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Disentangling the Association between Statins, Cholesterol, and Colorectal Cancer: A Nested Case-Control Study
BACKGROUND: Several prior studies have found an association between statin use and reduced risk of colorectal cancer. We hypothesized that these findings may be due to systematic bias and examined the independent association of colorectal cancer risk with statin use, serum cholesterol, and change in...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Public Library of Science
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4846028/ https://www.ncbi.nlm.nih.gov/pubmed/27116322 http://dx.doi.org/10.1371/journal.pmed.1002007 |
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author | Mamtani, Ronac Lewis, James D. Scott, Frank I. Ahmad, Tariq Goldberg, David S. Datta, Jashodeep Yang, Yu-Xiao Boursi, Ben |
author_facet | Mamtani, Ronac Lewis, James D. Scott, Frank I. Ahmad, Tariq Goldberg, David S. Datta, Jashodeep Yang, Yu-Xiao Boursi, Ben |
author_sort | Mamtani, Ronac |
collection | PubMed |
description | BACKGROUND: Several prior studies have found an association between statin use and reduced risk of colorectal cancer. We hypothesized that these findings may be due to systematic bias and examined the independent association of colorectal cancer risk with statin use, serum cholesterol, and change in cholesterol concentration. METHODS AND FINDINGS: 22,163 colorectal cancer cases and 86,538 matched controls between 1995 and 2013 were identified within The Health Improvement Network (THIN) a population-representative database. Conditional logistic regression models estimated colorectal cancer risk with statin use, serum total cholesterol (mmol/L), and change in total cholesterol level. We confirmed a decreased risk of colorectal cancer with statin use (long-term: odds ratio [OR], 0.95; 95% confidence interval [CI], 0.91–0.99; short-term: OR, 0.92; 95% CI, 0.85–0.99). However, to assess whether the observed association may result from indication bias, a subgroup analysis was conducted among patients prescribed a statin. In this subgroup (n = 5,102 cases, n = 19,032 controls), 3.1% of case subjects and 3.1% of controls discontinued therapy. The risk of colorectal cancer was not significantly different among those who continued statin therapy and those who discontinued (OR, 0.98; 95% CI, 0.79–1.22). Increased serum cholesterol was independently associated with decreased risk of colorectal cancer (OR, 0.89 per mmol/L increase; 95% CI, 0.87–0.91); the association was only present if serum cholesterol was measured near the cancer diagnosis (<6 mo: OR, 0.76; 95% CI, 0.47–0.61; >24 mo: OR, 0.98; 95% CI, 0.93–1.03). Decreases in serum total cholesterol >1 mmol/L ≥1 year prior to cancer diagnosis were associated with subsequent colorectal cancer (statin users: OR, 1.25; 95 CI%, 1.03–1.53; nonusers: OR, 2.36; 95 CI%, 1.78–3.12). As an observational study, limitations included incomplete data and residual confounding. CONCLUSIONS: Although the risk of colorectal cancer was lower in statin users versus nonusers, no difference was observed among those who continued versus discontinued statin therapy, suggesting the potential for indication bias. The association between decreased serum cholesterol and colorectal cancer risk suggests a cholesterol-lowering effect of undiagnosed malignancy. Clinical judgment should be used when considering causes of cholesterol reduction in patients, including those on statin therapy. |
format | Online Article Text |
id | pubmed-4846028 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | Public Library of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-48460282016-05-05 Disentangling the Association between Statins, Cholesterol, and Colorectal Cancer: A Nested Case-Control Study Mamtani, Ronac Lewis, James D. Scott, Frank I. Ahmad, Tariq Goldberg, David S. Datta, Jashodeep Yang, Yu-Xiao Boursi, Ben PLoS Med Research Article BACKGROUND: Several prior studies have found an association between statin use and reduced risk of colorectal cancer. We hypothesized that these findings may be due to systematic bias and examined the independent association of colorectal cancer risk with statin use, serum cholesterol, and change in cholesterol concentration. METHODS AND FINDINGS: 22,163 colorectal cancer cases and 86,538 matched controls between 1995 and 2013 were identified within The Health Improvement Network (THIN) a population-representative database. Conditional logistic regression models estimated colorectal cancer risk with statin use, serum total cholesterol (mmol/L), and change in total cholesterol level. We confirmed a decreased risk of colorectal cancer with statin use (long-term: odds ratio [OR], 0.95; 95% confidence interval [CI], 0.91–0.99; short-term: OR, 0.92; 95% CI, 0.85–0.99). However, to assess whether the observed association may result from indication bias, a subgroup analysis was conducted among patients prescribed a statin. In this subgroup (n = 5,102 cases, n = 19,032 controls), 3.1% of case subjects and 3.1% of controls discontinued therapy. The risk of colorectal cancer was not significantly different among those who continued statin therapy and those who discontinued (OR, 0.98; 95% CI, 0.79–1.22). Increased serum cholesterol was independently associated with decreased risk of colorectal cancer (OR, 0.89 per mmol/L increase; 95% CI, 0.87–0.91); the association was only present if serum cholesterol was measured near the cancer diagnosis (<6 mo: OR, 0.76; 95% CI, 0.47–0.61; >24 mo: OR, 0.98; 95% CI, 0.93–1.03). Decreases in serum total cholesterol >1 mmol/L ≥1 year prior to cancer diagnosis were associated with subsequent colorectal cancer (statin users: OR, 1.25; 95 CI%, 1.03–1.53; nonusers: OR, 2.36; 95 CI%, 1.78–3.12). As an observational study, limitations included incomplete data and residual confounding. CONCLUSIONS: Although the risk of colorectal cancer was lower in statin users versus nonusers, no difference was observed among those who continued versus discontinued statin therapy, suggesting the potential for indication bias. The association between decreased serum cholesterol and colorectal cancer risk suggests a cholesterol-lowering effect of undiagnosed malignancy. Clinical judgment should be used when considering causes of cholesterol reduction in patients, including those on statin therapy. Public Library of Science 2016-04-26 /pmc/articles/PMC4846028/ /pubmed/27116322 http://dx.doi.org/10.1371/journal.pmed.1002007 Text en © 2016 Mamtani et al http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited. |
spellingShingle | Research Article Mamtani, Ronac Lewis, James D. Scott, Frank I. Ahmad, Tariq Goldberg, David S. Datta, Jashodeep Yang, Yu-Xiao Boursi, Ben Disentangling the Association between Statins, Cholesterol, and Colorectal Cancer: A Nested Case-Control Study |
title | Disentangling the Association between Statins, Cholesterol, and Colorectal Cancer: A Nested Case-Control Study |
title_full | Disentangling the Association between Statins, Cholesterol, and Colorectal Cancer: A Nested Case-Control Study |
title_fullStr | Disentangling the Association between Statins, Cholesterol, and Colorectal Cancer: A Nested Case-Control Study |
title_full_unstemmed | Disentangling the Association between Statins, Cholesterol, and Colorectal Cancer: A Nested Case-Control Study |
title_short | Disentangling the Association between Statins, Cholesterol, and Colorectal Cancer: A Nested Case-Control Study |
title_sort | disentangling the association between statins, cholesterol, and colorectal cancer: a nested case-control study |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4846028/ https://www.ncbi.nlm.nih.gov/pubmed/27116322 http://dx.doi.org/10.1371/journal.pmed.1002007 |
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