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Risk of pancreatic cancer by alcohol dose, duration, and pattern of consumption, including binge drinking: a population-based study
Alcohol consumption is postulated to be a risk factor for pancreatic cancer (PCA), but clarification of degree of risk related to consumption characteristics is lacking. We examined the association between alcohol consumption and PCA in a population-based case–control study (532 cases, 1,701 control...
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Formato: | Texto |
Lenguaje: | English |
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Springer Netherlands
2010
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2883092/ https://www.ncbi.nlm.nih.gov/pubmed/20349126 http://dx.doi.org/10.1007/s10552-010-9533-6 |
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author | Gupta, Samir Wang, Furong Holly, Elizabeth A. Bracci, Paige M. |
author_facet | Gupta, Samir Wang, Furong Holly, Elizabeth A. Bracci, Paige M. |
author_sort | Gupta, Samir |
collection | PubMed |
description | Alcohol consumption is postulated to be a risk factor for pancreatic cancer (PCA), but clarification of degree of risk related to consumption characteristics is lacking. We examined the association between alcohol consumption and PCA in a population-based case–control study (532 cases, 1,701 controls) in the San Francisco Bay Area. Population-based controls were frequency-matched by sex, age within 5-year categories and county of residence to cases identified by the cancer registry’s rapid case ascertainment. Detailed alcohol consumption data, including binge drinking (≥5 drinks/day), were collected during in-person interviews. Odds ratios (OR) and 95% confidence intervals (95% CI) were computed using adjusted unconditional logistic regression. Depending on dose, duration, and pattern of drinking, ORs were increased 1.5- to 6-fold among men but not women. In men, ORs increased with increasing overall alcohol consumption (22–35 drinks/week OR = 2.2, 95% CI = 1.1–4.0; ≥35 drinks/week OR = 2.6, 95% CI = 1.3–5.1, p-trend = 0.04). Most notable were effects with a history of binge drinking (OR = 3.5, 95% CI = 1.6–7.5) including increased number of drinks per day (p-trend = 0.002), and increased years of binge drinking (p-trend = 0.0006). In fully adjusted models that included smoking and other confounders, ORs for binge drinking in men were somewhat higher than in age-adjusted models. Results from our detailed analyses provide support for heavy alcohol consumption (including binge drinking) as a risk factor for PCA in men. |
format | Text |
id | pubmed-2883092 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2010 |
publisher | Springer Netherlands |
record_format | MEDLINE/PubMed |
spelling | pubmed-28830922010-06-21 Risk of pancreatic cancer by alcohol dose, duration, and pattern of consumption, including binge drinking: a population-based study Gupta, Samir Wang, Furong Holly, Elizabeth A. Bracci, Paige M. Cancer Causes Control Original Paper Alcohol consumption is postulated to be a risk factor for pancreatic cancer (PCA), but clarification of degree of risk related to consumption characteristics is lacking. We examined the association between alcohol consumption and PCA in a population-based case–control study (532 cases, 1,701 controls) in the San Francisco Bay Area. Population-based controls were frequency-matched by sex, age within 5-year categories and county of residence to cases identified by the cancer registry’s rapid case ascertainment. Detailed alcohol consumption data, including binge drinking (≥5 drinks/day), were collected during in-person interviews. Odds ratios (OR) and 95% confidence intervals (95% CI) were computed using adjusted unconditional logistic regression. Depending on dose, duration, and pattern of drinking, ORs were increased 1.5- to 6-fold among men but not women. In men, ORs increased with increasing overall alcohol consumption (22–35 drinks/week OR = 2.2, 95% CI = 1.1–4.0; ≥35 drinks/week OR = 2.6, 95% CI = 1.3–5.1, p-trend = 0.04). Most notable were effects with a history of binge drinking (OR = 3.5, 95% CI = 1.6–7.5) including increased number of drinks per day (p-trend = 0.002), and increased years of binge drinking (p-trend = 0.0006). In fully adjusted models that included smoking and other confounders, ORs for binge drinking in men were somewhat higher than in age-adjusted models. Results from our detailed analyses provide support for heavy alcohol consumption (including binge drinking) as a risk factor for PCA in men. Springer Netherlands 2010-03-27 2010 /pmc/articles/PMC2883092/ /pubmed/20349126 http://dx.doi.org/10.1007/s10552-010-9533-6 Text en © The Author(s) 2010 https://creativecommons.org/licenses/by-nc/4.0/ This article is distributed under the terms of the Creative Commons Attribution Noncommercial License which permits any noncommercial use, distribution, and reproduction in any medium, provided the original author(s) and source are credited. |
spellingShingle | Original Paper Gupta, Samir Wang, Furong Holly, Elizabeth A. Bracci, Paige M. Risk of pancreatic cancer by alcohol dose, duration, and pattern of consumption, including binge drinking: a population-based study |
title | Risk of pancreatic cancer by alcohol dose, duration, and pattern of consumption, including binge drinking: a population-based study |
title_full | Risk of pancreatic cancer by alcohol dose, duration, and pattern of consumption, including binge drinking: a population-based study |
title_fullStr | Risk of pancreatic cancer by alcohol dose, duration, and pattern of consumption, including binge drinking: a population-based study |
title_full_unstemmed | Risk of pancreatic cancer by alcohol dose, duration, and pattern of consumption, including binge drinking: a population-based study |
title_short | Risk of pancreatic cancer by alcohol dose, duration, and pattern of consumption, including binge drinking: a population-based study |
title_sort | risk of pancreatic cancer by alcohol dose, duration, and pattern of consumption, including binge drinking: a population-based study |
topic | Original Paper |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2883092/ https://www.ncbi.nlm.nih.gov/pubmed/20349126 http://dx.doi.org/10.1007/s10552-010-9533-6 |
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