Faculty of Pharmacy, Université de Montréal, H3T 1J4, Montreal, Quebec, Canada.
Montreal Heart Institute, H1T 1C8, Montreal, Quebec, Canada.
Pharmacogenomics. 2023 Jun;24(8):441-448. doi: 10.2217/pgs-2023-0067. Epub 2023 Jun 12.
Few genome-wide association studies (GWASs) have been conducted to identify predictors of drug concentrations. The authors therefore sought to discover the pharmacogenomic markers involved in metoprolol pharmacokinetics. The authors performed a GWAS of a cross-sectional study of 993 patients from the Montreal Heart Institute Biobank taking metoprolol. A total of 391 and 444 SNPs reached the significance threshold of 5 × 10 for metoprolol and α-OH-metoprolol concentrations, respectively. All were located on chromosome 22 at or near the gene, encoding CYP450 2D6, metoprolol's main metabolizing enzyme. The results reinforce previous findings of the importance of the locus for metoprolol concentrations and confirm that large biobanks can be used to identify genetic determinants of drug pharmacokinetics at a GWAS significance level.
很少有全基因组关联研究(GWAS)来确定药物浓度的预测因子。因此,作者试图发现与美托洛尔药代动力学相关的药物基因组标记物。作者对来自蒙特利尔心脏研究所生物库的 993 名服用美托洛尔的患者进行了一项横断面研究的 GWAS。共有 391 个和 444 个 SNP 分别达到了美托洛尔和 α-OH-美托洛尔浓度的 5×10 显著性阈值。所有 SNP 均位于染色体 22 上,位于或靠近编码美托洛尔主要代谢酶 CYP450 2D6 的 基因附近。这些结果加强了先前关于 基因座对美托洛尔浓度重要性的发现,并证实大型生物库可用于在全基因组关联研究显著性水平上确定药物药代动力学的遗传决定因素。