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HPV prevalence among young adult women living with and without HIV in Botswana for future HPV vaccine impact monitoring
INTRODUCTION: In 2015, Botswana introduced quadrivalent human papillomavirus (HPV) vaccine for girls aged 9–13 years. To establish a baseline HPV prevalence for future HPV vaccine impact monitoring, we evaluated HPV prevalences among the youngest unvaccinated women in Botswana and compared HPV preva...
Autores principales: | , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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BioMed Central
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8862300/ https://www.ncbi.nlm.nih.gov/pubmed/35193517 http://dx.doi.org/10.1186/s12879-022-07130-x |
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author | McClung, Nancy Mathoma, Anikie Gargano, Julia W. Nyepetsi, Naledi Gape Querec, Troy D. Onyekwuluje, Juanita Mine, Madisa Morroni, Chelsea Luckett, Rebecca Markowitz, Lauri E. Ramogola-Masire, Doreen |
author_facet | McClung, Nancy Mathoma, Anikie Gargano, Julia W. Nyepetsi, Naledi Gape Querec, Troy D. Onyekwuluje, Juanita Mine, Madisa Morroni, Chelsea Luckett, Rebecca Markowitz, Lauri E. Ramogola-Masire, Doreen |
author_sort | McClung, Nancy |
collection | PubMed |
description | INTRODUCTION: In 2015, Botswana introduced quadrivalent human papillomavirus (HPV) vaccine for girls aged 9–13 years. To establish a baseline HPV prevalence for future HPV vaccine impact monitoring, we evaluated HPV prevalences among the youngest unvaccinated women in Botswana and compared HPV prevalences among women living with HIV (WLHIV) and without HIV. METHODS: Women aged 18–22 years were recruited from the University of Botswana and HIV clinics in Gaborone from October 2019–January 2021. Demographic and behavioral characteristics were self-reported during structured interviews; HIV clinical characteristics were abstracted from medical charts. Self-collected vaginal swabs were tested for 28 HPV types using Seegene Anyplex II HPV28. We compared prevalence of any HPV, high risk (HR)-HPV, and quadrivalent HPV vaccine types (HPV6/11/16/18) among WLHIV and women without HIV and evaluated risk factors for prevalence of HR-HPV. RESULTS: A total of 306 WLHIV and 500 women without HIV were recruited. Compared to women without HIV, WLHIV were more likely to be sexually experienced (86.6% versus 74.4%) and have ≥ 3 lifetime sex partners (55.3% versus 27.8%). All HPV type prevalences were significantly higher among WLHIV compared to women without HIV, including prevalence of any HPV (82.7% versus 63.0%), HR-HPV (72.9% versus 53.8%), and quadrivalent vaccine HPV types (34.3% versus 21.0%). Among WLHIV, there were no differences between those perinatally and non-perinatally infected for HPV prevalences, number of HPV types detected, CD4 count, or viral load. CONCLUSIONS: Over one-third of WLHIV and nearly a quarter of those without HIV had vaccine-type HPV detected. This study supports need for the national HPV vaccination program in Botswana and provides important baseline data for future evaluation of impact of the program. |
format | Online Article Text |
id | pubmed-8862300 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-88623002022-02-23 HPV prevalence among young adult women living with and without HIV in Botswana for future HPV vaccine impact monitoring McClung, Nancy Mathoma, Anikie Gargano, Julia W. Nyepetsi, Naledi Gape Querec, Troy D. Onyekwuluje, Juanita Mine, Madisa Morroni, Chelsea Luckett, Rebecca Markowitz, Lauri E. Ramogola-Masire, Doreen BMC Infect Dis Research INTRODUCTION: In 2015, Botswana introduced quadrivalent human papillomavirus (HPV) vaccine for girls aged 9–13 years. To establish a baseline HPV prevalence for future HPV vaccine impact monitoring, we evaluated HPV prevalences among the youngest unvaccinated women in Botswana and compared HPV prevalences among women living with HIV (WLHIV) and without HIV. METHODS: Women aged 18–22 years were recruited from the University of Botswana and HIV clinics in Gaborone from October 2019–January 2021. Demographic and behavioral characteristics were self-reported during structured interviews; HIV clinical characteristics were abstracted from medical charts. Self-collected vaginal swabs were tested for 28 HPV types using Seegene Anyplex II HPV28. We compared prevalence of any HPV, high risk (HR)-HPV, and quadrivalent HPV vaccine types (HPV6/11/16/18) among WLHIV and women without HIV and evaluated risk factors for prevalence of HR-HPV. RESULTS: A total of 306 WLHIV and 500 women without HIV were recruited. Compared to women without HIV, WLHIV were more likely to be sexually experienced (86.6% versus 74.4%) and have ≥ 3 lifetime sex partners (55.3% versus 27.8%). All HPV type prevalences were significantly higher among WLHIV compared to women without HIV, including prevalence of any HPV (82.7% versus 63.0%), HR-HPV (72.9% versus 53.8%), and quadrivalent vaccine HPV types (34.3% versus 21.0%). Among WLHIV, there were no differences between those perinatally and non-perinatally infected for HPV prevalences, number of HPV types detected, CD4 count, or viral load. CONCLUSIONS: Over one-third of WLHIV and nearly a quarter of those without HIV had vaccine-type HPV detected. This study supports need for the national HPV vaccination program in Botswana and provides important baseline data for future evaluation of impact of the program. BioMed Central 2022-02-22 /pmc/articles/PMC8862300/ /pubmed/35193517 http://dx.doi.org/10.1186/s12879-022-07130-x Text en © The Author(s) 2022 https://creativecommons.org/licenses/by/4.0/Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/ (https://creativecommons.org/publicdomain/zero/1.0/) ) applies to the data made available in this article, unless otherwise stated in a credit line to the data. |
spellingShingle | Research McClung, Nancy Mathoma, Anikie Gargano, Julia W. Nyepetsi, Naledi Gape Querec, Troy D. Onyekwuluje, Juanita Mine, Madisa Morroni, Chelsea Luckett, Rebecca Markowitz, Lauri E. Ramogola-Masire, Doreen HPV prevalence among young adult women living with and without HIV in Botswana for future HPV vaccine impact monitoring |
title | HPV prevalence among young adult women living with and without HIV in Botswana for future HPV vaccine impact monitoring |
title_full | HPV prevalence among young adult women living with and without HIV in Botswana for future HPV vaccine impact monitoring |
title_fullStr | HPV prevalence among young adult women living with and without HIV in Botswana for future HPV vaccine impact monitoring |
title_full_unstemmed | HPV prevalence among young adult women living with and without HIV in Botswana for future HPV vaccine impact monitoring |
title_short | HPV prevalence among young adult women living with and without HIV in Botswana for future HPV vaccine impact monitoring |
title_sort | hpv prevalence among young adult women living with and without hiv in botswana for future hpv vaccine impact monitoring |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8862300/ https://www.ncbi.nlm.nih.gov/pubmed/35193517 http://dx.doi.org/10.1186/s12879-022-07130-x |
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