Azathioprine Metabolites in Erythrocytes and DNA for Therapy Monitoring in Very Early Onset Inflammatory Bowel

Giulia Zudeh1, Martina Franzin1, Marianna Lucafò2

  • 1Department of Translational and Advanced Diagnostics, Institute for Maternal and Child Health I.R.C.C.S. Burlo Garofolo, Trieste 34137, Italy.

Insights

Very early onset inflammatory bowel disease (VEO-IBD) patients exhibit enhanced azathioprine metabolism, requiring higher doses. Thioguanine nucleotides (TGN) and deoxythioguanosine (DNA-TG) levels serve as reliable biomarkers for azathioprine metabolism in these young patients.

Area of Science:

  • Pharmacogenomics
  • Gastroenterology
  • Pediatric Medicine

Background:

  • Azathioprine is a key therapy for inflammatory bowel disease (IBD).
  • Very early onset IBD (VEO-IBD) patients (<6 years) present unique metabolic profiles, including higher thiopurine-methyltransferase (TPMT) activity.
  • Genetic polymorphisms in TPMT and PACSIN2 influence azathioprine efficacy.

Purpose of the Study:

  • To investigate the impact of age on azathioprine active metabolites and disease activity in IBD.
  • To evaluate the combined effects of age, TPMT, and PACSIN2 polymorphisms on azathioprine metabolism and disease outcomes.

Main Methods:

  • Quantification of erythrocyte thioguanine nucleotides (TGN) using HPLC.
  • Measurement of leukocyte-incorporated deoxythioguanosine (DNA-TG) via LC-MS/MS.
  • Analysis of VEO-IBD patients, IBD children, and IBD adolescents, assessing azathioprine dosage, metabolite levels, and disease scores.

Main Results:

  • VEO-IBD patients required higher azathioprine doses and exhibited lower DNA-TG/dose and TGN/dose ratios, indicating enhanced metabolism.
  • DNA-TG levels positively correlated with TGN and disease activity scores.
  • TPMT rs1142345 polymorphism was linked to increased DNA-TG and TGN concentrations.
  • PACSIN2 rs2413739 polymorphism correlated with disease scores.

Conclusions:

  • VEO-IBD patients demonstrate accelerated azathioprine metabolism, necessitating dose adjustments.
  • TGN and DNA-TG are validated biomarkers reflecting azathioprine metabolism and disease activity in VEO-IBD.
  • Genetic factors (TPMT, PACSIN2) and age significantly influence azathioprine pharmacokinetics and therapeutic response in IBD.

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