Joint effects of different human papillomaviruses and Chlamydia trachomatis infections on risk of squamous cell carcinoma of the cervix uteri

被引:28
作者
Luostarinen, T
Lehtinen, M
Bjorge, T
Abeler, V
Hakama, M
Hallmans, G
Jellum, E
Koskela, P
Lenner, P
Lie, AK
Paavonen, J
Pukkala, E
Saikku, P
Sigstad, E
Thoresen, S
Youngman, LD
Dillner, J
Hakulinen, T
机构
[1] Finnish Canc Registry, Inst Stat & Epidemiol Canc Res, FIN-00171 Helsinki, Finland
[2] Natl Publ Hlth Inst, Dept Infect Dis Epidemiol, FIN-00300 Helsinki, Finland
[3] Norwegian Radium Hosp, Dept Pathol, NO-0310 Oslo, Norway
[4] Tampere Univ, Sch Publ Hlth, FIN-33014 Tampere, Finland
[5] Umea Univ, Dept Publ Hlth & Clin Med, SE-90185 Umea, Sweden
[6] Norwegian Canc Soc, Janus Comm, NO-0369 Oslo, Norway
[7] Natl Publ Hlth Inst, Dept Microbiol, FIN-90101 Oulu, Finland
[8] Umea Univ, Dept Oncol, SE-90187 Umea, Sweden
[9] Univ Helsinki, Dept Obstet & Gynecol, FIN-00029 Helsinki, Finland
[10] Univ Oulu, Dept Med Microbiol, FIN-90014 Oulu, Finland
[11] Canc Registry Norway, Inst Epidemiol Canc Res, NO-0310 Oslo, Norway
[12] US Dept Hlth & Human Serv, Res Off, Laurel, MD 20708 USA
[13] Lund Univ, MAS Univ Hosp, Dept Med Microbiol, SE-20502 Malmo, Sweden
[14] Univ Helsinki, Dept Publ Hlth, FIN-00014 Helsinki, Finland
基金
芬兰科学院;
关键词
cervix; interaction; neoplasms; papillomaviruses; Chlamydia trachomatis;
D O I
10.1016/j.ejca.2003.11.032
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
This case-control study based in Nordic serum banks evaluated the joint effects of infections with genital human papillomavirus (HPV) types, and Chlamydia trachomatis in the aetiology of cervical squamous cell carcinoma. Through a linkage with the cancer registries, 144 cases were identified and 420 controls matched to them. Exposure to past infections was defined by the presence of specific IgG antibodies. The odds ratio (OR) for the second-order interaction of HPV16, HPV6/11 and C. trachomatis was small (1.0) compared to the expected multiplicative OR, 57, and the additive OR, 11. The interactions were not materially different among HPV16 DNA-positive squamous cell carcinomas. When HPV16 was replaced with HPV18/33 in the analysis of second-order interactions with HPV6/11 and C. trachomatis, there was no evidence of interaction, the joint effect being close to the expected additive OR. Possible explanations for the observed antagonism include misclassification, selection bias or a true biological phenomenon with HPV6/11 and C. trachomatis exposures antagonizing the carcinogenic effects of HPV16. (C) 2004 Elsevier Ltd. All rights reserved.
引用
收藏
页码:1058 / 1065
页数:8
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