Register for email alerts and news feeds:
This journal | BMJ Group
rss
Published Online First: 30 June 2005. doi:10.1136/gut.2005.070896
Gut 2005;54:1573-1578
Copyright © 2005 BMJ Publishing Group Ltd & British Society of Gastroenterology.

INFLAMMATORY BOWEL DISEASE

5-Aminosalicylate use and colorectal cancer risk in inflammatory bowel disease: a large epidemiological study

T P van Staa1, T Card2, R F Logan2, H G M Leufkens3

1 Department of Pharmacoepidemiology and Pharmacotherapy, University of Utrecht,, Utrecht, the Netherlands, and Procter and Gamble Pharmaceuticals, Egham, UK
2 Division of Epidemiology and Public Health, University of Nottingham Medical School, Nottingham, UK
3 Department of Pharmacoepidemiology and Pharmacotherapy, University of Utrecht, Utrecht, the Netherlands

Correspondence to:
Professor R F Logan
Division of Epidemiology and Public Health, School of Community Health Sciences, University of Nottingham Medical School, Nottingham NG7 2UH, UK; richard.logan{at}nottingham.ac.uk

Background and aims: The objective of this study was to evaluate the risk of colorectal cancer (CRC) in patients taking aminosalicylates (5-ASA) for inflammatory bowel disease (IBD).

Methods: The General Practice Research Database (GPRD) which contains the primary care records of five million people in the UK was used to identify users of mesalazine, balsalazide, olsalazine, or sulfasalazine with a history of IBD. In a nested case control analysis, each incident CRC case with any use of a 5-ASA in the six months before the CRC diagnosis was matched by age, sex, and calendar time to six control patients who were also currently using a 5-ASA. Patients were then classified according to regularity of use. The analysis was controlled for body mass index, IBD duration, history of colorectal polyps, use of non-steroidal anti-inflammatory drugs, paracetamol, aspirin, immunosuppressants, oral and rectal glucocorticoids, prior gastrointestinal hospitalisation, recorded colonoscopy, and number of visits to the general practitioner for IBD symptoms in the 6–24 months before diagnosis.

Results: The study population included 18 969 patients, of whom 100 had developed CRC during 5-ASA exposure. Most of these cases had a history of ulcerative colitis (76 patients). In the case control analysis, regular users, defined as having six or more 5-ASA prescriptions in the previous 12 months, were found to have a decreased risk of CRC compared with irregular users (crude odds ratio (OR) 0.7 (0.44–1.03); adjusted OR 0.60 (0.38–0.96)). Regular users of sulfasalazine with 6–12 prescriptions before had an adjusted OR of 0.95 (0.22–4.11); with 13–30 prior prescriptions this was 0.41 (0.14–1.20) and with >30 prior prescriptions this was 0.77 (0.37–1.60). For mesalazine users, these values were 1.13 (0.49–2.59), 0.30 (0.11–0.83), and 0.31 (0.11–0.84), respectively.

Conclusion: These results show that regular 5-ASA use is associated with some reduction in the risk of CRC developing in ulcerative colitis.

Abbreviations: 5-ASA, 5-aminosalicylate; CRC, colorectal cancer; NSAIDs, non-steroidal anti-inflammatory drugs; IBD, inflammatory bowel disease; UC, ulcerative colitis; CD, Crohn’s disease; GPRD, General Practice Research Database; OR, odds ratio; RR, relative rate; RA, rheumatoid arthritis

Keywords: Crohn’s disease; ulcerative colitis; inflammatory bowel disease; colorectal cancer; 5-aminosalicylate


Add to CiteULike CiteULike   Add to Complore Complore   Add to Connotea Connotea   Add to Del.icio.us Del.icio.us   Add to Digg Digg   Add to Reddit Reddit   Add to Technorati Technorati    What's this?

Relevant Articles

JournalScan
Gut 2007 56: 283. [Extract] [Full Text] [PDF]

Digest
Robin Spiller
Gut 2005 54: 1509. [Extract] [Full Text] [PDF]

This article has been cited by other articles:

  • Hemminki, K., Li, X., Sundquist, J., Sundquist, K. (2009). Cancer risks in Crohn disease patients. Ann Oncol 20: 574-580 [Abstract] [Full Text]  
  • Schwab, M., Reynders, V., Loitsch, S., Shastri, Y. M., Steinhilber, D., Schroder, O., Stein, J. (2008). PPAR{gamma} is involved in mesalazine-mediated induction of apoptosis and inhibition of cell growth in colon cancer cells. Carcinogenesis 29: 1407-1414 [Abstract] [Full Text]  
  • Stolfi, C., Fina, D., Caruso, R., Caprioli, F., Fantini, M. C., Rizzo, A., Sarra, M., Pallone, F., Monteleone, G. (2008). Mesalazine negatively regulates CDC25A protein expression and promotes accumulation of colon cancer cells in S phase. Carcinogenesis 29: 1258-1266 [Abstract] [Full Text]  
  • Kitiyakara, T, Chapman, R W (2008). Chemoprevention and screening in primary sclerosing cholangitis. Postgrad. Med. J. 84: 228-237 [Abstract] [Full Text]  
  • Nam, S. Y., Kim, J. S., Kim, J. M., Lee, J. Y., Kim, N., Jung, H. C., Song, I. S. (2008). DA-6034, a Derivative of Flavonoid, Prevents and Ameliorates Dextran Sulfate Sodium-Induced Colitis and Inhibits Colon Carcinogenesis. Exp. Biol. Med. 233: 180-191 [Abstract] [Full Text]  
  • Di Mari, J. F., Saada, J. I., Mifflin, R. C., Valentich, J. D., Powell, D. W. (2007). HETEs enhance IL-1-mediated COX-2 expression via augmentation of message stability in human colonic myofibroblasts. Am. J. Physiol. Gastrointest. Liver Physiol. 293: G719-G728 [Abstract] [Full Text]  

eLetters:

Read all eLetters

5-Aminosalicylate use and colorectal cancer risk in inflammatory bowel disease
Dr Prem Chattoo, et al.
Gut Online, 12 Jan 2006 [Full text]

This Article

Services
Citing Articles
Google Scholar
PubMed
Topic Collections
Bookmark with

Register for free content

The full back archive is now available for all BMJ Journals. Institutional subscribers may access the entire archive as part of their subscription. Personal subscribers will also have access to all content when logged in. Non-subscribers who register have free access to all articles published before 2006 right back to volume 1 issue 1. Register here to access the free archive of all BMJ Journals.

Don't forget to sign up for content alerts so you keep up to date with all the articles as they are published.

Cardiology Jobs

Gastroenterology Jobs