Cargando…
Chlamydia trachomatis infection and risk of cervical intraepithelial neoplasia
OBJECTIVES: High-risk human papillomavirus (hrHPV) is the primary cause of cervical cancer. As Chlamydia trachomatis is also linked to cervical cancer, its role as a potential co-factor in the development of cervical intraepithelial neoplasia (CIN) grade 2 or higher was examined. METHODS: The placeb...
Autores principales: | , , , , , , , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BMJ Group
2011
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3252607/ https://www.ncbi.nlm.nih.gov/pubmed/21471141 http://dx.doi.org/10.1136/sti.2010.044354 |
_version_ | 1782220649231548416 |
---|---|
author | Lehtinen, Matti Ault, Kevin A Lyytikainen, Erika Dillner, Joakim Garland, Suzanne M Ferris, Daron G Koutsky, Laura A Sings, Heather L Lu, Shuang Haupt, Richard M Paavonen, Jorma |
author_facet | Lehtinen, Matti Ault, Kevin A Lyytikainen, Erika Dillner, Joakim Garland, Suzanne M Ferris, Daron G Koutsky, Laura A Sings, Heather L Lu, Shuang Haupt, Richard M Paavonen, Jorma |
author_sort | Lehtinen, Matti |
collection | PubMed |
description | OBJECTIVES: High-risk human papillomavirus (hrHPV) is the primary cause of cervical cancer. As Chlamydia trachomatis is also linked to cervical cancer, its role as a potential co-factor in the development of cervical intraepithelial neoplasia (CIN) grade 2 or higher was examined. METHODS: The placebo arms of two large, multinational, clinical trials of an HPV6/11/16/18 vaccine were combined. A total of 8441 healthy women aged 15–26 years underwent cervicovaginal cytology (Papanicolaou (Pap) testing) sampling and C trachomatis testing at day 1 and every 12 months thereafter for up to 4 years. Protocol-specified guidelines were used to triage participants with Pap abnormalities to colposcopy and definitive therapy. The main outcome measured was CIN. RESULTS: At baseline, 2629 (31.1%) tested positive for hrHPV DNA and 354 (4.2%) tested positive for C trachomatis. Among those with HPV16/18 infection (n=965; 11.4%) or without HPV16/18 infection (n=7382, 87.5%), the hazard ratios (HRs) associated with development of any CIN grade 2 according to baseline C trachomatis status were 1.82 (95% CI: 1.06 to 3.14) and 1.74 (95% CI 1.05 to 2.90), respectively. The results were comparable when only the 12 most common hrHPV infections were considered, but the excess risk disappeared when the outcome was expanded to include CIN grade 3 or worse. CONCLUSION: Further studies based on larger cohorts with longitudinal follow-up in relation to the C trachomatis acquisition and a thorough evaluation of temporal relationships of infections with hrHPV types, C trachomatis and cervical neoplasia are needed to demonstrate whether and how in some situations C trachomatis sets the stage for cervical carcinogenesis. TRIAL REGISTRATION: NCT00092521 and NCT00092534. |
format | Online Article Text |
id | pubmed-3252607 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2011 |
publisher | BMJ Group |
record_format | MEDLINE/PubMed |
spelling | pubmed-32526072012-01-17 Chlamydia trachomatis infection and risk of cervical intraepithelial neoplasia Lehtinen, Matti Ault, Kevin A Lyytikainen, Erika Dillner, Joakim Garland, Suzanne M Ferris, Daron G Koutsky, Laura A Sings, Heather L Lu, Shuang Haupt, Richard M Paavonen, Jorma Sex Transm Infect Epidemiology OBJECTIVES: High-risk human papillomavirus (hrHPV) is the primary cause of cervical cancer. As Chlamydia trachomatis is also linked to cervical cancer, its role as a potential co-factor in the development of cervical intraepithelial neoplasia (CIN) grade 2 or higher was examined. METHODS: The placebo arms of two large, multinational, clinical trials of an HPV6/11/16/18 vaccine were combined. A total of 8441 healthy women aged 15–26 years underwent cervicovaginal cytology (Papanicolaou (Pap) testing) sampling and C trachomatis testing at day 1 and every 12 months thereafter for up to 4 