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A population-based cohort study of the risk of colorectal and other cancers among users of low-dose aspirin
Using data from the population-based Prescription Database of North Jutland County and the Danish Cancer Registry, we compared cancer incidence among 29 470 individuals prescribed low-dose aspirin at maximum doses of 150 mg with expected incidence based on county-specific cancer rates, during a 9-ye...
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Formato: | Texto |
Lenguaje: | English |
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Nature Publishing Group
2003
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2376336/ https://www.ncbi.nlm.nih.gov/pubmed/12618874 http://dx.doi.org/10.1038/sj.bjc.6600760 |
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author | Friis, S Sørensen, H T McLaughlin, J K Johnsen, S P Blot, W J Olsen, J H |
author_facet | Friis, S Sørensen, H T McLaughlin, J K Johnsen, S P Blot, W J Olsen, J H |
author_sort | Friis, S |
collection | PubMed |
description | Using data from the population-based Prescription Database of North Jutland County and the Danish Cancer Registry, we compared cancer incidence among 29 470 individuals prescribed low-dose aspirin at maximum doses of 150 mg with expected incidence based on county-specific cancer rates, during a 9-year study period. We observed 2381 cancer cases compared with 2187 expected, yielding a standardised incidence ratio (SIR) of 1.09 (95% confidence interval (CI), 1.05–1.13). No apparent risk reductions were found for cancers of the colon (SIR, 0.9; 95% CI, 0.7–1.1) or rectum (SIR, 1.0; 95% CI, 0.8–1.2), or for other site-specific cancers. Increased SIRs were observed for kidney cancer (SIR, 1.4; 95% CI, 1.1–1.7) and brain cancer (SIR, 1.7; 95% CI, 1.3–2.2), although the excess in the latter was confined to the first year of follow-up. Stratification by number of prescriptions and duration of follow-up revealed no apparent trends. The SIR for colorectal cancer was close to unity (SIR, 0.9; 95% CI, 0.6–1.2) among persons with 10 or more prescriptions who were followed for at least 5 years. Our results do not support a major protective effect of low-dose aspirin on the development of colorectal or other cancers. The observed excesses of kidney and brain cancers are not likely to be causally related to the use of low-dose aspirin. |
format | Text |
id | pubmed-2376336 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2003 |
publisher | Nature Publishing Group |
record_format | MEDLINE/PubMed |
spelling | pubmed-23763362009-09-10 A population-based cohort study of the risk of colorectal and other cancers among users of low-dose aspirin Friis, S Sørensen, H T McLaughlin, J K Johnsen, S P Blot, W J Olsen, J H Br J Cancer Epidemiology Using data from the population-based Prescription Database of North Jutland County and the Danish Cancer Registry, we compared cancer incidence among 29 470 individuals prescribed low-dose aspirin at maximum doses of 150 mg with expected incidence based on county-specific cancer rates, during a 9-year study period. We observed 2381 cancer cases compared with 2187 expected, yielding a standardised incidence ratio (SIR) of 1.09 (95% confidence interval (CI), 1.05–1.13). No apparent risk reductions were found for cancers of the colon (SIR, 0.9; 95% CI, 0.7–1.1) or rectum (SIR, 1.0; 95% CI, 0.8–1.2), or for other site-specific cancers. Increased SIRs were observed for kidney cancer (SIR, 1.4; 95% CI, 1.1–1.7) and brain cancer (SIR, 1.7; 95% CI, 1.3–2.2), although the excess in the latter was confined to the first year of follow-up. Stratification by number of prescriptions and duration of follow-up revealed no apparent trends. The SIR for colorectal cancer was close to unity (SIR, 0.9; 95% CI, 0.6–1.2) among persons with 10 or more prescriptions who were followed for at least 5 years. Our results do not support a major protective effect of low-dose aspirin on the development of colorectal or other cancers. The observed excesses of kidney and brain cancers are not likely to be causally related to the use of low-dose aspirin. Nature Publishing Group 2003-03-10 2003-03-04 /pmc/articles/PMC2376336/ /pubmed/12618874 http://dx.doi.org/10.1038/sj.bjc.6600760 Text en Copyright © 2003 Cancer Research UK https://creativecommons.org/licenses/by/4.0/This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made.The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material.If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit https://creativecommons.org/licenses/by/4.0/. |
spellingShingle | Epidemiology Friis, S Sørensen, H T McLaughlin, J K Johnsen, S P Blot, W J Olsen, J H A population-based cohort study of the risk of colorectal and other cancers among users of low-dose aspirin |
title | A population-based cohort study of the risk of colorectal and other cancers among users of low-dose aspirin |
title_full | A population-based cohort study of the risk of colorectal and other cancers among users of low-dose aspirin |
title_fullStr | A population-based cohort study of the risk of colorectal and other cancers among users of low-dose aspirin |
title_full_unstemmed | A population-based cohort study of the risk of colorectal and other cancers among users of low-dose aspirin |
title_short | A population-based cohort study of the risk of colorectal and other cancers among users of low-dose aspirin |
title_sort | population-based cohort study of the risk of colorectal and other cancers among users of low-dose aspirin |
topic | Epidemiology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2376336/ https://www.ncbi.nlm.nih.gov/pubmed/12618874 http://dx.doi.org/10.1038/sj.bjc.6600760 |
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