Antibodies Against Chlamydia trachomatis and Ovarian Cancer Risk in Two Independent Populations.


Journal

Journal of the National Cancer Institute
ISSN: 1460-2105
Titre abrégé: J Natl Cancer Inst
Pays: United States
ID NLM: 7503089

Informations de publication

Date de publication:
01 02 2019
Historique:
received: 09 01 2018
revised: 20 03 2018
accepted: 03 04 2018
pubmed: 24 5 2018
medline: 12 3 2020
entrez: 24 5 2018
Statut: ppublish

Résumé

Pelvic inflammatory disease (PID) has been associated with ovarian cancer risk. To clarify the role of Chlamydia trachomatis and other infectious agents in the development of ovarian cancer, we evaluated the association of serologic markers with incident ovarian cancer using a staged approach in two independent populations. Studies included: 1) a case-control study in Poland (244 ovarian cancers/556 control subjects) and 2) a prospective nested case-control study in the PLCO Cancer Screening Trial (160 ovarian cancers/159 control subjects). Associations of serologic marker levels with ovarian cancer risk at diagnostic as well as higher thresholds, identified in Poland and independently evaluated in PLCO, were estimated using multivariable adjusted logistic regression. In the Polish study, antibodies (based on laboratory cut-point) against the chlamydia plasmid-encoded Pgp3 protein (serological gold standard) were associated with increased ovarian cancer risk (adjusted odds ratio [OR] = 1.63, 95% confidence interval [CI] = 1.20 to 2.22); when a positive result was redefined at higher levels, ovarian cancer risk was increased (cut-point 2: OR = 2.00, 95% CI = 1.38 to 2.89; cut-point 3 [max OR]: OR = 2.19, 95% CI = 1.29 to 3.73). In the prospective PLCO study, Pgp3 antibodies were associated with elevated risk at the laboratory cut-point (OR = 1.43, 95% CI = 0.78 to 2.63) and more stringent cut-points (cut-point 2: OR = 2.25, 95% CI = 1.07 to 4.71); cut-point 3: OR = 2.53, 95% CI = 0.63 to 10.08). In both studies, antibodies against other infectious agents measured were not associated with risk. In two independent populations, antibodies against prior/current C. trachomatis (Pgp3) were associated with a doubling in ovarian cancer risk, whereas markers of other infectious agents were unrelated. These findings lend support for an association between PID and ovarian cancer.

Sections du résumé

BACKGROUND
Pelvic inflammatory disease (PID) has been associated with ovarian cancer risk. To clarify the role of Chlamydia trachomatis and other infectious agents in the development of ovarian cancer, we evaluated the association of serologic markers with incident ovarian cancer using a staged approach in two independent populations.
METHODS
Studies included: 1) a case-control study in Poland (244 ovarian cancers/556 control subjects) and 2) a prospective nested case-control study in the PLCO Cancer Screening Trial (160 ovarian cancers/159 control subjects). Associations of serologic marker levels with ovarian cancer risk at diagnostic as well as higher thresholds, identified in Poland and independently evaluated in PLCO, were estimated using multivariable adjusted logistic regression.
RESULTS
In the Polish study, antibodies (based on laboratory cut-point) against the chlamydia plasmid-encoded Pgp3 protein (serological gold standard) were associated with increased ovarian cancer risk (adjusted odds ratio [OR] = 1.63, 95% confidence interval [CI] = 1.20 to 2.22); when a positive result was redefined at higher levels, ovarian cancer risk was increased (cut-point 2: OR = 2.00, 95% CI = 1.38 to 2.89; cut-point 3 [max OR]: OR = 2.19, 95% CI = 1.29 to 3.73). In the prospective PLCO study, Pgp3 antibodies were associated with elevated risk at the laboratory cut-point (OR = 1.43, 95% CI = 0.78 to 2.63) and more stringent cut-points (cut-point 2: OR = 2.25, 95% CI = 1.07 to 4.71); cut-point 3: OR = 2.53, 95% CI = 0.63 to 10.08). In both studies, antibodies against other infectious agents measured were not associated with risk.
CONCLUSIONS
In two independent populations, antibodies against prior/current C. trachomatis (Pgp3) were associated with a doubling in ovarian cancer risk, whereas markers of other infectious agents were unrelated. These findings lend support for an association between PID and ovarian cancer.

Identifiants

pubmed: 29790947
pii: 5001107
doi: 10.1093/jnci/djy084
pmc: PMC6376903
doi:

Substances chimiques

Antibodies, Bacterial 0
Antigens, Bacterial 0
Bacterial Proteins 0
pgp3 protein, Chlamydia 0

Types de publication

Journal Article Research Support, N.I.H., Intramural

Langues

eng

Sous-ensembles de citation

IM

Pagination

129-136

Informations de copyright

Published by Oxford University Press 2018.

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Auteurs

Britton Trabert (B)

Division of Cancer Epidemiology and Genetics, National Cancer Institute, National Institutes of Health, Bethesda, MD.

Tim Waterboer (T)

Infections and Cancer Epidemiology, German Cancer Research Center (DKFZ), Heidelberg, Germany.

Annika Idahl (A)

Department of Clinical Science, Obstetrics and Gynecology, Umeå University, Umeå, Sweden.

Nicole Brenner (N)

Infections and Cancer Epidemiology, German Cancer Research Center (DKFZ), Heidelberg, Germany.

Louise A Brinton (LA)

Division of Cancer Epidemiology and Genetics, National Cancer Institute, National Institutes of Health, Bethesda, MD.

Julia Butt (J)

Infections and Cancer Epidemiology, German Cancer Research Center (DKFZ), Heidelberg, Germany.

Sally B Coburn (SB)

Division of Cancer Epidemiology and Genetics, National Cancer Institute, National Institutes of Health, Bethesda, MD.

Patricia Hartge (P)

Division of Cancer Epidemiology and Genetics, National Cancer Institute, National Institutes of Health, Bethesda, MD.

Katrin Hufnagel (K)

Infections and Cancer Epidemiology, German Cancer Research Center (DKFZ), Heidelberg, Germany.

Federica Inturrisi (F)

Infections and Cancer Epidemiology, German Cancer Research Center (DKFZ), Heidelberg, Germany.

Jolanta Lissowska (J)

Department of Epidemiology and Cancer Prevention, Cancer Center and M. Sklodowska-Curie Institute of Oncology, Warsaw, Poland.

Alexander Mentzer (A)

Wellcome Centre for Human Genetics, Oxford, UK.

Beata Peplonska (B)

Department of Environmental Epidemiology, Nofer Institute of Occupational Medicine, Lodz, Poland.

Mark E Sherman (ME)

Department of Pulmonary Medicine, Mayo Clinic, Jacksonville, FL.

Gillian S Wills (GS)

Jefferiss Research Trust Laboratories, Imperial College London, St Mary's Campus, London, UK.

Sarah C Woodhall (SC)

National Infection Service, Public Health England, London, UK.
Research Department of Infection and Population Health, UCL, London, UK.
Gloucestershire Hospitals NHS Foundation Trust, Cheltenham, UK.

Michael Pawlita (M)

Molecular Diagnostics of Oncogenic Infections Division, German Cancer Research Center (DKFZ), Heidelberg, Germany.

Nicolas Wentzensen (N)

Division of Cancer Epidemiology and Genetics, National Cancer Institute, National Institutes of Health, Bethesda, MD.

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Classifications MeSH