Identifying risk factors for prevalent anal human papillomavirus type 16 infection in women living with HIV

Women living with HIV (WLHIV) have a high risk of anal cancer. Identifying risk factors for anal HPV 16 infection, the most significant risk factor for anal cancer, is essential for prevention and screening strategies. In the EVVA Cohort study, 151 WLHIV had cervical and anal HPV testing with genoty...

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Published inPloS one Vol. 17; no. 5; p. e0268521
Main Authors Kaufman, Elaina, Williamson, Tyler, Mayrand, Marie-Hélène, Burchell, Ann N, Klein, Marina, Charest, Louise, Rodrigues-Coutlée, Sophie, Coutlée, François, de Pokomandy, Alexandra
Format Journal Article
LanguageEnglish
Published United States Public Library of Science 19.05.2022
Public Library of Science (PLoS)
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Summary:Women living with HIV (WLHIV) have a high risk of anal cancer. Identifying risk factors for anal HPV 16 infection, the most significant risk factor for anal cancer, is essential for prevention and screening strategies. In the EVVA Cohort study, 151 WLHIV had cervical and anal HPV testing with genotyping every 6 months for 2 years, while demographic and clinical data were collected via questionnaires and chart reviews. Here, we present results of baseline data analyzed using multivariable logistic regression. Among 150 women with adequate HPV test results at baseline, HPV 16 DNA was detected anally in 23 (15.3%; 95%CI:10.4-22.1) and cervically in 5 (3.3%; 95%CI:1.4-7.8). In multivariable analysis, current smoking (OR = 6.0; 95%CI: 1.5-23.9), nadir CD4 count ≤ 200 cells/μL (OR = 8.4; 95%CI: 2.0-34.3), prevalent cervical HPV 16 (OR = 14.7; 95%CI: 1.0-222.5) and anogenital herpes in previous 6 months (OR = 9.8, 95%CI: 1.7-56.8) were associated with prevalent anal HPV 16. Knowledge of risk factors can help identify WLHIV at greatest risk of anal HPV 16 infection and, potentially, developing subsequent anal cancer. Identification of the subgroup of these women in whom HPV 16 persists could be an early step in the algorithm of anal cancer screening.
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Competing Interests: I have read the journal’s policy and the authors of this manuscript have the following competing interests: The clinic of ADP and MK participates in several pharmaceutical clinical trials for HIV antiretrovirals and HCV treatments in which they are either site principal investigator or site co-investigator (ViiV Healthcare, Janssen, Merck, Gilead). ADP received financial support for participation in advisory boards on HIV antiretroviral therapy for ViiV Healthcare and Merck. MK received grants for research projects by Merck (HIV division) and ViiV Healthcare, and received consulting fees from ViiV Healthcare, Bristol-Myers Squibb, Merck, Gilead, and AbbVie. LC received financial support for participation to advisory boards on HIV antiretroviral therapy for Merck (HIV division), Gilead, and ViiV Healthcare. FC received grants to his research institution for research projects from Roche Diagnostics, Becton Dickinson and Merck Sharp and Dome, honorariums for presentations from Merck Sharp and Dome and Roche diagnostics, and has participated in an expert group by Merck Sharp and Dome. This does not alter our adherence to PLOS ONE policies on sharing data and materials.
Membership list of the EVVA study group is provided in Acknowledgments.
ISSN:1932-6203
1932-6203
DOI:10.1371/journal.pone.0268521