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Alcohol consumption and PSA-detected prostate cancer risk—A case-control nested in the ProtecT study
Alcohol is an established carcinogen but not an established risk factor for prostate cancer, despite some recent prospective studies suggesting increased risk among heavy drinkers. The aim of this study was to investigate the role of alcohol on prostate-specific antigen (PSA) levels and prostate can...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Wiley Subscription Services, Inc., A Wiley Company
2013
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3786564/ https://www.ncbi.nlm.nih.gov/pubmed/23024014 http://dx.doi.org/10.1002/ijc.27877 |
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author | Zuccolo, Luisa Lewis, Sarah J Donovan, Jenny L Hamdy, Freddie C Neal, David E Smith, George Davey |
author_facet | Zuccolo, Luisa Lewis, Sarah J Donovan, Jenny L Hamdy, Freddie C Neal, David E Smith, George Davey |
author_sort | Zuccolo, Luisa |
collection | PubMed |
description | Alcohol is an established carcinogen but not an established risk factor for prostate cancer, despite some recent prospective studies suggesting increased risk among heavy drinkers. The aim of this study was to investigate the role of alcohol on prostate-specific antigen (PSA) levels and prostate cancer risk. Two thousand four hundred PSA detected prostate cancer cases and 12,700 controls matched on age and general practice were identified through a case-control study nested in the PSA-testing phase of a large UK-based randomized controlled trial for prostate cancer treatment (ProtecT). Linear and multinomial logistic regression models were used to estimate ratios of geometric means (RGMs) of PSA and relative risk ratios (RRRs) of prostate cancer by stage and grade, with 95% confidence intervals (CIs), associated with weekly alcohol intake and drinking patterns. We found evidence of lower PSA (RGM 0.98, 95% CI: 0.98–0.99) and decreased risk of low Gleason-grade (RRR 0.96; 95%CI 0.93–0.99) but increased risk of high-grade prostate cancer (RRR 1.04; 95%CI 0.99–1.08; p(difference)=0.004) per 10 units/week increase in alcohol consumption, not explained by current BMI, blood pressure, comorbidities, or reverse causation. This is the first large population-based study to find evidence of lower PSA levels for increasing alcohol consumption, with potential public health implications for the detection of prostate cancer. Our results also support a modestly higher risk of high-grade disease for heavy drinkers, but require independent replication to establish the nature of the association of alcohol with low-grade disease, preferably in cohorts with a heterogeneous case-mix. WHAT'S NEW? Alcohol is not an established risk factor for prostate cancer; however, the current work suggests that heavy drinking could cause a small increase in risk of the more aggressive forms. If the results are confirmed to be causal, prostate cancer risk will be added to the many long-term health risks of heavy drinking, and public health strategies will then also reduce high-risk, poorer prognosis prostate cancer. The authors also found that heavy drinkers have lower PSA levels, suggesting that heavy alcohol consumption could be used as a marker to identify men in whom some cancers might be missed. |
format | Online Article Text |
id | pubmed-3786564 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2013 |
publisher | Wiley Subscription Services, Inc., A Wiley Company |
record_format | MEDLINE/PubMed |
spelling | pubmed-37865642013-10-04 Alcohol consumption and PSA-detected prostate cancer risk—A case-control nested in the ProtecT study Zuccolo, Luisa Lewis, Sarah J Donovan, Jenny L Hamdy, Freddie C Neal, David E Smith, George Davey Int J Cancer Epidemiology Alcohol is an established carcinogen but not an established risk factor for prostate cancer, despite some recent prospective studies suggesting increased risk among heavy drinkers. The aim of this study was to investigate the role of alcohol on prostate-specific antigen (PSA) levels and prostate cancer risk. Two thousand four hundred PSA detected prostate cancer cases and 12,700 controls matched on age and general practice were identified through a case-control study nested in the PSA-testing phase of a large UK-based randomized controlled trial for prostate cancer treatment (ProtecT). Linear and multinomial logistic regression models were used to estimate ratios of geometric means (RGMs) of PSA and relative risk ratios (RRRs) of prostate cancer by stage and grade, with 95% confidence intervals (CIs), associated with weekly alcohol intake and drinking patterns. We found evidence of lower PSA (RGM 0.98, 95% CI: 0.98–0.99) and decreased risk of low Gleason-grade (RRR 0.96; 95%CI 0.93–0.99) but increased risk of high-grade prostate cancer (RRR 1.04; 95%CI 0.99–1.08; p(difference)=0.004) per 10 units/week increase in alcohol consumption, not explained by current BMI, blood pressure, comorbidities, or reverse causation. This is the first large population-based study to find evidence of lower PSA levels for increasing alcohol consumption, with potential public health implications for the detection of prostate cancer. Our results also support a modestly higher risk of high-grade disease for heavy drinkers, but require independent replication to establish the nature of the association of alcohol with low-grade disease, preferably in cohorts with a heterogeneous case-mix. WHAT'S NEW? Alcohol is not an established risk factor for prostate cancer; however, the current work suggests that heavy drinking could cause a small increase in risk of the more aggressive forms. If the results are confirmed to be causal, prostate cancer risk will be added to the many long-term health risks of heavy drinking, and public health strategies will then also reduce high-risk, poorer prognosis prostate cancer. The authors also found that heavy drinkers have lower PSA levels, suggesting that heavy alcohol consumption could be used as a marker to identify men in whom some cancers might be missed. Wiley Subscription Services, Inc., A Wiley Company 2013-05-01 2012-10-25 /pmc/articles/PMC3786564/ /pubmed/23024014 http://dx.doi.org/10.1002/ijc.27877 Text en Copyright © 2012 UICC http://creativecommons.org/licenses/by/2.5/ Re-use of this article is permitted in accordance with the Creative Commons Deed, Attribution 2.5, which does not permit commercial exploitation. |
spellingShingle | Epidemiology Zuccolo, Luisa Lewis, Sarah J Donovan, Jenny L Hamdy, Freddie C Neal, David E Smith, George Davey Alcohol consumption and PSA-detected prostate cancer risk—A case-control nested in the ProtecT study |
title | Alcohol consumption and PSA-detected prostate cancer risk—A case-control nested in the ProtecT study |
title_full | Alcohol consumption and PSA-detected prostate cancer risk—A case-control nested in the ProtecT study |
title_fullStr | Alcohol consumption and PSA-detected prostate cancer risk—A case-control nested in the ProtecT study |
title_full_unstemmed | Alcohol consumption and PSA-detected prostate cancer risk—A case-control nested in the ProtecT study |
title_short | Alcohol consumption and PSA-detected prostate cancer risk—A case-control nested in the ProtecT study |
title_sort | alcohol consumption and psa-detected prostate cancer risk—a case-control nested in the protect study |
topic | Epidemiology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3786564/ https://www.ncbi.nlm.nih.gov/pubmed/23024014 http://dx.doi.org/10.1002/ijc.27877 |
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