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Article: Population-based prevalence of cervical infection with human papillomavirus genotypes 16 and 18 and other high risk types in Tlaxcala, Mexico

TitlePopulation-based prevalence of cervical infection with human papillomavirus genotypes 16 and 18 and other high risk types in Tlaxcala, Mexico
Authors
KeywordsHPV16/18
Human papillomavirus DNA testing
Mexico
Prevalence
Risk factors
Issue Date2016
Citation
BMC Infectious Diseases, 2016, v. 16, n. 1, article no. 461 How to Cite?
AbstractBackground: Cervical cancer remains an important cause of cancer mortality for Mexican women. HPV 16/18 typing may help to improve cervical cancer screening. Here we present the prevalence of high-risk human papillomavirus (hrHPV) including HPV16 and HPV18 from the FRIDA (Forwarding Research for Improved Detection and Access) population. Methods: Beginning in 2013, we recruited 30,829 women aged 30-64 in Tlaxcala, Mexico. Cervical samples were collected and tested for 14 hrHPV genotypes (16, 18, 31, 33, 35, 39, 45, 51, 52, 56, 58, 59, 66, and 68). We used logistic regression to estimate odds ratios with 95 % confidence intervals for hrHPV infections according to putative risk factors. Results: Prevalence of infection with any of the 14 hrHPV types was 11.0 %. The age-specific prevalence of all hrHPV formed a U-shaped curve with a higher prevalence for women aged 30-39 and 50-64 than women aged 40-49. Across all age groups, 2.0 % of women were positive for HPV16 and/or HPV18 (HPV16/18), respectively. HPV16/18 prevalence also showed a U-shaped curve with increased prevalence estimates for women aged both 30-39 and 60-64. Both prevalence curves had a significant quadratic age coefficient. Infections with hrHPV were positively associated with an increased number of lifetime sexual partners, a history of sexually transmitted disease, being unmarried, use of hormonal contraception, having a history of smoking and reported condom use in the multivariate model. Conclusions: The FRIDA population has a bimodal distribution of both hrHPV and HPV16/18 positivity with higher prevalences at ages 30-39 and 60-64. These findings will help to evaluate triage algorithms based on HPV genotyping. Trial registration: The trial is registered with ClinicalTrials.gov, number NCT02510027.
Persistent Identifierhttp://hdl.handle.net/10722/327117

 

DC FieldValueLanguage
dc.contributor.authorRudolph, Samantha E.-
dc.contributor.authorLorincz, Attila-
dc.contributor.authorWheeler, Cosette M.-
dc.contributor.authorGravitt, Patti-
dc.contributor.authorLazcano-Ponce, Eduardo-
dc.contributor.authorTorres-Ibarra, Leticia-
dc.contributor.authorLeón-Maldonado, Leith-
dc.contributor.authorRamírez, Paula-
dc.contributor.authorRivera, Berenice-
dc.contributor.authorHernández, Rubí-
dc.contributor.authorFranco, Eduardo L.-
dc.contributor.authorCuzick, Jack-
dc.contributor.authorMéndez-Hernández, Pablo-
dc.contributor.authorSalmerón, Jorge-
dc.contributor.authorWheeler, Cosette M.-
dc.contributor.authorLazcano, Eduardo-
dc.contributor.authorLeón, Leith-
dc.contributor.authorMéndez, Pablo-
dc.contributor.authorHernández, Mauricio-
dc.contributor.authorWright, Thomas C.-
dc.contributor.authorMoscicki, Anna Barbara-
dc.contributor.authorFlores, Yvonne-
dc.contributor.authorStoler, Mark H.-
dc.contributor.authorCarmona, Enrique-
dc.contributor.authorSchmeler, Kathleen M.-
dc.contributor.authorBishai, David-
dc.contributor.authorHernández, Pilar-
dc.contributor.authorAlvarez, Daniel-
dc.contributor.authorBarrios, Elizabeth-
dc.contributor.authorMendiola, Indira-
dc.contributor.authorGonzález, Vicente-
dc.date.accessioned2023-03-31T05:28:55Z-
dc.date.available2023-03-31T05:28:55Z-
dc.date.issued2016-
dc.identifier.citationBMC Infectious Diseases, 2016, v. 16, n. 1, article no. 461-
dc.identifier.urihttp://hdl.handle.net/10722/327117-
dc.description.abstractBackground: Cervical cancer remains an important cause of cancer mortality for Mexican women. HPV 16/18 typing may help to improve cervical cancer screening. Here we present the prevalence of high-risk human papillomavirus (hrHPV) including HPV16 and HPV18 from the FRIDA (Forwarding Research for Improved Detection and Access) population. Methods: Beginning in 2013, we recruited 30,829 women aged 30-64 in Tlaxcala, Mexico. Cervical samples were collected and tested for 14 hrHPV genotypes (16, 18, 31, 33, 35, 39, 45, 51, 52, 56, 58, 59, 66, and 68). We used logistic regression to estimate odds ratios with 95 % confidence intervals for hrHPV infections according to putative risk factors. Results: Prevalence of infection with any of the 14 hrHPV types was 11.0 %. The age-specific prevalence of all hrHPV formed a U-shaped curve with a higher prevalence for women aged 30-39 and 50-64 than women aged 40-49. Across all age groups, 2.0 % of women were positive for HPV16 and/or HPV18 (HPV16/18), respectively. HPV16/18 prevalence also showed a U-shaped curve with increased prevalence estimates for women aged both 30-39 and 60-64. Both prevalence curves had a significant quadratic age coefficient. Infections with hrHPV were positively associated with an increased number of lifetime sexual partners, a history of sexually transmitted disease, being unmarried, use of hormonal contraception, having a history of smoking and reported condom use in the multivariate model. Conclusions: The FRIDA population has a bimodal distribution of both hrHPV and HPV16/18 positivity with higher prevalences at ages 30-39 and 60-64. These findings will help to evaluate triage algorithms based on HPV genotyping. Trial registration: The trial is registered with ClinicalTrials.gov, number NCT02510027.-
dc.languageeng-
dc.relation.ispartofBMC Infectious Diseases-
dc.subjectHPV16/18-
dc.subjectHuman papillomavirus DNA testing-
dc.subjectMexico-
dc.subjectPrevalence-
dc.subjectRisk factors-
dc.titlePopulation-based prevalence of cervical infection with human papillomavirus genotypes 16 and 18 and other high risk types in Tlaxcala, Mexico-
dc.typeArticle-
dc.description.naturelink_to_subscribed_fulltext-
dc.identifier.doi10.1186/s12879-016-1782-x-
dc.identifier.pmid27585544-
dc.identifier.scopuseid_2-s2.0-84984832903-
dc.identifier.volume16-
dc.identifier.issue1-
dc.identifier.spagearticle no. 461-
dc.identifier.epagearticle no. 461-
dc.identifier.eissn1471-2334-

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