<HashMap><database>biostudies-literature</database><scores/><additional><omics_type>Unknown</omics_type><submitter>Sierra MS</submitter><funding>National Institutes of Health Office of Research on Women’s Health</funding><funding>World Health Organization</funding><funding>National Cancer Institute</funding><funding>NCI NIH HHS</funding><pubmed_abstract>&lt;h4>Introduction&lt;/h4>Human papillomavirus (HPV) vaccines protect against incident HPV infections, which cause cervical cancer.&lt;h4>Objectives&lt;/h4>We estimated the prevalence and incidence of HPV infections in young adult women to understand the impact of an HPV vaccination programme in this population.&lt;h4>Methods&lt;/h4>We collected cervical specimens from 6322 unvaccinated women, aged 18-37 years, who participated in the Costa Rica Vaccine Trial and its long-term follow-up. Women were followed for (median) 4.8 years and had (median) 4.0 study visits. Cervical specimens were tested for the presence/absence of 25 HPV genotypes. For each age band, we estimated the percentage of women with 1+ prevalent or 1+ incident HPV infections using generalised estimating equations. We also estimated the pre</pubmed_abstract><journal>Sexually transmitted infections</journal><pagination>sextrans-2022-055434</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC10176398</full_dataset_link><repository>biostudies-literature</repository><pubmed_title>Analysis of cervical HPV infections among unvaccinated young adult women to inform vaccine strategies in this age group: the Costa Rica HPV Vaccine Trial.</pubmed_title><pmcid>PMC10176398</pmcid><funding_grant_id>001</funding_grant_id><funding_grant_id>N01 CP011005</funding_grant_id><funding_grant_id>N01-CP-11005</funding_grant_id><pubmed_authors>Sampson JN</pubmed_authors><pubmed_authors>Hu S</pubmed_authors><pubmed_authors>Cortes B</pubmed_authors><pubmed_authors>Rodriguez AC</pubmed_authors><pubmed_authors>Schussler J</pubmed_authors><pubmed_authors>Stoler MH</pubmed_authors><pubmed_authors>Sidawy MK</pubmed_authors><pubmed_authors>Struijk L</pubmed_authors><pubmed_authors>Lowy DR</pubmed_authors><pubmed_authors>Gonzalez P</pubmed_authors><pubmed_authors>Sherman M</pubmed_authors><pubmed_authors>Wacholder S</pubmed_authors><pubmed_authors>Carvajal L</pubmed_authors><pubmed_authors>Jimenez SE</pubmed_authors><pubmed_authors>Quint W</pubmed_authors><pubmed_authors>Kemp TJ</pubmed_authors><pubmed_authors>Porras C</pubmed_authors><pubmed_authors>Schiffman M</pubmed_authors><pubmed_authors>Costa Rica HPV Vaccine Trial (CVT) Group</pubmed_authors><pubmed_authors>Kreimer AR</pubmed_authors><pubmed_authors>Sierra MS</pubmed_authors><pubmed_authors>Tsang SH</pubmed_authors><pubmed_authors>Schiller JT</pubmed_authors><pubmed_authors>Darragh TM</pubmed_authors><pubmed_authors>Palefsky JM</pubmed_authors><pubmed_authors>Romero B</pubmed_authors><pubmed_authors>Wagner S</pubmed_authors><pubmed_authors>Pinto LA</pubmed_authors><pubmed_authors>van Doorn LJ</pubmed_authors><pubmed_authors>Herrero R</pubmed_authors><pubmed_authors>Hildesheim A</pubmed_authors></additional><is_claimable>false</is_claimable><name>Analysis of cervical HPV infections among unvaccinated young adult women to inform vaccine strategies in this age group: the Costa Rica HPV Vaccine Trial.</name><description>&lt;h4>Introduction&lt;/h4>Human papillomavirus (HPV) vaccines protect against incident HPV infections, which cause cervical cancer.&lt;h4>Objectives&lt;/h4>We estimated the prevalence and incidence of HPV infections in young adult women to understand the impact of an HPV vaccination programme in this population.&lt;h4>Methods&lt;/h4>We collected cervical specimens from 6322 unvaccinated women, aged 18-37 years, who participated in the Costa Rica Vaccine Trial and its long-term follow-up. Women were followed for (median) 4.8 years and had (median) 4.0 study visits. Cervical specimens were tested for the presence/absence of 25 HPV genotypes. For each age band, we estimated the percentage of women with 1+ prevalent or 1+ incident HPV infections using generalised estimating equations. We also estimated the pre</description><dates><release>2022-01-01T00:00:00Z</release><publication>2022 Jul</publication><modification>2026-06-14T07:48:41.64Z</modification><creation>2025-04-04T11:50:41.352Z</creation></dates><accession>S-EPMC10176398</accession><cross_references><pubmed>35842229</pubmed><doi>10.1136/sextrans-2022-055434</doi></cross_references></HashMap>