Comparison between MassARRAY and pyrosequencing for CYP2C19 and ABCB1 gene variants of clopidogrel efficiency genotyping.

Q3 Biochemistry, Genetics and Molecular Biology
Juan Liu, Zesheng Xu, Ya Li, Shipeng Dai, Junying Liu, Junjun Pan, Yang Jiang
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引用次数: 10

Abstract

Clopidogrel is one of the most frequently used drugs in patients to reduce cardiovascular events. Since patients with different genetic variations respond quite differently to clopidogrel therapy, the related genetic testing plays a vital role in its dosage and genetic testing related to clopidogrel therapy is currently considered as routine test worldwide. In this study, we aim to use two different methods MALDI-TOF mass spectrometry and pyrosequencing to detect gene variant of CYP2C19 and ABCB1. Six single nucleotides polymorphisms (SNP) within CYP2C19 (*2, *3, *4, *5, *17) and ABCB1 C3435T in 458 Chinese Han patients were determined using both MassARRAY and Pyrosequencing. Sanger sequencing was used for verification. Results of both methods were analyzed and compared. Allele frequencies of each SNP and distribution of different genotypes were calculated based on the MassARRAY and Sanger sequencing results. Both methods provided 100% call rates for gene variants, while results of six samples were different with two methods. With Sanger sequencing as the reference results, MassARRAY generated all the same results. The minor allele frequencies of the above six SNPs were 27.1% (CYP2C19*), 5.9% (CYP2C19*3), 0% (CYP2C19*4), 0% (CYP2C19*5), 1.1% (CYP2C19*17), 40.9% (ABCB1), respectively. MassARRAY provides accurate clopidogrel related genotyping with relatively high cost-efficiency, throughput and short time when compared with pyrosequencing.

氯吡格雷效率基因分型CYP2C19和ABCB1基因变异的MassARRAY和焦磷酸测序比较
氯吡格雷是患者减少心血管事件最常用的药物之一。由于不同基因变异的患者对氯吡格雷治疗的反应大不相同,相关基因检测在其剂量中起着至关重要的作用,氯吡格雷治疗相关基因检测目前在世界范围内被认为是常规检测。在本研究中,我们旨在采用MALDI-TOF质谱法和焦磷酸测序两种不同的方法检测CYP2C19和ABCB1基因变异。采用MassARRAY和Pyrosequencing检测了458例中国汉族患者CYP2C19(*2、*3、*4、*5、*17)和ABCB1 C3435T基因的6个单核苷酸多态性(SNP)。采用Sanger测序进行验证。对两种方法的结果进行分析比较。根据MassARRAY和Sanger测序结果计算每个SNP的等位基因频率和不同基因型的分布。两种方法对基因变异的检出率均为100%,但两种方法对6个样本的检出率存在差异。以Sanger测序作为参考结果,MassARRAY生成所有相同的结果。上述6个snp的次要等位基因频率分别为27.1% (CYP2C19*)、5.9% (CYP2C19*3)、0% (CYP2C19*4)、0% (CYP2C19*5)、1.1% (CYP2C19*17)、40.9% (ABCB1)。与焦磷酸测序相比,MassARRAY提供准确的氯吡格雷相关基因分型,具有较高的成本效率、通量和较短的时间。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Molecular Membrane Biology
Molecular Membrane Biology 生物-生化与分子生物学
CiteScore
4.80
自引率
0.00%
发文量
0
审稿时长
>12 weeks
期刊介绍: Cessation. Molecular Membrane Biology provides a forum for high quality research that serves to advance knowledge in molecular aspects of biological membrane structure and function. The journal welcomes submissions of original research papers and reviews in the following areas: • Membrane receptors and signalling • Membrane transporters, pores and channels • Synthesis and structure of membrane proteins • Membrane translocation and targeting • Lipid organisation and asymmetry • Model membranes • Membrane trafficking • Cytoskeletal and extracellular membrane interactions • Cell adhesion and intercellular interactions • Molecular dynamics and molecular modelling of membranes. • Antimicrobial peptides.
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