Influence of 5-aminosalicylic acid on 6-thioguanosine phosphate metabolite levels: a prospective study in patients under steady thiopurine therapy

被引:49
作者
de Graaf, P. [1 ]
de Boer, N. K. H. [1 ]
Wong, D. R. [2 ]
Karner, S. [3 ,4 ]
Jharap, B. [1 ]
Hooymans, P. M. [2 ]
Veldkamp, A. I. [1 ]
Mulder, C. J. J. [1 ]
van Bodegraven, A. A. [1 ]
Schwab, M. [3 ,4 ,5 ]
机构
[1] Vrije Univ Amsterdam Med Ctr, NL-1007 MB Amsterdam, Netherlands
[2] Orbis Med Ctr, Sittard Geleen, Netherlands
[3] Dr Margarete Fischer Bosch Inst Clin Pharmacol St, Tubingen, Germany
[4] Univ Tubingen, Tubingen, Germany
[5] Univ Tubingen Hosp, Inst Expt & Clin Pharmacol & Toxicol, Dept Clin Pharmacol, Tubingen, Germany
关键词
azathioprine; 6-mercaptopurine; 5-aminosalicylates; mesalazine; inflammatory bowel disease; 6-thioguanine nucleotides; 6-methyl-mercaptopurine ribonucleotides; 6-thioguanosine triphosphate; drug interaction; clinical pharmacology; INFLAMMATORY-BOWEL-DISEASE; CROHNS-DISEASE; S-METHYLTRANSFERASE; AZATHIOPRINE THERAPY; DRUG-INTERACTION; 6-MERCAPTOPURINE; MESALAZINE; PHARMACOKINETICS; AMINOSALICYLATES; HEPATOTOXICITY;
D O I
10.1111/j.1476-5381.2010.00731.x
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Background and purpose: 5-aminosalicylate (5-ASA) raises levels of 6-thioguanine nucleotides (6-TGN), the active metabolites of thiopurines such as azathioprine (AZA). Changes in levels of each individual TGN - 6-thioguanosine mono-, di- and triphosphate (6-TGMP, 6-TGDP, 6-TGTP) - and of 6-methylmercaptopurine ribonucleotides (6-MMPR) after 5-ASA are not known. Experimental approach: Effects of increasing 5-ASA doses on AZA metabolites were investigated prospectively in 22 patients with inflammatory bowel disease in 4-week study periods. Patients started with 2 g 5-ASA daily, and then were increased to 4 g daily and followed by a washout period. Thiopurine doses remained unchanged throughout the entire study. Levels of 6-TGMP, 6-TGDP, 6-TGTP and 6-MMPR as well as of 5-ASA and N-acetyl-5-aminosalicylic acid (N-Ac-5-ASA) were determined each study period. Key results: Median baseline levels in 17 patients of 6-TGDP, 6-TGTP and 6-MMPR were 52, 319 and 1676 pmol per 8 x 108 red blood cells respectively. After co-administration of 2 g 5-ASA daily, median 6-TGDP and 6-TGTP levels increased but median 6-MMPR levels were unchanged. Increasing 5-ASA to 4 g daily did not affect median 6-TGDP and 6-TGTP levels, but median 6-MMPR levels decreased. After discontinuation of 5-ASA, both 6-TGDP and 6-TGTP levels decreased and median 6-MMPR levels increased. The 6-TGTP/(6-TGDP+6-TGTP)-ratio did not change during the study, but 6-MMPR/6-TGN ratios decreased. Conclusions and implications: Individual 6-TGN metabolites increased after addition of 5-ASA, but 6-MMPR-levels and the 6-MMPR/6-TGN ratios decreased. Further studies are needed to decide whether this pharmacokinetic interaction would result in improvement of efficacy and/or increased risk of toxicity of AZA.
引用
收藏
页码:1083 / 1091
页数:9
相关论文
共 33 条
[1]   COLONIC N-ACETYLATION OF 5-AMINOSALICYLIC ACID IN INFLAMMATORY BOWEL-DISEASE [J].
ALLGAYER, H ;
AHNFELT, NO ;
KRUIS, W ;
KLOTZ, U ;
FRANKHOLMBERG, K ;
SODERBERG, HNA ;
PAUMGARTNER, G .
