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1.
Braz. j. med. biol. res ; 43(5): 445-450, May 2010. tab, ilus
Artigo em Inglês | LILACS | ID: lil-546338

RESUMO

The functional effect of the A>G transition at position 2756 on the MTR gene (5-methyltetrahydrofolate-homocysteine methyltransferase), involved in folate metabolism, may be a risk factor for head and neck squamous cell carcinoma (HNSCC). The frequency of MTR A2756G (rs1805087) polymorphism was compared between HNSCC patients and individuals without history of neoplasias. The association of this polymorphism with clinical histopathological parameters was evaluated. A total of 705 individuals were included in the study. The polymerase chain reaction-restriction fragment length polymorphism technique was used to genotype the polymorphism. For statistical analysis, the chi-square test (univariate analysis) was used for comparisons between groups and multiple logistic regression (multivariate analysis) was used for interactions between the polymorphism and risk factors and clinical histopathological parameters. Using univariate analysis, the results did not show significant differences in allelic or genotypic distributions. Multivariable analysis showed that tobacco and alcohol consumption (P < 0.05), AG genotype (P = 0.019) and G allele (P = 0.028) may be predictors of the disease and a higher frequency of the G polymorphic allele was detected in men with HNSCC compared to male controls (P = 0.008). The analysis of polymorphism regarding clinical histopathological parameters did not show any association with the primary site, aggressiveness, lymph node involvement or extension of the tumor. In conclusion, our data provide evidence that supports an association between the polymorphism and the risk of HNSCC.


Assuntos
Feminino , Humanos , Masculino , Pessoa de Meia-Idade , /genética , Carcinoma de Células Escamosas/genética , Neoplasias de Cabeça e Pescoço/genética , Polimorfismo Genético/genética , Estudos de Casos e Controles , Carcinoma de Células Escamosas/enzimologia , Frequência do Gene , Predisposição Genética para Doença , Genótipo , Neoplasias de Cabeça e Pescoço/enzimologia , Reação em Cadeia da Polimerase , Polimorfismo de Fragmento de Restrição , Fatores de Risco
2.
Arq. bras. cardiol ; 37(2): 95-9, 1981.
Artigo em Português | LILACS | ID: lil-5169

RESUMO

Os autores relatam a experiencia inicial no reconhecimento e manuseio de disritmias cardiacas diagnosticadas no bercario de um hospital geral. Apos discussao de possibilidades etiologicas, demonstraram a preponderancia de disritmias supraventriculares no grupo etario e o efeito terapeutico com o uso do esquema digoxina e/ou propranolol. A ocorrencia na serie analidada de dois casos de parassistolia atrial e realcada, levantando a questao da real frequencia desta rara disritmia no recem-nascido e seus aspectos evoluativos


Assuntos
Arritmias Cardíacas , Doenças do Recém-Nascido
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