Wojtczak Anna, Wojtczak Maciej, Skrętkowicz Jadwiga
Department of Pharmacogenetics, Medical University of Lodz, Łódź, Poland.
Institute of Chemical Technology of Food, Lodz University of Technology, Łódź, Poland.
Pharmacol Rep. 2014 Jun;66(3):511-4. doi: 10.1016/j.pharep.2013.12.010. Epub 2014 Apr 3.
Metoprolol is the one of the most commonly used β-blockers in the treatment of ischemic heart disease and it is extensively metabolized in the liver undergoing oxidation by CYP2D6 isoenzyme of cytochrome P450. Gene encoding the CYP2D6 enzyme is characterized by genetic polymorphism. The CYP2D6 oxidation polymorphism has a major impact on the effectiveness and safety of the treatment. The aim of the study was to evaluate the relationship between plasma concentration of metoprolol and the CYP2D6 genotype in patients with ischemic heart disease.
Fifty patients were interviewed and subsequently enrolled into the study. The patients received metoprolol twice daily at a dose of 50mg. The blood samples were analyzed for two major defective alleles for CYP2D6 - CYP2D64 and CYP2D63--by the polymerase chain reaction-restriction fragment length polymorphism (PCR-RFLP) method. Metoprolol concentration in plasma was determined by using the new and unique high-performance liquid chromatography (HPLC) method in the author's own modification with Corona CAD detector (Charged Aerosol Detection).
In the test group, genotypes conditioning poor oxidation (PM) occurred in 3 patients (6%), while 47 patients (94%) had genotypes coding for extensive metabolism (EM). Patients with PM genotypes had significantly higher plasma concentrations of metoprolol than the patients with EM genotype (mean 92.25 ± SD 36.78 ng/ml vs. mean 168.22 ± SD 5.61 ng/ml, respectively). Established relationships were statistically significant (NIR test, p=0.0009).
This study demonstrated that the CYP2D6 genotype remains a major determinant of the metoprolol plasma concentrations. The pharmacogenetic effect is likely to have consequences on both, the clinical benefit of metoprolol treatment and adverse drug reactions. The use of Corona CAD detector seems to be a very good alternative method for the determination of metoprolol concentration in plasma.
美托洛尔是治疗缺血性心脏病最常用的β受体阻滞剂之一,它在肝脏中通过细胞色素P450的CYP2D6同工酶进行氧化而广泛代谢。编码CYP2D6酶的基因具有遗传多态性。CYP2D6氧化多态性对治疗的有效性和安全性有重大影响。本研究的目的是评估缺血性心脏病患者美托洛尔血浆浓度与CYP2D6基因型之间的关系。
对50名患者进行访谈并随后纳入研究。患者每天两次接受50mg剂量的美托洛尔治疗。通过聚合酶链反应-限制性片段长度多态性(PCR-RFLP)方法分析血样中CYP2D6的两个主要缺陷等位基因——CYP2D64和CYP2D63。采用作者自行改良的配备电晕CAD检测器(带电气溶胶检测)的新型独特高效液相色谱(HPLC)法测定血浆中美托洛尔的浓度。
在试验组中,3名患者(6%)出现了导致氧化不良的基因型(PM),而47名患者(94%)具有编码广泛代谢(EM)的基因型。PM基因型患者的美托洛尔血浆浓度显著高于EM基因型患者(分别为平均92.25±标准差36.78ng/ml和平均168.22±标准差5.61ng/ml)。所建立的关系具有统计学意义(NIR检验,p = 0.0009)。
本研究表明,CYP2D6基因型仍然是美托洛尔血浆浓度的主要决定因素。药物遗传学效应可能对美托洛尔治疗的临床益处和药物不良反应都产生影响。使用电晕CAD检测器似乎是测定血浆中美托洛尔浓度的一种非常好的替代方法。