Pharmacy Department, Beijing Anzhen Hospital, Capital Medical University, Beijing, China.
PLoS One. 2020 Mar 16;15(3):e0230445. doi: 10.1371/journal.pone.0230445. eCollection 2020.
Single-nucleotide polymorphisms (SNPs) is associated with efficacy of specific drugs. Although there are several methods for SNP genotyping in clinical settings, alternative methods with lower cost, higher throughout and less complexity are still needed. In this study, we modified Kompetitive Allele Specific PCR to enable multiplex SNP genotyping by introducing additional fluorescent cassettes that specifically help to differentiate more amplification signals in a single reaction. This new format of assay achieved a limit of detection down to 310 copies/ reactions for simultaneous detection of 2 SNPs with only standard end-point PCR workflow for synthetic controls, and genotyped 117 clinical samples with results that were in 100% agreement with hospital reports. This study presented a simplified, cost-effective high-throughput SNP genotyping alternative for pharmacogenetic variants, and enabled easier access to pharmaceutical guidance when needed.
单核苷酸多态性 (SNP) 与特定药物的疗效相关。虽然在临床环境中有几种 SNP 基因分型方法,但仍需要成本更低、通量更高、复杂性更低的替代方法。在这项研究中,我们通过引入额外的荧光盒对 Kompetitive Allele Specific PCR 进行了修改,从而能够通过单一反应来区分更多的扩增信号,从而实现多重 SNP 基因分型。这种新的检测方法仅使用标准终点 PCR 工作流程即可对合成对照进行检测,其检测下限达到了 310 个拷贝/反应,可同时检测 2 个 SNP,并对 117 个临床样本进行了基因分型,结果与医院报告完全一致。本研究提出了一种简化、经济高效的高通量 SNP 基因分型替代方法,可在需要时更容易获得药物指导。