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Good agreements between self and clinician-collected specimens for the detection of human papillomavirus in Brazilian patients
Authors:Karla Lopes Mandu de Campos  Ana Paula Machado  Flávia Gatto de Almeida  Camila Mareti Bonin  Thiago Theodoro Martins Prata  Larissa Zatorre Almeida  Cacilda Tezelli Junqueira Padovani  Alda Maria Teixeira Ferreira  Carlos Eurico dos Santos Fernandes  Inês Aparecida Tozetti
Affiliation:1. Laboratório de Imunologia e Biologia Molecular de Vírus, Centro de Ciências Biológicas e da Saúde;2. Programa de Pós-Graduação em Doenças Infecciosas e Parasitárias, Faculdade de Medicina, Universidade Federal de Mato Grosso do Sul, Campo Grande, MS, Brasil
Abstract:Women infected with human papillomavirus (HPV) are at a higher risk of developingcervical lesions. In the current study, self and clinician-collected vaginal andcervical samples from women were processed to detect HPV DNA using polymerase chainreaction (PCR) with PGMY09/11 primers. HPV genotypes were determined usingtype-specific PCR. HPV DNA detection showed good concordance between self andclinician-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-riskHPV (HR-HPV). HPV16 was the most frequently detected among the HR-HPV types. LR-HPVwas detected at a higher frequency in self-collected; however, HR-HPV types were morefrequently identified in clinician-collected samples than in self-collected samples.HPV infections of multiple types were detected in 20.5% of clinician-collectedsamples and 15.5% of self-collected samples. In this study, we demonstrated that theHPV DNA detection rate in self-collected samples has good agreement with that ofclinician-collected samples. Self-collected sampling, as a primary preventionstrategy in countries with few resources, could be effective for identifying cases ofHR-HPV, being more acceptable. The use of this method would enhance the coverage ofscreening programs for cervical cancer.
Keywords:human papillomavirus   self-collected   clinician-collected   PCR
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