Željka Celinšćak, Institute for Anthropological Research, Gajeva ulica 32, 10000 Zagreb, Croatia,
Croat Med J. 2022 Apr 30;63(2):117-125. doi: 10.3325/cmj.2022.63.117.
To compare the Croatian and European population in terms of allele frequencies of clinically relevant polymorphisms in drug absorption, distribution, metabolism, and excretion (ADME) genes.
In 429 Croatian participants, we genotyped 27 loci in 20 ADME genes. The obtained frequencies were merged with the published frequencies for the Croatian population by sample size weighting. The study sample obtained in this way was compared with the average data for the European population from the gnomAD database.
Variant allele frequencies in the Croatian population were higher in three and lower in two polymorphisms (Benjamini-Hochberg-corrected P values: 0.0027 for CYP2B64 rs2279343, CYP2C92 rs1799853, and VKORC1 rs9923231; 0.0297 for GSTP1 rs1695; 0.0455 for CYP2A6 rs1801272) compared with the European population. The most marked difference was observed for CYP2B64 (9.3% in Europe vs 24.3% in Croatia). The most clinically relevant findings were higher variant allele frequencies in two polymorphisms related to lower warfarin requirements: VKORC12 (34.9% in Europe vs 40.1% in Croatia) and CYP2C9*2 (12.3% in Europe vs 14.7% in Croatia). This indicates that three-quarters of Croatian people have at least one variant allele at these loci. Variants in genes GSTP1 and CYP2A6 were significantly less frequently observed in Croatia.
Croatian population has a higher bleeding and over-anticoagulation risk, which is why we recommend the prescription of lower doses of anticoagulation drugs such as warfarin and acenocoumarol. Lower phenytoin, and higher bupropion and efavirenz doses are also recommended in the Croatian population.
比较克罗地亚和欧洲人群在药物吸收、分布、代谢和排泄(ADME)相关基因中临床相关多态性的等位基因频率。
在 429 名克罗地亚参与者中,我们对 20 个 ADME 基因中的 27 个基因座进行了基因分型。通过样本量加权,将获得的频率与克罗地亚人群中已发表的频率合并。通过这种方式获得的研究样本与 gnomAD 数据库中欧洲人群的平均数据进行了比较。
与欧洲人群相比,克罗地亚人群中三种多态性的变异等位基因频率较高,两种多态性的变异等位基因频率较低(经 Benjamini-Hochberg 校正的 P 值:CYP2B64 rs2279343、CYP2C92 rs1799853 和 VKORC1 rs9923231 为 0.0027;GSTP1 rs1695 为 0.0297;CYP2A6 rs1801272 为 0.0455)。CYP2B64 的差异最为显著(欧洲为 9.3%,克罗地亚为 24.3%)。与华法林需求降低相关的两种多态性的变异等位基因频率较高,这是最具临床意义的发现:VKORC12(欧洲为 34.9%,克罗地亚为 40.1%)和 CYP2C9*2(欧洲为 12.3%,克罗地亚为 14.7%)。这表明,这些基因座中四分之三的克罗地亚人至少有一种变异等位基因。基因 GSTP1 和 CYP2A6 的变体在克罗地亚人群中明显较少见。
克罗地亚人群出血和过度抗凝的风险更高,因此我们建议处方抗凝药物(如华法林和醋硝香豆素)的剂量较低。在克罗地亚人群中,还建议使用较低剂量的苯妥英,较高剂量的苯并呋喃、丁丙诺啡和依非韦伦。