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Urinary estrogen metabolites and prostate cancer : a case-control study and meta-analysis
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Barba, Maddalena, Yang, Li, Ph.D., Schünemann, Holger J., Sperati, Francesca, Grioni, Sara, Stranges, Saverio, Westerlind, Kim C., Blandino, Giovanni, Gallucci, M. (Michele), Lauria, Rossella, Malorni, Luca and Muti, Paola (2009) Urinary estrogen metabolites and prostate cancer : a case-control study and meta-analysis. Journal of Experimental and Clinical Cancer Research, Vol.28 (Article 135). doi:10.1186/1756-9966-28-135 ISSN 1756-9966.
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Official URL: http://dx.doi.org/10.1186/1756-9966-28-135
Abstract
Objective: To investigate prostate cancer (Pca) risk in relation to estrogen metabolism, expressed as urinary 2-hydroxyestrone (2-OHE1), 16α-hydroxyestrone (16α-OHE1) and 2-OHE1 to 16α-OHE1 ratio.
Methods: We conducted a case-control study within the Western New York Health Cohort Study (WNYHCS) from 1996 to 2001. From January 2003 through September 2004, we completed the re-call and follow-up of 1092 cohort participants. Cases (n = 26) and controls (n = 110) were matched on age, race and recruitment period according to a 1:4 ratio. We used the unconditional logistic regression to compute crude and adjusted odds ratios (OR) and 95% confident interval (CI) of Pca in relation to 2-OHE1, 16αOHE1 and 2-OHE1 to 16α-OHE1 by tertiles of urine concentrations (stored in a biorepository for an average of 4 years). We identified age, race, education and body mass index as covariates. We also conducted a systematic review of the literature which revealed no additional studies, but we pooled the results from this study with those from a previously conducted case-control study using the DerSimonian-Laird random effects method.
Results: We observed a non-significant risk reduction in the highest tertile of 2-OHE1 (OR 0.72, 95% CI 0.25-2.10). Conversely, the odds in the highest tertile of 16α-OHE1 showed a non-significant risk increase (OR 1.76 95% CI 0.62-4.98). There was a suggestion of reduced Pca risk for men in the highest tertile of 2-OHE1 to 16α-OHE1 ratio (OR 0.56, 95% CI 0.19-1.68). The pooled estimates confirmed the association between an increased Pca risk and higher urinary levels of 16α-OHE1 (third vs. first tertile: OR 1.82, 95% CI 1.09-3.05) and the protective effect of a higher 2-OHE 1 to 16α-OHE1 ratio (third vs. first tertile: OR 0.53, 95% CI 0.31-0.90).
Conclusion: Our study and the pooled results provide evidence for a differential role of the estrogen hydroxylation pathway in Pca development and encourage further study.
Item Type: | Journal Article | ||||
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Subjects: | R Medicine > RC Internal medicine > RC0254 Neoplasms. Tumors. Oncology (including Cancer) Q Science > QP Physiology |
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Divisions: | Faculty of Science, Engineering and Medicine > Medicine > Warwick Medical School > Health Sciences Faculty of Science, Engineering and Medicine > Medicine > Warwick Medical School |
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Library of Congress Subject Headings (LCSH): | Prostate -- Cancer -- Research, Cancer -- Endocrine aspects, Estrogen -- Physiological effect, Hydroxylation | ||||
Journal or Publication Title: | Journal of Experimental and Clinical Cancer Research | ||||
Publisher: | BioMed Central Ltd. | ||||
ISSN: | 1756-9966 | ||||
Official Date: | 8 October 2009 | ||||
Dates: |
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Volume: | Vol.28 | ||||
Number: | Article 135 | ||||
DOI: | 10.1186/1756-9966-28-135 | ||||
Status: | Peer Reviewed | ||||
Publication Status: | Published | ||||
Access rights to Published version: | Open Access (Creative Commons) |
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