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 Bodegraven Adriaan A
Gastroenterology and Hepatology, VU University Medical Center, Amsterdam, The Netherlands.
Am J Gastroenterol. 2007 Dec;102(12):2747-53. doi: 10.1111/j.1572-0241.2007.01511.x. Epub 2007 Aug 31.
Studies indicated that 5-aminosalicylates (5-ASA) may influence the metabolism of thiopurines; however, conclusions were restricted as a result of number of patients or study design.
To determine the influence of 5-ASA on thiopurine metabolism, we performed a prospective multicenter pharmacokinetic interaction study of two different 5-ASA dosages (2 g daily followed by 4 g daily) in 26 inflammatory bowel disease (IBD) patients during steady-state AZA or 6-MP therapy.
The 4-wk coadministration of 2 g 5-ASA daily, followed by a 4-wk period of 4 g 5-ASA daily, led to a statistical significant increase of 40% (absolute 84 pmol/8x10(8) RBC) and 70% (absolute 154 pmol/8x10(8) RBC) in 6-thioguaninenucleotide levels (6-TGN), respectively. A rise in 6-TGN levels was observed in 100% of patients after a 4-wk period of 4 g 5-ASA daily. The 6-methylmercaptopurine-ribonucleotide levels did not change. Signs of myelotoxicity were observed in 7.7% of patients (N=2).
The level of the pharmacologically active 6-TGN significantly increases in a dose-dependent manner during 5-ASA coadministration. IBD patients who are unresponsive or refractory to standard thiopurine therapy may benefit from the coadministration of 5-ASA, leading to an increase in 6-TGN levels.
研究表明,5-氨基水杨酸酯(5-ASA)可能会影响硫嘌呤的代谢;然而,由于患者数量或研究设计的原因,结论受到限制。
为了确定5-ASA对硫嘌呤代谢的影响,我们对26例炎症性肠病(IBD)患者在接受稳态硫唑嘌呤(AZA)或6-巯基嘌呤(6-MP)治疗期间,进行了两种不同剂量5-ASA(每日2g,随后每日4g)的前瞻性多中心药代动力学相互作用研究。
每日服用2g 5-ASA共4周,随后每日服用4g 5-ASA共4周,导致6-硫鸟嘌呤核苷酸水平(6-TGN)分别有统计学意义地显著升高40%(绝对值84 pmol/8×10⁸红细胞)和70%(绝对值154 pmol/8×10⁸红细胞)。在每日服用4g 5-ASA共4周后,100%的患者观察到6-TGN水平升高。6-甲基巯基嘌呤核糖核苷酸水平未发生变化。7.7%的患者(N = 2)出现骨髓毒性迹象。
在联合使用5-ASA期间,药理活性6-TGN水平以剂量依赖方式显著升高。对标准硫嘌呤治疗无反应或难治的IBD患者可能受益于联合使用5-ASA,从而导致6-TGN水平升高。