Literature DB >> 20049951

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

Hiroyuki Hanai1, Takayuki Iida, Ken Takeuchi, Osamu Arai, Fumitoshi Watanabe, Jinrou Abe, Yasuhiko Maruyama, Akihiko Oohata, Kentarou Ikeya, Masanobu Kageoka, Ichita Miwa, Satou Yoshirou, Yoshisuke Hosoda, Takahiro Kubota.   

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.

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Year:  2010        PMID: 20049951     DOI: 10.1002/ibd.21190

Source DB:  PubMed          Journal:  Inflamm Bowel Dis        ISSN: 1078-0998            Impact factor:   5.325


  8 in total

1.  Nucleoside diphosphate-linked moiety X-type motif 15 R139C genotypes impact 6-thioguanine nucleotide cut-off levels to predict thiopurine-induced leukopenia in Crohn's disease patients.

Authors:  Xia Zhu; Kang Chao; Miao Li; Wen Xie; Hong Zheng; Jin-Xin Zhang; Pin-Jin Hu; Min Huang; Xiang Gao; Xue-Ding Wang
Journal:  World J Gastroenterol       Date:  2019-10-14       Impact factor: 5.742

2.  Personalized medicine to implementation science: Thiopurines set for the leap.

Authors:  Vishal Sharma; Saurabh Kedia; Vineet Ahuja
Journal:  JGH Open       Date:  2022-10-17

Review 3.  Thiopurine monitoring in children with inflammatory bowel disease: a systematic review.

Authors:  Anastasia Konidari; Antonios Anagnostopoulos; Laura J Bonnett; Munir Pirmohamed; Wael El-Matary
Journal:  Br J Clin Pharmacol       Date:  2014-09       Impact factor: 4.335

4.  Utility of maternal 6-thioguanine nucleotide levels in predicting neonatal pancytopenia.

Authors:  Hidehiko Maruyama; Katsuhiko Tada; Takuzo Fujiwara; Kosuke Ota; Misao Kageyama
Journal:  AJP Rep       Date:  2012-12-03

5.  A Prospective Study Evaluating Metabolic Capacity of Thiopurine and Associated Adverse Reactions in Japanese Patients with Inflammatory Bowel Disease (IBD).

Authors:  Shunichi Odahara; Kan Uchiyama; Takahiro Kubota; Zensho Ito; Shinichiro Takami; Hiroko Kobayashi; Keisuke Saito; Shigeo Koido; Toshifumi Ohkusa
Journal:  PLoS One       Date:  2015-09-11       Impact factor: 3.240

6.  The Impact of Azathioprine-Associated Lymphopenia on the Onset of Opportunistic Infections in Patients with Inflammatory Bowel Disease.

Authors:  Marius Vögelin; Luc Biedermann; Pascal Frei; Stephan R Vavricka; Sylvie Scharl; Jonas Zeitz; Michael C Sulz; Michael Fried; Gerhard Rogler; Michael Scharl
Journal:  PLoS One       Date:  2016-05-23       Impact factor: 3.240

7.  Genetic Polymorphism of Thiopurine S-methyltransferase in Children with Acute Lymphoblastic Leukemia in Jordan

Authors:  Mervat Alsous; Al-Motassem Yousef; Mariam Abdel Jalil; Mohammed Zawiah; Shorouq Yacoub; Deema Momani; Alia Gharabli; Suha Omar; Rawad Rihani
Journal:  Asian Pac J Cancer Prev       Date:  2018-01-27

8.  NUDT15 R139C Variants Increase the Risk of Azathioprine-Induced Leukopenia in Chinese Autoimmune Patients.

Authors:  Xiang Fei; Qing Shu; Huaijun Zhu; Bingzhu Hua; Shiying Wang; Ling Guo; Yun Fang; Weihong Ge
Journal:  Front Pharmacol       Date:  2018-05-07       Impact factor: 5.810

  8 in total

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