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Meta-Analysis on Prevalence and Attribution of Human Papillomavirus Types 52 and 58 in Cervical Neoplasia Worldwide

OBJECTIVE: To estimate the prevalence and attribution of two non-vaccine-covered HPV types (HPV52 and HPV58) across the world. METHODS: Meta-analysis on studies reported in English and Chinese between 1994 and 2012. RESULTS: The pooled prevalence and attribution rates of HPV52 and HPV58 in invasive...

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Autores principales: Chan, Paul K. S., Ho, Wendy C. S., Chan, Martin C. W., Wong, Martin C. S., Yeung, Apple C. M., Chor, Josette S. Y., Hui, Mamie
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4168000/
https://www.ncbi.nlm.nih.gov/pubmed/25229350
http://dx.doi.org/10.1371/journal.pone.0107573
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author Chan, Paul K. S.
Ho, Wendy C. S.
Chan, Martin C. W.
Wong, Martin C. S.
Yeung, Apple C. M.
Chor, Josette S. Y.
Hui, Mamie
author_facet Chan, Paul K. S.
Ho, Wendy C. S.
Chan, Martin C. W.
Wong, Martin C. S.
Yeung, Apple C. M.
Chor, Josette S. Y.
Hui, Mamie
author_sort Chan, Paul K. S.
collection PubMed
description OBJECTIVE: To estimate the prevalence and attribution of two non-vaccine-covered HPV types (HPV52 and HPV58) across the world. METHODS: Meta-analysis on studies reported in English and Chinese between 1994 and 2012. RESULTS: The pooled prevalence and attribution rates of HPV52 and HPV58 in invasive cervical cancers were significantly higher in Eastern Asia compared to other regions (HPV52 prevalence: 5.7% vs. 1.8–3.6%, P<0.001; HPV52 attribution: 3.7% vs. 0.2–2.0%; HPV58 prevalence: 9.8% vs. 1.1–2.5%, P<0.001; HPV58 attribution: 6.4% vs. 0.7–2.2%, P<0.001). Oceania has an insufficient number of studies to ascertain the prevalence of HPV52. Within Eastern Asia, the attribution of HPV58 to invasive cervical cancer was 1.8-fold higher than that of HPV52. Similarly, HPV52 and HPV58 shared a higher prevalence and attribution among cervical intraepithelial neoplasia in Eastern Asia. In contrast to the classical high-risk type, HPV16, the prevalence and attribution of HPV52 and HPV58 decreased with increasing lesion severity. Thus, HPV52 and HPV58 behave as an “intermediate-risk” type. CONCLUSION: The attribution of HPV52 and HPV58 to cervical intraepithelial neoplasia and invasive cancer in Eastern Asia were respectively 2.5–2.8 and 3.7–4.9 folds higher than elsewhere. Changes in the attributed disease fraction can serve as a surrogate marker for cross-protection or type replacement following widespread use of HPV16/18-based vaccines. This unique epidemiology should be considered when designing HPV screening assays and vaccines for Eastern Asia.
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spelling pubmed-41680002014-09-22 Meta-Analysis on Prevalence and Attribution of Human Papillomavirus Types 52 and 58 in Cervical Neoplasia Worldwide Chan, Paul K. S. Ho, Wendy C. S. Chan, Martin C. W. Wong, Martin C. S. Yeung, Apple C. M. Chor, Josette S. Y. Hui, Mamie PLoS One Research Article OBJECTIVE: To estimate the prevalence and attribution of two non-vaccine-covered HPV types (HPV52 and HPV58) across the world. METHODS: Meta-analysis on studies reported in English and Chinese between 1994 and 2012. RESULTS: The pooled prevalence and attribution rates of HPV52 and HPV58 in invasive cervical cancers were significantly higher in Eastern Asia compared to other regions (HPV52 prevalence: 5.7% vs. 1.8–3.6%, P<0.001; HPV52 attribution: 3.7% vs. 0.2–2.0%; HPV58 prevalence: 9.8% vs. 1.1–2.5%, P<0.001; HPV58 attribution: 6.4% vs. 0.7–2.2%, P<0.001). Oceania has an insufficient number of studies to ascertain the prevalence of HPV52. Within Eastern Asia, the attribution of HPV58 to invasive cervical cancer was 1.8-fold higher than that of HPV52. Similarly, HPV52 and HPV58 shared a higher prevalence and attribution among cervical intraepithelial neoplasia in Eastern Asia. In contrast to the classical high-risk type, HPV16, the prevalence and attribution of HPV52 and HPV58 decreased with increasing lesion severity. Thus, HPV52 and HPV58 behave as an “intermediate-risk” type. CONCLUSION: The attribution of HPV52 and HPV58 to cervical intraepithelial neoplasia and invasive cancer in Eastern Asia were respectively 2.5–2.8 and 3.7–4.9 folds higher than elsewhere. Changes in the attributed disease fraction can serve as a surrogate marker for cross-protection or type replacement following widespread use of HPV16/18-based vaccines. This unique epidemiology should be considered when designing HPV screening assays and vaccines for Eastern Asia. Public Library of Science 2014-09-17 /pmc/articles/PMC4168000/ /pubmed/25229350 http://dx.doi.org/10.1371/journal.pone.0107573 Text en © 2014 Chan et al http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited.
spellingShingle Research Article
Chan, Paul K. S.
Ho, Wendy C. S.
Chan, Martin C. W.
Wong, Martin C. S.
Yeung, Apple C. M.
Chor, Josette S. Y.
Hui, Mamie
Meta-Analysis on Prevalence and Attribution of Human Papillomavirus Types 52 and 58 in Cervical Neoplasia Worldwide
title Meta-Analysis on Prevalence and Attribution of Human Papillomavirus Types 52 and 58 in Cervical Neoplasia Worldwide
title_full Meta-Analysis on Prevalence and Attribution of Human Papillomavirus Types 52 and 58 in Cervical Neoplasia Worldwide
title_fullStr Meta-Analysis on Prevalence and Attribution of Human Papillomavirus Types 52 and 58 in Cervical Neoplasia Worldwide
title_full_unstemmed Meta-Analysis on Prevalence and Attribution of Human Papillomavirus Types 52 and 58 in Cervical Neoplasia Worldwide
title_short Meta-Analysis on Prevalence and Attribution of Human Papillomavirus Types 52 and 58 in Cervical Neoplasia Worldwide
title_sort meta-analysis on prevalence and attribution of human papillomavirus types 52 and 58 in cervical neoplasia worldwide
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4168000/
https://www.ncbi.nlm.nih.gov/pubmed/25229350
http://dx.doi.org/10.1371/journal.pone.0107573
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