Cuffari C, Théorêt Y, Latour S, Seidman G
Department of Pediatrics, Université de Montréal, Canada.
Gut. 1996 Sep;39(3):401-6. doi: 10.1136/gut.39.3.401.
6-Mercaptopurine (6-MP) has confirmed short and longterm efficacy in the treatment of IBD. However, the relation between its metabolism, efficacy, and side effects is not well understood.
To assay 6-MP metabolites and to correlate levels with drug compliance, disease activity, and adverse effects of treatment.
Heparinised blood was obtained prior to daily administration of 6-MP in 25 adolescent Crohn's disease patients (14 ileocolitis, 11 colitis) receiving 1.2 (range 0.4-1.6) mg/kg/day for a mean of 17 (range 4-65) months.
Erythrocyte free bases 6-thioguanine (6-TG) and 6-methyl-mercaptopurine (6-MMP) were measured (pmol/8 x 10(8) red blood cells) using reverse phase high performance liquid chromatography.
Disease activity (modified Harvey-Bradshaw index) improved significantly with 6-MP (p = 0.001). Clinical remission was achieved in 72% of patients, who stopped taking prednisone, or were successfully weaned to a low alternate day dose (< 0.4 mg/kg/OD). Remission correlated well with erythrocyte 6-TG (p < 0.05), but not 6-MMP levels. Neutropenia was associated with 6-MP use (p < 0.005), but did not correlate with erythrocyte 6-MP metabolite levels. One patient refractory to 6-MP had 6-TG, but no measureable 6-MMP production, suggesting deficient thiopurine methyl-transferase activity or poor compliance. 6-MP induced complications (hepatitis, pancreatitis, and marrow suppression) were generally associated with increased 6-MMP levels.
These results suggest that high performance liquid chromatography measurement of erythrocyte 6-MP metabolites may provide a quantitative assessment of patient responsiveness and compliance to treatment. The data support an immunosuppressive role for 6-TG, and potential cytotoxicity of raised 6-MMP levels.
6-巯基嘌呤(6-MP)在治疗炎症性肠病(IBD)方面已证实具有短期和长期疗效。然而,其代谢、疗效和副作用之间的关系尚未完全明确。
检测6-MP代谢产物,并将其水平与药物依从性、疾病活动度及治疗不良反应相关联。
对25例青少年克罗恩病患者(14例回结肠型,11例结肠型)在每日服用6-MP前采集肝素化血液,这些患者接受1.2(范围0.4 - 1.6)mg/kg/天的治疗,平均治疗时间为17(范围4 - 65)个月。
采用反相高效液相色谱法测定红细胞游离碱6-硫鸟嘌呤(6-TG)和6-甲基巯基嘌呤(6-MMP)(pmol/8×10⁸红细胞)。
6-MP治疗后疾病活动度(改良哈维-布拉德肖指数)显著改善(p = 0.001)。72%的患者实现临床缓解,这些患者停用了泼尼松,或成功减至隔日低剂量(< 0.4 mg/kg/隔日)。缓解与红细胞6-TG水平密切相关(p < 0.05),但与6-MMP水平无关。中性粒细胞减少与使用6-MP有关(p < 0.005),但与红细胞6-MP代谢产物水平无关。1例对6-MP耐药的患者有6-TG,但未检测到6-MMP生成,提示硫嘌呤甲基转移酶活性不足或依从性差。6-MP诱导的并发症(肝炎、胰腺炎和骨髓抑制)通常与6-MMP水平升高有关。
这些结果表明,通过高效液相色谱法测定红细胞6-MP代谢产物可能为评估患者对治疗的反应性和依从性提供定量依据。数据支持6-TG的免疫抑制作用以及6-MMP水平升高的潜在细胞毒性。