2 resultados para ICC.
em Universidade do Minho
Resumo:
Objetivo: realizar a adaptação cultural e a avaliação das propriedades psicométricas do Questionário do Comportamento Planeado no Diabetes – Cuidado Com os Pés. Metodologia: investigação metodológica em que foi realizada análise semântica por um comitê de juízes, pré-teste e, posteriormente, teste-reteste, análise de consistência interna e análise fatorial exploratória, em uma amostra de 130 pessoas com diabetes mellitus de uma Estratégia de Saúde da Família. Instituiu-se 6,35% de alteração semântica na escala original. Resultados: o questionário se mostrou estável (p>0,05 para a maioria dos itens, ICC=0,675); boa consistência interna (Alfa de Cronbach:>0,7 em quatro domínios), ótima relação entre os domínios (KMO=0,741) e estabilidade na estrutura fatorial. Conclusão: O instrumento demonstrou ser adequado para ser replicado no cenário brasileiro.
Resumo:
Invasive cervical cancer (ICC) is the third most frequent cancer among women worldwide and is associated with persistent infection by carcinogenic human papillomaviruses (HPVs). The combination of large populations of viral progeny and decades of sustained infection may allow for the generation of intra-patient diversity, in spite of the assumedly low mutation rates of PVs. While the natural history of chronic HPVs infections has been comprehensively described, within-host viral diversity remains largely unexplored. In this study we have applied next generation sequencing to the analysis of intra-host genetic diversity in ten ICC and one condyloma cases associated to single HPV16 infection. We retrieved from all cases near full-length genomic sequences. All samples analyzed contained polymorphic sites, ranging from 3 to 125 polymorphic positions per genome, and the median probability of a viral genome picked at random to be identical to the consensus sequence in the lesion was only 40%. We have also identified two independent putative duplication events in two samples, spanning the L2 and the L1 gene, respectively. Finally, we have identified with good support a chimera of human and viral DNA. We propose that viral diversity generated during HPVs chronic infection may be fueled by innate and adaptive immune pressures. Further research will be needed to understand the dynamics of viral DNA variability, differentially in benign and malignant lesions, as well as in tissues with differential intensity of immune surveillance. Finally, the impact of intralesion viral diversity on the long-term oncogenic potential may deserve closer attention.