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Prevalence of human papillomavirus genotypes among women with cervical cancer in Ghana

BACKGROUND: Human Papillomavirus (HPV) infections have been shown to be a necessary risk factor for the development of cervical cancer. However, HPV genotype distribution varies geographically, both in type and relative prevalence. In order to ensure a successful introduction of available vaccines,...

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Autores principales: Awua, A. K., Sackey, S. T., Osei, Y. D., Asmah, R. H., Wiredu, E. K.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4727324/
https://www.ncbi.nlm.nih.gov/pubmed/26816527
http://dx.doi.org/10.1186/s13027-016-0050-4
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author Awua, A. K.
Sackey, S. T.
Osei, Y. D.
Asmah, R. H.
Wiredu, E. K.
author_facet Awua, A. K.
Sackey, S. T.
Osei, Y. D.
Asmah, R. H.
Wiredu, E. K.
author_sort Awua, A. K.
collection PubMed
description BACKGROUND: Human Papillomavirus (HPV) infections have been shown to be a necessary risk factor for the development of cervical cancer. However, HPV genotype distribution varies geographically, both in type and relative prevalence. In order to ensure a successful introduction of available vaccines, there is the need to identify pre-vaccination HPV genotype prevalence in Ghana and the extent of single and multiple-infections. METHODS: Paraffin-embedded cervical tissues of 256 confirmed cervical cancer cases diagnosed at the Korle-Bu Teaching Hospital during the period January 2004 to December 2006 were selected after hematoxylin and eosin staining and confirmation. Following a heat-proteinase K-based tissue lysis, HPV was detected and typed by a nested-multiplex PCR assay using an E6/E7 consensus primer and type-specific primers. RESULTS: Of the 256 cases, 230 (89.8 %, 95 % CI 85.7–93.4 %) were positive for HPV DNA. HPV18 (47.4 %), HPV59 (42.2 %), HPV45 (37.4 %) and HPV16 (9.0 %) were the four common HPV genotypes detected. A total of 110 (47.8 %) of the 230 HPV DNA positive tissues, were infected by a single HPV genotype while the other 120 (52.2 %) were infected by multiple HPV genotypes. A significant association was determined between each of the following HPV genotypes and multiple-infection; HPV18 (OR = 6.97; 95 % CI, 3.89–12.50), HPV59 (OR = 9.56; 95 % CI, 5.57–20.02) and HPV45 (OR = 1.94; 95 % CI, 1.12–3.35). CONCLUSION: The prevalence of the following high risk HPV genotypes (HPV18, HPV59, HPV45) were relatively high among the cases of cervical cancers reported at this hospital in Ghana during the study period. Additionally, there was a high frequency of HPV multiple-infections among these cases.
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spelling pubmed-47273242016-01-27 Prevalence of human papillomavirus genotypes among women with cervical cancer in Ghana Awua, A. K. Sackey, S. T. Osei, Y. D. Asmah, R. H. Wiredu, E. K. Infect Agent Cancer Research Article BACKGROUND: Human Papillomavirus (HPV) infections have been shown to be a necessary risk factor for the development of cervical cancer. However, HPV genotype distribution varies geographically, both in type and relative prevalence. In order to ensure a successful introduction of available vaccines, there is the need to identify pre-vaccination HPV genotype prevalence in Ghana and the extent of single and multiple-infections. METHODS: Paraffin-embedded cervical tissues of 256 confirmed cervical cancer cases diagnosed at the Korle-Bu Teaching Hospital during the period January 2004 to December 2006 were selected after hematoxylin and eosin staining and confirmation. Following a heat-proteinase K-based tissue lysis, HPV was detected and typed by a nested-multiplex PCR assay using an E6/E7 consensus primer and type-specific primers. RESULTS: Of the 256 cases, 230 (89.8 %, 95 % CI 85.7–93.4 %) were positive for HPV DNA. HPV18 (47.4 %), HPV59 (42.2 %), HPV45 (37.4 %) and HPV16 (9.0 %) were the four common HPV genotypes detected. A total of 110 (47.8 %) of the 230 HPV DNA positive tissues, were infected by a single HPV genotype while the other 120 (52.2 %) were infected by multiple HPV genotypes. A significant association was determined between each of the following HPV genotypes and multiple-infection; HPV18 (OR = 6.97; 95 % CI, 3.89–12.50), HPV59 (OR = 9.56; 95 % CI, 5.57–20.02) and HPV45 (OR = 1.94; 95 % CI, 1.12–3.35). CONCLUSION: The prevalence of the following high risk HPV genotypes (HPV18, HPV59, HPV45) were relatively high among the cases of cervical cancers reported at this hospital in Ghana during the study period. Additionally, there was a high frequency of HPV multiple-infections among these cases. BioMed Central 2016-01-26 /pmc/articles/PMC4727324/ /pubmed/26816527 http://dx.doi.org/10.1186/s13027-016-0050-4 Text en © Awua et al. 2016 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.
spellingShingle Research Article
Awua, A. K.
Sackey, S. T.
Osei, Y. D.
Asmah, R. H.
Wiredu, E. K.
Prevalence of human papillomavirus genotypes among women with cervical cancer in Ghana
title Prevalence of human papillomavirus genotypes among women with cervical cancer in Ghana
title_full Prevalence of human papillomavirus genotypes among women with cervical cancer in Ghana
title_fullStr Prevalence of human papillomavirus genotypes among women with cervical cancer in Ghana
title_full_unstemmed Prevalence of human papillomavirus genotypes among women with cervical cancer in Ghana
title_short Prevalence of human papillomavirus genotypes among women with cervical cancer in Ghana
title_sort prevalence of human papillomavirus genotypes among women with cervical cancer in ghana
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4727324/
https://www.ncbi.nlm.nih.gov/pubmed/26816527
http://dx.doi.org/10.1186/s13027-016-0050-4
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