conditions was evaluated through the results in 22 CSF samples obtained from patients with any evidence of central nervous system diseases as well with any disease that might interfer with general metabolic conditions. For comparative purposes it was studied the serum osmolality in a series of 22 healthy people. The osmolality was evaluated by the Fiske's osmometer. Results are presented in table 1 (CSF), table 2 (blood sera) and their estimatives are grouped in table 3. The results reported confirm that there are any significative differences between the values of CSF and of blood serum osmolality in normal conditions.