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本文引用的文献

1
Cellular pharmacology of 6-mercaptopurine in acute lymphoblastic leukemia.6-巯基嘌呤在急性淋巴细胞白血病中的细胞药理学
Am J Pediatr Hematol Oncol. 1993 Feb;15(1):80-6.
2
Immunosuppressive therapy in pediatric inflammatory bowel disease: results of a survey of the North American Society for Pediatric Gastroenterology and Nutrition. Subcommittee on Immunosuppressive Use of the Pediatric IBD Collaborative Research Forum.儿童炎症性肠病的免疫抑制治疗:北美儿科胃肠病学与营养学会的一项调查结果。儿科炎症性肠病协作研究论坛免疫抑制应用小组委员会。
Am J Gastroenterol. 1993 Jan;88(1):44-8.
3
Reversal of 6-mercaptopurine and 6-methylmercaptopurine ribonucleoside cytotoxicity by amidoimidazole carboxamide ribonucleoside in Molt F4 human malignant T-lymphoblasts.
Biochem Pharmacol. 1993 Aug 3;46(3):547-50. doi: 10.1016/0006-2952(93)90534-4.
4
Long-term experience with 6-mercaptopurine in the treatment of Crohn's disease.6-巯基嘌呤治疗克罗恩病的长期经验
Am J Gastroenterol. 1993 Aug;88(8):1198-205.
5
Azathioprine combined with prednisolone or monotherapy with prednisolone in active Crohn's disease.硫唑嘌呤联合泼尼松龙或泼尼松龙单药治疗活动性克罗恩病。
Gastroenterology. 1993 Aug;105(2):367-72. doi: 10.1016/0016-5085(93)90709-l.
6
Congenital thiopurine methyltransferase deficiency and 6-mercaptopurine toxicity during treatment for acute lymphoblastic leukaemia.先天性硫嘌呤甲基转移酶缺乏与急性淋巴细胞白血病治疗期间的6-巯基嘌呤毒性
Arch Dis Child. 1993 Nov;69(5):577-9. doi: 10.1136/adc.69.5.577.
7
The role of leukopenia in the 6-mercaptopurine-induced remission of refractory Crohn's disease.白细胞减少症在6-巯基嘌呤诱导难治性克罗恩病缓解中的作用。
Am J Gastroenterol. 1994 Mar;89(3):362-6.
8
High-performance liquid chromatographic assay of human red blood cell thiopurine methyltransferase activity.人红细胞硫嘌呤甲基转移酶活性的高效液相色谱测定法。
J Chromatogr B Biomed Appl. 1994 Nov 4;661(1):25-33. doi: 10.1016/0378-4347(94)00327-0.
9
Azathioprine and 6-mercaptopurine in Crohn disease. A meta-analysis.硫唑嘌呤和6-巯基嘌呤用于克罗恩病的荟萃分析
Ann Intern Med. 1995 Jul 15;123(2):132-42. doi: 10.7326/0003-4819-123-2-199507150-00009.
10
6-Mercaptopurine: cytotoxicity and biochemical pharmacology in human malignant T-lymphoblasts.6-巯基嘌呤:人恶性T淋巴母细胞中的细胞毒性及生化药理学
Biochem Pharmacol. 1993 Apr 6;45(7):1455-63. doi: 10.1016/0006-2952(93)90045-x.

克罗恩病中6-巯基嘌呤的代谢:与疗效和毒性的相关性

6-Mercaptopurine metabolism in Crohn's disease: correlation with efficacy and toxicity.

作者信息

Cuffari C, Théorêt Y, Latour S, Seidman G

机构信息

Department of Pediatrics, Université de Montréal, Canada.

出版信息

Gut. 1996 Sep;39(3):401-6. doi: 10.1136/gut.39.3.401.

DOI:10.1136/gut.39.3.401
PMID:8949645
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC1383347/
Abstract

BACKGROUND

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.

AIMS

To assay 6-MP metabolites and to correlate levels with drug compliance, disease activity, and adverse effects of treatment.

PATIENTS

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.

METHODS

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.

RESULTS

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.

CONCLUSIONS

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.

摘要

背景

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。

目的

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。

患者

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。

方法

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)。

结果

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。

结论

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。