Suppr超能文献

MassARRAY与焦磷酸测序法在氯吡格雷疗效基因分型的CYP2C19和ABCB1基因变异检测中的比较。

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

作者信息

Liu Juan, Xu Zesheng, Li Ya, Dai Shipeng, Liu Junying, Pan Junjun, Jiang Yang

机构信息

a Department of Cardiology , Hebei Cangzhou Central Hospital , Cangzhou , China.

出版信息

Mol Membr Biol. 2019 Dec;35(1):1-8. doi: 10.1080/09687688.2019.1597194.

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% (CYP2C193), 0% (CYP2C194), 0% (CYP2C195), 1.1% (CYP2C1917), 40.9% (ABCB1), respectively. MassARRAY provides accurate clopidogrel related genotyping with relatively high cost-efficiency, throughput and short time when compared with pyrosequencing.

摘要

氯吡格雷是患者中最常用的药物之一,用于降低心血管事件的发生风险。由于具有不同基因变异的患者对氯吡格雷治疗的反应差异很大,因此相关基因检测在其剂量确定中起着至关重要的作用,并且与氯吡格雷治疗相关的基因检测目前在全球范围内被视为常规检测。在本研究中,我们旨在使用两种不同的方法,即基质辅助激光解吸电离飞行时间质谱(MALDI-TOF质谱)和焦磷酸测序,来检测CYP2C19和ABCB1的基因变异。使用MassARRAY和焦磷酸测序技术对458名中国汉族患者的CYP2C19(2、3、4、5、17)内的六个单核苷酸多态性(SNP)和ABCB1 C3435T进行了测定。采用桑格测序法进行验证。对两种方法的结果进行了分析和比较。根据MassARRAY和桑格测序结果计算每个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%,但有六个样本的两种方法结果不同。以桑格测序结果为参考,MassARRAY得出的所有结果均相同。上述六个SNP的次要等位基因频率分别为27.1%(CYP2C19)、5.9%(CYP2C193)、0%(CYP2C194)、0%(CYP2C195)、1.1%(CYP2C1917)、40.9%(ABCB1)。与焦磷酸测序相比,MassARRAY提供了准确的氯吡格雷相关基因分型,具有相对较高的成本效益、通量和较短的时间。

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验