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

被引:47
|
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
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