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Oral contraceptive use is associated with prostate cancer: an ecological study

BACKGROUND: Several recent studies have suggested that oestrogen exposure may increase the risk of prostate cancer (PCa). OBJECTIVES: To examine associations between PCa incidence and mortality and population-based use of oral contraceptives (OCs). It was hypothesised that OC by-products may cause e...

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Autores principales: Margel, David, Fleshner, Neil E
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BMJ Group 2011
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3221291/
https://www.ncbi.nlm.nih.gov/pubmed/22102643
http://dx.doi.org/10.1136/bmjopen-2011-000311
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author Margel, David
Fleshner, Neil E
author_facet Margel, David
Fleshner, Neil E
author_sort Margel, David
collection PubMed
description BACKGROUND: Several recent studies have suggested that oestrogen exposure may increase the risk of prostate cancer (PCa). OBJECTIVES: To examine associations between PCa incidence and mortality and population-based use of oral contraceptives (OCs). It was hypothesised that OC by-products may cause environmental contamination, leading to an increased low level oestrogen exposure and therefore higher PCa incidence and mortality. METHODS: The hypothesis was tested in an ecological study. Data from the International Agency for Research on Cancer were used to retrieve age-standardised rates of prostate cancer in 2007, and data from the United Nations World Contraceptive Use 2007 report were used to retrieve data on contraceptive use. A Pearson correlation and multivariable linear regression were used to associate the percentage of women using OCs, intrauterine devices, condoms or vaginal barriers to the age standardised prostate cancer incidence and mortality. These analyses were performed by individual nations and by continents worldwide. RESULTS: OC use was significantly associated with prostate cancer incidence and mortality in the individual nations worldwide (r=0.61 and r=0.53, respectively; p<0.05 for all). PCa incidence was also associated with OC use in Europe (r=0.545, p<0.05) and by continent (r=0.522, p<0.05). All other forms of contraceptives (ie, intra-uterine devices, condoms or vaginal barriers) were not correlated with prostate cancer incidence or mortality. On multivariable analysis the correlation with OC was independent of a nation's wealth. CONCLUSION: A significant association between OCs and PCa has been shown. It is hypothesised that the OC effect may be mediated through environmental oestrogen levels; this novel concept is worth further investigation.
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spelling pubmed-32212912011-12-01 Oral contraceptive use is associated with prostate cancer: an ecological study Margel, David Fleshner, Neil E BMJ Open Occupational & Environmental Medicine BACKGROUND: Several recent studies have suggested that oestrogen exposure may increase the risk of prostate cancer (PCa). OBJECTIVES: To examine associations between PCa incidence and mortality and population-based use of oral contraceptives (OCs). It was hypothesised that OC by-products may cause environmental contamination, leading to an increased low level oestrogen exposure and therefore higher PCa incidence and mortality. METHODS: The hypothesis was tested in an ecological study. Data from the International Agency for Research on Cancer were used to retrieve age-standardised rates of prostate cancer in 2007, and data from the United Nations World Contraceptive Use 2007 report were used to retrieve data on contraceptive use. A Pearson correlation and multivariable linear regression were used to associate the percentage of women using OCs, intrauterine devices, condoms or vaginal barriers to the age standardised prostate cancer incidence and mortality. These analyses were performed by individual nations and by continents worldwide. RESULTS: OC use was significantly associated with prostate cancer incidence and mortality in the individual nations worldwide (r=0.61 and r=0.53, respectively; p<0.05 for all). PCa incidence was also associated with OC use in Europe (r=0.545, p<0.05) and by continent (r=0.522, p<0.05). All other forms of contraceptives (ie, intra-uterine devices, condoms or vaginal barriers) were not correlated with prostate cancer incidence or mortality. On multivariable analysis the correlation with OC was independent of a nation's wealth. CONCLUSION: A significant association between OCs and PCa has been shown. It is hypothesised that the OC effect may be mediated through environmental oestrogen levels; this novel concept is worth further investigation. BMJ Group 2011-11-14 /pmc/articles/PMC3221291/ /pubmed/22102643 http://dx.doi.org/10.1136/bmjopen-2011-000311 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 Occupational & Environmental Medicine
Margel, David
Fleshner, Neil E
Oral contraceptive use is associated with prostate cancer: an ecological study
title Oral contraceptive use is associated with prostate cancer: an ecological study
title_full Oral contraceptive use is associated with prostate cancer: an ecological study
title_fullStr Oral contraceptive use is associated with prostate cancer: an ecological study
title_full_unstemmed Oral contraceptive use is associated with prostate cancer: an ecological study
title_short Oral contraceptive use is associated with prostate cancer: an ecological study
title_sort oral contraceptive use is associated with prostate cancer: an ecological study
topic Occupational & Environmental Medicine
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3221291/
https://www.ncbi.nlm.nih.gov/pubmed/22102643
http://dx.doi.org/10.1136/bmjopen-2011-000311
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