Wang Ziran, Yi Jie, Yu Qi, Liu Yiwei, Zhang Rui, Zhang Dong, Yang Wenhang, Xu Yingchun, Chen Yu
Department of Clinical Laboratory, Peking Union Medical College Hospital, Chinese Academy of Medical Sciences, Beijing, China.
Pract Lab Med. 2023 Aug 14;36:e00330. doi: 10.1016/j.plabm.2023.e00330. eCollection 2023 Aug.
The real-time PCR system is one of the most powerful research tools available in the life sciences field. The aim of this study was to preliminarily evaluate the analytical performance of QuantStudio 1 Plus real-time PCR system (QS 1 plus) for clinical procedures.
The consistency of QS 1 plus with the reference system in terms of various clinical procedures was evaluated. For qualitative data, the Kappa test was used to analyze the agreement of the results. For the quantitative data, Passing-Bablok regression analysis and Bland-Altman plot analysis were used to assess the concordance between QS 1 plus and the reference instrument.
Passing-Bablok regression showed an excellent agreement between the QS 1 plus and LC 480 systems for HBV DNA quantification (y = 0.928 + 0.970x), whereas Bland-Altman plot analysis showed very small mean deviations between the two systems. The QS 1 plus yielded perfectly consistent results with the reference instrument for methylenetetrahydrofolate reductase (MTHFR) C677T melting curve genotyping analysis, MTHFR C677T genotyping analysis, Norovirus RNA negative/positive analysis, influenza B virus (Flu B) RNA negative/positive analysis, (MTB) DNA negative/positive analysis, Human Papillomavirus (HPV) genotyping analysis, epidermal growth factor receptor (EGFR) gene mutation analysis. Both the relative quantitative analysis and the relative quantitative analysis (standard curve) confirmed the satisfactory concordance between the QS 1 plus instrument and the ABI 7500 instrument by Passing-Bablok regression analysis (y = 0.180 + 0.817x and y = 0.012 + 1.000x, respectively) and Bland-Altman plot analysis.
Our research has proven that QS 1 plus is adaptable to most test procedures in the clinical laboratory. This may provide the basis for its further application.
实时荧光定量聚合酶链反应(PCR)系统是生命科学领域中最强大的研究工具之一。本研究旨在初步评估QuantStudio 1 Plus实时荧光定量PCR系统(QS 1 plus)在临床检测中的分析性能。
评估QS 1 plus在各种临床检测中与参考系统的一致性。对于定性数据,采用Kappa检验分析结果的一致性。对于定量数据,采用Passing-Bablok回归分析和Bland-Altman图分析评估QS 1 plus与参考仪器之间的一致性。
Passing-Bablok回归分析显示,QS 1 plus与LC 480系统在乙肝病毒(HBV)DNA定量检测方面具有良好的一致性(y = 0.928 + 0.970x),而Bland-Altman图分析显示两者之间的平均偏差非常小。在亚甲基四氢叶酸还原酶(MTHFR)C677T熔解曲线基因分型分析、MTHFR C677T基因分型分析、诺如病毒RNA阴性/阳性分析、乙型流感病毒(Flu B)RNA阴性/阳性分析、结核分枝杆菌(MTB)DNA阴性/阳性分析、人乳头瘤病毒(HPV)基因分型分析、表皮生长因子受体(EGFR)基因突变分析中,QS 1 plus与参考仪器的结果完全一致。通过Passing-Bablok回归分析(分别为y = 0.180 + 0.817x和y = 0.012 + 1.000x)和Bland-Altman图分析,相对定量分析和相对定量分析(标准曲线)均证实QS 1 plus仪器与ABI 7500仪器之间具有令人满意的一致性。
我们的研究证明,QS 1 plus适用于临床实验室的大多数检测程序。这可能为其进一步应用提供依据。