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Dynamics of genotype-specific HPV clearance and reinfection in rural Ghana may compromise HPV screening approaches

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. I...

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Autores principales: Krings, Amrei, Boateng, Gifty, Dunyo, Priscilla, Amuah, Joseph E., Adams, Rashid A., Adunyame, Lois, Nkansah, Dinah O., Wormenor, Comfort M., Hansen, Benjamin T., Gedzah, Isaac, Asmah, Richard H., Wiredu, Edwin K., Kaufmann, Andreas M.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6350109/
https://www.ncbi.nlm.nih.gov/pubmed/30625379
http://dx.doi.org/10.1016/j.pvr.2018.12.004
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author Krings, Amrei
Boateng, Gifty
Dunyo, Priscilla
Amuah, Joseph E.
Adams, Rashid A.
Adunyame, Lois
Nkansah, Dinah O.
Wormenor, Comfort M.
Hansen, Benjamin T.
Gedzah, Isaac
Asmah, Richard H.
Wiredu, Edwin K.
Kaufmann, Andreas M.
author_facet Krings, Amrei
Boateng, Gifty
Dunyo, Priscilla
Amuah, Joseph E.
Adams, Rashid A.
Adunyame, Lois
Nkansah, Dinah O.
Wormenor, Comfort M.
Hansen, Benjamin T.
Gedzah, Isaac
Asmah, Richard H.
Wiredu, Edwin K.
Kaufmann, Andreas M.
author_sort Krings, Amrei
collection PubMed
description 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.
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spelling pubmed-63501092019-02-05 Dynamics of genotype-specific HPV clearance and reinfection in rural Ghana may compromise HPV screening approaches Krings, Amrei Boateng, Gifty Dunyo, Priscilla Amuah, Joseph E. Adams, Rashid A. Adunyame, Lois Nkansah, Dinah O. Wormenor, Comfort M. Hansen, Benjamin T. Gedzah, Isaac Asmah, Richard H. Wiredu, Edwin K. Kaufmann, Andreas M. Papillomavirus Res Article 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. Elsevier 2019-01-06 /pmc/articles/PMC6350109/ /pubmed/30625379 http://dx.doi.org/10.1016/j.pvr.2018.12.004 Text en © 2019 The Authors http://creativecommons.org/licenses/by-nc-nd/4.0/ This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).
spellingShingle Article
Krings, Amrei
Boateng, Gifty
Dunyo, Priscilla
Amuah, Joseph E.
Adams, Rashid A.
Adunyame, Lois
Nkansah, Dinah O.
Wormenor, Comfort M.
Hansen, Benjamin T.
Gedzah, Isaac
Asmah, Richard H.
Wiredu, Edwin K.
Kaufmann, Andreas M.
Dynamics of genotype-specific HPV clearance and reinfection in rural Ghana may compromise HPV screening approaches
title Dynamics of genotype-specific HPV clearance and reinfection in rural Ghana may compromise HPV screening approaches
title_full Dynamics of genotype-specific HPV clearance and reinfection in rural Ghana may compromise HPV screening approaches
title_fullStr Dynamics of genotype-specific HPV clearance and reinfection in rural Ghana may compromise HPV screening approaches
title_full_unstemmed Dynamics of genotype-specific HPV clearance and reinfection in rural Ghana may compromise HPV screening approaches
title_short Dynamics of genotype-specific HPV clearance and reinfection in rural Ghana may compromise HPV screening approaches
title_sort dynamics of genotype-specific hpv clearance and reinfection in rural ghana may compromise hpv screening approaches
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6350109/
https://www.ncbi.nlm.nih.gov/pubmed/30625379
http://dx.doi.org/10.1016/j.pvr.2018.12.004
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