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Re-detection vs. new acquisition of high-risk human papillomavirus in mid-adult women.
Fu, Tsung-Chieh Jane; Carter, Joseph J; Hughes, James P; Feng, Qinghua; Hawes, Stephen E; Schwartz, Stephen M; Xi, Long Fu; Lasof, Taylor; Stern, Joshua E; Galloway, Denise A; Koutsky, Laura A; Winer, Rachel L.
Affiliation
  • Fu TC; Department of Epidemiology, University of Washington, Seattle, WA, 98195.
  • Carter JJ; Fred Hutchinson Cancer Research Center, Seattle, WA, 98109.
  • Hughes JP; Department of Biostatistics, University of Washington, Seattle, WA, 98195.
  • Feng Q; FIDALAB, Seattle, WA, 98177.
  • Hawes SE; Department of Epidemiology, University of Washington, Seattle, WA, 98195.
  • Schwartz SM; Department of Epidemiology, University of Washington, Seattle, WA, 98195.
  • Xi LF; Fred Hutchinson Cancer Research Center, Seattle, WA, 98109.
  • Lasof T; Department of Pathology, University of Washington, Seattle, WA, 98195.
  • Stern JE; University of California San Diego, La Jolla, CA, 92093.
  • Galloway DA; Department of Global Health, University of Washington, Seattle, WA, 98195.
  • Koutsky LA; Fred Hutchinson Cancer Research Center, Seattle, WA, 98109.
  • Winer RL; Department of Microbiology, University of Washington, Seattle, WA, 98195.
Int J Cancer ; 139(10): 2201-12, 2016 11 15.
Article in En | MEDLINE | ID: mdl-27448488
ABSTRACT
To understand high-risk (hr) human papillomavirus (HPV) epidemiology in mid-adulthood, we assessed whether associations between incident detection of hrHPV DNA and recent sexual behavior differed according to whether or not there was serologic evidence of prior infection. From 2011 to 2012, we enrolled 409 women aged 30-50 years into a 6-month longitudinal study. We collected health and sexual behavior histories, enrollment sera for HPV antibody testing, and monthly self-collected vaginal swabs for HPV DNA genotyping. Generalized estimating equations logistic regression identified risk factors for type-specific incident hrHPV DNA, stratified by type-specific hrHPV serostatus at enrollment. Population attributable risks of hrHPV due to prior and recent exposure were estimated. When type-specific hrHPV serology was negative, recent sexual risk behavior was positively associated with incident hrHPV DNA (odds ratio in women reporting ≥3 recent sexual risk behaviors [e.g., new or multiple partners] vs. no recent sexual activity = 9.8, 95% CI 2.4-40.6). No associations with recent sexual behavior were observed with positive type-specific hrHPV serology. Thirty percent of incident hrHPV DNA detection was attributable to prior infection (with positive serology) and 40% was attributable to recent sexual risk behavior (with negative serology). The proportion of incident hrHPV DNA detection attributable to recent sexual risk behavior decreased with increasing age. Among women with serologic evidence of prior infection, re-detection of the same hrHPV type is likely due to reactivation or intermittent detection of persistent infection. Without serologic evidence of prior infection, new detection is likely due to new acquisition or to intermittent detection of persisting infection.
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Papillomaviridae / Sexually Transmitted Diseases, Viral / Papillomavirus Infections Type of study: Diagnostic_studies / Etiology_studies / Observational_studies / Prognostic_studies / Risk_factors_studies Limits: Adult / Female / Humans Country/Region as subject: America do norte Language: En Journal: Int J Cancer Year: 2016 Type: Article

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Papillomaviridae / Sexually Transmitted Diseases, Viral / Papillomavirus Infections Type of study: Diagnostic_studies / Etiology_studies / Observational_studies / Prognostic_studies / Risk_factors_studies Limits: Adult / Female / Humans Country/Region as subject: America do norte Language: En Journal: Int J Cancer Year: 2016 Type: Article