Literature DB >> 26510636

Thiopurine metabolite testing in inflammatory bowel disease.

Rimma Goldberg1,2, Gregory Moore1,3, Georgina Cunningham2, Julien Schulberg2, Philip Marsh1, Steven Brown2, William Connell2, Mark Lust2, Michael A Kamm2,4,5, Sally Bell2.   

Abstract

BACKGROUND: Thiopurine use in inflammatory bowel disease (IBD) is limited by drug toxicity and lack of therapeutic efficacy. We assessed the utility of thiopurine metabolite testing and the relationship between disease activity, dose, and metabolite levels in a real world setting.
METHODS: Patients identified from pathology databases (2007-2012) at two tertiary IBD centers were included if they had thiopurines for at least four weeks. Demographics, dose, test indication, clinical status, action taken, and outcome were obtained by retrospective medical record review.
RESULTS: A total of 169 patients were included. 6-Thioguanine (TGN) levels were sub-therapeutic in 52%, therapeutic in 34%, and supratherapeutic in 14%. Test indication was active disease (79%), adverse effect (11%), or adherence assessment (7%). TGN trended lower in the active disease group compared to those with adverse effects (273 (+/- 23.2) versus 447 (+/- 117.7) pmol/8 × 10(8) RBC, P = 0.05). Weight-based dosing did not improve rates of therapeutic TGN levels (under-dosed 31.5% vs standard dose 35.4%), but was significantly associated with shunting toward 6-MMP (23.1% vs 6.8%, P = 0.008, OR = 4.1). Testing resulted in a change in patient treatment in 86% of patients with active disease and subtherapeutic levels and in 68% of tested patients overall.
CONCLUSIONS: Metabolite testing resulted in a change in management in most patients not responding to thiopurines or experiencing adverse events. Weight-based dosing did not increase rates of therapeutic levels but was associated with increased 6MMP shunting.
© 2015 Journal of Gastroenterology and Hepatology Foundation and Wiley & Sons Australia, Ltd.

Entities:  

Keywords:  IBD; metabolite testing; thiopurines

Mesh:

Substances:

Year:  2016        PMID: 26510636     DOI: 10.1111/jgh.13210

Source DB:  PubMed          Journal:  J Gastroenterol Hepatol        ISSN: 0815-9319            Impact factor:   4.029


  6 in total

1.  The glutathione transferase Mu null genotype leads to lower 6-MMPR levels in patients treated with azathioprine but not with mercaptopurine.

Authors:  M M T J Broekman; D R Wong; G J A Wanten; H M Roelofs; C J van Marrewijk; O H Klungel; A L M Verbeek; P M Hooymans; H-J Guchelaar; H Scheffer; L J J Derijks; M J H Coenen; D J de Jong
Journal:  Pharmacogenomics J       Date:  2017-01-03       Impact factor: 3.550

2.  Clinical utility of thiopurine metabolite monitoring in inflammatory bowel disease and its impact on healthcare utilization in Singapore.

Authors:  Jia Qi Yeo; Hua Heng McVin Cheen; Amanda Wong; Teong Guan Lim; Balram Chowbay; Wai Fook Leong; Chunyan Wang; Ennaliza Salazar; Webber Pak Wo Chan; San Choon Kong; Wan Chee Ong
Journal:  JGH Open       Date:  2022-08-01

3.  Allopurinol in combination with thiopurine induces mucosal healing and improves clinical and metabolic outcomes in IBD.

Authors:  Brigitte Moreau; Pierre Clement; Yves Theoret; Ernest G Seidman
Journal:  Therap Adv Gastroenterol       Date:  2017-10-11       Impact factor: 4.409

4.  Weight and Body Composition Compartments do Not Predict Therapeutic Thiopurine Metabolite Levels in Inflammatory Bowel Disease.

Authors:  Darcy Q Holt; Boyd Jg Strauss; Gregory T Moore
Journal:  Clin Transl Gastroenterol       Date:  2016-10-27       Impact factor: 4.488

Review 5.  Can We Predict the Toxicity and Response to Thiopurines in Inflammatory Bowel Diseases?

Authors:  Raphael P Luber; Sailish Honap; Georgina Cunningham; Peter M Irving
Journal:  Front Med (Lausanne)       Date:  2019-11-28

6.  Thiopurine metabolite level and toxicity in Indians with inflammatory bowel disease.

Authors:  Suruchi P Parkar; Alpa J Dherai; Devendra C Desai; Tester F Ashavaid
Journal:  JGH Open       Date:  2017-09-18
  6 in total

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