GASTROENTEROLOGY, 1989, 97 (01) :38-41
[2]   Long-term outcome of using allopurinol co-therapy as a strategy for overcoming thiopurine hepatotoxicity in treating inflammatory bowel disease [J].
Ansari, A. ;
Elliott, T. ;
Baburajan, B. ;
Mayhead, P. ;
O'Donohue, J. ;
Chocair, P. ;
Sanderson, J. ;
Duley, J. .
ALIMENTARY PHARMACOLOGY & THERAPEUTICS, 2008, 28 (06) :734-741
[3]   Adherence to thiopurine treatment in out-patients with Crohn's disease [J].
Bokemeyer, B. ;
Teml, A. ;
Roggel, C. ;
Hartmann, P. ;
Fischer, C. ;
Schaeffeler, E. ;
Schwab, M. .
ALIMENTARY PHARMACOLOGY & THERAPEUTICS, 2007, 26 (02) :217-225
[4]   Genotypic analysis of thiopurine S-methyltransferase in patients with Crohn's disease and severe myelosuppression during azathioprine therapy [J].
Colombel, JF ;
Ferrari, N ;
Debuysere, H ;
Marteau, P ;
Gendre, JP ;
Bonaz, B ;
Soulé, JC ;
Modgliani, R ;
Touze, Y ;
Catala, P ;
Libersa, C ;
Broly, F .
GASTROENTEROLOGY, 2000, 118 (06) :1025-1030
[5]   Drug Insight: pharmacology and toxicity of thiopurine therapy in patients with IBD [J].
de Boer, Nanne K. H. ;
van Bodegraven, Adriaan A. ;
Jharap, Bindia ;
de Graaf, Peer ;
Mulder, Chris J. J. .
NATURE CLINICAL PRACTICE GASTROENTEROLOGY & HEPATOLOGY, 2007, 4 (12) :686-694
[6]   Dose-dependent influence of 5-aminosalicylates on thiopurine metabolism [J].
de Boer, Nanne K. H. ;
Wong, Dennis R. ;
Jharap, Bindia ;
de Graaf, Peer ;
Hooymans, Piet M. ;
Mulder, Chris J. J. ;
Rijmen, Frank ;
Engels, Leopold G. J. B. ;
van Bodergraven, Adrian A. .
AMERICAN JOURNAL OF GASTROENTEROLOGY, 2007, 102 (12) :2747-2753
[7]   Stability of thiopurine metabolites: A potential analytical bias [J].
de Graaf, Peer ;
de Boer, Nanne K. H. ;
Jharap, Bindia ;
Mulder, Chris J. J. ;
van Bodegraven, Ad A. ;
Veldkamp, Agnes I. .
CLINICAL CHEMISTRY, 2008, 54 (01) :216-218
[8]   Pharmacokinetics of 6-mercaptopurine in patients with inflammatory bowel disease - Implications for therapy [J].
Derijks, LJJ ;
Gilissen, LPL ;
Engels, LGJB ;
Bos, LP ;
Bus, PJ ;
Lohman, JJHM ;
Curvers, WL ;
van Deventer, SJH ;
Hommes, DW ;
Hooymans, PM .
THERAPEUTIC DRUG MONITORING, 2004, 26 (03) :311-318
[9]   Interaction between azathioprine and aminosalicylates:: an in vivo study in patients with Crohn's disease [J].
Dewit, O ;
Vanheuverzwyn, R ;
Desager, JP ;
Horsmans, Y .
ALIMENTARY PHARMACOLOGY & THERAPEUTICS, 2002, 16 (01) :79-85
[10]   Monitoring of thiopurine methyltransferase activity in postsurgical patients with Crohn's disease during 1 year of treatment with azathioprine or mesalazine [J].
Dilger, Karin ;
Schaeffeler, Elke ;
Lukas, Milan ;
Strauch, Ulrike ;
Herfarth, Hans ;
Mueller, Ralph ;
Schwab, Matthias .
THERAPEUTIC DRUG MONITORING, 2007, 29 (01) :1-5