Suppr超能文献

巯嘌呤维持治疗溃疡性结肠炎:监测 6-硫代鸟嘌呤核苷酸的临床意义。

Thiopurine maintenance therapy for ulcerative colitis: the clinical significance of monitoring 6-thioguanine nucleotide.

机构信息

Centre for Gastroenterology and Inflammatory Bowel Disease Research, Hamamatsu South Hospital, Hamamatsu, Japan.

出版信息

Inflamm Bowel Dis. 2010 Aug;16(8):1376-81. doi: 10.1002/ibd.21190.

Abstract

BACKGROUND

6-Mercaptopurine (6-MP) is an effective maintenance medication in patients with ulcerative colitis (UC), but toxic effects like myelosuppression limit its clinical benefit. In the blood, 6-thioguanine (6-TGN) is formed from 6-MP and mediates the therapeutic efficacy and most of the toxicities of 6-MP. The level of 6-TGN depends on the activity of thiopurine methyltransferase (TPMT), inherited as 1 of its 3 polymorphic forms with low, moderate, or normal/high activity. Accordingly, the 6-MP dose needs to be pharmacogenetically guided.

METHODS

Patients with quiescent UC received 6-MP as maintenance therapy and 6-TGN was assayed as its concentrations in red blood cells (RBCs) done by high-performance liquid chromatography. In a preliminary investigation, 30 mg/day 6-MP (n = 50) was given orally over 12 weeks to determine the time course of blood 6-TGN level. Then 257 patients were given 6-MP at 15-80 mg/day in a stepwise manner based on RBC 6-TGN, white blood cell count, and body weight to monitor 6-MP efficacy and safety profiles.

RESULTS

At 30 mg/day 6-MP, RBC 6-TGN peaked over 4-8 weeks. In the main dosing study, the mean RBC 6-TGN level in patients who remained in remission during the 1-year observation time (n = 151) was 322.3 +/- 119.5 pmole/8 x 10(8) RBC versus 204.8 +/- 78.7 pmole/8 x 10(8) RBC in patients (n = 19) who relapsed (P < 0.001). Bone marrow suppression was seen almost exclusively at high 6-TGN concentration ranges. Further, a regression plot showed an inverse relationship between 6-TGN levels in RBC and TPMT enzyme activity.

CONCLUSIONS

By regularly measuring RBC 6-TGN in patients with quiescent UC receiving 6-MP as maintenance therapy, we could monitor bone marrow suppression as well as other toxic side effects. Potentially, this strategy should enable physicians to avoid thiopurine-related adverse effects and identify individuals who may benefit most from 6-MP maintenance therapy.

摘要

背景

6-巯基嘌呤(6-MP)是溃疡性结肠炎(UC)患者的有效维持治疗药物,但骨髓抑制等毒性作用限制了其临床获益。在血液中,6-硫鸟嘌呤(6-TGN)由 6-MP 形成,介导 6-MP 的治疗效果和大多数毒性作用。6-TGN 的水平取决于硫嘌呤甲基转移酶(TPMT)的活性,其以低、中、高活性的 3 种多态形式遗传。因此,6-MP 剂量需要进行药物遗传学指导。

方法

处于缓解期的 UC 患者接受 6-MP 作为维持治疗,并通过高效液相色谱法检测红细胞(RBC)中的 6-TGN 浓度。在初步研究中,50 例患者接受 6-MP 30mg/天,口服,共 12 周,以确定血液 6-TGN 水平的时间过程。然后,根据 RBC 6-TGN、白细胞计数和体重,257 例患者以逐步方式接受 15-80mg/天的 6-MP,以监测 6-MP 的疗效和安全性特征。

结果

6-MP 30mg/天,RBC 6-TGN 于 4-8 周达到峰值。在主要给药研究中,在 1 年观察时间内仍处于缓解期的患者(n=151)的平均 RBC 6-TGN 水平为 322.3±119.5pmol/8×10^8 RBC,而复发患者(n=19)的平均 RBC 6-TGN 水平为 204.8±78.7pmol/8×10^8 RBC(P<0.001)。骨髓抑制几乎仅在高 6-TGN 浓度范围内出现。此外,回归图显示 RBC 6-TGN 水平与 TPMT 酶活性呈负相关。

结论

通过定期测量接受 6-MP 维持治疗的处于缓解期的 UC 患者的 RBC 6-TGN,我们可以监测骨髓抑制和其他毒性副作用。潜在地,这种策略应该使医生能够避免与硫嘌呤相关的不良反应,并确定最有可能从 6-MP 维持治疗中获益的个体。

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验