Please use this identifier to cite or link to this item: https://hdl.handle.net/2440/132953
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dc.contributor.authorJamieson, L.M.-
dc.contributor.authorGarvey, G.-
dc.contributor.authorHedges, J.-
dc.contributor.authorLeane, C.-
dc.contributor.authorHill, I.-
dc.contributor.authorBrown, A.-
dc.contributor.authorJu, X.-
dc.contributor.authorSethi, S.-
dc.contributor.authorRoder, D.-
dc.contributor.authorLogan, R.M.-
dc.contributor.authorJohnson, N.-
dc.contributor.authorSmith, M.-
dc.contributor.authorAntonsson, A.-
dc.contributor.authorCanfell, K.-
dc.date.issued2021-
dc.identifier.citationBMJ Open, 2021; 11(6):e046928-1-e046928-11-
dc.identifier.issn2044-6055-
dc.identifier.issn2044-6055-
dc.identifier.urihttps://hdl.handle.net/2440/132953-
dc.description.abstractPurpose Our aims are to: (1) estimate prevalence, incidence, clearance and persistence of oral human papillomavirus (HPV) infection among Indigenous Australians; (2) identify risk factors associated with oropharyngeal squamous cell carcinoma (OPSCC)-related HPV types (HPV 16 or 18); (3) develop HPV-related health state valuations and; (4) determine the impact on OPSCC and cervical cancers, and the cost-effectiveness of extending publicly-funded HPV vaccination among Indigenous Australians. Participants Participants were recruited from February 2018 to January 2019. Twelve-month follow-up occurred from March 2019 to March 2020. Participants provided socio-demographic characteristics, health-related behaviours including tobacco and alcohol use and sexual history. Health state preferences in regard to HPV vaccination, knowledge regarding HPV infection, OPSCC and cervical cancer were collected using a two-stage standard gamble approach. Participants provided saliva samples and DNA for microbial genotyping was extracted. Findings to date Of the 910 participants who were positive for β-globin at baseline, 35% had any oral HPV infection. The most prevalent HPV types were 13 or 32 (Heck’s disease; 23%). The second most prevalent types were associated with OPSCC (HPV 16 or 18; 3.3%). Of the 645 participants who were positive for β-globin at 12-month follow-up, 43% had any HPV infection. Of these, 33% were HPV types 13 or 32 and 2.5% were HPV 16 or 18. Some 588 participants had β-globin positive oral samples at baseline and 12-month follow-up. The prevalence of any oral HPV infection increased from 34% at baseline to 44% at 12-month follow-up; due to increases in HPV types 13 or 32 (20% at baseline and 34% at 12-month follow-up). Future plans Further funding will be sought to continue follow-up of this cohort, and to include (after a full medical history) a thorough clinical examination of the external head and neck; a complete oral examination and examination of the oropharynx. Blood tests for early stage OPSCC will also be undertaken.-
dc.description.statementofresponsibilityLisa M Jamieson, Gail Garvey, Joanne Hedges, Cathy Leane, Isaac Hill, Alex Brown ... et al.-
dc.language.isoen-
dc.publisherBMJ-
dc.rights© Author(s) (or their employer(s)) 2021. Re-use permitted under CC BY-NC. No commercial re-use. See rights and permissions. Published by BMJ.-
dc.source.urihttps://www.bmj.com/-
dc.subjectHumans-
dc.subjectPapillomaviridae-
dc.subjectPapillomavirus Infections-
dc.subjectCarcinoma, Squamous Cell-
dc.subjectHead and Neck Neoplasms-
dc.subjectOropharyngeal Neoplasms-
dc.subjectProspective Studies-
dc.subjectAustralia-
dc.subjectFemale-
dc.subjectAlphapapillomavirus-
dc.subjectSquamous Cell Carcinoma of Head and Neck-
dc.subject.meshHumans-
dc.subject.meshPapillomaviridae-
dc.subject.meshPapillomavirus Infections-
dc.subject.meshCarcinoma, Squamous Cell-
dc.subject.meshHead and Neck Neoplasms-
dc.subject.meshOropharyngeal Neoplasms-
dc.subject.meshProspective Studies-
dc.subject.meshAustralia-
dc.subject.meshFemale-
dc.subject.meshAlphapapillomavirus-
dc.subject.meshSquamous Cell Carcinoma of Head and Neck-
dc.titleCohort profile: indigenous human papillomavirus and oropharyngeal squamous cell carcinoma study - a prospective longitudinal cohort-
dc.typeJournal article-
dc.identifier.doi10.1136/bmjopen-2020-046928-
dc.relation.granthttp://purl.org/au-research/grants/nhmrc/1120215-
dc.relation.granthttp://purl.org/au-research/grants/nhmrc/1102587-
dc.relation.granthttp://purl.org/au-research/grants/nhmrc/1159491-
dc.relation.granthttp://purl.org/au-research/grants/nhmrc/1176651-
pubs.publication-statusPublished-
dc.identifier.orcidJamieson, L.M. [0000-0001-9839-9280]-
dc.identifier.orcidHedges, J. [0000-0002-2413-5992]-
dc.identifier.orcidBrown, A. [0000-0003-2112-3918]-
dc.identifier.orcidJu, X. [0000-0003-4759-3918]-
dc.identifier.orcidSethi, S. [0000-0002-3571-5298]-
dc.identifier.orcidRoder, D. [0000-0001-6442-4409]-
dc.identifier.orcidLogan, R.M. [0000-0002-9331-1814]-
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