Literature DB >> 11600468

Leucopenia resulting from a drug interaction between azathioprine or 6-mercaptopurine and mesalamine, sulphasalazine, or balsalazide.

P W Lowry1, C L Franklin, A L Weaver, C L Szumlanski, D C Mays, E V Loftus, W J Tremaine, J J Lipsky, R M Weinshilboum, W J Sandborn.   

Abstract

AIM: We evaluated the effect of coadministration of sulphasalazine, mesalamine, and balsalazide on the pharmacokinetics and pharmacodynamics of azathioprine and 6-mercaptopurine.
METHODS: Thirty four patients with Crohn's disease receiving azathioprine or 6-mercaptopurine were enrolled in an eight week non-randomised parallel group drug interaction study and treated with mesalamine 4 g/day, sulphasalazine 4 g/day, or balsalazide 6.75 g/day. The primary outcome measure was the occurrence of clinically important leucopenia during the study, defined separately as total leucocyte counts < 3.0 x 10(9)/l and < or = 3.5 x 10(9)/l. Whole blood 6-thioguanine nucleotide concentrations were determined.
RESULTS: Three patients could not be evaluated for the primary outcome measure. In the remaining 31 patients, the frequency of total leucocyte counts < 3.0 and < or = 3.5 were: 1/10 and 5/10 in the mesalamine group; 1/11 and 6/11 in the sulphasalazine group; and 0/10 and 2/10 in the balsalazide group. There were significant increases in mean whole blood 6-thioguanine nucleotide concentrations from baseline at most time points in the mesalamine and sulphasalazine groups but not in the balsalazide group.
CONCLUSIONS: In patients with Crohn's disease receiving azathioprine or 6-mercaptopurine, coadministration of mesalamine, sulphasalazine, and possibly balsalazide results in an increase in whole blood 6-thioguanine nucleotide concentrations and a high frequency of leucopenia.

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Year:  2001        PMID: 11600468      PMCID: PMC1728490          DOI: 10.1136/gut.49.5.656

Source DB:  PubMed          Journal:  Gut        ISSN: 0017-5749            Impact factor:   23.059


  24 in total

1.  Balsalazide and azathiprine or 6-mercaptopurine: evidence for a potentially serious drug interaction.

Authors:  P W Lowry; C L Szumlanski; R M Weinshilboum; W J Sandborn
Journal:  Gastroenterology       Date:  1999-06       Impact factor: 22.682

2.  Measurement of thiopurine methyltransferase activity and azathioprine metabolites in patients with inflammatory bowel disease.

Authors:  P W Lowry; C L Franklin; A L Weaver; M G Pike; D C Mays; W J Tremaine; J J Lipsky; W J Sandborn
Journal:  Gut       Date:  2001-11       Impact factor: 23.059

3.  Pharmacogenomics and metabolite measurement for 6-mercaptopurine therapy in inflammatory bowel disease.

Authors:  M C Dubinsky; S Lamothe; H Y Yang; S R Targan; D Sinnett; Y Théorêt; E G Seidman
Journal:  Gastroenterology       Date:  2000-04       Impact factor: 22.682

4.  Adverse reactions during salicylazosulfapyridine therapy and the relation with drug metabolism and acetylator phenotype.

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5.  Human thiopurine methyltransferase pharmacogenetics: gene sequence polymorphisms.

Authors:  D Otterness; C Szumlanski; L Lennard; B Klemetsdal; J Aarbakke; J O Park-Hah; H Iven; K Schmiegelow; E Branum; J O'Brien; R Weinshilboum
Journal:  Clin Pharmacol Ther       Date:  1997-07       Impact factor: 6.875

6.  Lack of effect of intravenous administration on time to respond to azathioprine for steroid-treated Crohn's disease. North American Azathioprine Study Group.

Authors:  W J Sandborn; W J Tremaine; D C Wolf; S R Targan; C A Sninsky; L R Sutherland; S B Hanauer; J W McDonald; B G Feagan; R N Fedorak; K L Isaacs; M G Pike; D C Mays; J J Lipsky; S Gordon; C S Kleoudis; R H Murdock
Journal:  Gastroenterology       Date:  1999-09       Impact factor: 22.682

7.  6-Mercaptopurine metabolism in Crohn's disease: correlation with efficacy and toxicity.

Authors:  C Cuffari; Y Théorêt; S Latour; G Seidman
Journal:  Gut       Date:  1996-09       Impact factor: 23.059

8.  Mercaptopurine pharmacogenetics: monogenic inheritance of erythrocyte thiopurine methyltransferase activity.

Authors:  R M Weinshilboum; S L Sladek
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9.  Thiopurine methyltransferase genotype predicts therapy-limiting severe toxicity from azathioprine.

Authors:  A J Black; H L McLeod; H A Capell; R H Powrie; L K Matowe; S C Pritchard; E S Collie-Duguid; D M Reid
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10.  Studies of two novel sulfasalazine analogs, ipsalazide and balsalazide.

Authors:  R P Chan; D J Pope; A P Gilbert; P J Sacra; J H Baron; J E Lennard-Jones
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  45 in total

1.  Measurement of thiopurine methyltransferase activity and azathioprine metabolites in patients with inflammatory bowel disease.

Authors:  P W Lowry; C L Franklin; A L Weaver; M G Pike; D C Mays; W J Tremaine; J J Lipsky; W J Sandborn
Journal:  Gut       Date:  2001-11       Impact factor: 23.059

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5.  Interruption of mesalamine and reduction of the blood concentration of the active metabolites of azathioprine: possible causes of ulcerative colitis relapse.

Authors:  Gabriele Stocco; Stefano Martelossi; Noelia Malusa'; Sara Marino; Giuliana Decorti; Fiora Bartoli; Alessandro Ventura
Journal:  Dig Dis Sci       Date:  2008-05-10       Impact factor: 3.199

Review 6.  Update on the management of Crohn's disease.

Authors:  Anna M Buchner; Wojciech Blonski; Gary R Lichtenstein
Journal:  Curr Gastroenterol Rep       Date:  2011-10

7.  Is less more: does leukopenia predict remission in patients with inflammatory bowel disease receiving thiopurine treatment?

Authors:  Javier P Gisbert
Journal:  Dig Dis Sci       Date:  2015-01       Impact factor: 3.199

Review 8.  Interactions Between Inflammatory Bowel Disease Drugs and Chemotherapy.

Authors:  Galen Leung; Marianna Papademetriou; Shannon Chang; Francis Arena; Seymour Katz
Journal:  Curr Treat Options Gastroenterol       Date:  2016-12

9.  Usefulness of salicylate and thiopurine coprescription in steroid-dependent ulcerative colitis and withdrawal strategies.

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Review 10.  Balsalazide: a review of its therapeutic use in mild-to-moderate ulcerative colitis.

Authors:  Richard B R Muijsers; Karen L Goa
Journal:  Drugs       Date:  2002       Impact factor: 9.546

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