Literature DB >> 8160249

Kinetics of mercaptopurine and thioguanine nucleotides in renal transplant recipients during azathioprine treatment.

S Bergan1, H E Rugstad, O Bentdal, L Endresen, O Stokke.   

Abstract

The purpose of this study was to examine the pharmacokinetics of mercaptopurine (6-MP) and thioguanine nucleotides (6-TGN) during azathioprine treatment. Plasma profiles and urinary excretion of 6-MP and 6-TGN concentrations in red blood cells (RBCs) were measured repeatedly during the first 3 weeks following transplantation in 10 adults, who had received kidney grafts from living related donors. Mean maximal 6-MP plasma concentration (Cmax) was 340 nmol/L (SD = 290), mean time to Cmax (Tmax) was 2 h (SD = 1.8), and mean area under the plasma concentration-time curve (AUC) was 930 nmol/L/h (SD = 770). The mean fraction of azathioprine dose excreted as 6-MP in urine was 1.32% (SD = 1.11). Up to eightfold variability of Cmax and AUC was observed from day to day within each patient. The correlation between 6-MP AUC and amount excreted in the urine was weak (r = 0.37, 95% CI from 0.02 to 0.64). In this group of patients the observed 6-TGN levels in RBCs were low; maxima during the observation period ranged from undetectable to 250 pmol/8 x 10(8) RBCs. In individual patients, 6-TGN levels were relatively stable throughout the dosing interval ("within-dose-interval-CV" < 19%), even when sharp and high 6-MP peaks in plasma were observed.

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Year:  1994        PMID: 8160249     DOI: 10.1097/00007691-199402000-00002

Source DB:  PubMed          Journal:  Ther Drug Monit        ISSN: 0163-4356            Impact factor:   3.681


  4 in total

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Authors:  T N Witte; A L Ginsberg
Journal:  Can J Gastroenterol       Date:  2008-02       Impact factor: 3.522

2.  Therapeutic drug monitoring in patients with inflammatory bowel disease and established azathioprine therapy.

Authors:  L P L Gilissen; L J J Derijks; L P Bos; P J Bus; P M Hooymans; L G J B Engels
Journal:  Clin Drug Investig       Date:  2004       Impact factor: 2.859

3.  Model-based contextualization of in vitro toxicity data quantitatively predicts in vivo drug response in patients.

Authors:  Christoph Thiel; Henrik Cordes; Isabel Conde; José Vicente Castell; Lars Mathias Blank; Lars Kuepfer
Journal:  Arch Toxicol       Date:  2016-05-09       Impact factor: 5.153

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

  4 in total

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