Literature DB >> 30610277

Do clinical and laboratory parameters predict thiopurine metabolism and clinical outcome in patients with inflammatory bowel diseases?

Sven Frick1, Daniel Müller2, Gerd A Kullak-Ublick1, Alexander Jetter3.   

Abstract

PURPOSE: The thiopurines azathioprine and 6-mercaptopurine are frequently used for remission maintenance in patients with inflammatory bowel diseases. However, there are therapy failures, and it is unclear whether clinical and laboratory parameters can be used to predict thiopurine metabolite concentrations (as a surrogate for adequate remission maintenance therapy) and clinical outcome in these patients.
METHODS: In this retrospective analysis of clinical routine patient data, multivariate statistical models based on Linear Mixed Models regression and Generalized Estimating Equations logistic regression were developed. The adequacy of the models was assessed using Pearson's correlation and a receiver operating characteristic curve.
RESULTS: This study included 273 patients and 1158 thiopurine metabolite measurements as well as routine laboratory and clinical data. In the statistical models, thiopurine metabolite concentrations and the odds of non-remission based on different clinical and laboratory parameters were computed. Correlation (r2) between predicted and measured thiopurine metabolites were 0.40 (p < 0.001) for 6-thioguanine nucleotides and 0.53 (p < 0.001) for 6-methyl-mercaptopurine nucleotides, respectively. The model for remission classified data sets in remission and non-remission with a sensitivity of 63% and a specificity of 73%. The area under the receiver operating characteristic curve of the model was 0.72.
CONCLUSIONS: Although the models are not yet accurate enough to be used in clinical routine, model-based prediction of thiopurine metabolite concentrations and of outcome is feasible. Until more accurate models are developed and validated, traditional therapeutic drug monitoring of thiopurine metabolites in patients with inflammatory bowel diseases under thiopurine therapy stays the best tool to individualize therapy.

Entities:  

Keywords:  Azathioprine; Inflammatory bowel diseases; Linear and logistic regression models; Therapeutic drug monitoring; Thiopurines

Mesh:

Substances:

Year:  2019        PMID: 30610277     DOI: 10.1007/s00228-018-02616-7

Source DB:  PubMed          Journal:  Eur J Clin Pharmacol        ISSN: 0031-6970            Impact factor:   2.953


  30 in total

1.  6-MP metabolite profiles provide a biochemical explanation for 6-MP resistance in patients with inflammatory bowel disease.

Authors:  Marla C Dubinsky; Huiying Yang; Philip V Hassard; Ernest G Seidman; Lori Y Kam; Maria T Abreu; Stephan R Targan; Eric A Vasiliauskas
Journal:  Gastroenterology       Date:  2002-04       Impact factor: 22.682

2.  Pharmacogenomics and metabolite measurement for 6-mercaptopurine therapy in inflammatory bowel disease.

Authors:  M C Dubinsky; S Lamothe; H Y Yang; S R Targan; D Sinnett; Y Théorêt; E G Seidman
Journal:  Gastroenterology       Date:  2000-04       Impact factor: 22.682

3.  Therapeutic drug monitoring of thiopurine metabolites in adult thiopurine tolerant IBD patients on maintenance therapy.

Authors:  Lennard P L Gilissen; Dennis R Wong; Leopold G J B Engels; Jörgen Bierau; Jaap A Bakker; Aimée D C Paulussen; Mariëlle J Romberg-Camps; Arnold Stronkhorst; Paul Bus; Laurens P Bos; Piet M Hooymans; Reinhold W Stockbrügger; Cees Neef; Ad A M Masclee
Journal:  J Crohns Colitis       Date:  2012-01-10       Impact factor: 9.071

4.  Thiopurine methyltransferase (TPMT) activity and adverse effects of azathioprine in inflammatory bowel disease: long-term follow-up study of 394 patients.

Authors:  Javier P Gisbert; Pilar Niño; Luis Rodrigo; Carlos Cara; Luis G Guijarro
Journal:  Am J Gastroenterol       Date:  2006-10-06       Impact factor: 10.864

5.  6-Mercaptopurine metabolism in Crohn's disease: correlation with efficacy and toxicity.

Authors:  C Cuffari; Y Théorêt; S Latour; G Seidman
Journal:  Gut       Date:  1996-09       Impact factor: 23.059

6.  Relevance of thiopurine methyltransferase activity in inflammatory bowel disease patients maintained on low-dose azathioprine.

Authors:  S Campbell; K Kingstone; S Ghosh
Journal:  Aliment Pharmacol Ther       Date:  2002-03       Impact factor: 8.171

7.  Clinical significance of azathioprine active metabolite concentrations in inflammatory bowel disease.

Authors:  S Wright; D S Sanders; A J Lobo; L Lennard
Journal:  Gut       Date:  2004-08       Impact factor: 23.059

8.  Thiopurine methyltransferase activity influences clinical response to azathioprine in inflammatory bowel disease.

Authors:  Carmen Cuffari; Themistocles Dassopoulos; Lisa Turnbough; Richard E Thompson; Theodore M Bayless
Journal:  Clin Gastroenterol Hepatol       Date:  2004-05       Impact factor: 11.382

9.  Thiopurine methyltransferase activity and the use of azathioprine in inflammatory bowel disease.

Authors:  A Ansari; C Hassan; J Duley; A Marinaki; E-M Shobowale-Bakre; P Seed; J Meenan; A Yim; J Sanderson
Journal:  Aliment Pharmacol Ther       Date:  2002-10       Impact factor: 8.171

10.  Thiopurine methyltransferase activity combined with 6-thioguanine metabolite levels predicts clinical response to thiopurines in patients with inflammatory bowel disease.

Authors:  L Y Kwan; S M Devlin; J M Mirocha; K A Papadakis
Journal:  Dig Liver Dis       Date:  2008-03-04       Impact factor: 4.088

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