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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.
Abstract:
Azathioprine is used for inflammatory bowel disease (IBD) therapy. Patients under 6 years of age (very early onset, VEO-IBD) showed distinctive clinical characteristics, such as increased activity of thiopurine-methyltransferase (TPMT), a crucial enzyme for thiopurine metabolism. TPMT and PACSIN2 polymorphisms were associated with azathioprine efficacy. This study investigated the role of age in thiopurine active metabolites and disease activity. Also, the effects of age, TPMT and PACSIN2 polymorphisms on azathioprine metabolites and disease activity were evaluated. Erythrocytes thioguanine nucleotides (TGN) were measured by HPLC, and leukocytes incorporated deoxythioguanosine (DNA-TG) byLC-MS/MS in 12 VEO-IBD patients (median age 4.13 ± 0.98, 7 females, 6 Crohn's disease (CD)), 11 IBD children (median age 9.36 ± 1.52, 8 females, 1 CD ), and 73 IBD adolescents (median age 14.92 ± 1.81, 33 females, 37 CD). VEO-IBD subjects required a higher azathioprine dose (p-value = 0.048) and showed a lower DNA-TG/azathioprine dose ratio (p-value = 0.049) and TGN/azathioprine dose ratio (p-value = 0.013). DNA-TG was positively correlated with TGN (p-value = 4.15 × 10-5) and disease score (p-value = 1.54 × 10-4). TPMT rs1142345 (76 wild type, 10 heterozygous) was associated with increased concentrations of DNA-TG and TGN (p-value = 0.024 and 0.00038, respectively), whereas PACSIN2 rs2413739 (37 wild types, 34 heterozygous, 16 homozygous variants) was associated with the disease score (p-value = 0.04). Together, these data confirmed that VEO-IBD patients show enhanced azathioprine metabolism, which can be accurately reflected by both TGN and DNA-TG levels, highlighting their ability to be good biomarkers of azathioprine metabolism.
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