Predição dos campos elétricos na faixa de ondas médias em ambiente rural utilizando equações parabólicas

O Brasil está realizando testes para selecionar o padrão de transmissão digital a ser adotado. Sistemas como Digital Radio Mondiale (DRM) e Rádio de Alta Definição (HD Radio), desenvolvido apenas para frequências abaixo de 30 MHz permitem a operação com largura de banda compatível com a utilizada no país, abrindo a possibilidade de coexistência de radiodifusão analógica e digital. Para qualquer sistema a ser adotado são necessários estudos que permitem uma melhor gestão do espectro eletromagnético, que exige conhecimento real do alcance do sinal. A propagação de ondas eletromagnéticas na faixa de ondas médias (MW) é caracterizada pela dependência do campo em relação aos parâmetros elétricos do solo. Para contribuir para o planejamento e adaptação do Plano Básico de Radiodifusão em Onda Média – PMWB, a inclusão de novas estações que operam principalmente em simulcast-canal, torna-se necessário desenvolver ferramentas que permitem a avaliação das características do solo onde não fornece dados precisos, permitindo uma revisão de modelos teóricos para prever a adoção, contribuindo para a implantação do rádio digital em nosso país. Este trabalho apresenta os resultados dos ensaios de campo realizados pela ANATEL (Agência Nacional de Telecomunicações) e Radiobrás para analisar um sistema de DRM (Digital Radio Mondiale) na faixa de ondas médias. Foi gerada uma potência de 50kW, com antenas omni-direcionais operando na frequência de 980kHz e utilizando um veículo de medição para recepção fixa e móvel. Várias vias radiais foram percorridas a partir do transmissor localizado em uma área urbana e rural nos entorno da capital do Brasil, Brasília. A partir desses dados é proposto um modelo para avaliação das características elétricas do solo correspondente ao campo elétrico, através da aplicação do método de Equações Parabólicas e comprovação da eficácia do modelo proposto.

Mitochondrial DNA mapping of social-biological interactions in Brazilian Amazonian African-descendant populations

ABSTRACT: The formation of the Brazilian Amazonian population has historically involved three main ethnic groups, Amerindian, African and European. This has resulted in genetic investigations having been carried out using classical polymorphisms and molecular markers. To better understand the genetic variability and the micro-evolutionary processes acting in human groups in the Brazilian Amazon region we used mitochondrial DNA to investigate 159 maternally unrelated individuals from five Amazonian African-descendant communities. The mitochondrial lineage distribution indicated a contribution of 50.2% from Africans (L0, L1, L2, and L3), 46.6% from Amerindians (haplogroups A, B, C and D) and a small European contribution of 1.3%. These results indicated high genetic diversity in the Amerindian and African lineage groups, suggesting that the Brazilian Amazonian African-descendant populations reflect a possible population amalgamation of Amerindian women from different Amazonian indigenous tribes and African women from different geographic regions of Africa who had been brought to Brazil as slaves. The present study partially mapped the historical biological and social interactions that had occurred during the formation and expansion of Amazonian African-descendant communities.

Pharmacogenetic polymorphisms in Brazilian-born, first-generation japanese descendants

Brazil hosts the largest Japanese community outside Japan, estimated at 1.5 million individuals, one third of whom are first-generation, Brazilian-born with native Japanese parents. This large community provides a unique opportunity for comparative studies of the distribution of pharmacogenetic polymorphisms in native Japanese versus their Brazilian-born descendants. Functional polymorphisms in genes that modulate drug disposition (CYP2C9, CYP2C19 and GSTM3) or response (VKORC1) and that differ significantly in frequency in native Japanese versus Brazilians with no Japanese ancestry were selected for the present study. Healthy subjects (200 native Japanese and 126 first-generation Japanese descendants) living in agricultural colonies were enrolled. Individual DNA was genotyped using RFLP (GSTM3*A/B) or TaqMan Detection System assays (CYP2C9*2 and *3; CYP2C19*2 and *3; VKORC1 3673G>A, 5808T>G, 6853G>C, and 9041G>A). No difference was detected in the frequency of these pharmacogenetic polymorphisms between native Japanese and first-generation Japanese descendants. In contrast, significant differences in the frequency of each polymorphism were observed between native or first-generation Japanese and Brazilians with no Japanese ancestry. The VKORC1 3673G>A, 6853G>C and 9041G>A single nucleotide polymorphisms were in linkage disequilibrium in both native and first-generation Japanese living in Brazil. The striking similarity in the frequency of clinically relevant pharmacogenetic polymorphisms between Brazilian-born Japanese descendants and native Japanese suggests that the former may be recruited for clinical trials designed to generate bridging data for the Japanese population in the context of the International Conference on Harmonization.

Increased risk of venous thrombosis by AB alleles of the ABO blood group and Factor V Leiden in a Brazilian population

Most cases of a predisposition to venous thrombosis are caused by resistance to activated protein C, associated in 95% of cases with the Factor V Leiden allele (FVL or R506Q). Several recent studies report a further increased risk of thrombosis by an association between the AB alleles of the ABO blood group and Factor V Leiden. The present study investigated this association with deep vein thrombosis (DVT) in individuals treated at the Hemocentro de Pernambuco in northeastern Brazil. A case-control comparison showed a significant risk of thrombosis in the presence of Factor V Leiden (OR = 10.1), which was approximately doubled when the AB alleles of the ABO blood group were present as well (OR = 22.3). These results confirm that the increased risk of deep vein thrombosis in the combined presence of AB alleles and Factor V Leiden is also applicable to the Brazilian population suggesting that ABO blood group typing should be routinely added to FVL in studies involving thrombosis.