Alan G Nyitray1, Roberto J Carvalho da Silva2, Mihyun Chang3, Maria Luiza Baggio4, Donna J Ingles5, Martha Abrahamsen6, Mary Papenfuss6, Hui-Yi Lin7, Jorge Salmerón8,9, Manuel Quiterio10, Eduardo Lazcano-Ponce10, Luisa L Villa11, Anna R Giuliano6. 1. Center for Infectious Diseases, University of Texas School of Public Health at Houston. 2. Centro de Referência e Treinamentoem Doenças Sexualmente Transmissíveis/AIDS, São Paulo, Brazil. 3. Division of Biostatistics, University of Texas School of Public Health at Houston. 4. Center of Translational Oncology, Instituto do Câncer do Estado de São Paulo (ICESP), Brazil. 5. Vanderbilt Institute for Global Health, Nashville, Tennessee. 6. Center for Infection Research in Cancer,Moffitt Cancer Center and Research Institute, Tampa, Florida. 7. Biostatistics, School of Public Health, Louisiana State University Health Sciences Center, New Orleans. 8. Instituto Nacional de Salud Pública. 9. Instituto Mexicano del Seguro Social, and. 10. Instituto Nacional de Salud Pública, Cuernavaca, México; and. 11. Faculdade de Medicina, Universidade de São Paulo Department of Radiology and Oncology, Centro de Investigação Translacional em Oncologia, ICESP, Brazil.
Abstract
BACKGROUND: Given high rates of anal disease, we investigated the natural history of high-risk anal human papillomavirus (HPV) among a multinational group of men who have sex with men (MSM) aged 18-64 years. METHODS: Anal specimens from human immunodeficiency virus-negative men from Brazil, Mexico, and the United States were genotyped. Over 2 years, 406 MSM provided evaluable specimens every 6 months for ≥2 visits. These men were stratified into men who have sex only with men (MSOM, n = 70) and men who have sex with women and men (MSWM, n = 336). Persistence was defined as ≥12 months' type-specific duration and could begin with either a prevalent or incident infection. Prevalence ratios and 95% confidence intervals were calculated by Poisson regression. RESULTS: Median follow-up time was 2.1 years. Retention was 82%. Annual cumulative incidence of 9-valent vaccine types was 19% and 8% among MSOM and MSWM, respectively (log-rank P = .02). Duration of anal HPV did not differ for MSOM and MSWM and was a median of 6.9 months for HPV-16 after combining men from the 2 groups. Among men with prevalent high-risk infection (n = 106), a total of 36.8%, retained the infection for at least 24 months. For those with prevalent HPV-16 (n = 27), 29.6% were persistent for at least 24 months. Persistence of high-risk HPV was associated with number of male anal sex partners and inversely associated with number of female sex partners. CONCLUSIONS: MSM with prevalent high-risk HPV infection should be considered at increased risk for nontransient infection.
BACKGROUND: Given high rates of anal disease, we investigated the natural history of high-risk anal human papillomavirus (HPV) among a multinational group of men who have sex with men (MSM) aged 18-64 years. METHODS: Anal specimens from human immunodeficiency virus-negative men from Brazil, Mexico, and the United States were genotyped. Over 2 years, 406 MSM provided evaluable specimens every 6 months for ≥2 visits. These men were stratified into men who have sex only with men (MSOM, n = 70) and men who have sex with women and men (MSWM, n = 336). Persistence was defined as ≥12 months' type-specific duration and could begin with either a prevalent or incident infection. Prevalence ratios and 95% confidence intervals were calculated by Poisson regression. RESULTS: Median follow-up time was 2.1 years. Retention was 82%. Annual cumulative incidence of 9-valent vaccine types was 19% and 8% among MSOM and MSWM, respectively (log-rank P = .02). Duration of anal HPV did not differ for MSOM and MSWM and was a median of 6.9 months for HPV-16 after combining men from the 2 groups. Among men with prevalent high-risk infection (n = 106), a total of 36.8%, retained the infection for at least 24 months. For those with prevalent HPV-16 (n = 27), 29.6% were persistent for at least 24 months. Persistence of high-risk HPV was associated with number of male anal sex partners and inversely associated with number of female sex partners. CONCLUSIONS: MSM with prevalent high-risk HPV infection should be considered at increased risk for nontransient infection.
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