6 research outputs found

    Infecção por mĂșltiplos tipos de Papilomavirus humano em mulheres jovens sexualmente ativas

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    Modelo do estudo: transversal. Objetivo do estudo: estimar a frequĂȘncia e a distribuição dos tipos de PapilomavĂ­rus humano (HPV) em mulheres jovens sexualmente ativas. Metodologia: foram coletadas amostras do canal vaginal e endocĂ©rvice de 158 mulheres, com idade entre 18 e 35 anos, por meio da tĂ©cnica de autocoleta. O DNA-HPV foi extraĂ­do e amplificado pela tĂ©cnica de PCR end point utilizando os primers consensus PGMY09/11. A genotipagem foi executada pela tĂ©cnica de PCR tipo especĂ­fico (TSPCR) e por anĂĄlise dos fragmentos obtidos com o uso de enzimas de restrição (RFLP). Resultados: DNA-HPV foi detectado em 23% das amostras, 92% foram genĂłtipos de alto risco oncogĂȘnico (HR), sendo prevalente o HPV45, seguido do HPV16 e 31. InfecçÔes por mĂșltiplos tipos de HPV foram detectadas em 35% das amostras, demonstrando infecção por mais de dois tipos em 22,2% das genotipadas. Maior frequĂȘncia do DNA-HPV foi observada entre mulheres com idade ≀ 25 anos. ConclusĂŁo: Este estudo demostrou alta frequĂȘncia da infecção pelo HPV em mulheres jovens sexualmente ativas, assim como uma alta prevalĂȘncia de infecção mĂșltipla com tipos de alto risco oncogĂȘnicoStudy design: cross. Study objective: estimate the frequency and distribution types of human papillomavirus (HPV) in sexually active young women. Methods: samples of vaginal and endocervical canal of 158 women, aged between 18 and 35 years were collected through self-collection technique. The HPV DNA was extracted and amplified by PCR end point using the consensus primers PGMY09/11 and genotyping was performed by PCR specific type (TS-PCR) and by analysis of the fragments obtained from the use of restriction enzymes (RFLP). Results: HPV DNA was detected in 23% of participants, 92% were high-risk HPV genotypes (HR), being the prevalent HPV45, followed by HPV16 and 31 infections with multiple HPV types were detected in 35% of samples, indicating infection by more than two types in 22.2% of the genotyped. Higher frequency of HPV DNA was detected in women ≀ 25 old. Conclusion: this demonstrated a high frequency of HPV infection in sexually active young women, as well as a high prevalence of infection with multiple types of high oncogenic ris

    Presence of highly oncogenic human papillomavirus in the oral mucosa of asymptomatic men

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    Objectives: The aim of this study was to identify highly oncogenic forms of human papillomavirus in the oral mucosa of asymptomatic men. Methods: In this study, we analyzed samples of exfoliated cells from the oral cavity of 559 asymptomatic men. DNA-human papillomavirus was detected using the consensus primers PGMY09/11; viral genotyping was performed using type-specific PCR and restriction fragment length polymorphism. Results: DNA-human papillomavirus was detected in 1.3% of the study participants and of those 42.8% were infected by more than one type of virus. Viral types included HPV6, 11, 89 (low oncogenic risk), and HPV52, 53 (high oncogenic risk). Increased vulnerability to human papillomavirus infection was observed in individuals aged over 26 years, among those who reported oral sex practices, and in those who have had more than 16 sexual partners since first engaging in sexual intercourse. Conclusions: There was a low prevalence of human papillomavirus detection in the oral mucosa of asymptomatic men. Highly oncogenic human papillomavirus types and infection by more than one viral type was observed. Oral sex practices and a large number of sexual partners may increase the risk of acquiring human papillomavirus infection. Keywords: Human papilomavĂ­rus, Men, Viral type, Oral mucosa

    Good agreements between self and clinician-collected specimens for the detection of human papillomavirus in Brazilian patients

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    Women infected with human papillomavirus (HPV) are at a higher risk of developing cervical lesions. In the current study, self and clinician-collected vaginal and cervical samples from women were processed to detect HPV DNA using polymerase chain reaction (PCR) with PGMY09/11 primers. HPV genotypes were determined using type-specific PCR. HPV DNA detection showed good concordance between self and clinician-collected samples (84.6%; kappa = 0.72). HPV infection was found in 30% women and genotyping was more concordant among high-risk HPV (HR-HPV) than low-risk HPV (HR-HPV). HPV16 was the most frequently detected among the HR-HPV types. LR-HPV was detected at a higher frequency in self-collected; however, HR-HPV types were more frequently identified in clinician-collected samples than in self-collected samples. HPV infections of multiple types were detected in 20.5% of clinician-collected samples and 15.5% of self-collected samples. In this study, we demonstrated that the HPV DNA detection rate in self-collected samples has good agreement with that of clinician-collected samples. Self-collected sampling, as a primary prevention strategy in countries with few resources, could be effective for identifying cases of HR-HPV, being more acceptable. The use of this method would enhance the coverage of screening programs for cervical cancer
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