TY - JOUR
T1 - Trichomonas vaginalis infection and risk of prostate cancer
T2 - associations by disease aggressiveness and race/ethnicity in the PLCO Trial
AU - Marous, Miguelle
AU - Huang, Wen Yi
AU - Rabkin, Charles S.
AU - Hayes, Richard B.
AU - Alderete, John F.
AU - Rosner, Bernard
AU - Grubb, Robert L.
AU - Winter, Anke C.
AU - Sutcliffe, Siobhan
N1 - Funding Information:
The authors thank the National Cancer Institute (NCI) for providing the human material collected by PLCO; Karen Pettit, Sally Larson, and Amy Hutchinson for performing or coordinating serum specimen retrieval and aliquoting; Mike Furr, Craig Williams, and Ryan Noble for managing study data; Calvin Neace and Patrick A. Joyce for performing T. vaginalis antibody testing; Drs. Raphael P. Viscidi, Francis K. Lee, Yun F. Wang, and Denise Whitby and their staff for performing or supervising STI testing in the previous nested case–control study in PLCO; and Dr. Graham A. Colditz for helpful review of our NCI Grant. PLCO is supported by the Intramural Research Program of the Division of Cancer Epidemiology and Genetics, and by contracts from the Division of Cancer Prevention, NCI, National Institutes of Health, the Department of Health and Human Services. This study was funded by NCI Grant R03 CA143949; the Intramural Research Program of the Division of Cancer Epidemiology and Genetics, NCI, the National Institutes of Health, the Department of Health and Human Services; the Barnes-Jewish Hospital Foundation; and the Alvin J. Siteman Cancer Center.
Publisher Copyright:
© 2017, Springer International Publishing AG.
PY - 2017/8/1
Y1 - 2017/8/1
N2 - Purpose: Results from previous sero-epidemiologic studies of Trichomonas vaginalis infection and prostate cancer (PCa) support a positive association between this sexually transmitted infection and aggressive PCa. However, findings from previous studies are not entirely consistent, and only one has investigated the possible relation between T. vaginalis seropositivity and PCa in African-American men who are at highest risk of both infection and PCa. Therefore, we examined this possible relation in the Prostate, Lung, Colorectal, and Ovarian Cancer Screening Trial, including separate analyses for aggressive PCa and African-American men. Methods: We included a sample of participants from a previous nested case–control study of PCa, as well as all additional Caucasian, aggressive, and African-American cases diagnosed since the previous study (total n = 438 Gleason 7 Caucasian cases, 487 more advanced Caucasian cases (≥Gleason 8 or stage III/IV), 201 African-American cases, and 1216 controls). We tested baseline sera for T. vaginalis antibodies. Results: No associations were observed for risk of Gleason 7 (odds ratio (OR) = 0.87, 95% confidence interval (CI) 0.55–1.37) or more advanced (OR = 0.90, 95% CI 0.58–1.38) PCa in Caucasian men, or for risk of any PCa (OR = 1.06, 95% CI 0.67–1.68) in African-American men. Conclusions: Our findings do not support an association between T. vaginalis infection and PCa.
AB - Purpose: Results from previous sero-epidemiologic studies of Trichomonas vaginalis infection and prostate cancer (PCa) support a positive association between this sexually transmitted infection and aggressive PCa. However, findings from previous studies are not entirely consistent, and only one has investigated the possible relation between T. vaginalis seropositivity and PCa in African-American men who are at highest risk of both infection and PCa. Therefore, we examined this possible relation in the Prostate, Lung, Colorectal, and Ovarian Cancer Screening Trial, including separate analyses for aggressive PCa and African-American men. Methods: We included a sample of participants from a previous nested case–control study of PCa, as well as all additional Caucasian, aggressive, and African-American cases diagnosed since the previous study (total n = 438 Gleason 7 Caucasian cases, 487 more advanced Caucasian cases (≥Gleason 8 or stage III/IV), 201 African-American cases, and 1216 controls). We tested baseline sera for T. vaginalis antibodies. Results: No associations were observed for risk of Gleason 7 (odds ratio (OR) = 0.87, 95% confidence interval (CI) 0.55–1.37) or more advanced (OR = 0.90, 95% CI 0.58–1.38) PCa in Caucasian men, or for risk of any PCa (OR = 1.06, 95% CI 0.67–1.68) in African-American men. Conclusions: Our findings do not support an association between T. vaginalis infection and PCa.
KW - Epidemiology
KW - Prostate cancer
KW - Prostate, Lung, Colorectal, and Ovarian Cancer Screening Trial
KW - Sexually transmitted infections
KW - Trichomonas vaginalis
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U2 - 10.1007/s10552-017-0919-6
DO - 10.1007/s10552-017-0919-6
M3 - Article
C2 - 28669054
AN - SCOPUS:85021768810
SN - 0957-5243
VL - 28
SP - 889
EP - 898
JO - Cancer Causes and Control
JF - Cancer Causes and Control
IS - 8
ER -