Optimizing clinical use of mesalazine (5-aminosalicylic acid) in inflammatory bowel disease
- PMID: 21765868
- PMCID: PMC3131170
- DOI: 10.1177/1756283X11405250
Optimizing clinical use of mesalazine (5-aminosalicylic acid) in inflammatory bowel disease
Abstract
Mesalazine [5-aminosalicylic acid (5-ASA)] has been used for over 30 years in the treatment of inflammatory bowel disease (IBD). It is a highly effective, safe, and well-tolerated drug for treatment of mild to moderate ulcerative colitis, which represents most patients with this disease. Recent studies of patient adherence to 5-ASA therapies in ulcerative colitis have highlighted the need for regimens that enable long-term compliance to significantly reduce the risk of troublesome and debilitating flares in the short term, and possibly colon cancer in the long term. Indeed, much of the recent innovation in clinical use of 5-ASA in colitis has come from studies of novel delivery mechanisms and simplified oral dosing schedules. These studies have provided much needed clarity on essential matters such as starting dose, dose escalation, and efficacy in terms of the ideal clinical endpoint - mucosal healing. Various manufacturers are re-evaluating their products to determine the safety and efficacy of such dosing regimens. Although once widely employed in the treatment of Crohn's disease (CD), the accumulated body of evidence now suggests that there is a much more limited role for 5-ASA in this particular form of inflammatory bowel disease. Recent 5-ASA randomized-controlled trials, comparative studies, and outcomes research have led to refined treatment strategies and awareness for practitioners to better inform, engage and facilitate patients in optimal use of 5-ASA in inflammatory bowel disease.
Keywords: 5-aminosalicylic acid; Crohn’s disease; delayed-action preparations; inflammatory bowel disease; mesalazine; ulcerative colitis.
Conflict of interest statement
The authors declare the following potential conflicts of interest. Dr Chad Williams is a clinical IBD Fellow sponsored in part by Centocor. Dr Remo Panaccione has received research support and consultancy fees from Astra Zeneca, Ferring, Abbott, Byk Solvay, Axcan, Jansen, Schering-Plough, Shire, Centocor, Elan, Prometheus, Glaxo Smith Kline, Proctor & Gamble, UCB, Bristol Meyers Squibb, and Millennium Pharmaceuticals. Dr Subrata Ghosh has received research support and participated in advisory panels and speaking engagements for Shire, Ferring Abbott, Merck, Centocor, and Pfizer. Dr Kevin Rioux has participated in advisory boards for Abbott, UCB, Schering-Plough, and Ferring Pharmaceuticals.
References
-
- Akobeng A.K., Gardener E. (2005) Oral 5-aminosalicylic acid for maintenance of medically-induced remission in Crohn's Disease. Cochrane Database Syst Rev 1: CD003715–CD003715. - PubMed
-
- Allgayer H. (1992) Sulfasalazine and 5-ASA compounds. Gastroenterol Clin North Am 21: 643–658. - PubMed
-
- Asano T.K., McLeod R.S. (2004) Nonsteroidal anti-inflammatory drugs and aspirin for the prevention of colorectal adenomas and cancer: a systematic review. Dis Colon Rectum 47: 665–673. - PubMed
-
- Baert F., Moortgat L., Van Assche G., Caenepeel P., Vergauwe P., De Vos M., et al. (2010) Mucosal healing predicts sustained clinical remission in patients with early-stage Crohn's disease. Gastroenterology 138: 463–468. quiz e410-e461. - PubMed
-
- Bernstein C.N., Blanchard J.F., Kliewer E., Wajda A. (2001) Cancer risk in patients with inflammatory bowel disease: a population-based study. Cancer 91: 854–862. - PubMed
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