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dc.contributor.authorMandishora, Racheal S. Dube
dc.contributor.authorRounge, Trine Ballestad
dc.contributor.authorFitzpatrick, Megan
dc.contributor.authorChristiansen, Hanne Irene Kraus
dc.contributor.authorAmbur, Ole Herman
dc.contributor.authorLagström, Sonja
dc.contributor.authorStray-Pedersen, Babill
dc.contributor.authorTommasino, Massimo
dc.contributor.authorPalefsky, Joel
dc.contributor.authorChirenje, Zvavahera M.
dc.coverage.spatialZimbabween_US
dc.date.accessioned2022-03-24T15:24:27Z
dc.date.available2022-03-24T15:24:27Z
dc.date.created2021-06-24T11:12:57Z
dc.date.issued2021-04-26
dc.identifier.citationPLOS ONE. 2021, 16 (4), .en_US
dc.identifier.issn1932-6203
dc.identifier.urihttps://hdl.handle.net/11250/2987470
dc.description.abstractBackground & aim: Women with HIV/HPV coinfection and cervical lesions are at increased risk of developing HPV related anal cancer. Self-collection of anal swabs may facilitate HPV molecular testing in anal cancer screening, especially in high-risk groups, and yet it is not adequately studied. We evaluated level of agreement between self-collected anal swabs (SCAS) and clinician-collected anal swabs (CCAS) when used for HPV genotyping. We also described the anal HPV genotype distribution and HIV/HPV coinfection. Methods: We performed a cross sectional study with participants from a visual-inspection-with-acetic-acid and cervicography (VIAC) clinic, in Harare, Zimbabwe. In a clinic setting, the women aged ≥ 18 years provided anal swabs in duplicate; first CCAS and then SCAS immediately after. HPV detection and genotyping were performed using next generation amplicon sequencing of a 450bp region of the HPV L1 gene. Level of agreement of HPV genotypes between CCAS and SCAS was calculated using the kappa statistic. McNemar tests were used to evaluate agreement in the proportion of genotypes detected by either method. Results: Three-hundred women provided 600 samples for HPV genotyping. HPV genotypes were detected in 25% of SCAS and in 22% of CCAS. The most common genotypes with CCAS were HPV52, HPV62 and HPV70 and with SCAS were HPV62, HPV44, HPV52, HPV53 and HPV68. Total HPV genotypes detected in CCAS were more than those detected in SCAS, 32 versus 27. The agreement of HPV genotypes between the two methods was 0.55 in kappa value (k). The test of proportions using McNemar gave a Chi-square value of 0.75 (p = 0.39). Multiple HPV infections were detected in 28/75 and 29/67 women for CCAS and SCAS respectively. Conclusions: SCAS and CCAS anal swabs showed moderate agreement, with no statistically significant difference in the proportion of genotypes detected by either methods. Although the differences between the two methods were not statistically significant, CCAS detected more HPV genotypes than SCAS and more HPV infections were detected in SCAS than in CCAS. Our data suggest that self-collected anal swabs can be used as an alternative to clinician-collected anal swabs for HPV genotyping.en_US
dc.description.sponsorshipTwo organisations funded the research reported in this publication; Letten Foundation Norway and The Fogarty International Center of the National Institutes of Health under Award Number D43TW010137 within the University of Zimbabwe PERFECT program.en_US
dc.language.isoengen_US
dc.publisherPublic Library of Scienceen_US
dc.relation.ispartofseriesPLOS ONE;16 (4): e0250426
dc.rightsNavngivelse 4.0 Internasjonal*
dc.rights.urihttp://creativecommons.org/licenses/by/4.0/deed.no*
dc.subjectHuman papillomavirus infectionsen_US
dc.subjectHuman papillomavirusen_US
dc.subjectAnal canceren_US
dc.subjectGenotypingen_US
dc.subjectCervical canceren_US
dc.subjectHIVen_US
dc.titleSelf-collected and clinician-collected anal swabs show modest agreement for HPV genotypingen_US
dc.typePeer revieweden_US
dc.typeJournal articleen_US
dc.description.versionpublishedVersionen_US
dc.rights.holder© 2021 Dube Mandishora et al.en_US
dc.source.articlenumbere0250426en_US
cristin.ispublishedtrue
cristin.fulltextoriginal
cristin.qualitycode1
dc.identifier.doihttps://doi.org/10.1371/journal.pone.0250426
dc.identifier.cristin1918109
dc.source.journalPLOS ONEen_US
dc.source.volume16en_US
dc.source.issue4en_US
dc.source.pagenumber1-13en_US


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