years. Protocol-specified guidelines were used to triage participants with Pap abnormalities to colposcopy and definitive therapy. The main outcome measured was CIN. RESULTS: At baseline, 2629 (31.1%) tested positive for hrHPV DNA and 354 (4.2%) tested positive for C trachomatis. Among those with HPV16/18 infection (n=965; 11.4%) or without HPV16/18 infection (n=7382, 87.5%), the hazard ratios (HRs) associated with development of any CIN grade 2 according to baseline C trachomatis status were 1.82 (95% CI: 1.06 to 3.14) and 1.74 (95% CI 1.05 to 2.90), respectively. The results were comparable when only the 12 most common hrHPV infections were considered, but the excess risk disappeared when the outcome was expanded to include CIN grade 3 or worse. CONCLUSION: Further studies based on larger cohorts with longitudinal follow-up in relation to the C trachomatis acquisition and a thorough evaluation of temporal relationships of infections with hrHPV types, C trachomatis and cervical neoplasia are needed to demonstrate whether and how in some situations C trachomatis sets the stage for cervical carcinogenesis. TRIAL REGISTRATION: NCT00092521 and NCT00092534. BMJ Group 2011-04-06 2011-08 /pmc/articles/PMC3252607/ /pubmed/21471141 http://dx.doi.org/10.1136/sti.2010.044354 Text en © 2011, Published by the BMJ Publishing Group Limited. For permission to use (where not already granted under a licence) please go to http://group.bmj.com/group/rights-licensing/permissions. This is an open-access article distributed under the terms of the Creative Commons Attribution Non-commercial License, which permits use, distribution, and reproduction in any medium, provided the original work is properly cited, the use is non commercial and is otherwise in compliance with the license. See: http://creativecommons.org/licenses/by-nc/2.0/ and http://creativecommons.org/licenses/by-nc/2.0/legalcode. |
spellingShingle | Epidemiology Lehtinen, Matti Ault, Kevin A Lyytikainen, Erika Dillner, Joakim Garland, Suzanne M Ferris, Daron G Koutsky, Laura A Sings, Heather L Lu, Shuang Haupt, Richard M Paavonen, Jorma Chlamydia trachomatis infection and risk of cervical intraepithelial neoplasia |
title | Chlamydia trachomatis infection and risk of cervical intraepithelial neoplasia |
title_full | Chlamydia trachomatis infection and risk of cervical intraepithelial neoplasia |
title_fullStr | Chlamydia trachomatis infection and risk of cervical intraepithelial neoplasia |
title_full_unstemmed | Chlamydia trachomatis infection and risk of cervical intraepithelial neoplasia |
title_short | Chlamydia trachomatis infection and risk of cervical intraepithelial neoplasia |
title_sort | chlamydia trachomatis infection and risk of cervical intraepithelial neoplasia |
topic | Epidemiology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3252607/ https://www.ncbi.nlm.nih.gov/pubmed/21471141 http://dx.doi.org/10.1136/sti.2010.044354 |
work_keys_str_mv | AT lehtinenmatti chlamydiatrachomatisinfectionandriskofcervicalintraepithelialneoplasia AT aultkevina chlamydiatrachomatisinfectionandriskofcervicalintraepithelialneoplasia AT lyytikainenerika chlamydiatrachomatisinfectionandriskofcervicalintraepithelialneoplasia AT dillnerjoakim chlamydiatrachomatisinfectionandriskofcervicalintraepithelialneoplasia AT garlandsuzannem chlamydiatrachomatisinfectionandriskofcervicalintraepithelialneoplasia AT ferrisdarong chlamydiatrachomatisinfectionandriskofcervicalintraepithelialneoplasia AT koutskylauraa chlamydiatrachomatisinfectionandriskofcervicalintraepithelialneoplasia AT singsheatherl chlamydiatrachomatisinfectionandriskofcervicalintraepithelialneoplasia AT lushuang chlamydiatrachomatisinfectionandriskofcervicalintraepithelialneoplasia AT hauptrichardm chlamydiatrachomatisinfectionandriskofcervicalintraepithelialneoplasia AT paavonenjorma chlamydiatrachomatisinfectionandriskofcervicalintraepithelialneoplasia AT chlamydiatrachomatisinfectionandriskofcervicalintraepithelialneoplasia |