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Risk of cancer in a large cohort of nonaspirin NSAID users: a population-based study
There is increasing evidence of an inverse association between use of nonsteroidal anti-inflammatory drugs (NSAIDs) and risk of colorectal cancer. However, data regarding other cancer sites are limited. Using data from the population-based North Jutland Prescription Database and the Danish Cancer Re...
Autores principales: | , , , , , , , |
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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/PMC2377131/ https://www.ncbi.nlm.nih.gov/pubmed/12771981 http://dx.doi.org/10.1038/sj.bjc.6600945 |
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author | Sørensen, H T Friis, S Nørgård, B Mellemkjær, L Blot, W J McLaughlin, J K Ekbom, A Baron, J A |
author_facet | Sørensen, H T Friis, S Nørgård, B Mellemkjær, L Blot, W J McLaughlin, J K Ekbom, A Baron, J A |
author_sort | Sørensen, H T |
collection | PubMed |
description | There is increasing evidence of an inverse association between use of nonsteroidal anti-inflammatory drugs (NSAIDs) and risk of colorectal cancer. However, data regarding other cancer sites are limited. Using data from the population-based North Jutland Prescription Database and the Danish Cancer Registry, we compared cancer incidence among 172 057 individuals prescribed nonaspirin NSAIDs with expected incidence (based on county-specific cancer rates) during a 9-year study period. A total of 6081 incident cancer cases were diagnosed among NSAID users vs 5722 expected (standardised incidence ratio (SIR) 1.1, 95% confidence interval (CI)1.0–1.1). The SIRs for colon and rectal cancer among persons who obtained 10 or more prescriptions were 0.7 (95% CI 0.6–0.9) and 0.6 (95% CI 0.4–0.9), respectively. Similarly, reduced risk estimates were found for stomach (SIR 0.7, 95% CI 0.4–1.1) and ovarian cancer (SIR 0.7, 95% CI 0.4–1.0). Standardised incidence ratios for other cancers among those with 10 or more prescriptions tended to be close to 1.0, except for lung, kidney, and prostate cancers with SIRs of 1.3 (95% CI 1.1–1.6), 1.4 (95% CI 0.9–2.1), and 1.6 (95% CI 1.3–2.0), respectively. We found protective associations of NSAIDs against colon, rectal, stomach, and ovarian cancer. Reasons for the increased risk for some cancer sites are not clear. |
format | Text |
id | pubmed-2377131 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2003 |
publisher | Nature Publishing Group |
record_format | MEDLINE/PubMed |
spelling | pubmed-23771312009-09-10 Risk of cancer in a large cohort of nonaspirin NSAID users: a population-based study Sørensen, H T Friis, S Nørgård, B Mellemkjær, L Blot, W J McLaughlin, J K Ekbom, A Baron, J A Br J Cancer Epidemiology There is increasing evidence of an inverse association between use of nonsteroidal anti-inflammatory drugs (NSAIDs) and risk of colorectal cancer. However, data regarding other cancer sites are limited. Using data from the population-based North Jutland Prescription Database and the Danish Cancer Registry, we compared cancer incidence among 172 057 individuals prescribed nonaspirin NSAIDs with expected incidence (based on county-specific cancer rates) during a 9-year study period. A total of 6081 incident cancer cases were diagnosed among NSAID users vs 5722 expected (standardised incidence ratio (SIR) 1.1, 95% confidence interval (CI)1.0–1.1). The SIRs for colon and rectal cancer among persons who obtained 10 or more prescriptions were 0.7 (95% CI 0.6–0.9) and 0.6 (95% CI 0.4–0.9), respectively. Similarly, reduced risk estimates were found for stomach (SIR 0.7, 95% CI 0.4–1.1) and ovarian cancer (SIR 0.7, 95% CI 0.4–1.0). Standardised incidence ratios for other cancers among those with 10 or more prescriptions tended to be close to 1.0, except for lung, kidney, and prostate cancers with SIRs of 1.3 (95% CI 1.1–1.6), 1.4 (95% CI 0.9–2.1), and 1.6 (95% CI 1.3–2.0), respectively. We found protective associations of NSAIDs against colon, rectal, stomach, and ovarian cancer. Reasons for the increased risk for some cancer sites are not clear. Nature Publishing Group 2003-06-02 2003-05-27 /pmc/articles/PMC2377131/ /pubmed/12771981 http://dx.doi.org/10.1038/sj.bjc.6600945 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 Sørensen, H T Friis, S Nørgård, B Mellemkjær, L Blot, W J McLaughlin, J K Ekbom, A Baron, J A Risk of cancer in a large cohort of nonaspirin NSAID users: a population-based study |
title | Risk of cancer in a large cohort of nonaspirin NSAID users: a population-based study |
title_full | Risk of cancer in a large cohort of nonaspirin NSAID users: a population-based study |
title_fullStr | Risk of cancer in a large cohort of nonaspirin NSAID users: a population-based study |
title_full_unstemmed | Risk of cancer in a large cohort of nonaspirin NSAID users: a population-based study |
title_short | Risk of cancer in a large cohort of nonaspirin NSAID users: a population-based study |
title_sort | risk of cancer in a large cohort of nonaspirin nsaid users: a population-based study |
topic | Epidemiology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2377131/ https://www.ncbi.nlm.nih.gov/pubmed/12771981 http://dx.doi.org/10.1038/sj.bjc.6600945 |
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