Hande Scott, Wilson-Rich Noah, Bousvaros Athos, Zholudev Anna, Maurer Rie, Banks Peter, Makrauer Frederick, Reddy Sarathchandra, Burakoff Robert, Friedman Sonia
Brigham and Women's Hospital, Boston, Massachusetts, USA.
Inflamm Bowel Dis. 2006 Apr;12(4):251-7. doi: 10.1097/01.MIB.0000206544.05661.9f.
BACKGROUND: Small uncontrolled trials have suggested that 5-aminosalicylate (5-ASA) medications increase 6-thioguanine nucleotide (6-TGn) levels in adults with Crohn's disease (CD) on azathioprine (AZA) or 6-mercaptopurine (6-MP), presumably through the inhibition of thiopurine methyltransferase (TPMT). We tested the theory that coadministration of 5-ASA agents with AZA/6-MP results in higher 6-TGn levels in a large cohort of children and adults with CD or ulcerative colitis (UC). METHODS: A retrospective cohort study identified all children and adults treated for IBD with AZA/6-MP at 2 tertiary medical centers. Patients were included if their TPMT genotype was known and 6-TGn and 6-methymercaptopurine (6-MMP) levels had been obtained after 3 months of clinical remission at a stable dose of AZA/6-MP. 6-TGn and 6-MMP levels were compared between patients taking and those not taking 5-ASA medications through the use of linear regression models to identify and adjust for potentially confounding variables. RESULTS: Of the 126 patients included, 88 were taking 5-ASA medications. Patients on 5-ASA agents had higher mean 6-TGn levels after adjustment for confounding variables (Delta6-TGn, 47.6 +/- 21.8 pmol/8 x 10 red blood cells; P = 0.03). CD and TPMT heterozygosity was independently associated with higher 6-TGn levels (P = 0.01 and P = 0.03, respectively). 5-ASA exposure was not associated with a change in 6-MMP levels. CONCLUSIONS: We found that 5-ASA therapy is associated with higher 6-TGn levels in children and adults with IBD on 6-MP/AZA. TPMT inhibition may not explain this effect because 5-ASA exposure did not affect 6-MMP levels. The observed association of CD with higher 6-TGn levels is novel and needs to be verified in prospective studies.
背景:小型非对照试验表明,5-氨基水杨酸(5-ASA)类药物可使接受硫唑嘌呤(AZA)或6-巯基嘌呤(6-MP)治疗的克罗恩病(CD)成年患者的6-硫鸟嘌呤核苷酸(6-TGn)水平升高,推测其机制是抑制硫嘌呤甲基转移酶(TPMT)。我们验证了以下理论:在一大群患有CD或溃疡性结肠炎(UC)的儿童和成人中,5-ASA制剂与AZA/6-MP联合使用会使6-TGn水平升高。 方法:一项回顾性队列研究纳入了在两家三级医疗中心接受AZA/6-MP治疗的所有IBD儿童和成人。如果患者的TPMT基因型已知,且在以稳定剂量的AZA/6-MP达到临床缓解3个月后获得了6-TGn和6-甲基巯基嘌呤(6-MMP)水平,则纳入研究。通过线性回归模型比较服用和未服用5-ASA药物的患者的6-TGn和6-MMP水平,以识别和调整潜在的混杂变量。 结果:纳入的126例患者中,88例正在服用5-ASA药物。在对混杂变量进行调整后,服用5-ASA制剂的患者的平均6-TGn水平更高(Δ6-TGn,47.6±21.8 pmol/8×10⁶红细胞;P=0.03)。CD和TPMT杂合性分别与较高的6-TGn水平独立相关(P=0.01和P=0.03)。5-ASA暴露与6-MMP水平的变化无关。 结论:我们发现,在接受6-MP/AZA治疗的IBD儿童和成人中,5-ASA治疗与较高的6-TGn水平相关。TPMT抑制可能无法解释这种效应,因为5-ASA暴露并未影响6-MMP水平。观察到的CD与较高6-TGn水平之间的关联是新发现,需要在前瞻性研究中进行验证。
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