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<p>Personalized thiopurine therapy is among the most established examples of pharmacogenomics translated into clinical practice. Variants in <i>TPMT</i> (rs1800462, rs1800460, rs1142345) and <i>NUDT15</i> (rs116855232) are recognized clinical predictors of thiopurine efficacy and toxicity. Additional variants in genes such as <i>PACSIN2</i> (rs2413739), <i>ITPA</i> (rs1127354) and <i>MTHFR</i> (rs1801133 and rs1801131), also contribute to variability in drug response. Here we characterize the frequency of the pharmacogenetic variants involved in thiopurine metabolism in a healthy population of Kosovo. We genotyped 299 healthy blood donors for polymorphisms. Among <i>TPMT</i> variant alleles, <i>TPMT*3A</i> was observed at a frequency of 2.0%, and the <i>TPMT*3C</i> at 0.1%. Notably, the <i>MTHFR</i> 677T variant (rs1801133) was significantly more frequent in the Kosovo population (49.8%) compared with the global and European frequencies. The minor allele frequency of <i>MTHFR</i> rs1801131 was 27.4%. Minor allele frequencies for <i>PACSIN2</i> rs2413739 and <i>ITPA</i> rs1127354 variants were 48.8% and 4.0%, respectively. Sequencing of <i>NUDT15</i> revealed six variants, with rs116855232 present at frequency of 0.8%. These findings provide important insights into the pharmacogenomic profile of the Kosovo population and support the implementation of pre-emptive genotyping to improve the safety and efficacy of thiopurine therapy in the region.</p>

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Population frequencies of thiopurine-related pharmacogenes in healthy individuals from Kosovo

  • 期刊论文

  • 出版模式：

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  • 发表日期：

    2026年2月27日

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  • Flaka Pasha,
  • Dunja Urbančič,
  • Gordana Gosheva,
  • Bukurije Zhubi,
  • Safete Maliqi Qormemeti,
  • Shaip Krasniqi,
  • Irena Mlinarič-Raščan

摘要

Personalized thiopurine therapy is among the most established examples of pharmacogenomics translated into clinical practice. Variants in TPMT (rs1800462, rs1800460, rs1142345) and NUDT15 (rs116855232) are recognized clinical predictors of thiopurine efficacy and toxicity. Additional variants in genes such as PACSIN2 (rs2413739), ITPA (rs1127354) and MTHFR (rs1801133 and rs1801131), also contribute to variability in drug response. Here we characterize the frequency of the pharmacogenetic variants involved in thiopurine metabolism in a healthy population of Kosovo. We genotyped 299 healthy blood donors for polymorphisms. Among TPMT variant alleles, TPMT*3A was observed at a frequency of 2.0%, and the TPMT*3C at 0.1%. Notably, the MTHFR 677T variant (rs1801133) was significantly more frequent in the Kosovo population (49.8%) compared with the global and European frequencies. The minor allele frequency of MTHFR rs1801131 was 27.4%. Minor allele frequencies for PACSIN2 rs2413739 and ITPA rs1127354 variants were 48.8% and 4.0%, respectively. Sequencing of NUDT15 revealed six variants, with rs116855232 present at frequency of 0.8%. These findings provide important insights into the pharmacogenomic profile of the Kosovo population and support the implementation of pre-emptive genotyping to improve the safety and efficacy of thiopurine therapy in the region.