dc.contributor.author
Krings, Amrei
dc.contributor.author
Boateng, Gifty
dc.contributor.author
Dunyo, Priscilla
dc.contributor.author
Amuah, Joseph E.
dc.contributor.author
Adams, Rashid A.
dc.contributor.author
Adunyame, Lois
dc.contributor.author
Nkansah, Dinah O.
dc.contributor.author
Wormenor, Comfort M.
dc.contributor.author
Hansen, Benjamin T.
dc.contributor.author
Gedzah, Isaac
dc.contributor.author
Asmah, Richard H.
dc.contributor.author
Wiredu, Edwin K.
dc.contributor.author
Kaufmann, Andreas M.
dc.date.accessioned
2019-06-25T13:27:50Z
dc.date.available
2019-06-25T13:27:50Z
dc.identifier.uri
https://refubium.fu-berlin.de/handle/fub188/24925
dc.identifier.uri
http://dx.doi.org/10.17169/refubium-2685
dc.description.abstract
Persistent Human Papillomavirus (HPV) infection is a prerequisite for cervical cancer development. Few studies investigated clearance of high-risk HPV in low-and-middle-income countries. Our study investigated HPV clearance and persistence over four years in women from North Tongu District, Ghana. In 2010/2011, cervical swabs of 500 patients were collected and HPV genotyped (nested multiplex PCR) in Accra, Ghana. In 2014, 104 women who previously tested positive for high-risk HPV and remained untreated were re-tested for HPV. Cytobrush samples were genotyped (GP5+/6+ PCR & Luminex-MPG readout) in Berlin, Germany. Positively tested patients underwent colposcopy and treatment if indicated. Of 104 women, who tested high-risk HPV+ in 2010/2011, seven (6,7%; 95%CI: 2.7-13.4%) had ≥1 persistent high-risk-infection after ~4 years (mean age 39 years). Ninety-seven (93,3%; 95%CI: 86.6-97.3%) had cleared the original infection, while 22 (21.2%; 95%CI: 13.8-30.3%) had acquired new high-risk infections with other genotypes. Persistent types found were HPV 16, 18, 35, 39, 51, 52, 58, and 68. Among those patients, one case of CIN2 (HPV 68) and one micro-invasive cervical cancer (HPV 16) were detected. This longitudinal observational data suggest that single HPV screening rounds may lead to over-referral. Including type-specific HPV re-testing or additional triage methods could help reduce follow-up rates.
en
dc.rights.uri
https://creativecommons.org/licenses/by-nc-nd/4.0/
dc.subject
Cervical screening
en
dc.subject
HPV screening
en
dc.subject
Natural history
en
dc.subject.ddc
600 Technik, Medizin, angewandte Wissenschaften::610 Medizin und Gesundheit::610 Medizin und Gesundheit
dc.title
Dynamics of genotype-specific HPV clearance and reinfection in rural Ghana may compromise HPV screening approaches
dc.type
Wissenschaftlicher Artikel
dcterms.bibliographicCitation.doi
10.1016/j.pvr.2018.12.004
dcterms.bibliographicCitation.journaltitle
Papillomavirus Research
dcterms.bibliographicCitation.originalpublishername
Elsevier
dcterms.bibliographicCitation.pagestart
45
dcterms.bibliographicCitation.pageend
51
dcterms.bibliographicCitation.volume
7
refubium.affiliation
Charité - Universitätsmedizin Berlin
refubium.resourceType.isindependentpub
no
dcterms.accessRights.openaire
open access
dcterms.bibliographicCitation.pmid
30625379
dcterms.isPartOf.eissn
2405-8521