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Baseline assessment of prevalence and geographical distribution of HPV types in Chile using self-collected vaginal samples

BACKGROUND: Chile has broad variations in weather, economics and population from the far desert north (Region 1) to the cold, icy south (Region 12). A home-based self-collected vaginal sampling was nested in the 2003 Chilean population-based health survey in order to explore the possibility of a typ...

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Autores principales: Ferreccio, Catterina, Corvalán, Alejandro, Margozzini, Paula, Viviani, Paola, González, Claudia, Aguilera, Ximena, Gravitt, Patti E
Formato: Texto
Lenguaje:English
Publicado: BioMed Central 2008
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2291464/
https://www.ncbi.nlm.nih.gov/pubmed/18304362
http://dx.doi.org/10.1186/1471-2458-8-78
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author Ferreccio, Catterina
Corvalán, Alejandro
Margozzini, Paula
Viviani, Paola
González, Claudia
Aguilera, Ximena
Gravitt, Patti E
author_facet Ferreccio, Catterina
Corvalán, Alejandro
Margozzini, Paula
Viviani, Paola
González, Claudia
Aguilera, Ximena
Gravitt, Patti E
author_sort Ferreccio, Catterina
collection PubMed
description BACKGROUND: Chile has broad variations in weather, economics and population from the far desert north (Region 1) to the cold, icy south (Region 12). A home-based self-collected vaginal sampling was nested in the 2003 Chilean population-based health survey in order to explore the possibility of a type-specific geographical variation for human papillomavirus METHODS: The population was a national probability sample of people 17 years of age and over. Consenting women provided self-collected cervicovaginal swabs in universal collection media (UCM). DNA was extracted and typed to 37 HPV genotypes using PGMY consensus PCR and line blot assay. Weighted prevalence rates and adjusted OR were calculated. RESULTS: Of the 1,883 women participating in the health survey, 1,219 (64.7%) provided a cervicovaginal sample and in 1,110 (56.2% of participants and 66.5% of those eligible) the samples were adequate for analysis. Refusal rate was 16.9%. HPV prevalence was 29.2% (15.1% high-risk HPV and 14.1% low-risk HPV). Predominant high-risk types were HPV 16, 52, 51, 56 and 58. Predominant low-risk HPVs were HPV 84, CP6108, 62, 53 and 61. High-risk and low-risk HPV rates were inversely correlated between the regions. High-risk HPV prevalence was highest among the youngest women, whereas low-risk HPV increased slightly with age. CONCLUSION: Self-obtained vaginal sampling is adequate for monitoring HPV in the community, for identifying high-risk areas, and for surveying the long term impact of interventions.
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spelling pubmed-22914642008-04-10 Baseline assessment of prevalence and geographical distribution of HPV types in Chile using self-collected vaginal samples Ferreccio, Catterina Corvalán, Alejandro Margozzini, Paula Viviani, Paola González, Claudia Aguilera, Ximena Gravitt, Patti E BMC Public Health Research Article BACKGROUND: Chile has broad variations in weather, economics and population from the far desert north (Region 1) to the cold, icy south (Region 12). A home-based self-collected vaginal sampling was nested in the 2003 Chilean population-based health survey in order to explore the possibility of a type-specific geographical variation for human papillomavirus METHODS: The population was a national probability sample of people 17 years of age and over. Consenting women provided self-collected cervicovaginal swabs in universal collection media (UCM). DNA was extracted and typed to 37 HPV genotypes using PGMY consensus PCR and line blot assay. Weighted prevalence rates and adjusted OR were calculated. RESULTS: Of the 1,883 women participating in the health survey, 1,219 (64.7%) provided a cervicovaginal sample and in 1,110 (56.2% of participants and 66.5% of those eligible) the samples were adequate for analysis. Refusal rate was 16.9%. HPV prevalence was 29.2% (15.1% high-risk HPV and 14.1% low-risk HPV). Predominant high-risk types were HPV 16, 52, 51, 56 and 58. Predominant low-risk HPVs were HPV 84, CP6108, 62, 53 and 61. High-risk and low-risk HPV rates were inversely correlated between the regions. High-risk HPV prevalence was highest among the youngest women, whereas low-risk HPV increased slightly with age. CONCLUSION: Self-obtained vaginal sampling is adequate for monitoring HPV in the community, for identifying high-risk areas, and for surveying the long term impact of interventions. BioMed Central 2008-02-28 /pmc/articles/PMC2291464/ /pubmed/18304362 http://dx.doi.org/10.1186/1471-2458-8-78 Text en Copyright © 2008 Ferreccio et al; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License ( (http://creativecommons.org/licenses/by/2.0) ), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research Article
Ferreccio, Catterina
Corvalán, Alejandro
Margozzini, Paula
Viviani, Paola
González, Claudia
Aguilera, Ximena
Gravitt, Patti E
Baseline assessment of prevalence and geographical distribution of HPV types in Chile using self-collected vaginal samples
title Baseline assessment of prevalence and geographical distribution of HPV types in Chile using self-collected vaginal samples
title_full Baseline assessment of prevalence and geographical distribution of HPV types in Chile using self-collected vaginal samples
title_fullStr Baseline assessment of prevalence and geographical distribution of HPV types in Chile using self-collected vaginal samples
title_full_unstemmed Baseline assessment of prevalence and geographical distribution of HPV types in Chile using self-collected vaginal samples
title_short Baseline assessment of prevalence and geographical distribution of HPV types in Chile using self-collected vaginal samples
title_sort baseline assessment of prevalence and geographical distribution of hpv types in chile using self-collected vaginal samples
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2291464/
https://www.ncbi.nlm.nih.gov/pubmed/18304362
http://dx.doi.org/10.1186/1471-2458-8-78
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